I PUC Chem Chapterwise Q and Answers
I PUC Chem Chapterwise Q and Answers
1 mark questions
1. What is Chemistry?
Ans: It is a Branch of science deals with the study of composition,
properties and interaction of matter.
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13. Define Significant figure
Ans: Significant figures are meaningful digits which are known with
certainty.
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22. What is a stoichiometry?
Ans: The quantitative relationships between the various reactants and
products interms of moles, masses, molecules and volumes is called
stoichiometry.
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30. Define mole
Ans: Mole can be defined as the amount of a substance that contains as
many particles or entities as there are atoms in exactly 12 gms of carbon
– 12 isotope.
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5. Define atom with an example.
Ans: Atom is the smallest particle of an element which may or may not
be capable of independent existence.
Ex: Atoms of iron, copper, hydrogen
9. Give the units of S.I. systems for the following a) Electric current
b) Amount of substance
Ans: a) Electric current – Ampere (A)
b) Amount of substance – Mole (mol)
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12. Define significant figures
Ans: The total number of digits in a number including the last digit
whose value is uncertain is called the number of significant figures.
Ans: a) 6.005 = Four because the zeroes between the non zero digits
are significant figures
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18. State Gay Lussac’s law of Gaseous volumes
Ans: It can be defined as when gases combine or are produced in a
chemical reaction they do so in a simple ratio by volume provided all
gases are at same temperature and pressure.
22. A piece of copper wire is 2.00 inch long. What is its length in centimeter
Ans: 1 inch = 2.54 cm
Therefore 2 inch = 2.54 x 2 = 5.08 Cms
1
23. A plastic Jug contains 3.5 Ltrs of milk calculate the volume of milk in
meter 3
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1 minute = 60 seconds
3 day = 3 x 24 Hrs x 60 min x 60 sec
= 259 200 seconds
25. Calculate the molecular mass of the following a) Ethane (C2H6)
b) Ammonia (NH3)
Ans: a) Ethane (C2H6)
Ethane = C2H6 2 x atomic mass of carbon + 6 x atomic mass of
Hydrogen
= 2 x (12.011u) + 6 x (1.008 U)
= 24.022u + 6.048u
= 30.070u
b) Ammonia (NH3)
Ammonia=(NH3) = 1x atomic mass of Nitrogen + 3 x atomic mass of Hydrogen
= 1x(14.01u) + 3 (1.008u)
= 14.01u + 3.024u = 17.034u
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Percent composition of Hydrogen = Mass of Hydrogen x 100
Molecular mass of CH3OH
= 4.032 x 100 = 12.5%
32.042
30. How many moles of methane required to produce 88 gms of CO2 after
combustion
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= 25 Kg N2 + 5 Kg H2 NH3
1 Kg of N2 = 1000gm N2
25 Kg of N2 = 25 x 1000 = 25000/28 = 892.85 mol
1 Kg of H2 = 1000 gm H2
5 Kg of H2 = 5x 1000 = 5000/2.016 = 2480.15 mol
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34. The density of 2M solution of sodium chloride (NaCl) 1.13 g mol/litre.
Calculate molality of the solution. M= 2 mol per litre.
4 Marks questions
11
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Ans:
Element % At mass % at mass Nearest
whole no
Carbon 57.14 12 57.14/12 4.76 4.76/0.68=7
Hydrogen 6.16 1 6.16/1 6.16 6.16/0.68=9.06
Nitrogen 9.52 14 9.52/14 0.68 0.68/0.68=1
Oxygen 27.18 16 27.18/16 1.698 1.698/0.68=2.45
Ans:
Element Symbol % of At mass of Moles of the Simpler molar
element element element = % mass
Hydrogen H 4.07 1 4.07/1 = 4.07 4.04/2.018=2.01
Carbon C 24.27 12 24.27/12 2.022/2.018
= 2.022 =1.0019
Chlorine Cl 71.65 35.5 71.65/35.5 2.018/2.018 = 1
= 2.018
12
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Therefore Empirical formula = H2C Cl = CH2Cl
Empirical formula weight = 1x12 + 2x1 + 35.5x1
= 12+2+35.5 = 49.5
Step 2
To calculate the empirical formula mass
Empirical formula C2H3O2
Therefore Empirical formula mass 2x12+3x1+2x16 = 59
13
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Step 3
To calculate the molecular mass of the compound
The vapour density of the compound = 59
Molecular mass = Vapour density x 2
= 59 x 2 = 118
Step 4
To calculate the value of ‘n’
n= molecular mass = 118 =2
Empirical formula mass 59
Step 5
Molecular formula = Empirical formula x n
= C2H3O2 x 2
= C4H6O4
Therefore Molecular formula is C4H6O4
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CHAPTER 2: STRUCTURE OF ATOM
NUMBER OF TEACHING HOURS: 10 HOURS
1. Name the person who first proposed the atomic theory of matter on scientific
basis.
4. Under what conditions of pressure and voltage, the electrical discharge through the
gases can be observed?
7. Name the phosphorescent material coated inside the discharge tube behind the
anode.
8. Give the conditions under which cathode rays travel in straight line.
9. What is the name given to the particles which constitute the cathode rays?
10. Does the nature of cathode ray depend on the nature of gas in the discharge tube or
the electrode material?
11. Name the scientist who was able to determine e/m value of an electron.
15. Name the fundamental particle of an atom that has highest value for its e/m value.
16. Does the e/m value of canal rays depend on the nature of gas in the discharge
tube?
17. Name the gas to be filled in the discharge tube to obtain the smallest and the
lightest positive ion.
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18. Name the smallest and lightest positive ion obtained when hydrogen gas is
subjected to electrical discharge.
22. Name the electrically neutral particle obtained by bombarding beryllium with α-
particles.
26. Name the metal foil used in Rutherford’s α-particle scattering experiment.
38. Name the fundamental particle of an atom which determines the chemical
properties of an element.
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42. What is the SI unit of wave number?
43. What is the relation between energy (E) and frequency ( )الof an electromagnetic
radiation?
44. What is the name given to the smallest quantity of energy that can be emitted or
absorbed in the form of electromagnetic radiation?
55. Name the series of spectral line of hydrogen obtained in visible region.
56. Write the mathematical expression for the calculation of angular momentum of an
electron in a given stationary state.
57. Write an expression for the calculation of energy associated with an electron in a
given stationary state.
58. Write an expression to calculate the wave number of a spectral line in the
hydrogen spectrum.
59. What is the value of the radius of the first stationary state (Bohr orbit)?
61. Write the relationship between wave length ( λ), velocity (c) and frequency ( )الof
a radiation.
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63. What is Stark effect?
71. What is the significance of (a) principal quantum number(n); (b) azimuthal
quantum number (l); (c) magnetic quantum number (ml); (d) spin quantum number
(ms)?
73. What are the possible values of ‘l’ (azimuthal quantum number) for a given value
of ‘n’?
74. What are the possible values for ml (magnetic quantum number) for a given value
of ‘l’?
76. What is the total value of ml (magnetic quantum number) for a given value of ‘l’?
77. What is the value of ‘l’ for:- (a) s- sub shell; (b) p- sub shell; (c) d-sub shell; (d)
f-sub shell; (e) g-sub shell; (f) h- sub shell?
78. Write the possible values of magnetic quantum number (ml) for l= 2.
79. Name the quantum number that specifies the shape of an atomic orbital.
80. Name the quantum number that specifies the size of an atomic orbital.
81. Name the quantum number that designates the orientation of the atomic orbital.
83. Write the total number of nodes for a given value of ‘n’.
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85. What is the shape of: (a) s-orbital: (b) p- orbital; (c) d-orbital?
88. What is the maximum number of electrons that can be accommodated in: (a) s-
orbital: (b) p- orbitals; (c) d-orbitals; (d) f-orbitals?
89. How many number of orbital are possible for f-sub shell?
90. Using s, p, d, notations, write the orbitals having following quantum numbers: (a)
n=4, l=0; (b) n=5, l=1; (c) n=3, l= 2.
95. How many electrons in an atom may have the following quantum numbers: n=3,
l= 0?
97. Write the electronic configuration of the following elements: (a) Cr (Z=24) (b) Cu
(Z=29) (c) Ca (Z=20).
98. Write the electronic configuration of the following: (a) Na+ (b) Cl- (c) O-2.
100. How many unpaired electrons are present in the following: (a) Na (b) P (c) O?
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107. State Pauli’s exclusion principle.
110. Write the schematic diagram to remember sequences of filling atomic orbitals.
111. Name two series of hydrogen spectra which fall in infra red region.
117. Calculate the wave length of the radiation emitted with a frequency of 1,200kHz
(c =3.0x108m/s)
119. Calculate the energy of one mole of photon of radiation whose frequency is 4
X1012 Hz.
120. The threshold frequency ال0 for a metal is 6.0 X 1013 s-1. Calculate the kinetic
energy of an electron when the radiation of frequency = ال1.0 X 1014 s-1 hits the
metal.
121. What will be the wavelength of a ball of mass 0.2 kg moving with velocity of 10
ms-1?
122. Calculate the wave number of the spectral line of shortest wavelength appearing in
the Balmer series of hydrogen spectrum (Given RH = 1.09 X 107 m-1)
123. What are the results drawn from the Cathode ray discharge experiment?
125. What are the observations made out of Ruther ford’s α-ray scattering experiment?
126. What are the conclusions drawn regarding the structure of the atom on the basis of
observations in the α-ray scattering experiment?
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127. Describe Rutherford’s nuclear model of the atom.
129. What are the factors that cannot be explained by electromagnetic theory?
130. What are the observations made by Hertz after conducting the photo electric effect
experiment?
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Answers
Chapter 2: Structure of atom
1. John Dalton
2. Protons, Neutrons and electrons
3. ‘Like charges repel each other and unlike charges attract each other’.
4. At very low pressure and at very high voltage
5. By using vacuum pump
6. The particles moving in the discharge tube from cathode to anode.
7. Zinc sulphide
8. In the absence of electrical or magnetic field.
9. Electrons
10. No. Neither nature of the gas nor electrode material
11. J.J. Thomson.
12. -1.6x10-19C.
13. 9.1094x10-31Kg.
14. The particles carrying positive charge in a discharge tube.
15. Electron.
16. Yes.
17. Hydrogen.
18. Proton.
19. James Chad Wick.
20. 1.672x10-27 Kg.
21. 1.675x10-27 Kg.
22. Neutron.
23. J. J. Thomson.
24. Plum pudding or raisin pudding or watermelon.
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25. Mass of the atom is uniformly distributed over the atom.
26. Gold.
27. The circular path of an electron moving around the nucleus of an atom.
28. No. of Protons present in the nucleus or No. of electrons in a neutral atom.
29. Protons and neutrons present in the Nucleus of an atom.
30. Total No. of Protons and neutrons present in the nucleus of an atom.
31. Atoms of the same element having identical atomic Number but different mass
No.
32. Atoms of different elements having same mass No. but different atomic No.
33. Protium, deuterium and Tritium.
34. A= Mass No, Z= Atomic No.
35. 18.
36. 6.
37. 11.
38. Electron
39. Hertz2
40. 3.0x108 m/s.
41. Number of wave lengths per unit length is called wave number ()ال.
42. m-1 or per meter
43. E =hال
44. Proton.
45. 400 nm to 750 nm
46. 6.626x10-34 Js.
47. The ideal body which emits and absorbs radiations of all frequency.
48. The ejection of electrons from metal surface when radiation strikes it.
49. Potassium or Caesium or Rubidium.
50. The minimum frequency below which photoelectric effect is not observed.
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51. The spectrum of radiation emitted by a substance that has absorbed energy is
called an emission spectrum.
52. The study of emission or absorption spectra is known as spectroscopy.
53. Rubidium or Caesium, or Thallium or Indium, or Gallium or Scandium or
Helium.
54. 2.18x10-18 J.
55. Balmer series
56. me vr = n h
2π
57. En= -RH 1
n2
58. = الRH 1 - 1 cm-1
n12 n22
59. a0 = 52.9 Pm.
60. rn = n 2 a 0
61. C= الλ
62. The splitting of spectral lines in the presence of magnetic field.
63. The splitting of spectral lines in an electric field.
64. λ= h = h
mv p
65.
66. It rules out existence of definite paths of electrons.
67. It deals with dual behavior of matter.
68. Hψ = Eψ
69. It is the region around the nucleus where electron will most probably be found.
70. Quantum Numbers specify the energy, size, shape and orientation of an orbital.
71. a) It determines the size and energy of the orbital.
b) It determines the three dimensional shape of the orbital.
c) It gives the spatial orientation of the orbital.
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d) It refers to orientation of the spin of the electron.
72. n=1,2,3 - - - - - ∞.
73. l=0,1,2,3 - - - - (n-1).
74. m=-l, -(l-1), -(l-2)- - - - 0,1 - - - (l-2), (l-1),l
75. + 1 and - 1
2 2
76. (2l+1) values.
77. a) l=0, b) l=1, c) l=2, d) l=3, e) l=4, f) l=5
78. ml = -2, -1, 0, + 1, + 2.
79. Azimuthal Q.no(l)
80. Principal Q. no (n)
81. Magnetic Q.no (ml)
82. The region where probability density function reduces to zero.
83. Total no. of nodes = (n-1).
84. No. of nodes = 2
85. a) Spherical b) dumb bell c) double dumb – bell.
86. px , py and pz
87. dxy, dyz, dzx, dx2 -y2 and dz2
88. a) 2 b) 6 c) 10 d) 14
89. 7
90. a) 4s b) 5p c) 3d
91. Orbital’s having the same energy.
92. Atom having electrons occupying lowest energy level.
93. The state of an atom having its electron in higher energy level.
94. The net positive charge experienced by the outer electrons.
95. 2 electrons.
96. The distribution of electrons into orbitals of an atom.
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97. a) 1s2 2s2 2p6 3s2 3p63d5 4s1 b) 1s2 2s2 2p6 3s2 3p63d10 4s1
c) 1s2 2s2 2p6 3s2 3p6 4s2
98. a) 1s2 2s2 2p6 b) 1s2 2s2 2p6 3s23p6 c) 1s2 2s2 2p6
99. 3d
100. a) 1 b) 3 c) 2
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106. “ In the ground state of the atom orbitals are filled in the order of their increasing
energies”.
107. “ No two electrons in an atom can have the same set of four quantum
numbers”.
108. “ Pairing of electrons in the orbital’s belonging to the same sub shell does not
takes place until each orbital belonging to that sub shell has got one electron
each.”
109. “ It is the three dimensional region of space where the probability of finding
the electron is maximum.”
The different orbitals are s, p, d, and f
110.
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113. De Broglie Equation λ= h
Mv
Where m is the mass of the particle?
v is the velocity of the particle
114. = الRH 1 - 1 cm-1
n12 n22
ال- wave number
RH – Rydberg constant
115. a. This model fails to account for the stability of an atom.
b. This model does not explain the line spectrum of an atom.
Or
This model does not have any specific radius for radius electron orbit.
116. “ Lower the value of (n+l) for an orbital , the lower is its energy . If two
orbital’s have the same value of (n + l) , the orbital with lower value of n will
have the lower energy.”
117. λ =C
ال
λ 3 X 10 8 ms-1
1200 X 103 s-1
λ = 0.0025 X 105 m
λ = 250 m
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119. Energy of photon E = h ال
h = 6.626 X 10-34 JS
= ال4 X 10 12 Hz (s-1)
E = 6.626 X 10-34 Js X 4 X 1012 S-1
= 26.504 X 10– 22
= 2.65 X 10– 21 J
120. Kinetic Energy = h (ال – الo)
= (6.626 X 10 -34 Js) (1.0x1014 s-1– 6.0 X 1013 s-1 )
= (6.626 X 10-34 Js) (4.0 X 1013 s-1)
= 2.65 X 10-20J
121. λ =h
mν
= (6.626 X 10 -34 Js)/ (0.2 Kg X 10 ms-1)
= 3.313 X 10 -34 m
122.
= الRH (1/n12 – 1/n22 )
n1 = 2 n2 = ∞
= 1.09 X 107 (¼ - 0 )
123. .
i. The Cathode rays start form cathode and move towards anode.
iii. In the absence of electrical or Magnetic field, Cathode rays travel in straight
lines.
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iv. In the presence of electrical or magnetic field, the direction of deflection of
cathode rays shows that they contain negatively charged particles.
v. The characteristics of cathode rays do not depend on the material of electrodes
and nature of the gas present in the cathode ray tube.
(Any Four Points)
124.
i. Positively charged particles (Canal Rays) depend upon the nature of the gas
present in the cathode-ray tube.
ii. The charge to mass ratio of the particles depend on the gas from which they
originate.
iii. Some of the positively charged particles carry a multiple of the fundamental
unit of electrical charge.
125.
i. Most of the α–particles passed through the gold foil undeflected.
iii. A very few α-particles bounced back, that is were defected nearly 1800
126.
i. Most of the space in the atom is empty
ii. The Positive charge of the atom is not spread through out the atom, but
concentrated in a very small volume
iii. The volume occupied by the nucleus is negligibly small as compared to the
total volume of the atom
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127.
i. The positive charge and most of the mass of the atom is concentrated in a small
region called nucleus
iii. The Electrons move around the nucleus in circular paths called orbits.
iv. The Electrons and the nucleus are held together by Electrostatic force of
attraction
128.
i. Electrical and Magnetic waves are perpendicular to each other and both are
perpendicular to the direction of the propagation of the wave.
ii. Electromagnetic waves do not require medium and they can move in vacuum
iii. There are many types of electromagnetic radiations. They differ from one
another in wavelength or frequency
v. radiation.
129.
i. The nature of emission of radiation from hot bodies (black body radiation)
ii. Ejection of electrons from metal surface when radiation strikes it (Photo
electric effect)
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130.
i. The electrons are ejected from the metal surface as soon as the beam of light
strikes the surface
iii. For each metal there is a characteristic minimum frequency called threshold
frequency below which photo electric effect is not observed.
iv. The kinetic energies of ejected electrons increase with increase of frequency of
light used.
131.
i. The electron in the hydrogen atom can move around the nucleus in a circular
path of fixed radius and energy and the paths are called orbits
ii. The energy of an electron in the orbit does not change with time
iii. The frequency of radiation absorbed or emitted when transition occurs between
two stationary states that differ in energy by ∆ E is given by
ال =∆E
h
= الE2-E1
h
iv. The angular momentum of an electron in a given stationary state is integral
multiple of h
2π
i.e., meVr = n h
2π
132.
i. Principal quantum number determines energy and size of the orbital
ii. Azimuthal quantum number defines three dimensional shape of the orbital.
iii. Magnetic quantum number gives the information about the spatial orientation
of the orbital.
iv. Spin quantum number refers to orientation of the spin of the electron.
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UNIT-3
Classification of elements and periodicity in properties
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26. Why are d block elements also called transition elements?
27. Write the general outer electronic configuration of f block elements.
28. What are transuranium elements?
29. What is the trend in the metallic character of elements down a group?
30. In bromine molecule (Br2) the bond distance is 228 pm. What is the covalent
radius of bromine?
31. What is covalent radius for a non-metal?
32. Define metallic radius.
33. Arrange the following in the decreasing order of their atomic radius:
K Be N Na
(Z=19) (Z=4) (Z=7) (Z=11)
34. For noble gases covalent radius cannot be defined. Why?
35. Name a group of non-metals for which covalent radius cannot be defined.
36. Size of the cation is smaller than the parent atom. Give reason.
37. Size of the anion is larger than the parent atom. Give reason.
38. Hydride ion (H−) is larger than hydrogen atom. Give reason.
39. Mention a species that is isoelectronic with neon.
40. Arrange the following in the increasing order of their ionic radii: F−, N−3, Na+, O−2.
41. X+ (s) → X+2 (g) + e−. Correct the equation to represent the 2nd ionisation
enthalpy of the element X.
42. Define second ionisation enthalpy.
43. 2nd ionisation enthalpy for an element is higher than the 1st ionisation enthalpy.
Give reason.
44. Using the graph, match the ionisation energy of Ar, Na, Ne, Li
with positions P, Q, R and S.
45. Define electron gain enthalpy.
46. Why is ionisation enthalpy always positive?
47. Arrange the below elements X, Y, Z in the increasing order of electron gain
enthalpy.
Element Electron gain enthalpy kJ/mol
X −48
Y +77
Z −295
48. What is electronegativity for an atom?
49. “Ability of an atom in a compound to attract the shared electrons to itself”. Which
periodic property does the above quote represent?
50. On the basis of Pauling scale what is the value of electronegativity of fluorine?
51. How is electronegativity related to non-metallic property of an element?
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52. Give reason for the anamalous properties of 2nd period elements when compared to
the elements in their respective groups.
53. Mention one property common to all actinoid elements.
54. How are H− and He related?
55. By what name do we know the 17th group elements?
56. Isoelectronic species do not have the same size. Why?
57. Arrange the following in the increasing order of their metallic character: Cu, K,
Ge, Br.
58. What is the difference between an amphoteric oxide and a neutral oxide?
59. Give an example for a basic oxide.
60. Give an example for a neutral oxide.
61. Name the element that is diagonally related to beryllium.
62. Why do 17th group elements have high negative electron gain enthalpy?
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17. Given: a) F, Cl, Br b) N, O, F : For which one of these set of elements does
the atomic radius increase? Justify your answer.
18. What are isoelectronic species? Give example.
19. Which among the following has i)largest ii)smallest ionic radii:Na+,Al+3,Mg+2, F−?
20. Define ionisation enthalpy. Give its SI unit.
21. Compare the 1st and 2nd ionisation enthalpies of magnesium with reason.
22. Which group of elements have maximum value for ionisation enthalpy. Give
reason.
23. Draw a graph showing the variation of ionisation enthalpy with atomic number for
the elements Li, Be, B and C.
24. How does ionisation enthalpy vary along a period? Give reason.
25. How does ionisation enthalpy vary down a group? Give reason.
26. Ionisation enthalpy of boron is less than that of beryllium. Give reason.
27. Why is ionisation enthalpy of oxygen less than that of nitrogen?
28. Ionisation enthalpy of aluminium is less than that of magnesium. Justify the
statement.
29. Give two differences between ionisation enthalpy and electron gain enthalpy for an
element.
30. How does electron gain enthalpy vary along a period? Give reason.
31. How does electron gain enthalpy vary down the group? Explain.
32. Between flourine and chlorine which one of these has low electron gain enthalpy.
Give reason.
33. Which among the following has the most positive and the most negative electron
gain enthalpy: O, Ar, Na, S?
34. How does electronegativity vary along a period? Give reason.
35. How does electronegativity vary down a group? Give reason.
36. Name any two periodic properties that increases along a period.
37. Name any two periodic properties that decreases down a group.
38. Arrange the elements in the following two sets in the increasing order of their
electronegativity values: a) [Cl, F, I, Br] b) [S, Cl, Al, Na]
− −3
39. Which one of these is possible: BF4 or BF6 . Justify your answer. (atomic number
of boron = 5)
40. Why is the chemical reactivity of elements at the two extremes (except noble
gases) of the periodic table very high?
41. Why are the elements placed in the extreme left of the periodic table most
metallic?
42. Mention two factors on which ionisation enthalpy depends.
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43. Mention one exception (anomaly) each found in the variation of i) ionisation
enthalpy in the 2nd period ii) electron gain enthalpy in the 16th period.
44. Classify these into acidic, basic, amphoteric and neutral oxide: CO, Na2O, Cl2O7,
Al2O3.
Four Marks:
1. a) What is the valence of 2nd group elements?
b) Using the table given below, evolve the formulae of i) aluminium oxide,
ii) aluminium nitride, iii) aluminium fluoride:
Group No. 13 15 16 17
Element Al N O F
2. a) When is a cation and an anion is formed from an atom?
b) Arrange H+, H−, H in decreasing order of their size.
c) What does the energy absorbed in the reaction represent?
X (g) → X (+g ) + e−
3. What does ionisation enthalpy, electron gain enthalpy and electronegativity
measure for an atom? Which one of these is not a measurable quantity?
4. Given:
Element Electronic configuration
P 1s2 2s2
Q 1s2 2s2 2p6 3s2 3p1
R 1s2 2s2 2p6 3s1
S 1s2 2s2 2p4
i) Arrange P, Q, R, S in decreasing order of their atomic radii.
ii) Which one among these is a chalcogen?
iii) Which one among these has more positive electron gain enthalpy?
iv) Give the formula of the oxide formed from R and S.
5. Mention any two characteristic properties each for s and p block elements.
6. How does metallic and non-metallic character vary along a period and down a
group. Give reasons.
7. Given the outer electronic configurations of A and B as .... 3s2 and .... 3s2 3p5.
a) Locate their position in the periodic table (group and period)
b) Which one of these has i) larger atomic size ii) higher ionisation energy
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Scheme of valuation with complete answers
Marks
Qn.No. Value points
allotted
1 23 1
2 Law of octaves 1
3 Atomic weight or atomic mass 1
Properties of the elements are periodic functions of their atomic
4 1
weight
5 Moseley or Henry Moseley 1
Physical and chemical properties or properties of the elements are
6 1
periodic functions of their atomic numbers
7 Atomic number 1
8 Principal quantum number 1
9 18 1
10 103 1
11 Unnilennium 1
12 5d 1
13 6th period or 6 1
14 7th period or 7 1
15 Actinoids or actinide series 1
16 14 1
Similar outermost electronic configuration or same number and
17 1
same distribution of electrons in their outermost orbital
It has completely filled value shell (1s2) and has properties
18 1
characteristic of noble gases
19 s block 1
20 6 1
21 s and p block 1
22 16th group or 16 1
23 (n−1) d1−10 ns0−2 1
24 d – block 1
25 d – block 1
They act as a bridge between chemically most active metals of s-
26 1
block and less active elements of groups 13 and 14.
27 (n−2) f1−14 (n−1) d0−1 ns2 1
28 Elements appearing after uranium 1
29 Metallic character increases 1
30 114 pm 1
It is one half the distance between two atoms bonded by a single
31 1
covalent bond
It is half the internuclear distance separating the metal cores in the
32 1
metallic crystal
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33 K > Na > Be > N 1
34 They are monoatomic gases 1
35 Noble gases 1
36 It has fewer electrons and nuclear charge remains same 1
37 It has more electrons and effective nuclear charge decreases 1
In H− due to more number of electrons the effect of nuclear charge
38 1
is less
39 Na+ (or Mg+2, Al+3 or any other) 1
40 Na+ < F− < O−2 < N−3 1
+ +2
41 X (g) → X (g) + e− 1
It is the energy required to remove the 2nd most loosely bound
42 1
electron
It is more difficult to remove an electron from a positively charged
43 1
ion than from a neutral atom
44 P = Li, Q = Ne, R = Na, S = Ar 1
It is the enthalpy change that occurs when an electron is added to a
45 1
neutral gaseous atom
It is an endothermic process or energy is always absorbed to
46 1
remove an electron
47 Y<X<Z 1
It is the ability of an atom in a compound to attract the shared
48 1
electrons to itself
49 Electronegativity 1
50 4 1
51 Electronegativity α non-metallic character 1
Same size, large charge / radius ratio, high electronegativity (any
52 1
two)
53 Radioactivity 1
54 Isoelectronic 1
55 Halogens 1
56 They have different nuclear charge 1
57 Br < Ge < Cu < K 1
Amphoteric oxide has both acidic and basic character. But a
58 1
neutral oxide is neither acidic nor basic.
59 Na2O 1
60 CO 1
61 Aluminium 1
62 By gaining one electron they attain noble gas configuration 1
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Two mark questions:
Marks
Qn.No. Value points
allotted
i) Position of some elements do not fit in with the scheme of 1
classification or element of lower atomic weight are placed
1
before the element with high atomic weight.
ii) He correctly predicted the existence of few elements. 1
Eka-aluminium 1
2
Gallium 1
The regularities in the x-ray spectra of elements could be 1
accounted if a plot of ν (ν is the frequency of x-rays emitted)
versus atomic number and not atomic mass was done. 1
3
or
A graph of ν versus atomic number and not atomic mass could 1
explain the characteristics of x-ray spectra of elements. 1
The vertical column of elements are called groups. 1
4
The horizontal rows of elements are called periods. 1
5 18 groups and 7 periods 1+1
8 elements 1
6 nd
In the 2 period (n = 2) the sub-shells filled are 2s and 2p only 1
st
1 period 1
7 th
6 period 1
i) 2s and 2p 1
8
ii) 4s, 3d and 4p 1
st
i) It has only one electron in 1 orbital and hence could be
placed in I group 1
9 ii) It can also gain one electron to achieve a noble gas
configuration like 17 group elements and hence can be placed 1
in 17 group.
Block – d 1
10
Period − 4 1
2 2 6 2 6 2 10 6 2 10 6 2 14 10 6 2
1s 2s 2p 3s 3p 4s 3d 4p 5s 4d 5p 6s 4f 5d 6p 7s 1
14 10 6 2 14 10 6
11 5f 6d 7p or [Rn] 7s 5f 6d 7p
18 group or noble gas group 1
Metals Non-metals
1. Have high melting point Have low melting point. (any
12 2. Good conductor of heat and Bad conductor of heat and two)
electricity electricity 1+1
3. Malleable and ductile Not malleable and ductile
Elements that show properties similar to both metals and non- 1
13 metals
Silicon (or any other) 1
i) Atom is very small 1
14
ii) Electron cloud of the atom does not have a sharp boundary 1
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It decreases along a period 1
15
It increases down a group 1
i) Along a period the electron is added to same valence shell and
1
effective nuclear charge increases.
16
ii) Down a group the electron is added to a new shell and
1
effective nuclear charge decreases.
Set a 1
17 The elements belong to a group and down the group the atomic
size increases. 1
Species containing same number of electrons. 1
18
E.g.: Na+, Mg+2 1
F− 1
19
Al+3 1
It is the energy required to remove an electron from an isolated 1
20 gaseous atom in its ground state.
kJ mol−1 or kJ 1
1st ionisation enthalpy of magnesium is less than the 2nd.
1
21 More energy is required to remove an electron from Mg+ than
1
from Mg
Noble gases or 18 group. 1
22
They have a very stable electronic configuration. 1
23 1+1
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Ionisation enthalpy Electron gain enthalpy
Its always positive It may be positive, negative or 1
29 zero
It measures the hold of the It measures the affinity of an 1
nucleus on its electron. atom to add an electron.
It increases or it becomes more negative. 1
30
Effective nuclear charge increases. 1
It decreases or it becomes less negative. 1
31
Size of the atom increases and effective nuclear charge decreases. 1
Fluorine 1
32 The electron is added to 2p orbital which is small and experiences
more repulsion from other electrons. 1
Ar 1
33
O 1
It increases 1
34
Atomic radius decreases 1
It decreases 1
35
Atomic radius increases 1
36 Ionisation enthalpy and electronegativity 2
37 Electron gain enthalpy and electronegativity 2
I < Br < F < Cl 1
38
Na < Al < S < Cl 1
[BF4]− 1
39
Boron has only 4 valence orbitals. 1
Towards the left, ionisation energy is the least and atoms have the
1
tendency to lose the electron.
40
Towards the right, electron gain enthalpy is more negative and
1
hence atoms have tendency to gain an electron.
The elements have low ionisation enthalpy and have high 1
41
tendency to form cations. 1
Attraction of electrons towards the nucleus. 1
42
Repulsion of electrons from each other. 1
Beryllium and Boron or oxygen and nitrogen 1
43
Oxygen and sulphur 1
44 CO- neutral, Na2O – basic, Al2O3 – amphoteric, Cl2O7 – acidic 2
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Four mark questions:
Marks
Qn.No. Value points
allotted
a) 2 1
b) i) Al2O3 1
1
ii) AlN 1
iii) AlF3 1
When an atom loses an electron and when an atom gains an 2
electron.
2
H− > H > H+ 1
st
1 ionisation enthalpy 1
Ionisation energy measures tendency of an atom to lose an 1
electron.
Electron gain enthalpy measures tendency of an atom to gain an 1
3 electron.
Electronegativity measures the ability of an atom in a compound 1
to attract shared electrons.
Electronegativity 1
Q>R>P>S 1
S 1
4
Q 1
R 2S 1
s block : They are metals and form basic oxides. 2
5
p block : They are non-metals and form acidic oxides. 2
Metallic character increases down a group. 1
Ionisation energy decreases. 1
6
Non-metallic character increases along a period. 1
Electron gain enthalpy increases. 1
nd rd th rd
A: 2 group, 3 period ; B: 17 group, 3 period 2
7
i) A ii) B 2
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I PUC QUESTION BANK
Chapter: 4
Chemical bonding
1 Mark Questions
1) Who were the first to propose a theory on chemical bonding using electrons?
2) What is a chemical bond?
3) Write Lewis dot symbols for atoms of the following elements
Mg, Na, B, O, N, and Br.
4) Draw the Lewis structures for the following molecules and ions.
H2, O2, CO2, C2H4, C2H2, HNO3, CO
5) In the periodic table, the group of highly electronegative elements is _____.
6) In the periodic table, the group of highly electropositive elements is _____.
7) Write the general electronic configuration of noble gases.
8) What type of bond is present in NaCl?
9) Which force holds oppositely charged ions together in an ionic bond?
10) Name a cation that contains cation having two non metallic elements in an ionic
compound.
11) How does resonance stabilize a molecule?
12) Give the mathematical expression for dipole moment.
13) Expand VSEPR
14) What is the basis of VSEPR theory?
15) Arrange the repulsive interaction between electron pairs (lp-bp, bp-bp, and lp-lp)
in increasing order.
16) What is lone pair of electrons?
17) What is bonded pair of electrons?
18) Among bonded pair of electron and lone pair of electron, which occupy more
space in a molecule?
19) How many lone pairs of electrons are present in a molecule of ammonia?
20) How many lone pairs of electrons are present in a molecule of water?
21) How many lone pairs of electrons are present in a molecule of ClF3?
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22) How many lone pairs of electrons are present in a molecule of SF4?
23) What is hybridization?
24) Write the shape and bond angle of sp hybrid orbitals?
25) Give an example of a molecule having sp hybridization?
26) What is the percentage of s character in sp hybridization?
27) What is the shape and bond angle of sp2 hybrid orbitals?
28) What is the percentage of s character in sp3 hybridizations?
29) Give an example for sp2 and sp3 hybrid molecules
30) Write the shape and bond angle of sp3 hybridized orbitals.
31) Write the shape, hybridization and bond angle of a) NH3 and, b) H2O
32) How many σ and π bonds are there in a) ethylene b) ethyne?
33) What is the type of hybridization found in PCl5?
34) What is the shape and hybridization of SF6?
35) Write the number of axial and equatorial bonds in PCl5
36) Give example of a molecule showing dsp2 hybridization.
37) Write the shape of Br F5 molecule.
38) Arrange the following orbitals in the increasing order of s- character.sp, sp2, sp3
39) Define hydrogen bond.
40) How is the magnitude of hydrogen bonding in different states of matter?
41) Is the force between two nuclei of hydrogen atoms attractive or repulsive?
42) Which of the force (i.e. attractive or repulsive) is stronger?
43) What is bond enthalpy?
44) The electrons present in valence shells should have ___spins in order to be
paired up.
45) Will a bond be stronger when there is more overlap or less overlap of atomic
orbitals?
46) Hydrogen molecule is formed due to overlap of ____ orbitals.
47) What is tetrahedral bond angle?
48) What are the types of overlap depending on the sign (phase) of orbital wave
function?
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49) If the wave functions of participating atomic orbitals are same phase, the overlap
is called _________.
50) The energy required for changing the electronic configuration from ground to
exited state is provided from where?
51) What is the angle between any two p orbitals?
52) What are the two types of covalent bonds?
53) What is a pi bond?
54) What is the shape of the electron cloud in a pi bond?
55) Can a pi bond exist without a sigma bond?
56) Is there greater overlap in sigma or pi bonds?
57) Define hydrogen bond.
2 Marks
1) Which type of elements is likely to form anions and give the reason for the same?
2) Which factor favours formation of cation? Explain.
3) Among KCl and NaCl, which is more stable? Give reason.
4) Under what conditions the concept of resonance is applied?
5) The dipole moment in BF3 is zero. Explain
6) The net dipole of NH3 is greater than that of NF3. Why?
7) Write the resonance structures of CO32- and CO2.
8) List the outcome of repulsive interaction between electron pairs in a molecule.
9) Account for the shape of the following molecules based on VSEPR theory
i) Water molecule.
ii) SO2 molecule
iii) Ammonia molecule
iv) SF4 molecule.
10) What are the causes of formation of hydrogen bond?
11) What are the conditions for hydrogen bonding?
12) Draw the shapes of following hybrid orbitals.
sp, sp2,sp3
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13) Considering X- axis as the internuclear axis, which out of the following will not
form sigma bond? Why?
1s and 2s b) 1s and 2px c) 2py and 2py d) 1s and 2s
14) Draw the shapes of H2O and C2H4 molecule
15) Describe the change in the hybridization of the Al atom in the following reaction.
AlCl3 + Cl- → AlCl4-
16) Is there any change in hybridization of B and N as a result of the reaction?
BF3 + NH3 → BF3.NH3
17) What are the various forces that arise between the two atoms of hydrogen as they
approach each other?
18) Give the ground and exited configuration of carbon for the formation of methane
molecule.
19) What is a sigma bond? Mention types.
20) Explain the LCAO method for the formation of molecular orbitals from the
atomic orbitals.
21) Distinguish between atomic orbital and molecular orbital.
22) Distinguish between bonding molecular orbital and anti-bonding molecular
orbital.
23) Define bond order and give the relationship between bond order and bond length
24) What are the causes of formation of hydrogen bond?
25) What are the conditions for formation of hydrogen bonds?
3 Mark questions
1) Explain the conditions for the combination of atomic orbitals to form molecular orbitals.
2) Write the assumptions of the molecular orbital theory.
3) Explain the diamagnetic behaviour of Hydrogen molecule on the basis of molecular
orbital theory.
4) Show the non-existence of helium molecule based on molecular orbital theory.
5) Explain the formation of Lithium molecule on the basis of molecular orbital.
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6) Show that oxygen molecule is paramagnetic based on molecular orbital theory.
7) Write the molecular orbital electronic configuration for carbon molecule and comment
on its magnetic property
8) Define octet rule. Write its significance and limitations.
9) Explain why crystal structure of NaCl is stable in spite of having sum of electron gain
energy and ionization enthalpy as positive. Substantiate with an example
10) Why it is required to take average bond enthalpy in case of polyatomic molecules?
Explain with example.
11) Among O2 and N2 which is more stable and why?
12) The net dipole moment of NH3 is greater than that of NF3. Why?
13) State the postulates of VSEPR theory
14) Indicate the geometry in the following compounds and give one example for each.
i) AB2
ii) AB3
iii) AB4
iv) AB5
v) AB6
15) What are the types of hydrogen bonds?
16) What are the salient features of hybridization?
17) With the help of potential energy diagram explain how bonding between two hydrogen
atoms takes place.
18) Explain the shape of methane molecule through valence bond theory.
19) Explain the formation of BeCl2 using hybridization.
20) Explain the sp2 hybridization with the example of BCl3.
21) Explain the shape of NH3 molecule using hybridization.
22) Explain the formation of SF6 using sp3d2 hybridization.
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1mark Answers:
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31) Ans: a) NH3
Shape: Pyramidal
Hybridization: sp3
Bond angle: 107o
b) H2O
Shape: V shape or angular shape
Hybridization: sp3
Bond angle: 104.5o
32) Ans: Ethylene σ bond = 5, π bond = 1
Ethyne σ bond = 3, π bond = 2
33) Ans: sp3d hybridization
34) Ans: Shape – Octahedral
Hybridization – sp3d2
35) Ans: Axial bond – 2
Equatorial bond -3
36) Ans: [PtCl4]2-
37) Ans: Square pyramidal
38) Ans: Sp3<sp2<sp
39) Ans: Hydrogen bond is defined as the attractive force which binds hydrogen atom
of one molecule with the electronegative atom (F, O or N) of another molecule.
40) Ans: It is maximum in solid state and minimum in the gaseous state.
41) Ans: Repulsive
42) Ans: Attractive
43) Ans: The energy released when a bond is formed between two atoms is called
bond enthalpy.
44) Ans: Opposite
45) Ans: More overlap
46) Ans: 1s
47) Ans: 109028′
48) Ans: Positive, negative, zero
49) Ans: Positive
50) Ans: When atomic orbitals overlap there is release in energy, this energy is used
to change the electronic configuration
51) Ans: 900
52) Ans: Sigma and pi
53) Ans: It is a type of covalent bond formed due to overlap of atomic orbitals side
ways.
54) Ans: A pi electron cloud consists of two saucer shaped clouds above and below
the plane of participating atoms.
55) Ans: No
56) Ans: Sigma bonds.
57) Ans: Hydrogen bond is defined as the attractive force which binds hydrogen atom
of one molecule with the electronegative atom (F, O or N) of same molecule or
another molecule.
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2 Marks answers
1) Ans: Non-metallic elements have high electron gain enthalpy to form anions which
is produced in the process
Cl (g) + e-1 → Cl-(g) ∆H = 348.7kJmol-1
2) Ans: Metallic elements have low ionization energy which facilitates the easy
release of electrons from the metal and formation of cation is
Na → Na+ + e –
5) Ans: In BF3 µ = 0, although the B-F bonds are oriented at an angle of 1200to one
another. This is because the bond moments give a net sum of zero as the
resultant of any two is equal and opposite of third.
6)Ans: In case of NH3 the 0rbital dipole due to lone pair of electron on nitrogen atom ,
is in the same direction as the resultant dipole moment of N-H bonds, where
as in NF3, it is in the direction opposite to resultant dipole moment of 3 N-F
bonds. The orbital dipole decreases the effect of the resultant N-F bond
moments which reduces dipole moment of NF3.
7) Ans: For the resonance structures of CO32- and CO2 refer to page no 106( Part-1)
8) Ans: a) Deviation in the shape of the molecule
b) Alterations in the bond angle in the molecule.
9) Ans: i) Water molecule belongs to type of AB2E2
The shape of water molecule should have been tetrahedral if there were all
bond pair. But because of the presence of two lone pair, the shape is distorted
tetrahedral or angular. The reason is lp-lp repulsion is more than bp-bp
repulsion. Thus the angle is reduced to 104.50 from 109.50.
Refer to page no 112 for structure.
ii) SO2 molecule
SO2 molecule belongs to AB2E
The shape of SO2 molecule should have been triangular planar but it is found
to be bent or V-shaped .This is due to the fact that lp-bp repulsion is much
more than bp-bp repulsion. So the angle is reduced to 119.50 from 1200.
iii) Ammonia molecule
Ammonia molecule belong to AB3E type
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The shape of NH3 molecule should have been tetrahedral if all the electrons
were bond pair. But because of the presence of one lp,ther is lp-bp repulsion
which is more than bp-bp repulsion and the angle is reduced from 1070 to 104.50.
iv) SF4 molecule.
SF4 molecule belongs to AB4E type.
The shape of SF4 molecule is distorted tetrahedron or a folded square or a
see- saw in which the lp is in an equatorial position where there are only two
lp-bp repulsions. This arrangement is more stable than the arrangement
where the lp is present at axial position where there are three lp-bp
repulsions at 900.
10) Ans: When there is formation of covalent bond between hydrogen and
electronegative elements, the electrons of the covalent bond are shifted
towards more electronegative atom as of which the positively charged
hydrogen forms a bond with the other electronegative atom .
11) Ans: a) Hydrogen atom should be bonded to highly electronegative atoms such as
fluorine, oxygen or nitrogen.
b) Size of the electronegative atoms should be small.
12) Ans: sp – Refer to page 117,fig 4.10
sp2 – Refer to page 117, fig 4.11
sp3 – Refer to page 118, fig 4.12
13) Ans: 2py and 2py will not form a sigma bond because taking x- axis as the
internuclear axis, there will be lateral overlapping between 2py orbitals forming a
pi bond.
14) Ans: For H2O refer page 118, fig 4.14 and for C2H4 refer page 119, Fig 4.15
15) Ans: Electronic configuration of Al = 1s22s22p63s23p2
Exited state configuration is 1s22s22p63s13px13py1
Hence hybridization is sp2
In AlCl4- empty 3pz orbital is also involved so the hybridization is sp3 and
shape is tetrahedral.
16) Ans: In BF3, B atom is sp2 hybridized. In NH3, N atom is sp3 hybridized. After
the reaction hybridization changes from sp2 to sp3.
17) Ans: a) Attractive force between nucleus and its own electron.
b) Attractive force between nucleus and electron of other atom
c) Repulsive force between the two nuclei
d) Repulsive force between two electrons.
18) Ans: Ground state [He] 2s22p2
Excited state [He] 2s12px12py12pz1
19) Ans: This type of covalent bond is formed by the head on overlap of atomic
orbitals along the internuclear axis. The sigma bonds result from the
following types of overlap
a) s-s b) s-p c) p-p
20) Ans: The molecular orbitals are formed by the linear combination of wave functions of
the participating atomic orbitals. They may combine either by addition or by
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subtraction. Let ψA and ψB represent the wave functions of the two combining
atomic orbitals A and B taking part in chemical combination.
Molecular orbitals
23) Ans: It is half of the difference between the number of electrons present in
bonding molecular orbitals and the number of electrons present in the
antibonding molecular orbitals.
24) Ans: When there is formation of covalent bond between hydrogen and
electronegative elements, the electrons of the covalent bond are shifted
towards more electronegative atom which makes the hydrogen atom
positive and it forms the hydrogen bond with other electronegative atom.
3 Mark answers
1) Ans: The conditions for the combination of atomic orbitals to form molecular orbitals are
1. The combining atomic orbitals must have same or nearly the same energy.
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2. The combining atomic orbitals must have the same symmetry about the molecular
axis.
3. The combining atomic orbitals must overlap to the maximum extent.
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6) Ans: It is formed by the combination of the two oxygen atoms.
Each oxygen atom has eight electrons and its electronic configuration is
1s2, 2s2, 2px2, 2py1, 2pz1.
Hence there are 16 electrons in oxygen molecule.
The molecular orbital configuration is
σ 1s2, σ *1s2, σ 2s2, σ *2s2, σ 2pz2, π2px2 = π2py2, π*2px1 = π*2py1
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Therefore Na (g) + Cl (g) → Na+ + Cl- ∆H = 147.1kJmol-1
This is compensated by the lattice energy of NaCl
Na+ (g) + Cl-(g) → NaCl(s) ∆H = -788 kJmol-1
Thus stability of ionic compound is due to enthalpy of lattice formation not just by
octet ionic species in gaseous state.
10) Ans: In polyatomic molecules the enthalpy required to break the same bond in different
chemical environment are different.
Example: H2O (g) → H (g) + OH (g) ∆H1 = 502 kJmol-1
OH (g) → H (g) + O (g) ∆H2 = 427 kJmol-1
Average bond enthalpy is 502+427/2 = 464.5 Kjmol-1
Greater the bond order, bond enthalpy (energy required to break the bond) increases,
bond length decreases. Hence stability of the molecule increases. Thus N2 is more
stable than O2.
12) Ans: In case of NH3 the orbital dipole due to lone pair of electrons on N atom , is in the
same direction as the resultant dipole moment of N-H bonds, whereas in NF3 it is in
the direction opposite to resultant dipole moment of three N-F bonds. The orbital
dipole decreases the effect of the resultant N-F bond moments which reduces µ of
NF3.
13) Ans: a) The shape of the molecule depends upon the number of valence shell electron
pairs (bonded or non bonded) around the central atom.
b) Pairs of electrons in the valence shell repel one another since their electron clouds
are negatively charged.
c) These pairs of electrons tend to occupy such positions in space that minimize
repulsion and thus maximize distance between them.
d) The valence shell is taken as a sphere with the electron pairs localizing on the
spherical surface at maximum distance from one another.
e) A multiple bond is treated as if it is a single electron pair and the two or three
electron pairs of a multiple bond are treated as a single super pair.
f) Where two or more resonance structure can represent a molecule, the VSEPR
model is applicable to any such structure.
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Trigonal bipyramidal geometry, Ex: PCl5
e) AB6
Octahedral geometry, Ex: SF6.
15) Ans: There are two types of hydrogen bonds
Intermolecular hydrogen bond: It is formed between two different molecules of the
same or different molecules of the same or different compounds.
Example: HF, H2O, Alcohols
Intramolecular hydrogen bond: It is formed when hydrogen atom is in between the
two highly electronegative atoms present within the same molecule.
Example: O-nitrophenol.
16) Ans: a) The number of hybrid orbitals is equal to the number of atomic orbitals
undergoing hybridization.
b) The hybridized orbitals are always equivalent in energy and shape
c) Hybrid orbitals are more effective in forming stable bonds than pure atomic
orbitals
d) Type of hybridization indicates the geometry of the molecule
e) The orbitals in the valence shell of atom are hybridized
f) The orbitals undergoing hybridization should have comparable energy.
g) Not only half filled orbitals but filled orbitals also take part in hybridization
17) Ans: When two atoms approach each other, a number of attractive and repulsive forces
operate. Experimentally it has been found that attractive forces have greater
magnitude and hence the atoms come closer together. A point is reached here net
attractive force balances net repulsive force and potential energy reaches a
minimum. At this stage the atoms are said to be bonded. Refer fig 4.8, pg: 114
18).Ans: In the formation of methane molecule the unpaired electrons in each of the orbital s
of carbon pair up with electron in 1s of hydrogen, resulting in formation of 4 C-H
bonds. As the angle between p-orbitals is 900 the H-C-H bond angle should also be
900 and as 1s orbital is spherical the overlap can occur in any direction and direction
of fourth C-H bond cannot be ascertained but CH4 has a tetrahedral structure hence
simple atomic overlap cannot explain the tetrahedral shape of methane.
19) Ans: The ground state electronic configuration of Be is 1s22s2. In the exited state one of
the 2s-electrons is promoted to vacant 2p orbital to account for its bivalency. One 2s
and one 2p orbitals get hybridized to form two sp hybridized orbitals. These two sp
hybrid orbitals are oriented in opposite direction forming an angle of 180o. Each of
the sp hybridized orbital overlaps with the 2p- orbital of chlorine axially and form
two Be-Cl sigma bonds. Ref Pg 117 , Fig 4.10 (b).
20).Ans: In BCl3 molecule, the ground state electronic configuration of central boron atom is
1s22s22p1. In the exited state, one of the 2s electrons is promoted to vacant 2p orbital
as a result boron has three unpaired electrons. These 3 orbitals (one 2s and two 2p)
hybridized to form three sp2 hybrid orbitals. The three hybrid orbitals so formed are
oriented in a trigonal planar arrangement and overlap with 2p orbitals of chlorine to
form three B – Cl bonds. Therefore, in BCl3, the geometry is trigonal planar with
Cl-B-Cl bond angle of 1200. Ref pg 117, Fig 4.11.
21) Ans: In ammonia, the valence shell electronic configuration of N in the ground state is
2s22px12py12pz1 having three unpaired electrons in the sp3 hybrid orbitals and a lone
pair of electrons is present in the fourth one. These 3 hybrid orbitals overlap with 1s
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orbitals of hydrogen atoms to form 3 N-H sigma bonds. Force of repulsion between a
lone pair and a bond pair is more than the force of repulsion between two bond pairs
of electrons. The molecules thus get distorted and the bond angle is reduced to 1070
from 109.50. The geometry of such a molecule will be pyramidal and can be
explained with sp3 hybridization. Ref Pg 118, Fig 4.13.
22).Ans: In SF6 the central sulphur atom has the ground state outer electronic configuration of
3s23p4. In the exited state the available 6 orbitals i.e., 1s, 3p and 2d are singly
occupied by electrons. These orbitals hybridise to form 6 new sp3d2 hybrid orbitals,
which are projected towards the 6 corners of a regular octahedron in SF6. These 6
sp3d2 hybrid orbitals overlap with singly occupied orbitals of Fluorine atoms to form
6 S-F sigma bonds. Thus it has regular octahedron shape. Ref pg121, Fig 4.18
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UNIT 5
States of matter
I. Questions carrying one mark
5.1 What are van der Waals forces?
5.2 What type of van der Waals force exists between HCl molecules?
5.3 Between which type of molecules does dipole – induced dipole forces exist?
5.4 Even though HF has lower molecular mass compared to HCl, HF is in the liquid
state and HCl is in the gaseous state at room temperature .why?
5.5 Why are liquids & solids are hard to compress?
5.6 State Boyle’s law
5.7 What happens to the pressure when the volume of a gas is doubled at constant
temperature?
5.8 Give the relationship between pressure and density of a gas
5.9 Mountaineers carry oxygen cylinders along with them . Which gas law will account
to the above statement?
5.10 Relate absolute temperature scale or Kelvin temperature to Celsius scale.
5.11 If a volume vs temperature graph is plotted in degree centigrade at constant
pressure, at what temperature the line cuts the temperature axis?
5.12 Each line of volume vs pressure graph at constant temperature is known as what?
5.13 Define absolute zero temperature
5.14 Represent Charles law graphically
5.15 What is the volume occupied by the gas at -273.15ºC?
5.16 State Gay – Lussac’s law
5.17 Equal volumes of all gases under the same condition of temperature and pressure
contain equal number of molecules. Name the gas law for the above statement
5.18 Which law relates temperature and pressure ?
5.19 If the numbers of moles of a gas are doubled by keeping the temperature and
pressure constant, what would be the new volume of the gas?
5.20 Relate density and molar mass of a gas molecule
5.21 Give the value of R in SI unit.
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5.22 Write the value of molar volume of an ideal gas at STP, when pressure is 1bar
5.23 State Dalton’s law of partial pressure
5.24 Write a postulate of kinetic molecular theory of gases that explains the great
compressibility of gases
5.25 Define aqueous tension
5.26 Why do the gases expand &occupy the entire space available to them?
5.27 How does a gas exert pressure?
5.28 Collision of the gas molecules does not change average kinetic energy.why?
5.29 Write van der Waals equation for ´n’ moles of a gas
5.30Write the expression for compressibility factor Z for one mole of a gas.
5.31Define Boyle temperature
5.32 The value of Van der walls constant ‘a’ for a gas is zero, what does it signify?
5.33 Define boiling point temperature at a given pressure for a liquid
5.34 Give the value for standard boiling point of water
5.35 Define surface energy
5.36 What would be SI unit of a quantity PV2 T2/n ?
5.37 The magnitude of coefficient of viscosity of liquid at 25°C ,45°C, 19ºC and 57°C
are p, q, r, s respectively. Arrange them in the increasing value of co-efficient of
viscosity
5.38 What is meant by most probable speed of gas molecule ?
5.39 Water has higher vapour pressure than mercury. Justify
5.40 Name the property of the liquid that measures the resistance to the flow of liquid
due to internal friction.
5.41 How does the volume of a gas under given temperature and pressure vary with
molar mass?
5.42. The size of the weather balloon becomes larger and larger as it ascends up into
higher attitude. Which gas law explains the above phenomenon?
5.43 Arrange Urms,Ump,Uav in the increasing value for a gas at a given temperature
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II. Questions carrying Two marks
5.1 Name two types of forces which determines the physical state of substances
5.2 Write any two important physical properties of gases.
5.3 How does pressure for a given amount of gas vary with volume at a given
temperature? Represent this graphically
5.4 In terms of Charles law, explain why -273.15ºC is the lowest possible temperature of
gases.
5.5 Represent Charles law graphically. What is each line in the graph known as?
5.6 Write the Avogadro’s law. Write the mathematical representation of the law.
5.7 Using ideal gas equation derive an equation that relates density and molar mass of a
gaseous substance .
5.8 Deduce the value of R in SI unit
5.9 State Daltons law of partial pressure. How is partial pressure of a gas is related to
mole fraction
5.10 Justify: collisions among the molecules in a gas are perfectly elastic
5.11 Two flasks of equal volumes contains nitrogen and oxygen gases at the same
temperature and pressure. Which will have greater number of molecules? Justify
the answer by stating the law.
5.12 If the number of moles of a gas is doubled by keeping the temperature and pressure
constant, what will happen to the volume? Give reason.
5.13 Which two postulates of the kinetic theory of gases are not applicable for real
gases?
5.14 Explain the physical significance of Van der Waals parameters ‘a’ & ‘b’for a real
gas.
5.15 Under what condition real gases tend to show ideal gas behaviour?
5.16 Draw Z vs P graph for ideal gas and CO2 gas.
5.17 At high attitude time required to cook food is more than at sea level.
Justify the statement.
5.18 Out of NH3 and N2, which will have higher value of ‘a’- the van der Waals
parameter and why?
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5.19 What happens to the compressibility factor for gases like CO2 at
i) Very high pressure & ordinary temperature
ii) Low pressure & ordinary temperature
5.20 Can Dalton’s law of partial pressure be used to calculate pressure of mixture of NH3
& HCl? Justify the answer .
5.21 Two gases A and B have critical temperature of 250K & 125K respectively. Which
one of these can be liquefied easily and why?
5.22 Define surface tension. Write the SI unit of surface tension.
5.23 A drop of liquid assumes spherical shape. why?
5.24 Name the two factors on which the magnitude of surface tension depends?
5.25 A balloon has a volume of 175dm3 when filled with hydrogen gas at a pressure of
1.0 bar. Calculate the volume of the balloon when the pressure is 0.8bar. Assume
that the temperature remains constant.
5.26 A gas cylinder containing cooking gas can withstand a pressure of 14.9bar. The
pressure gauge of the cylinder indicates 12bar at 27ºC. Due to sudden fire in the
building, the temperature starts rising. At what temperature will the cylinder
explode?
5.27 A weather balloon filled with hydrogen at 1 atm & 27ºC has volume equal to
1200dm3. On ascending it reaches a place where the temperature is -23ºC and
pressure is 0.5 atm. What is the volume of the balloon at this temperature?
5.28 Write two factors on which molecular speed of a gas depends?
5.29. The density of a gas is found to be 1.56g /dm3 at 0.98bar pressure & 65ºC.
Calculate the molar mass of the gas (R=0.083 bar dm3/K/mol).
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5.3. Enlist the three postulates of kinetic molecular theory of gases.
5.4. Define the terms
i) Critical temperature for a gas
ii) Aqueous tension
iii) Critical volume
5.5. What is the effect of temperature on -
i) Density ii) Surface tension iii) Vapour pressure of the liquid.
5.6 The mass of 0.5 dm3 of hydrogen gas at a pressure of 1bar of Hg and at a temperature
of 300K was found to be 4 x 10-2g. Calculate the molar mass of hydrogen (R= 0.083
bar dm3/K/mol).
5.7 2.9g of a gas at 95ºC occupies the same volume as 0.184 g of dihydrogen at 17 ºC
at the same pressure . What is the molar mass of the gas?
5.8 Calculate the total pressure of mixture of 8g of oxygen and 4g of hydrogen
confined in a vessel of 1dm3 at 27ºC (R=0.083 bar dm3/K/mol).
5.9 Calculate volume occupied by 8.8gof CO2 at 31.10C&1bar pressure
(R =0.083 bar LK-1 mol-1).
Answers
I. Answers for Questions carrying 1 mark
Q. NO Value point Marks
5.1 Attractive intermolecular forces 1
5.2 Dipole- dipole forces 1
5.3 Polar molecule &non-polar molecule 1
5.4 Due to the presence of hydrogen bonding between the 1
molecules in HF.
5.5 Intermolecular forces are very strong or 1
Particles in liquids &solids are very close to each other
5.6 At constant temperature, the pressure of fixed amount of a gas 1
varies inversely with its volume
5.7 Reduces to half of the initial pressure 1
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5.8 Pressure α density OR 1
PM=dRT
5.9 Boyles Law 1
5.10 T= 273+t 1
Where T is Kelvin temp scale and t is Celsius scale
5.11 -273.15ºC 1
5.12 Isotherms 1
5.13 lowest imaginary temperatures at which gases are supposed to 1
occupy zero volume
5.14 1
5.15 Zero or 0 1
5.16 At constant volume, pressure of fixed amount of a gas varies 1
directly with temperature
5.17 Avogadro’s law 1
5.18 Gay – Lussacs law 1
5.19 Doubles 1
5.20 Density α Molar mass 1
or
M= (d/P) RT
5.21 8.341J/K/mol 1
5.22 22.7 L/ mol 1
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5.23 The total pressure exerted by the mixture of non- reactive 1
gases is equal to the sum of the partial pressures of individual
gases under same conditions of volume &temperature.
5.24 Gases consists of large number of identical particles called 1
atoms or molecules .The volume of the molecule is negligible
in comparison to the empty space between them.
5.25 Pressure exerted by saturated water 1
5.26 There is no force of attraction between the particles of the 1
gases at ordinary temperature & pressure
5.27 collision of the gas molecule with the walls of the container 1
during their random motion
5.28 Collisions of the gas molecule is elastic. 1
5.29 (P+ an2/ v2) (v-nb) = n RT 1
5.30 Z= PV/RT 1
5.31 Temperature at which a real gas obeys ideal gas law over an 1
appreciable range of pressure
5.32 attractive forces among the gas molecules are absent 1
or
gas cannot be liquified
5.33 The temperature at which vapour pressure of liquid is equal to 1
the external pressure
5.34 99.6ºC 1
5.35 The energy required to increase the surface area of the liquid 1
by one unit
5.36 Nm4K2/mol 1
5.37 s<q< p < r 1
5.38 Speed possessed by maximum number of molecules. 1
5.39 The inter molecular attraction in water are lower than mercury 1
5.40 Viscosity 1
5.41 Volume is inversely proportional to molar mass or 1
Vα1/M or V= mRT/MP
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5.42 Boyles law 1
5.43 Ump < Uav < Urms 1
Or
Pα1
V
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5.4 Vt = V0 (273.15 + t) 1
273.15
Substitute t = -273.150 C Vt = 0
Or
volume of a gas at - 273.150 C is zero indicates that 1
substances fails to exist as gas below this temperature.
5.5
1
1
Isobar
5.6
It states that equal volumes of all gases under same
1
conditions of temperature and pressure contain equal
number of molecules
1
Vα n
5.7 PV=nRT 1
P=m RT
MXV 1
PM = d R T since m = d where M is the molar mass
V &d is the density
R = P V / n T = 105 x 22.7x10 -3
1 x 273 = 8.314 Pa m3/K/mol 1
= 8.314 J/K/mol.
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5.9
The total pressure of exerted by the mixture of non-reactive
1
gases is equal to the sum of the partial pressures of
individual gases.
1
Partial pressure = mole fraction x total pressure.
or
PA = XA X PTotal
5.10
It means that total energy of molecules before and after the
1
collision remains same.
5.11
The two gases will have equal number of molecules
1
.This is according to Avagadro’s law which states that equal 1
volumes of different gases under similar conditions of
temperature and pressure contains equal number of
molecules.
5.12 Volume will be doubled. 1
Since v α n - according to Avogadro’s law. 1
5.13
i) The volume occupied by the gas molecule is negligible as
1
compared to the total volume of the gas.
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5.16
2
Z=1
5.21 Gas A 1
Higher the critical temperature ,greater the inter molecular
force of attraction 1
5.22 Surface tension is defined as the force acting on unit length 1
perpendicular to the line drawn on the surface of the liquid.
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5.24 i) Attractive forces between the molecules 1
ii) Temperature. 1
V2 = 1x175 = 228.75 d m3 1
0.8
5.26 Gay-Lussac’s law P1 = T1 1
P2 T2
5.27 P1V1 = P2 V2 1
T1 T2
1x1200 = 0.5xV2 1
300 250
V2 = 2000 dm3
5.28 i)Temperature 1
ii) Molecular mass of a gas 1
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5.2 A gas that follows Boyle’s law, Charles law & Avogadro’s 1
law strictly is called an ideal gas
At constant T V α 1/P – Boyles law 1
At constant P V α T_ Charles Law
At constant P& T V α n Avogadro’s Law
1
.. . V α n T/p
PV= nRT where R is constant called as gas
constant.
5.3 1) Gases consists of large number of tiny particles, of 1
negligible volume , identical particles called as atoms or
molecules
1
2) There is no force of attraction between these particles
3) These particles are always in constant random motion
1
4) The particles of a gas move in all possible directions in a
straight line
5) Collisions of gas molecules are perfectly elastic
6) Different particles in the gas have different speeds & hence
different kinetic energies
7) The average kinetic energy of gas molecules is directly
proportional to the absolute temperature.
Note: Write any three- each carry 1 mark
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5.5 i) Density of liquid decreases with increase in temperature 1
ii) Surface tension decreases with increases in temperature
1
iii) vapour pressure of the liquid increases with increase in 1
temperature .
5.6 PV = nRT - ideal gas equation. 1
n = PV/RT.
n = 1x 0.5/ 0.083x300. 1
= 2x 10-2 mol.
n = m/M , M = m/n = 4x 10-2/2x 10-2 1
= 2g/mol
5.7 PV=n1 R T1=n2RT2 since pressure and volume kept 1
constant n1T1 = n2T2
(m 1/M1)T1=(m2/M2)T2 Where m & M are mass & 1
molecular mass
M2 =M1m2 T2/m1T1
Substituting
1
M2= (2x 2.9x368)/(0.184x290)
M2=40g mol-1
5.8 n=m/M 1
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I PUC – CHEMISTRY
CHAPTER - 06
Thermodynamics
One mark questions
1. Define System.
2. Define surroundings.
3. What is an open system? Give one example.
4. What is closed system? Give one example.
5. What is an isolated system? Give one example.
6. What is an extensive property? Give example.
7. What is an intensive property? Give example.
8. What is isothermal process?
9. What is an adiabatic process?
10. Write an expression for work done during an isothermal reversible expansion of an
ideal gas.
11. State I law of Thermodynamics.
12. Write mathematical expression to represent I law.
13. Define Enthalpy.
14. Write mathematical statement of enthalpy.
15. What is an exothermic reaction?
16. Give one example for exothermic reaction.
17. What is an endothermic reaction?
18. Give one example for endothermic reaction.
o
19. Define heat of a reaction (∆ H r)
20. Define standard enthalpy of formation.
21. State Hess’s law of constant heat summation.
22. What is spontaneous process?
23. Give one example for spontaneous reaction.
24. Define entropy.
25. Write the S.I.Unit of entropy.
26. State second law of thermodynamics.
27. Define free energy.
28. Write mathematical statement of free energy.
29. Define standard free energy change for a reaction.
30. Out of Diamond and graphite which one has zero value of standard free energy of
formation.
31. What is the change in entropy when sugar is dissolved in water?
32. What happens to entropy when water freezes?
33. Give the mathematical form of Gibbs-Helmholtz equation.
34. What is the state of a chemical reaction when i) ∆G = 0 ii) ∆G > 0 iii) ∆G <0
35. Mention the sign of ∆H for the formation of explosives.
36. Write the thermochemical equation for combustion of Benzene( l )
37. Write the mathematical statement of II law of thermodynamics.
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38. How is change in enthalpy related to change in internal energy?
39. What is meant by free expansion?
40. State III Law of thermodynamics.
41. Define reversible process.
42. Define irreversible process.
43. Define internal energy.
44. Give an expression for the work done during an adiabatic process.
45. Define the term state function.
46. What is state of a system?
47. What is standard state of a system?
48. Define Enthalpy of combustion.
49. How is standard free energy change of a reaction is related to equilibrium constant?
50. What is the change in internal energy of a system if 10 joules of heat is supplied to it
and 15 joules of work is done by it?
51. Give a chemical reaction for which ∆H = ∆U.
52. A closed thermos flask containing hot coffee represents what type of a system.
53. What is the relationship between ∆H and ∆U for the reaction.
PCl5(g) PCl3(g) + Cl2(g)
54. Choose the correct answer:
a) A thermodynamic state function is a quantity
i) used to determine heat changes
ii) whose value is independent of path
iii) used to determine pressure, volume work
iv) whose value depends on temperature only
b) For the process to occur under adiabatic conditions, the correct condition is,
i) ∆T = 0 ii) ∆p = 0 iii) q = 0 iv) w = 0
c) The enthalpies of all elements in their standard states are
i) unity ii) zero iii) < 0 iv) different for each element
d) ∆UΘ of combustion of methane is –XKJ mol-1. The value of ∆HΘ is
i) = ∆UΘ ii) >∆UΘ iii) <∆UΘ iv) 0
e) The enthalpy of combustion of methane, graphite and dihydrogen at 298K are
-890.3 kJ mol-1 , - 393.5 k J mol-1 and - 285.8 kJ mol-1 respectively. Enthalpy
of formation of CH4(g) will be
i) -74.8 k J mol-1 ii) -52.27 k J mol-1
iii) +74.8 k J mol-1 iv) + 52.26 k J mol-1
f) A reaction , A + B → C + D + q is found to have a positive entropy change.
The reaction will be
i ) possible at high temperature
ii) possible only at low temperature
iii) not possible at any temperature
iv) possible at any temperature
Two Marks questions
1. In a process, 701J of heat is absorbed by a system and 394J of work is done by the
system. What is the change in internal energy for the process?
2. For the reaction; 2Cl (g) → Cl2(g) ; what will be the signs of ∆H and ∆S?
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3. Define standard Enthalpy of vapourisation.
4. Write thermochemical equation for the vaporization of Ethanol.
5. Calculate the Enthalpy of vapourisation of Ethanol, given enthalpies of formation of
liquid ethanol and gaseous Ethanol as -277.6kJ and -235.4kJ respectively.
6. Define standard enthalpy of fusion or molar enthalpy of fusion.
7. Define standard enthalpy of sublimation.
Θ
8. Define enthalpy of atomization (∆aH )
9. Define bond dissociation enthalpy.
10. For a equilibrium reaction.
A + 2B C ∆H = + 400kJ and ∆S is +200 J/K. Calculate the
temperature above which the reaction becomes spontaneous
11. For Cl2 → 2Cl . Assign the signs for ∆H and ∆S
(g) (g)
Θ
12. Define enthalpy of a solution ∆solH
13. For the reaction
4Fe(s) +3O2(g) → 2Fe2O3(s) Entropy change and enthalpy change at 298K are
-549.4 J|K|mol and -1648 x 103 J | mol respectively. Calculate the free energy
change for the reaction.
14. For an isolated system ∆U = 0; what will be ∆S.
15. Comment on the thermodynamic stability of NO(g) and NO2(g) given
½ N2(g) + ½ O2(g) → NO(g) ; ∆fHΘ = 90 kJ mol-1
NO(g) + ½ O2(g) → NO2(g) ; ∆fHΘ = -74 kJ mol-1
Θ -1
16. Given : N2(g) + 3H2(g) → 2NH3(g) ; ∆rH = -92.4 kJ mol
What is the standard enthalpy of formation of NH3 gas.
17. Explain the spontaineity of Exothermic reactions using Gibb’s equation.
18. Explain the spontaineity of endothermic reactions using Gibb’s equation.
19. Calculate the entropy change in surroundings when 1.0 mol of H2O( l ) is formed
under standard conditions. Given ∆HΘ = -286 kJ mol-1
20. Under what conditions ∆H < ∆U. Give an example.
21. For an isolated system ∆U = 0; what will be ∆S?
-1 -1 -1
22. For a reaction at 298 K 2A + B → C ∆H = 400 kJ mol and ∆S = 0.2 kJ k mol .
At what temperature will the reaction become spontaneous considering ∆H and ∆S to
be constant over the temperature range?
23. Calculate the heat of formation of Carbon-monoxide from the following data.
i) C(s) + O2(g) → CO2(g) ; ∆fH = -393.5 kJ
ii) CO(g) + ½ O2(g) → CO2(g) ; ∆fH = -282.8 kJ
24. Calculate the work done when a gas expands at a constant temperature from volume
2 x 10-3 m3 to 4 x 10-3 m3 against a constant pressure of 1.2 x 105 Nm-2.
25. Define : specific heat capacity, Molar heat capacity.
-1
26. Standard enthalpy of vapourisation of water at 373 K is 40.66 k J mol . Calculate
internal energy of vapourisation.
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3 and 4 marks questions.
1. The reaction of cyanamide, NH2CN(s) with oxygen was affected in a bomb
calorimeter and ∆U was found to be -742.7 kJ mol-1 of cyanamide at 298K. Calculate
the enthalpy change for the reaction at 298 K.
NH2CN(s) + 3/2 O2 (g) → N2(g) + CO2(g) +H2O( l )
2. Calculate the number of kJ necessary to raise the temperature of 60 g of aluminium
from 35o to 55o C. Molar heat capacity of Al is 24 J mol-1 K-1.
3. Calculate the enthalpy change on freezing of 1.0 mol of water at 10.0oC to ice at -
10.0oC. ∆fusH = 6.03 kJ mol-1 at 0oC. Cp [H2O( l )] = 75.3 J mol-1 k-1.
Cp[H2O(s)] = 36.8 J mol-1 k-1.
4. Enthalpy of combustion of carbon to carbon-di-oxide is -393.5 k J mol-1. Calculate
the heat released upon formation of 35.2g of CO2 from carbon and oxygen gas.
5. Calculate the enthalpy of the reaction
N2O4 (g) + 3CO(g) → N2O(g) + 3CO2(g)
Given that : ∆fH CO(g) = -11- k J mol-1
∆fH CO2(g) = -393 k J mol-1
∆fHN2O(g) = 81 k J mol-1
∆fH N2O4(g) = 9.7 k J mol-1
6. Calculate the standard enthalpy of formation of CH3OH( l ) from the following data.
i) CH3OH( l ) + 3 O2(g) → CO2(g) + 2H2O( l ) ; ∆fHΘ = -726 kJ mol-1 → (i)
2
ii) C(s) + O2(g) → CO2(g); ∆cHΘ = -393 kJ mol-1 → (ii)
Θ -1
iii) H2(g) + ½ O2(g) → H2O( l ) ; ∆fH = -286 kJ mol →(iii)
7. Calculate the enthalpy change for the process
CCl4(g) → C(g) + 4 Cl(g) and calculate bond enthalpy of C – Cl in CCl4(g)
Given : ∆vapHΘ (CCl4) = 30.5 kJ mol-1
∆fHΘ (CCl4) = -135.5 kJ mol-1
∆aHΘ ( C) = 715.0 kJ mol-1 where ∆aHΘ is enthalpy of atomisation
∆aHΘ (Cl2) = 242 kJ mol-1
8. For a reaction ; 2A (g) + B(g) → 2D(g)
∆U298 = -10.5 kJ and ∆SΘ = -44.1 J k-1.
Calculate ∆U298 for the reaction and predict whether the reaction is spontaneous
or not.
9. The equilibrium constant for the reaction is 10. Calculate the value of ∆GΘ ; given
R = 8 J k-1 mol-1 ; T = 300 K
10. Explain the determination of ∆U using bomb caloriemeter.
11. Explain the determination of ∆H using caloriemeter.
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Thermodynamics
One mark Answers
1. It is the specific part of the universe in which energy changes are taking place.
2. Rest of the universe which surrounds the system.
3. A system is said to be open if both matter and energy can be exchanged with the
surroundings. Example: Water kept in an open beaker.
4. A system is said to be closed if it exchanges only energy with the surroundings.
Example. Water kept in a closed container.
5. A system is said to be isolated if it neither exchanges matter nor energy. Example:
Coffee taken in a thermos flask.
6. Extensive properties of a system are the properties which depend upon the quantity of
the matter present in the system. Example: Volume, internal energy, Enthalpy, heat
capacity etc.
7. Intensive properties of a system are the properties which do not depend upon the
quantity of the matter present in the system. Example: pressure, temperature, density,
specific heat, surface tension etc.
8. A process is said to be isothermal if the temperature of the system remains constant.
(dT = 0 )
9. A process is said to be adiabatic if no heat exchange between the system and
surroundings takes place. (dq = 0)
P
10. W = -2.303 nRT log 1
P2
V
W = - 2.303 nRT log 2
V1
11. Energy can neither be created nor destroyed, it can be transformed from one form to
another.
12. ∆U = q + w, ∆U = change in internal energy
q = heat supplied
w = work done on the system
13. It is the sum of the internal energy and pressure volume energy.
14. H = U + PV H = Enthalpy
U = Internal energy
PV = pressure volume energy
15. A reaction in which heat energy is evolved is an exothermic reaction.
16. C (s) + O2 (g) CO2 (g) ; ∆H = -393.5 k J.
17. A reaction in which heat energy is absorbed is an endothermic reaction.
18. N2(g) + O2 (g) 2 NO (g)
19. The change in heat that takes place in a chemical reaction represented by balanced
chemical equation.
20. The change in enthalpy that takes place when one mole of compound is formed from
its constituent elements, at standard conditions. [298 K, 101.3 k.Pa]
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21. The heat change that takes place in a chemical reaction is independent of time taken
and number of intermediate steps involved.
22. A process that can take place on its own with or without initiation is called
spontaneous process.
23. Zn + H2SO4 Zn SO4 + H2 ↑
24. Entropy is a measure of randomness or disorder of a system.
25. Joule / Kelvin / mole or JK-1 mol-1
26. All spontaneous processes are thermodynamically irreversible
27. The amount of energy available for doing useful work under conditions of constant
temperature and pressure.
28. G = H – TS. G = free energy
H = Enthalpy
S = Entropy
T = Temperature on Kelvin scale
29. The change in free energy that takes place when the reactants in their standard states
are converted into product in their standard states at 298K and 101.3kPa.
30. Graphite.
31. Increases (or) positive
32. Decreases (or) negative
33. ∆G = ∆H - T∆S
34. i) Reaction attains equilibrium
ii) Reaction is non spontaneous
iii) Reaction is spontaneous
35. Positive
36. C6H6 ( l ) ) + 15 O2 ( g ) → 6 CO2(g) + 3 H2O( l) ∆H = - qkJ
2
37. ∆S > 0 or ∆S system + ∆S surrounding > 0
38. ∆H = ∆U + ∆(g)nRT
39. Expansion of a gas in vacuum is called free expansion.
40. Entropy of perfectly crystalline solid at absolute zero is zero.
41. A process which can be reversed at any instant of time by increasing the opposing
force by an infinitesimal amount.
42. A process which is carried out rapidly so that the system does not get a chance to
attain equilibrium.
43. The energy possessed by the system due to its nature, chemical composition and
thermodynamic state.
44. W = n Cv(T2 – T1) for ‘n’ moles of a gas.
45. The variables like temperature, pressure, volume etc, which define the state of a
system are called state functions.
46. Condition of the system expressed by giving definite values for its properties such as
temperature, pressure, volume.
47. The state of a system at 298K and 101.3 k.Pa is known as standard state of a system.
48. The change in enthalpy that takes place when one mole of a substance is completely
burnt in air or oxygen at a given temperature.
49. ∆Go = - 2.303 RT log KP
50. ∆U = q – w
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∆U = 10 – 15
∆U = - 5 joules
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6. The enthalpy change that accompanies melting of one mole of a solid substance in
standard state is called standard enthalpy of fusion or molar enthalpy of fusion.
∆fus HΘ
Θ
7. Standard enthalpy of sublimation, ∆subH is the change in enthalpy when one mole of
a solid substance sublimes at a constant temperature and under standard pressure.
(1 bar)
8. It is the enthalpy change on breaking one mole of bonds completely to obtain atoms
in the gas phase.
9. It is the change in enthalpy when one mole of covalent bonds of the gaseous covalent
compound is broken to form products in the gaseous phase.
10. ∆G = ∆H – T ∆S
At equilibrium ∆G = 0, ∆H = T ∆S
∆H 400 × 10 3
T= =
∆S 200
T = 2000 K
11. ∆H = + ve , ∆S = + ve
12. It is the change in enthalpy when one mole of a substance is dissolved in a specified
amount of a solvent.
13. ∆G = ∆H - T∆S
∆G = -1648 X 103 – [(298) (-549.4)]
= -1648000 + 163721.2
= -1484278.8 J/mol = -1484.27 kJ/mol
14. Change in internal energy (∆U) for an isolated system is zero because it does not
exchange any energy with the surroundings. But entropy tends to increase in case of
spontaneous reaction. Therefore, ∆S > 0 or positive.
Θ
15. for NO(g) ; ∆fH = +ve : unstable in nature
For NO2(g) ; ∆fHΘ = -ve : stable in nature.
Θ -1
16. ∆fH NH3(g) = -(92.4) / 2 = -46.2 kJ mol
17. Gibb’s equation is ∆G = ∆H – T ∆S (1)
For exothermic reaction ∆H is –ve
i) If ∆S is +ve according to equation (1)
∆G is –ve, reaction is spontaneous at all temperature.
ii) If ∆S is –ve, according to equation (1)
∆G is –ve at low temperature such that
T ∆S < ∆H. Reaction is spontaneous.
18. Gibb’s equation is ∆G = ∆H – T ∆S (1)
For endothermic reaction, ∆H is +ve
i) If ∆S is +ve according to equation (1)
∆G is –ve, at high temperature
such that T ∆S > ∆H. Reaction is spontaneous
ii) If ∆S is –ve, according to equation (1)
∆G is always +ve. Reaction is nonspontaneous at all temperature.
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q rev (286000 Jmol −1 )
∆S(surroundings) = =
T 298K
= 959 J k-1 mol-1
ng
20. ∆H < ∆U ; if ∆ is negative
Example: N2(g) + 3H2(g) → 2NH3(g)
∆ng = 2 – 4 = -2
21. Change in internal energy (∆U) for an isolated system is zero because it does not
exchange any energy with the surroundings. But entropy tends to increase in case of
spontaneous reaction. Therefore, ∆S > 0 or positive.
22. According to Gibbs – Helmholtz equation;
∆G = ∆H – T ∆S
∆H
For ∆G = O ; ∆H = T∆S or T =
∆S
−1
(400kJmol )
T= = 2000 k
(0.2kJk −1 mol −1 )
Thus, reaction will be in a state of equilibrium at 2000K and will be spontaneous
above this temperature.
23. Required equation
C(s) + ½ O2(g) → CO(g) ; ∆fH = ?
Subtract equation (ii) from (i)
C(s) + O2(g) → CO2(g) ; ∆H = - 393.5 kJ
CO(g) + ½ O2(g) → CO2(g) ; ∆H = - 282.8 kJ
(Subtract) C(s) + ½ O2(g) - CO(g) → ∆H = (-393.5 + 282.8)
Or C(s) + ½ O2(g) → CO(g); ∆fH = -110.7kJ
24. W = -P∆V
P = 1.2 × 105 Nm-2
∆V = V2 – V1 = (4 × 10-3) – (2 × 10-3) – 2 × 10-3 m3 W = ?
= - 1.2 × 105 Nm-2 × 2 × 10-3 m3
= -2.4 × 102 Nm
= - 2.4 × 102 J (since Nm = J)
Work done by the system = -2.4 × 102 J
25. Specific heat capacity : It is defined as the quantity of heat required to raise the
temperature of 1 gram of a substance by 1oC or 1 K.
Molar heat capacity: It is defined as the quantity of heat required to raise the
temperature of 1 mol of a substance by one degree celsius or one Kelvin.
26. H2O( l ) H2O(g)
∆n = ηgp - ηgR
=1–0
=1
∆H = ∆U + ∆ηgRT
∆U = ∆H - ∆ηgRT
= 40.66 – (1) × 8.314 × 10-3 × 373
= 40.66 – 3.1011
= 37.5589 k J mol-1
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3 and 4 marks Answers
1
1. ∆U – 742.7 kJ mol-1 ; ∆ng = 2 – 3/2 = + mol
2
R= 8.314 x 10-3 kJ k-1 mol-1 ; T = 298 K
According to the relation, ∆H = ∆U + ∆ng RT
∆H = (-742.7 kJ) + ( ½ mol) x (8.314 x 10-3 kJ k-1 mol-1) x 298K
= - 742.7 kJ + 1.239 kJ = -741.5 kJ
60 g
2. No. of moles of Al(m) = = 2.22 mol
(27 gmol −1 )
Molar heat capacity (c ) = 24 J mol-1 k-1
Rise in temperature (∆T) = 55 – 35 = 20oC = 20 K
Heat evolved (q) = c × m × T
= (24 J mol-1 k-1) × (2.22 mol) ×20 K
= 1065.6 J = 1.067 kJ
10
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C(s) + 2H2(g) + ½ O2(g) → CH3OH( l ) ; ∆fHΘ = ± ?
Multiply equation (iii) by 2 and add to equation (ii)
C(s) + 2H2(g) + 2O2(g) → CO2(g) + 2H2O( l )
∆H = -(393 + 522) = - 965 kJ mol-1
Subtract equation (i) from equation (iv)
CH3OH( l ) + 3 O2(g) → CO2(g) + 2H2O( l ) ; ∆H = -726 kJ mol-1
2
Subtract C(s) +2H2(g) + ½ O2(g) → CH3OH( l ) ; ∆fHΘ = -239 kJ mol-1
7. The available data is
i) CCl4( l )→ CCl4(g) ∆vapHΘ = 30.5 kJ mol-1
ii) C(s) + 2Cl2(g) → CCl4 ( l ), ∆fHΘ = - 135.5 kJ mol-1
iii)C(s) → C(g), ∆aHΘ = 715.0 kJ mol-1
iv) Cl2(g) → 2Cl(g) , ∆aHΘ = 242 kJ mol-1
The equation we aim at is
CCl4(g) → C(g) + 4Cl(g); ∆H = ?
Equation (iii) + 2 x equation (iv) – equation (i) – equation (ii) gives the required
equation with
∆H = 715.0 + 2(242) – 30.5 – (-135.5) kJ mol-1
= 1304 kJ mol-1
Bond enthalpy of C-Cl in CCl4 (average value)
1304
= = 326 kJ mol-1
4
8. ∆HΘ = ∆UΘ + ∆ngRT
∆UΘ = -10.5 kJ ; ∆ng = 2 – 3 = -1 mol
R = 8.314 x 10-3 kJ mol-1 ; T = 298 K
∴∆HΘ = (-10.5 kJ ) + [(-1mol) x 8.314 x 10-3 kJ k-1mol-1 x (298K)]
= - 10.5 kJ – 2.478 kJ = -12.978 kJ
According to Gibb’s Hemholtz equation
∆GΘ = ∆HΘ - T∆SΘ
∆GΘ = (-12.978 kJ ) – (298K) x (-0.0441 kJ k-1)
= - 12.978 + 13.142
= - 12.978 + 13.142
= 0.164 kJ
Since ∆GΘ is positive, the reaction is non spontaneous in nature.
9. ∆GΘ = - RT in K = -2.303 RT log K
R = 8.0 J k-1 mol-1 ; T = 300 K ; k = 10
∆GΘ = - 2.303 x ( 8 J k-1 mol-1) x (300K) x log 10
= - 5527 J mol-1 = - 5.527 kJ mol-1 .
10. Refer page 163 and 164 of the prescribed text book
11. Refer page 164 of the prescribed text book
***********
11
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CHAPTER-7
EQUILIBRIUM
ONE MARK QUESTIONS WITH ANSWERS. CHAPTER WEIGHTAGE: 13
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15. Write the relationship between Kp and Kc for the reaction
CS2(g) + 4H2(g) CH4 (g) + 2H2S (g)
Ans. np= 1 + 2 = 3, nR = 1 + 4 = 5, ∆n = np – nR = 3-5 = -2
∴ Kp = Kc (RT)∆n , Kp = Kc(RT) -2
∴ Kp = Kc ⇒ Kc > Kp
(RT)2
16. Write Kc expression for the reaction N2(g) + 3H2(g) 2NH3 (g)
Ans. Kc = [NH3]2
[N2] [H2]3
17. The equilibrium constant for the reaction A+B C + D is 10. If the initial concentration
of A and B is doubled then what is the value of equilibrium constant?
Ans. It remains same.
22. In a reversible reaction Qc > K, predict the direction in which the reaction proceeds?
Ans. Net reaction goes from right to left i.e., towards backward direction.
23. Give the relationship Gibb’s free energy change and equilibrium constant
Ans. ∆Go = - 2.303 RTlogK
24. What happens to the rate of forward reaction when the pressure increases
COCl2(g) CO(g) + Cl2 (g) ?
Ans. Increase in pressure decreases the rate of forward reaction.
25. The rate constant values of a certain reaction is 7.2 x 10-10 and 3.9 x 10-7 at 600K and
800K. predict whether reaction is exothermic or endothermic?
Ans. Since rate constant values are increasing with temperature, the reaction is endothermic.
26. In a certain chemical reaction change in pressure does not influence the equilibrium
state. What does it signify?
Ans.The number of moles of gaseous products and reactants are same in the reaction.
27. For the reaction 2SO2 (g) + O2(g) 2SO2(g) ∆H = -qkJ. State whether rate of forward
reaction increases or decreases when temperature is decreased.
Ans. Rate of forward reaction increases.
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28. What happens to rate of forward reaction
N2(g) + O2(g) 2NO(g) ∆H = +qkJ, when pressure is increased?
Ans. Rate of the reaction remains same.
34. Give the conjugate acid of H2O, CO32-, HSO-4, O2- and CH3COO-.
Ans. a) H2O ---- H3+O.
b) CO32- ---- HCO3-
c) HSO-4 ---- H2SO4
d) O2- ---- OH-
e) CH3COO- ---- CH3COOH.
35. Write the conjugate base of H2O, NH+4, H2CO3, HS-, HCl.
Ans. a) H2O --- OH-
b) NH+4 --- NH3
c) H2CO3 --- HCO-3
d) HS - --- S2-
e) HCl --- Cl-
-
36. OH is a Lewis base. Why?
Ans. Since it can donate a pair of electrons.
39. The pKa values of acids x, y and z are 4.2, 9.8 and 6.1 respectively. Which among the
above acid is strongest?
Ans. X
41. A small amount of NH4Cl is added to NH4OH, what happens to ionization of NH4OH?
Ans. Ionisation of NH4OH decreases.
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42. Write solubility product expression of Ag2CrO4.
Ans. Ag2CrO4 2Ag+(aq) + CrO42- (aq)
Ksp= (2s)2 x s Ksp =4s3.
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8) What is homogeneous equilibrium? given an example
Ans. It is an equilibrium in which all the reactants and products are in same phase.
Example: H2(g)+I2(g) 2HI(g)
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19) With an example explain Bronsted Lowry concept of acid and base?
Ans. Consider a reaction CH3COOH + H2O CH3COO- + H3+O
In the above example acetic acid donates a proton hence it is an acid and water
accepts a proton and it is a base.
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29) What is hydrolysis of salt? Give an Example.
Ans. The interaction of cations and anions of salt with water to give acidic or basic or neutral
solution is called hydrolysis.
Example: when sodium acetate undergoes hydrolysis in water it gives basic
solution due to formation of strong base NaOH and weak acid CH3COOH.
2) For the equilibrium 4NH3 (g) +5O2 (g) 4NO (g) +6H2O (g) Discuss the effect of
a) Addition of NH3 b) Addition of oxygen
c) Addition of H2O d) Removal of H2O
Ans. a) Addition of NH3: Addition of ammonia (reactant) increases the concentration of
product that is rate of forward reaction increases.
b) Addition of oxygen: Addition of oxygen increases the concentration of product that
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is rate of forward reaction increases.
c) Addition of water: Addition of water (product) increases the concentration of
reactant that is rate of backward reaction increases.
d) Removal of water: Removal of water (product) decreases the concentration of
reactant i.e. rate of forward reaction increases.
4) Which of the following reactions is affected by increase in pressure? Also mention the
change in direction of equilibrium.
a) CO2 (g) +C(s) 2CO (g) b) C2H4 (g) +H2 (g)C2H6 (g)
c) COCl2 (g) CO (g) +Cl2 (g) d) H2(g) +Br2 (g) 2HBr (g)
Ans. a) Increase in pressure increases rate of backward reaction because nP(2) >nR(1)
b) Increase in pressure increases rate of forward reaction because nR(2) >nP(1)
c) Increase in pressure increases rate of backward reaction because nP(2) <nR(1)
d) Increase in pressure has no effect on effect on the reaction because nP(2) = nR(2)
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7) Explain the factors affecting acidic strength of acids.
Ans. The important factors affecting acidic strengths are
1)The bond strength of H-A: The strength of H-A bond is weak in case of strong acids
hence cleavage of bond becomes easier, whereas the strength of H-A bond is high in
case of weak acids.
2) Polarity of H-A bond: In case of strong acids the electronegativity difference between
H and A is large, hence H-A bond become more polar therefore cleavage of bond
becomes easier ,where as polarity of H-A bond is less in case of weak acids.
8) Derive an expression for ionization constant Ka of weak acid.
Ans. Consider a weak acid HX which partially ionizes in aqueous solution as
HX(aq) H+(aq) + X-(aq)
Initial concentration C 0 0
Equilibrium concentration C-Cα Cα Cα
Where C is the initial concentration in mol/L of the acid, α is the extent of ionization. The
ionization constant of the acid is given by
Ka = [H+] [X-]/[HX] = Cα . Cα / C – Cα
Ka = Cα2 / 1 – α
The above expression is called as mathematical form of Ostwald’s dilution law.
2 Marks Problems
1) The Kc for a certain reaction is 4.5 x 107 at 750K, what is Kc for the reverse reaction?
Ans. Kc1 = 1/Kc = 1/4.5x107 = 0.2222x10-7
Kc 1 =
2.222x10-8
2) For a reversible reaction PCl3(g) + Cl2(g) PCl5(g) Kc is 3.0 at 2700 C find the value of Kp?
Ans. Given
t=2700C For the above reaction
T= t+273 nP=1 , nR=2
=270+273=543K ∆n = nP – nR = 1 – 2 = -1
R=0.0831barlitre/mol K W.K.T KP = Kc(RT)∆n
Kc=3.0 KP = 3.0x(0.0831x543)-1
KP = 3.0/0.0831x543 = 0.06648
3) For the synthesis of ammonia N2(g) + 3H2(g) 2NH3(g) the KP value is 41 at 400K.
Calculate KC for the reaction?
Ans. Given For the above reaction
KP = 41 nP=2 , nR=4
T = 400K ∆n = nP – nR = 2 – 4 = -2
R = 0.0831bar litre / mol K W.K.T KP = Kc(RT)∆n
Kc = Kp/(RT)∆n = 41/(0.0831x400)-2
KC = 41x(0.0831x400)2 = 45300.8
4) For the reaction 2NOCl(g) 2NO(g) + Cl2(g), The equilibrium constant is 3.75 X 10-6
at 1069K. What is equilibrium constant for the reaction 2NO(g) + Cl2(g) 2NOCl(g)?
Ans. Given Kc = 3.75x10-6
W.K.T KC1 =1/Kc = 1/3.75x10-6
= 0.2666x106 = 2.666x10+5
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5) The equilibrium concentrations of ammonia, hydrogen and Nitrogen for synthesis of
ammonia are 1.2x10-2M, 3x10-2 M and 1.5x10-2M respectively, at given temperature
calculate equilibrium constant Kc.
Ans. Given [NH3] = 1.2x10-2M N2 + 3H2 2NH3(g)
-2
[H2] = 3x10 M Kc = [NH3]2/[N2][H2]3
[N2] = 1.5x10-2M = (1.2x10-2)2/(1.5x10-2)x(3x10-2)3
= 0.03556x10—4+2+6
= 0.03556x10+4 = 3.556x102
6) The equilibrium concentrations of hydrogen iodide and hydrogen for the reaction
H2(g) + I2(g) 2HI(g) are 5.86x10-2M and 0.86x10-2M respectively. At given temperature
calculate equilibrium constant Kc.
Ans. Given [HI] = 5.86x10-2 Kc = [HI]2/[H2][I2]
[H2] = [I2] = 0.86x10-2 =
(5.86x10-2)2/0.86x10-2 x 0.86x10-2
=
42.43x10-4+2+2 = 42.43
7) For the reaction 2NO(g) + Br2(g) 2NOBr(g) the equilibrium concentrations of Nitric
oxide, bromine and nitrosyl bromide are 0.0352M, 0.0178M and 0.0518M respectively at
constant temperature, calculate equilibrium constant KC.
Ans. Given [NO] = 0.0352 KC = [NOBr]2/[NO]2[Br2]
[Br2] = 0.0178 KC = (0.0518)2/(0.0352)2(0.0178)
[NOBr] = 0.0518 = 121.66
8) The equillibricum partial pressure of HI , H2 and I2 for the reaction 2HI(g) I2(g) + H2(g)
are 0.04 atm , 0.08atm and 0.08 atm respectively, Calculate equilibrium constant KP for the
reaction.
Ans. Given PHI = 0.04atm KP = PH2xPI2/P2HI
PI2 = 0.08atm = 0.08x0.08/(0.04)2
PH2 = 0.08atm = 0.16
9) For the reaction A+3B 4C,the partial pressure of B and C are 0.8atm and 0.4 atm
respectively. The equilibrium constant KP for the reaction is 24, what is the partial pressure
of A at equilibrium?
Ans. Given KP = 24 KP = Pc4/PA.PB3
PB = 0.8tm PA = Pc4/KP.PB3
Pc = 0.4atm = (0.4)4/24x(0.8)3
PA = ? PA = 0.00208atm
10) The equilibrium constant KC for a reaction is 1.3x102 at 300K. Calculate standard free
energy change for the reaction. State whether the reaction is spontaneous or non-
spontaneous.
Ans. Given R = 8.314J mol-1 K-1 ΔG0 = -2.303RT log KC
T = 300K = -2.302x8.314JK-1mol-1x300Klog 1.3x102
Kc=1.3 x 102 = -5744.14(2 + log 1.3)
ΔG = -12142.54 Jmol-1
0
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Since ΔG0 is negative the reaction is spontaneous
11) standard free energy change for a reaction is 12 KJ at 300K. Calculate equilibrium
constant for the reaction at same temperature.
Ans. Given ΔG0 = 12KJ = 12x103J ΔG0 =-2.303RT log KC
T = 300K log KC =- ΔG0/2.303RT
R = 8.314Jmol-1K-1 log KC =-12000J/2.303x8.314JK-1mol-1x300K
log KC = -2.0891
KC = antilog[+1-1-2.0891]
__
= antilog[ 3. 9109]
Kc = 8.145x10-3
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17) The ionization constant 0.05M propanoic acid is 1.3 x 10-5 . Calculate degree of
ionization.
Ans. Given Ka=1.3 x 10-5
C =0.05M
C =0.05M α = 1.87x10-2
20) The pKa of acetic acid and pKb of ammonium hydroxide are 5.75 and 5.70
respectively. Calculate the pH of ammonium acetate solution.
Ans. pH = 7 + ½[pKa + pKb] = 7 + ½[5.75 – 5.70]
= 7 + ½ X 0.05 = 7 + 0.025 = 7.025
21) The solubility of A2X in water is 1.1 x 10-5 mol/L calculate the solubility product of the
electrolyte.
Ans. S = 1.1 x 10-5 A 2X 2A+ + X2-
Ksp = [A+]2[X2-] = (2s)2 . s = 4s3
= 4 x (1.1 x 10-5)3
= 5.324 x 10-15(mol/L)3
22) The solubility product of silver bromide is 5.0 x 10-13 at 298K. find its solubility.
Ans. Ksp = 5 x 10-13 AgBr Ag+ + Br-
Ksp = [Ag+][Br-]
Ksp = s.s
-13
5 x 10 = s2
s = = 0.7071 x 10-6mol/L
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3 Marks Problems
1) For the reaction N2(g) + 3H2(g) 2NH3(g), The partial pressures of N2 and H2 are 0.8
and 0.4 atmosphere respectively at equilibrium. The total pressure of the system is 2.80
atmospheres. What is KP for the above reaction?
Ans. Given PN2 = 0.8atm PN2 + PH2 + PNH3 = P
PH2 = 0.4atm 0.8 + 0.4 +PNH3 = 2.8
P = 2.8atm PNH3 = 2.8 – 1.2 = 1.6atm
KP = P2NH3/PN2 .P3H2 = (1.6)2/0.8 x (0.4)3 = 50
2) The equilibrium constant at 298K for the reaction Cu(s) + 2Ag+(aq) Cu2(aq) + 2Ag(s)
is 2.0 x 1015. The concentration of Cu2+ and Ag+ in solution are 1.8 x 10-2 mol/L and
3.0 x 10-9mol/L respectively. Predict the direction in which reaction proceed.
Ans. Given[Cu2+] = 1.8 x 10-2 mol/L Qc = [Cu2+(aq)][Ag(s)] / [Cu(s)][Ag+(aq)]2
[Ag+] = 3.0 x 10-9 mol/L = 1.8 x 10-2/(3.0 x10-9)2
Kp = 2.0 x 1015 = 0.2 x 10-2+18 = 2 x 1015
By convention [Ag(s)] = 1 and [Cu(s)] = 1
Qc = KP = 2 x 1015 , hence reaction is at equilibrium
3) 2 moles of N2O4 taken in a flask of 10L capacity is heated to 350K. At equilibrium 50%
of N2O4 was found to be dissociated to give NO2. Find the equilibrium constant for the
reaction.
Ans. Initial concentration of N2O4 = 2/10 mol/L
50% of 2N2O4 is dissociated implies, x = 50/100 = 0.5
N2O4 2NO2
Initial concentration 2/10 0
Equilibrium concentration 2(1-x) /10 2(2x)/10
2(1-0.5) /10 = 0.1 2(2x0.5)/10 = 0.2
2
Kc = [NO4] /[N2O4]
=(0.2)2/0.1 = 0.4
4) Calculate the pKa value of 0.1M weak mono basic acid whose degree of ionisation
1.52 x 10-2
Ans. Given α = 1.52 x 10-2 Ka = Cα2
C = 0.1M =0.1 x (1.52 x 10-2)2= 0.2310 x 10-4
= 2.310 x 10-5
pKa = -log Ka
= - log[2.310 x 10-5] = -[log2.310 – (5)log10]
= +5 – log2.310 = +5 – 0.3636 = 4.6364
5) Calculate the hydrogen ion concentration of 0.1M weak mono basic acid whose
dissociation constant is 4 x 10-10 at 298K.
Ka = 4 x 10-10
Wkt [H+] = Cα = 0.1 x 6.324 x 10-5 = 0.6324x10-5M
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6) Find the pH of 0.05M acid which is 10% ionised at 298K.
Ans. Given c = 0.05
α = 10% = 10/100 = 0.1
wkt [H+] = Cα = 0.05 x 0.1 = 0.005 = 5 x 10-3M
4 Marks Problems
1) The initial molar concentration of reactants A and B are 0.1 M and 0.2M respectively
in the reaction A +B 2C at equilibrium. The concentration of A in the mixture was found to
be 0.06m. Calculate the equilibrium constant.
Ans. Initial concentration of A = 0.1M
Concentration of A at equilibrium = 0.06M
Concentration of A reacted = 0.1 – 0.06m = 0.04M
A + B 2C
Initial concentration 0.1 0.2 0
Equilibrium concentration 0.1 – 0.04 0.2 – 0.04 2 x 0.04 = 0.08
=0.06 =0.16
Kc = [C] /[A][B] = (0.08)2/0.06 x 0.16 = 0.6667
2
C = 0.025 =
α = 2.66 x 10-2
WKT, Ka X Kb = Kw
Ka= Kw/Kb = 10-14/1.77 x 10-5 = 0.5649 x 10-9
5) The Ksp values of BaSO4 and PbSO4 are 1.1 x 10-10 and 1.6 x 10-8 respectively. Which
salt is more soluble?
Ans. Let solubility of BaSO4 is s1 and solubility of PbSO4 is s2
BaSO4 Ba2+ + SO42-
Ksp = [Ba2+] [SO42-]
1.1 x 10-10 = s1.s1
S1 = = 1.0489 x 10-5mol/L
PbSO4 Pb2++ SO42-
Ksp = [Pb2+][SO42-]
1.6 x 10-8 = s2 . s2
S2 = = 1.2649 x 10-4mol/L
S2 > s1 hence PbSO4 is more soluble than BaSO4
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SUBJECT : CHEMISTRY
12. What happens to the oxidation number (O.N.) of an element during oxidation?
19. Name the cell obtained by coupling a zinc electrode with a copper electrode.
20. Identify the oxidant in the following reaction: H2O2 + O3 H2O + 2O2
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QUESTIONS CARRYING TWO MARKS:
3. Define oxidation and reduction in terms of oxygen and hydrogen. Give one example
for each.
6. How are the oxidizing agent and reducing agents defined in terms if oxidation number?
7. Write separate equations for the oxidation and reduction reactions occurring in the
following redox reaction: 2Fe + 2HCl FeCl2 + H2
11. What is a redox couple? Identify the redox couples in the reaction:
13. What is a spectator ion? Give an example of a reaction involving such an ion.
14. Write the formula for the following compounds represented using Stock notation:
15. Using Stock notation, represent the following compounds: Fe2O3, CuO, MnO and
MnO2
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(a) HPO3 2– and (b)PO43-
18. Assign oxidation number to the underlined elements in each of the following
19. Give an example of a redox combination reaction. Mention the species that undergo
oxidation and reduction.
20. Give an example of a redox decomposition reaction. Mention the species that
undergo oxidation and reduction.
21. Give an example of a redox displacement reaction. Mention the species that undergo
oxidation and reduction.
22. Give an example of a redox disproportionation reaction. Mention the species that
undergo oxidation and reduction.
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1. When blue coloured solution of copper sulphate is stirred with a zinc rod, the blue
colour of the solution fades off and the zinc rod is coated with reddish copper metal.
Write the chemical reaction taking place in the above observation and identify the
species undergoing oxidation and reduction.
2. A solution of silver nitrate turns blue slowly on stirring with a copper rod which in turn
gets coated with a white deposit of silver. Write a chemical reaction for this observation
and identify the oxidizing and reducing agents in it.
(iii) MnO4– (aq) + SO2 (g) →Mn2+ (aq) + HSO4– (aq) (in acidic solution)
(iv) H2O2 (aq) + Fe2+ (aq) →Fe3+ (aq) + H2O (l) (in acidic solution)
(v) Cr2O7 2– + SO2(g) → Cr3+ (aq) + SO42– (aq) (in acidic solution)
(a) MnO4– (aq) + SO2 (g) →Mn2+ (aq) + HSO4– (aq) (in acidic solution)
(b) MnO4– (aq) + I– (aq) → MnO2 (s) + I2(s) (in basic medium)
(c) H2O2 (aq) + Fe2+ (aq) → Fe3+ (aq) + H2O (l) (in acidic solution)
(d) Cr2O7 2– + SO2(g) →Cr3+ (aq) + SO42– (aq) (in acidic solution)
5. In the reactions given below, identify the species undergoing oxidation and reduction:
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ANSWERS:
4. Fluorine (F2).
6. Lithium (Li).
8. The term Oxidation number denotes the oxidation state of an element in a compound
ascertained according to a set of rules formulated on the basis that electron pair in a
11. Zero.
12. It increases.
13. It decreases
16. Zero.
17. A setup consisting of a metal in contact with its salt solution is called an electrode.
18. The potential attained by a metal in contact with a solution containing its own ions is
called electrode potential.
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19. The potential attained by a metal in contact with its salt solution of concentration 1
moldm-3 at 298 K.
21. +2
ANSWERS:
1. A chemical reaction in which both oxidation and reduction are taking place
simultaneously is called a redox reaction.
reduction
Oxidation
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5. In terms of oxidation number,
Oxidation:
Oxidation An increase in the oxidation number of an element in a given substance.
Reduction:
Reduction A decrease in the oxidation number of an element in a given substance.
6. Oxidising agent:
agent: A reagent which can increase the oxidation number of an element
Reducing agent: A reagent which lowers the oxidation number of an element in a given
9. +2 + 4 –2 +2 –2 +4 –2
CaCO3 (s) CaO(s) + CO2(g)
10.
10 (i) Let the O.N. of S be ‘ x’
11.
11 A redox couple is defined as having together the oxidized and reduced forms of a
substance taking part in an oxidation or reduction half reaction.
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12.
12 A series of electrode potential values arranged in the increasing or decreasing order
constitute an electrochemical series.
13.
13 An ion which is present in a redox reaction, but does not take part in a reaction during
electron transfer is called a spectator ion.
15.
15 Fe2O3 - Fe2(III)O3 , CuO – Cu(II)O
(+1) + x + 3(-2) = -2
∴ x = +3
X + 4(-2) = -3
∴ x = +5
17.
17 Step 1: Write skeletal equation with O.N of each element.
4+ 2- 0
SO2 + H2S S + H2O.
Step 2: Multiply H2S by 2 to equalize the oxidation numbers on either side of the
equation.
4+ 2 x (2-) 0
SO2 +2 H2S S + H2O.
Step 3: Now, balance S atoms on RHS.
18.
18 (a) NaH2PO4 : O.N. of P = (+1)+2(+1)+x+4(-2); x = +5.
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(b) NaHSO4: O.N of S = (+1) + (+1) + x + 4(-2); x = +6
19.
19 Example for Redox combination reaction:
0 0 +4 –2
C(s) + O2 (g) CO2(g)
In this reaction, the O.N. of ‘C’ increases from 0 to +4. So it is undergoing oxidation.
the O.N. of ‘O’ decreases from 0 to -2. So it is undergoing reduction.
20.
20 Example for Redox decomposition reaction:
-1+1 0 0
2NaH(s) 2Na(s) + H2(g)
In this reaction, the O.N. of ‘Na’ increases from -1 to 0. So it is undergoing oxidation.
the O.N. of ‘H’ decreases from +1 to 0. So it is undergoing reduction.
21.
21 Example for Redox displacement reaction:
+2 +6 -2 0 0 +2 +6 –2
CuSO4(aq) + Zn (s) Cu(s) + ZnSO4 (aq)
In this reaction, the O.N. of ‘Zn’ increases from 0 to +2. So it is undergoing oxidation.
the O.N. of ‘Cu’ decreases from +2 to 0. So it is undergoing reduction.
22.
22 Example for Redox disproportionation reaction:
+1 –1 +1 –2 0
2H2O2 (aq) 2H2O(l) + O2(g)
In this reaction, the O.N. of ‘O’ increases from -1 to 0 as well as decreases from -1 to -2.
So oxygen is undergoing both oxidation and reduction(disproportionation).
23.
23 Among halogens, fluorine (F2) is the most electronegative element; it cannot exhibit any
positive oxidation state. Hence it does not show a disproportionation tendency.
24.
24 (a) 3Mg(s) + N2(g) → Mg3N2(s) - Redox combination reaction
(c) Cr2O3 (s) + 2 Al (s) → Al2O3 (s) + 2Cr(s) - Redox displacement reaction
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(d) 2NO2(g) + 2OH–(aq) → NO2–(aq) +NO3– (aq)+H2O(l) - Redox disproportionation
reaction.
(ii) Starch.
Oxidation
Oxidation
In this reaction, Zn loses 2e - to Cu and hence is undergoing oxidation; Cu2+ is
undergoing reduction to Cu.
2. reduction
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oxidation
2+ 6+ 3+ 3+
Fe + H + Cr2O7 → Cr + Fe3+ + H2O
2+ + 2– 3+
reduction
Step 2: Multiply Cr3+ by 2 and Fe2+ and Fe3+ by 6 to equalize the oxidation numbers on
either side of the equation.
2+ 1+ 6+ 2x3+ 3+
6Fe + H + Cr2O7 → 2 Cr3+ +6 Fe3+ + H2O
2+ + 2–
Step 4: Finally balance H atoms by adding 14H+ on LHS to get a balanced equation as:
3. (ii) MnO4– (aq) + I– (aq) → MnO2 (s) + I2(s) (in basic medium)
. Step 1: Write skeletal equation with O.N of each element Undergoing change in
oxidation number.
Oxidation
7+ 1- 6+ 0
MnO4 (aq) + I– (aq) →
– MnO2 (s) + I2(s)
reduction
Step 2: Multiply I- by 6 and MnO4- by 2 to equalize the oxidation numbers on either side
of the equation.
Step 3: Now, add 8 OH- on RHS to balance –ve charges on either side.
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2MnO4– (aq) + 6I– (aq) → 2MnO2 (s) +3 I2(s) +8OH-
Step 4: Finally balance H and O atoms by adding 4H2O on LHS to get a balanced
equation as:
3. (iii) MnO4– (aq) + SO2 (g) →Mn2+ (aq) + HSO4– (aq) (in acidic solution)
. Step 1: Write skeletal equation with O.N of each element undergoing change in
oxidation number.
Oxidation-2e-
7+ 4+ 2+ 6+
MnO4– (aq) + SO2 (g) → Mn2+ (aq) + HSO4– (aq)
reduction-5e-
Step 2: Multiply SO2 by 5 and MnO4- by 2 to balance +ve charges on both sides.
2 MnO4– (aq) + 5SO2 (g) +2H2O +H+ → 2Mn2+ (aq) + 5HSO4– (aq)
3. (iv) H2O2 (aq) + Fe2+ (aq) →Fe3+ (aq) + H2O (l) (in acidic solution)
. Step 1: Write skeletal equation with O.N of each element undergoing change in
oxidation number
Oxidation-1e-
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1- 2+ 3+ 2-
2+ 3+
H2O2 (aq) + Fe (aq) →Fe (aq) + H2O (l))
reduction-2 x 1e-
Step 2: Since the number of charges on both sides are not equal, 2Fe2+ on LHS and
2Fe3+ on RHS
3.(v) Cr2O7 2– + SO2(g) → Cr3+ (aq) + SO42– (aq) (in acidic solution)
3.(v) solution)
Step 1: Write skeletal equation with O.N of each element Undergoing change in
oxidation number.
Oxidation-2e-
2 x (6+) 4+ 3+ 6+
2– 3+ 2–
Cr2O7 + SO2(g) → Cr (aq) + SO4 (aq)
reduction-3e-
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Cr2O7 2– + SO2(g) → 2Cr3+ (aq) + SO42– (aq)+ H2O(l)
oxidation-2e-
reduction-5e-
Step2: Write out oxidation and reduction separately and balance the atoms other than H
and O.
Step3: Multiply the oxidation reaction with the extent of reduction and reduction reaction
by the extent of oxidation and add.
Step4: Add H+ and 2H2O on LHS to balance H and O atoms in the acid medium to get a
balanced equation.
(b) MnO4– (aq) + I– (aq) → MnO2 (s) + I2(s) (in basic medium)
4.. (b)
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oxidation-2e-
Step2: Write out oxidation and reduction separately and balance the
Step3: Multiply the oxidation reaction with the extent of reduction and reduction reaction
Step4: Add 4OH- on RHS and 2H2O on LHS to balance H and O atoms in the basic medium to
get a balanced equation.
4. (c) H2O2 (aq) + Fe2+ (aq) → Fe3+ (aq) + H2O (l) (in acidic solution)
oxidation-1e-
reduction-2e-
Step2: Write out oxidation and reduction separately and balance the atoms other than H
and O.
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Step3: Multiply the oxidation reaction with the extent of reduction and reduction reaction
Step4: Add 2H+ on LHS and H2O on RHS to balance H and O atoms in the acid medium to get
a balanced equation.
oxidation-2e-
reduction-2x3e-
Step2: Write out oxidation and reduction separately and balance the atoms other than H
and O.
Step3: Multiply the oxidation reaction with the extent of reduction and reduction reaction
Step4: Add H+ and 2H2O on LHS to balance H and O atoms in the acid medium to get a
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balanced equation.
oxidation-2x1e-
reduction-5e-
Step2: Write out oxidation and reduction separately and balance the atoms other than H
and O.
Step3: Multiply the oxidation reaction with the extent of reduction and reduction reaction
Step4: Add required number H+ on LHS and H2O on RHS to balance H and O atoms in the
The species undergoing reduction is: Cl2 (∵ the O.N. of Cl decreases from 0 to -1)
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5.(ii) 2 Na (s) + H2 (g) 2 NaH (s)
In this reaction, the species undergoing oxidation is: Na (∵ the O.N. of Na increases
from 0 to +1).
The species undergoing reduction is: H2 (∵ the O.N. of H2 decreases from 0 to -1)
In this reaction, the species undergoing oxidation is: Fe (∵ the O.N. of Fe increases
from 0 to +2)
The species undergoing reduction is: HCl (∵ the O.N. of H in HCl decreases from +1 to 0 )
*******************
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I P U C QUESTION BANK
4. What is the chemical used in clarke’s process to remove the temporary hardness of
water?
5. What volume of oxygen is produced by one litre of “10 volume” H2O2 at STP?
12. Arrange LiH, NaH, and CsH in the increasing order of ionic character.
13. Arrange H2, D2, T2 in the increasing order of their boiling points.
21. What is the chemical name of zeolite used in softening of hard water?
1
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23. What is the bond angle in H2O molecule?
24. Name the gas liberated by the reaction of zinc with aqueous NaOH solution.
Boil
Mg(HCO3)2 (aq) → ____________ + 2 CO2.
27. Write the names of isotopes of hydrogen. What is the mass ratio of these isotopes?
28. Why does hydrogen occur in a diatomic form rather than in a monoatomic form
29. How can the production of dihydrogen obtained from ‘coal gasification’ be
increased?
30. Describe the bulk preparation of dihydrogen by electrolytic method. What is the role
∆
i) H2(g) + MmOo(s) →
∆
ii) CO(g) + H2(g) →
Catalyst
∆
iii) C3H8(g) + 3 H2O(g) →
Catalyst
Heat
iv) Zn(s) + NaOH (aq) →
32. Discuss the consequences of high enthalpy of H-H bond in terms of chemical
reactivity of dihydrogen.
33. What do you understand by (i) electron- deficient (ii) electron-precise (iii)
2
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34. How do you expect the metallic hydrides to be useful for hydrogen storage?
Explain.
35. How does the atomic hydrogen or oxy hydrogen torch function for cutting and
36. Among NH3, H2O, and HF, which has highest magnitude of hydrogen bonding and
why?
38. Consider the reaction of water with F2 and suggest, in terms of oxidation and
41. Discuss the principle and method of softening of hard water by synthetic ion
exchange resins.
42. Write chemical reactions to justify that H2O2 can function as an oxidizing as well as
reducing agent?
43. What properties of water make it useful as a solvent? What type of compounds can
44. How can saline hydrides remove traces of water from organic compounds?
45. What is the difference between the terms hydrolysis and hydration?
3
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48. With an example explain the oxidizing property of water.
50. With equations explain the action of washing soda on hard water in removing it’s
permanent hardness.
1. Hydrogen
2. Protium—1H1
3. A mixture of carbon monoxide and hydrogen or CO + H2
4. Lime or Ca(OH)2 or Calcium hydroxide.
5. 10 litres.
6. Tritium—1T3
7. As a moderator or to slow down fast moving neutrons.
8. A mixture of carbon monoxide and hydrogen (CO+H2)
9. LiH, BeH2, or MgH2
10. CH4, NH3, H2O, HF etc.
11. Water which does not contain cations and anions is called demineralised water.
12. LiH < NaH < CsH.
13. H2 < D2 < T2.
14. Tritium.
15. Temporary hardness is due to the presence of bicarbonates of calcium and
magnesium in water.
16. Permanent hardness is due to the presence of chlorides and sulphates of calcium
and magnesium.
17. H2O molecules associate due to intermolecular hydrogen bonding.
18. Non-stoichiometric hydrides are hydrogen deficient compounds formed by the
reaction of dihydrogen with d and f block elements.
19. Alkali metal oxides present in glass catalyse the decomposition of H2O2.
20. Sodium hexa metaphosphate or Na6P6O18.
21. Sodium Aluminium silicate-(NaAlSiO4)
4
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22. Ice has low density.
23. 104.50
24. Hydrogen gas
25. Mg(OH)2
Model answers for questions carrying two or three marks.
26. Resemblance of hydrogen with alkali metals:
i) Hydrogen has 1S1 configuration in it’s valence shell and has a tendency to
lose electron to form H+ ion.
ii) Similar to alkali metals hydrogen forms oxides, halides, and sulphides.
Resemblance of hydrogen with halogens:
i) Similar to halogens it can gain one electron and form hydride (H--) ion.
ii) It also forms covalent compounds and exists as a diatomic molecule “H2”
28. Hydrogen molecule has a very high bond dissociation enthalpy . It forms a covalent
bond with another H-atom and exists as a diatomic molecule.
∆
ii)CO(g) + H2(g) → CH3OH(l)
Catalyst
∆
iii)C3H8(g) + 3 H2O(g) → 3CO(g) + 7 H2(g)
Catalyst
5
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Heat
iv)Zn(s) + 2 NaOH (aq) → Na2znO2(aq) + H2(g).
32.Dihydrogen is chemically inert at room temperature due to it’s high H-H bond
dissociation enthalpy. At high temperature it accomplishes the reactions in which it is
converted to H+ or OH—ions and formation of covalent bond by sharing electrons.
33.I) An electron deficient hydride has less number of electrons for writing it’s
conventional lewis structure. Example: diborane-B2H6.
ii)An electron precise hydride has the required number of electrons to write the
conventional lewis structure. Example: methane-CH4.
iii)Electron rich hydrides have excess of electrons which are present as lone
pairs.Example: ammonia-NH3.
34. Metallic hydrides of Ni, Pd, Ce, Ac etc. have the property of absorption of
dihydrogen. The property of absorption of large volume of hydrogen on transition
metals like Pd and Pt is widely used in catalytic reduction / hydrogenation. This
property has high potential for hydrogen storage and as source of energy.
35. Atomic hydrogen produced by the dissociation of dihydrogen with the help of an
electric arc is made is made to combine on the surface to be welded which produces a
very high temperature of 4000k.
Oxy-hydrogen flame generates a high temperature used for cutting and welding
purposes.
36. Fluorine is the most electronegative atom and H-F bond is highly polar leading to
strong intermolecular bonding in H-F.
6
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39. I) PbS(s) + 4H2O2(l) 4H2O(l) + PbSO4 (Redox reaction)
41.Cation exchange resins contain large organic molecules like R—SO3H which are
water soluble. Ion exchange resin ( R—SO3H) is changed to R—Na by treating with
NaCl. The resin exchanges Na+ ions with Ca2+ and Mg2+ ions present in hard water
and make it soft. Here R is anion.
2R—Na(s) + M2+(aq) R2M(s) + 2Na+(aq)
The resin can be regenerated by adding aqueous NaCl solution.
43. Water is a universal solvent due to high value of dielectric constant and dipole
moment.
Ii) water can hydrolyse metallic and non-metallic oxides , hydrides ,carbides etc.
7
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44. Saline hydrides are ionic and contain H—ion which react with water liberating H2
gas.
45. Hydrolysis is reaction in which H+ and OH—ions of water react with a compound to
form products.Hydration is association of one or more molecules of water to form
hydrated compounds.
48. Highly electropositive metals like Na reacts with H2O and reduces H2O to
dihydrogen.
*******************
8
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Chapter 10
S -BLOCK ELEMENTS
s-block elements are those in which the last electron enters the
outermost s-orbital.
As the s-orbital can accommodate only two electrons, two groups (1 & 2) belong
to the s-block of the Periodic Table.
2. Name the elements present in the 1st Group of the Periodic Table
These are called so because they form hydroxides on reaction with water which are
strongly alkaline in nature.
4. Name the elements present in the 2nd Group of the Periodic Table:
These are called so because their oxides and hydroxides are alkaline in nature and
these metal oxides are found in the earth’s crust.
Diagonal relationship is due to the similarity in ionic sizes and /or charge/radius
ratio of the elements.
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7. Which is smaller in size between a metal ion and its parent atom?
The monovalent ions (M+) are smaller than the parent atom.
8. Which group elements show very low ionization enthalpy in the periodic
table?
First group elements (alkali metals)
10. Arrange the first group elements in the decreasing order of Hydration
Enthalpy
The hydration enthalpies of alkali metal ions decrease with increase in ionic sizes.
Li+> Na+ > K+ > Rb+ > Cs+
Li+ has maximum degree of hydration and for this reason lithium salts are mostly
hydrated, e.g., LiCl· 2H2O
Na2CO3·10H2O.
13. Give reason for the higher melting point and boiling point of alkali earth
metals than alkali metals.
The melting and boiling points of these metals are higher than the corresponding
alkali metals due to smaller sizes.
The electrons in beryllium and magnesium are too strongly bound to get excited by
flame. Hence, these elements do not impart any colour to the flame.
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15. Name the gas liberated when alkali metals react with dil acid?
The alkaline earth metals readily react with acids liberating dihydrogen gas .
M + 2HCl →→MCl2 + H2
Radium salts are used in radiotherapy, for example, in the treatment of cancer.
17. Give reason .the compounds of alkaline earth metals are less ionic than
alkali metals
→→→→→→→→
20. What happens when Calcium carbonate is heated to 1200 K?
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2. Lithium and beryllium, shows similarity with which elements .
3. Which elements of s- block are largely found in biological fluids & what is
its importance?
Mono valent sodium and potassium ions and divalent magnesium and calcium ions
are found in large proportions in biological fluids. These ions perform important
biological functions such as maintenance of ion balance and nerve impulse
conduction.
4. Why alkali metals are highly electro positive & they are not found in free
state ?
The loosely held s-electron in the outermost valence shell of these
elements makes them the most electropositive metals. They readily lose electron to
give monovalent M+ ions. Hence they are never found in free state in nature.
The atomic and ionic radii of alkali metals increase on moving down the group i.e.,
they increase in size while going from Li to Cs.
This is because, the Increase in atomic size is more predominant over increasing
nuclear charge and the outer most electrons are very well screened from the
nuclear charge by the inner shell electrons
7. Give reason .the melting point and boiling point of alkali metals are low
The melting and boiling points of the alkali metals are low indicating
weak metallic bonding due to the presence of only a single valence electron in
them.
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8. Give reason for the colour imparted to the flame by alkali metals
The alkali metal atoms have the largest sizes in a particular period of the
periodic table. With This property makes caesium and potassium useful as
electrodes in photoelectric cells.
11. Name the most power full reducing agent & give reason for it .
The alkali metals are strong reducing agents, lithium being the
most and sodium the least powerful reducing agent.
Note--- With the small size of its ion, lithium has the highest hydration enthalpy
which accounts for its high
negative E0 value and its high reducing power.
12.Give reason for the low solubility of LiF & CsI in water.
The low solubility of LiF in water is due to its high lattice enthalpy
whereas the low solubility of CsI is due to smaller hydration enthalpy of its two
ions. Other halides of lithium are soluble in ethanol, acetone and ethylacetate; LiCl
is soluble in pyridine also.
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13. What are Oxo-Acids?give ex .
15. Why Solvay process cannot be extended for the manufacture of potassium
carbonate?
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18.Mention any two Uses of NaCl :
It is used in
(i) The manufacture of soap, paper, artificial silk and a number of chemicals,
(ii) In petroleum refining,
(iii) In the purification of bauxite,
(iv) In the textile industries for mercerising cotton fabrics,
(v) For the preparation of pure fats and oils, and
(vi) As a laboratory reagent.
22. How does the atomic and Ionic Radii of alkaline earth metals vary in
comparison to alkali metals
The atomic and ionic radii of the alkaline earth metals are smaller than
those of the corresponding alkali metals in the same periods. This is due to the
increased nuclear charge in these elements. Within the group, the atomic and ionic
radii increase with increase in atomic number.
23. How does the of Ionization Enthalpy of alkaline earth metals vary in
comparison to alkali metals
The alkaline earth metals have low ionization enthalpies due to fairly
large size of the atoms. Since the atomic size increases down the group, their
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ionization enthalpy decreases The first ionisation enthalpies of the alkaline earth
metals are higher than those of the corresponding Group 1 metals. This is due to
their small size as compared to the corresponding alkali metals. It is interesting to
note that the second ionisation enthalpies of the alkaline earth metals are smaller
than those of the corresponding alkali metals.
24. How does the of Hydration Enthalpy of alkaline earth metals vary &
compare it with alkali metals
The hydration enthalpies of alkaline earth metal ions decrease with increase
in ionic size down the group. Be2+> Mg2+ > Ca2+ > Sr2+ > Ba2+ The hydration
enthalpies of alkaline earth metal ions are larger than those of alkali metal ions.
Thus, compounds of alkaline earth metals are more extensively hydrated than those
of alkali metals, e.g., MgCl2 and CaCl2 exist as MgCl2.6H2O and CaCl2· 6H2O
while NaCl and KCl do not form such hydrates.
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28. Account for the reducing nature of Be even though it has less negative
value of reduction potential .
Like alkali metals, the alkaline earth metals are strong reducing agents. This
is indicated by large negative values of their reduction potentials However their
reducing power is less than those of their corresponding alkali metals. Beryllium
has less negative value compared to other alkaline earth metals. However, its
reducing nature is due to large hydration energy associated with the small size of
Be2+ ion and relatively large value of the atomization enthalpy of the metal.
29. write the general equation for the reaction of alkali earth metals with NH3.
Alkaline earth metals dissolve in liquid ammonia to give deep blue black
solutions forming ammoniated ions.
→→→→→→→→→→→→
From these solutions, the ammoniates, [M(NH3)6]2+ can be recovered.
The sulphates of the alkaline earth metals are all white solids and stable to
heat. BeSO4, and MgSO4 are readily soluble in water; the solubility decreases from
CaSO4 to BaSO4. The greater hydration enthalpies of Be2+ and Mg2+ ions overcome
the lattice enthalpy factor and therefore their sulphates are soluble in water.
The nitrates are made by dissolution of the carbonates in dilute nitric acid.
Magnesium nitrate crystallises with six molecules of water, whereas barium nitrate
crystallises as the anhydrous salt. This again shows a decreasing tendency to form
hydrates with increasing size and decreasing hydration enthalpy. All of them
decompose on heating to give the oxide like lithium nitrate.
→→→ (M = Be, Mg, Ca, Sr, Ba)
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The carbon dioxide is removed as soon as it is produced to enable the reaction to
proceed to completion.
Note; The addition of limited amount of water breaks the lump of lime. This
process is called slaking of lime.
(i) It is an important primary material for manufacturing cement and is the cheapest
form of alkali.
(ii) It is used in the manufacture of sodium carbonate from caustic soda.
(iii) It is employed in the purification of sugar and in the manufacture of dye stuffs.
36.How lime water reacts with limited CO2 and excess CO2 ?
When carbon dioxide is passed through lime water it turns milky due to the
formation of calcium carbonate.
→→→→
On passing excess of carbon dioxide, the precipitate dissolves to form calcium
hydrogen carbonate.
→→→→
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(ii) It is used in white wash due to its disinfectant nature.
(iii) It is used in glass making, in tanning industry, for the preparation of bleaching
powder and for purification of sugar.
Note--Excess of carbon dioxide should be avoided since this leads to the formation
of water soluble calcium hydrogencarbonate.
39.Which gas is liberated when Calcium carbonate is reacted with dil acid ?
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property of setting with water. On mixing with an adequate quantity of water it
forms a plastic mass that gets into a hard solid in 5 to 15 minutes.
43.What are the Uses of cement? Cement has become a commodity of national
necessity for any country next to iron and steel. It is used in concrete and
reinforced concrete, in plastering and in the construction of bridges, dams and
buildings.
The alkali metals tarnish in dry air due to the formation of their oxides
which in turn react with moisture to form hydroxides. They burn vigorously in
oxygen forming oxides.
Lithium forms monoxide,
sodium forms peroxide,
the other metals form superoxides.
The superoxide O2 – ion is stable only in the presence of large cations such as
K, Rb, Cs.
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(M = K,
Rb, Cs)
In all these oxides the oxidation state of the alkali metal is +1. Lithium shows
exceptional behaviour in reacting directly with nitrogen of air to form the nitride,
Li3N as well. Because of their high reactivity towards air and water, they are
normally kept in kerosene oil.
The alkali metals react with water to form hydroxide and dihydrogen.
(M = an alkali metal)
It may be noted that although lithium has most negative E0 value, its reaction with
water is less vigorous than that of sodium which has the least negative E0 value
among the alkali metals. This behaviour of lithium is attributed to its small size and
very high hydration energy. Other metals of the group react explosively with
water.
They also react with proton donors such as alcohol, gaseous ammonia and
alkynes.
The alkali metals readily react vigorously with halogens to form ionic
halides, M+X–. However, lithium halides are somewhat covalent. It is because of
the high polarisation capability of lithium ion (The distortion of electron cloud of
the anion by the cation is called polarisation). The Li+ ion is very small in size and
has high tendency to distort electron cloud around the negative halide ion. Since
anion with large size can be easily distorted, among halides, lithium iodide is the
most covalent in nature.
5.Why do the the alkali metals give blue solution ,when treated with liq NH3?
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The blue colour of the solution is due to the ammoniated electron which absorbs
energy in the visible region of light and thus imparts blue colour to the solution.
The solutions are paramagnetic and on standing slowly liberate hydrogen resulting
in the formation of amide.
Lithium metal is used to make useful alloys, for example with lead to
make ‘white metal’ bearings for motor engines, with aluminium to make aircraft
parts, and with magnesium to make armour plates. It is used in thermonuclear
reactions. Lithium is also used to make electrochemical cells. Sodium is used to
make a Na/Pb alloy needed to make PbEt4 and PbMe4. These organolead
compounds were earlier used as anti-knock additives to petrol, but nowadays
vehicles use lead-free petrol. Liquid sodium metal is used as a coolant in fast
breeder nuclear reactors. Potassium has a vital role in biological systems.
Potassium chloride is used as a fertilizer. Potassium hydroxide is used in the
manufacture of soft soap. It is also used as an excellent absorbent of carbon
dioxide. Caesium is used in devising photoelectric cells.
7.What is the reason for the increasing stability of peroxide & superoxide of
alkali metals down the group?
On combustion in excess of air, lithium forms mainly the oxide, Li2O (plus
some peroxide Li2O2), sodium forms the peroxide, Na2O2 (and some superoxide
NaO2) whilst potassium, rubidium and caesium form the superoxides, MO2. Under
appropriate conditions pure compounds M2O, M2O2 and MO2 may be prepared.
The increasing stability of the peroxide or superoxide, as the size of the metal ion
increases, is due to the stabilisation of large anions by larger cations through lattice
energy effects. These oxides are easily hydrolysed by water to form the hydroxides
according to the following reactions :
The oxides and the peroxides are colourless when pure, but the superoxides are
yellow or orange in colour. The superoxides are also paramagnetic. Sodium
peroxide is widely used as an oxidising agent in inorganic chemistry.
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8. Explain the stability of carbonates & bicarbonates of alkali metals .
The alkali metals form salts with all the oxo-acids. They are generally
soluble in water and thermally stable. Their carbonates (M2CO3) and in most cases
the hydrogencarbonates (MHCO3) also are highly stable to heat. As the
electropositive character increases down the group, the stability of the carbonates
and hydorgencarbonates increases. Lithium carbonate is not so stable to heat;
lithium being very small in size polarises a large CO3 2– ion leading to the
formation of more stable Li2O and CO2. Its hydrogencarbonate does not exist as a
solid.
(i) Lithium is much harder. Its m.p. and b.p. are higher than the other alkali metals.
(ii) Lithium is least reactive but the strongest reducing agent among all the alkali
metals. On combustion in
air it forms mainly monoxide, Li2O and the nitride, Li3N unlike other alkali
metals.
(iii) LiCl is deliquescent and crystallises as a hydrate, LiCl.2H2O whereas other
alkali metal chlorides do not
form hydrates.
(iv) Lithium hydrogencarbonate is not obtained in the solid form while all other
elements form solid
hydrogen carbonates.
(v) Lithium unlike other alkali metals forms no ethynide on reaction with ethyne.
(vi) Lithium nitrate when heated gives lithium oxide, Li2O, whereas other alkali
metal nitrates decompose to
give the corresponding nitrite.
(vii) LiF and Li2O are comparatively much less soluble in water than the
corresponding compounds of other
alkali metals.
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The similarity between lithium and magnesium is particularly striking and arises
because of their similar sizes : (atomic radii, Li = 152 pm, Mg = 160 pm; ionic
radii : Li+ = 76 pm, Mg2+= 72 pm. )
The main points of similarity are:
(i) Both lithium and magnesium are harder and lighter than other elements in the
respective groups.
(ii) Lithium and magnesium react slowly with water. Their oxides and hydroxides
are much less soluble and
their hydroxides decompose on heating. Both form a nitride, Li3N and Mg3N2,
by direct combination
with nitrogen.
(iii) The oxides, Li2O and MgO do not combine with excess oxygen to give any
superoxide.
(iv) The carbonates of lithium and magnesium decompose easily on heating to
form the oxides and CO2.
Solid hydrogencarbonates are not formed by lithium and magnesium.
(v) Both LiCl and MgCl2 are soluble in ethanol.
(vi) Both LiCl and MgCl2 are deliquescent and crystallise from aqueous solution as
hydrates, LiCl·2H2O
and MgCl2·8H2O.
Recovery of some raw material--In this process NH3 is recovered when the
solution containing NH4Cl is treated with Ca(OH)2. Calcium chloride is obtained
as a by-product.
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→→→→
The most abundant source of sodium chloride is sea water which contains
2.7 to 2.9% by mass of the salt. In tropical countries like India, common salt is
generally obtained by evaporation of sea water. Approximately 50 lakh tons of salt
are produced annually in India by solar evaporation. Crude sodium chloride,
generally obtained by crystallization of brine solution, contains sodium sulphate,
calcium sulphate, calcium chloride and magnesium chloride as impurities.
Calcium chloride, CaCl2, and magnesium chloride, MgCl2 are deliquescent
impurities (because they absorb moisture easily from the atmosphere).
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The amalgam is treated with water to give sodium hydroxide and hydrogen gas.
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carbon. Calcium and barium metals, owing to their reactivity with oxygen and
nitrogen at elevated temperatures, have often been used to remove air from vacuum
tubes. Radium salts are used in radiotherapy, for example, in the treatment of
cancer.
Except for beryllium halides, all other halides of alkaline earth metals
are ionic in nature. Beryllium halides are essentially covalent and soluble in
organic solvents. Beryllium chloride has a chain structure in the solid state as
shown below:
In the vapour phase BeCl2 tends to form a chloro-bridged dimer which dissociates
into the linear monomer at high temperatures of the order of 1200 K.
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The ionic radius of Be2+ is estimated to be 31 pm; the charge/radius ratio is nearly
the same as that of the Al3+ ion. Hence beryllium resembles aluminium in some
ways. Some of the similarities are:
(i) Like aluminium, beryllium is not readily attacked by acids because of the
presence of an oxide film on
the surface of the metal.
(ii) Beryllium hydroxide dissolves in excess of alkali to give a beryllate ion,
[Be(OH)4]2– just as aluminium
hydroxide gives aluminate ion, [Al(OH)4]–.
(iii) The chlorides of both beryllium and aluminium have Cl– bridged chloride
structure in vapour phase.
Both the chlorides are soluble in organic solvents and are strong Lewis acids.
They are used as Friedel
Craft catalysts.
(iv) Beryllium and aluminium ions have strong tendency to form complexes,
BeF42–, AlF63–.
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22. How does the setting of cement takes place & what is the role of gypsum in
setting of cement ?
When mixed with water, the setting of cement takes place to give a hard mass.
This is due to the hydration of the molecules of the constituents and their
rearrangement. The purpose of adding gypsum is only to slow down the process of
setting of the cement so that it gets sufficiently hardened.
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Subject: Chemistry
Chapter – 11: P-Block Element
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It accepts electrons from OH – ion.
c) Aluminium is treated with dilute NaOH.
Sodium tetrahydroxoaluminate(III) and hydrogen gas is
liberated.
d) Boron trifluoride is reacted with ammonia.
Form an adduct and results in complete octet around boron.
7. Classify the following oxides as neutral,acidic ,basic or
amphoteric.
CO,B2O3 ,SiO2,CO2.Al2O3,PbO2,Tl2O3.
Acidic-B2O3,SiO2,CO2
Basic-Ti2O3
Neutral-CO
Amphoteric-Al2O3,PbO2.
8. What are allotropes? Name the allotropes of carbon?
Elements having different physical properties and same
chemical properties are known as Allotropes.
Allotropes of carbon – Graphite, Diamond, Fullerene .
9. Write the oxidation states exhibited by elements of group
14?
+2 and +4 .
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10. What is the nature of hybridization in diamond and
graphite?
SP3 and SP2 respectively.
11. write the valence shell electronic configuration of p-block
elements
ns2 np1-6 (except helium )
12. write the chemical composition of borax.
Na2 B4 O7 . 10H2O
13. Which is the catalyst used to convert alcohols directly into
gasoline?
ZSM-5
14. Which is the basic structural unit of silicates?
Sio44-
15. Which is the repeating unit of organosillicon polymer?
R2SiO
16. Name the important oxides of carbon?
CO,CO2
17. Why carbon shows allotropic forms?
Due to property of catenation and Pπ - Pπ bond formation.
18. What happens atomic and ionic radii of p-block elements
along a period?
Decreases.
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19. What happens to ionization enthalphy of p-block elements
of down a group?
Decreases.
20. Name the solid metalloid of p-block elements?
Boron.
21. Which is the most abundant metal in the earth crust?
Aluminium.
22. Which is the simplest boron hydride?
Di borane.
23. Which compound is known as inorganic benzene?
Borazine.
24. Who discovered fullerenes?
H.W.Kroto, E.Smalley and R.F.Curl.
25. What type of hybridization does carbon undergo in
diamond?
Sp3.
26. What type of hybridization does carbon undergo in
Graphite?
Sp2.
27. What is water gas ?
CO+H2.
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28. What is producer gas?
CO +N2.
29. What is dry ice?
Solid CO2.
30. What is the type of hybridization of boron in diborane?
Sp3.
31. Which gas is used in fizzy drinks and fire extinguisher?
CO2.
32. Why diamond donot conduct electricity?
Because it has no free electrons.
33. Name the allotropic form of carbon whose structure
resembles soccer ball?
Fullerene,
34. Why CH4 is more stable than SiH4?
Due to small size of carbon.
35. Mention one use of dry ice?
As a refrigerant for ice cream.
36. Write the equation for the decomposition of steam by tin?
∆
Sn+2H2O ՜ SnO2+2H2.
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Two marks questions:-
37. Write balanced equations for
a) B2H6+O2 →
B2H6+3O2 → B2O3+3H2O
b) BF3+NaH 450 K.
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42. Write the uses of the aluminium.
In making utensils,aeroplane and transportation industry etc.
43. Why Carbon monoxide is poisonous? Explain.
Because its ability to form a complex with heamoglobin.The CO-
Hb complex is more stable than O2-Hb complex and prevents
Hb to bind with oxygen, thus person dies due to lack of oxygen
44. Distinguish between diamond and graphite.
Diamond –each carbon atom is sp3 hybridised and bonded to 4
other carbon atoms. C-C bond length is 154 pm
Graphite-each carbon atom is sp2 hybridised and is bonded to 3
other carbon atoms. C-C bond length is 141.5 pm
45. Why does boron trifluoride behave as a lewis acid?
Octet remains incomplete hence electron deficient and acts as
a lewis acid
46. What is the action of borax on heating?
It first loses water molecules to form sodium metaborate. On
further heating forms glass like material known as borax bead
47. How is orthoboric acid is prepared from borax?
It can be prepared by acidifying an aqueous solution of borax
Na2B4O7+2HCl +5H2O → 2Nacl+4H3BO3
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48. Why is boric acid considered as a weak acid?
Because it is not able to relese H+ ions on its own. It
receives OH- ions from water molecule to complete its
octet in turn releases H+ ions.
49. How to prepare diborane on industrial scale?
Boran trifluride reacts with sodium hydride at 450k forms
diborane.
2BF3+6NaH 450K B2H6 +6NaF
50. Write the structure of diborane
Reffer text book.
51. What is catenation?
Carbon atoms have the tendency to link with one another
through covalent bonds to form chains and rings this property
is called catenation.
52. Why boric acid is considered as a weak acid?
Boric acid is considered as a weak acid because it is not able to
release H+ ions on its own. It receives OH- ions from water
molecules to complete its octet and in turn releases H+ ions.
53. Give one method for industrial preparation of CO.
C+H2O → CO+H2
54. Give one method for laboratory preparation of co.
HCOOH → H2O+CO
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55. Explain why is there a phenomenal decrease in ionization
enthalpy from carbon to silicon?
As carbon is very small in size its ionization energy is high .
however on moving down the group the size of silicon increases
and its ionization enthalpy decreases sharply.
56. How would explain the lower atomic radius of Ga as
compared to Al?
Although Ga has one extra shell than Al , atomic radius is less
than Al this is because the presence of additional 10d-electrons
offer poor screening effect for the outer electrons in Ga ,
hence atomic radius of Ga is less than that of Al
57. Why carbon differs from rest of the members of its family.?
Due to its smaller size, higher electronegetivity, higher
ionization enthalpy and unavailability of d orbitals.
58. Diamond is covalent yet it has high melting point. Why.?
Diamond has a three – dimensional network involving strong
C-C bonds, which are very difficult to break and in turn has high
melting point.
59. Why graphite is used as a dry lubricant in machines running
at high temperature.?
Graphite cleaves easily between the layers and therefore, it is
very soft and slippery for this reason it is used as dry lubricant.
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60. How to obtain carbon dioxide in laboratory?
By the action of dilute HCl on calcium carbonate.
CaCO3+2HCl → Ca Cl2+CO2+H2O
61. Write the equation for the chemical change during
photosynthesis?
6CO2+12H2O → C6H12O6+6O2+6H2O
62. Write the resonance structures of carbon dioxide?
Reffer text book.
63. What are the crystalline forms of silica? Are they
interconvertable?
Quartz,Cristobalite and trydymite.Yes
64. What are silicons.?
Group of organosilicon polymers, which have (R2SiO) as a
repeating unit.
65. Name the important man made silicates.
Glass and cement
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forces it to form only covalent compounds Al shows +3
oxidation state,on moving down the group, due to poor
shielding effect of intervening d and f orbitals and inert pair
effct,the two electrons present in the s-shell are stongly
attracted by the nucleus and not participating in bonding .
hence +1 state becomes more stable down the group. In Ga, In
and Tl, both +1 and +3 oxidation states are observed.
(2) the common oxidation state +4 and +2,down the group +2
oxidation statebecomes common.C and Si shows the +4
state.down the group higher oxidation state less stable because
of inert pair effct.
67. Explain the structure of diborane .
The four terminal hydrogen atoms and the boron atoms lie in
one plane .Above and below this plane ,there are two bridging
hydrogen atoms. The four terminal B-H bonds are regular two
centre –two electron bonds while the two bridge(B-H-B)bonds
are different and can be described in terms of three centre-two
electron bonds as in the figure(refer text book).
68. Explain the anomalus behavior of carbon.
Due to its smaller size ,higher electronegetivity,higher
ionization enthalpy and unavailability of d-orbitals only s and p
orbitals are available for bonding so maximum covalence is 4
and due to catenation it shows allotropic forms.
69. How can you explain higher stability of BCl3 as compared to
TlCl3.?
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Outer electronic configuration- ns2np1.
Bcl3 is more stable than TlCl3 because +3 oxidation state of B is
more stable than +3 oxidation state of Tl,+3 state is highly
oxidizing.
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73. How to synthesis organo silicon polymers?
***************************************
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Chapter -12
Organic Chemistry-Some Basic Principles and Technique
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TWO MARKS QUESTIONS
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ANSWERS TO ONE MARK QUESTIONS
1. a) sp3sp2 b) sp3sp c) sp2sp2 d) sp3sp sp
2.
3. Functional group may be defined as an atom (or) group of atoms which determine the
properties of an organic compound.
4. 1 –Pentanal
5. H3C – CH = CH – CH – CH2 – CH3
|
Cl
6. The polarization of one bond caused by polarization. of adjacent bond due to
difference in electronegativity.
7. Partial displacement of sigma bond pair of electrons away from the substituent is called +I
effect.
8. Partial displacement of bond pair of electrons towards substituent is called -I effect.
9. NO2, - CN, -F, -COOH, -Cl, -Br, -I, -OCH3 etc. are electron with drawing groups
10. Alkyl groups like methyl (-CH3) & ethyl (-CH2 – CH3) are usually considered as electron
donating groups.
11. The permanent polarity is produced by the interaction of lone pair & Pi electrons in
conjugate system of an organic molecule.
12. Shifting of electron pair away from substituent in a conjugate system.
13. Shifting of electron pair towards the substituent in a conjugate system.
14. –Cl, -Br, -I, -NH2, -NHR, -OH, -OR, -SH, -OCH3 etc.
15. –NO2,-CN, -CHO, - COOH, - COOR etc.
16. It is the complete transfer of Pi – electrons of a multiple bond to one of the atom in the
presence of attacking reagent.
17. When the transfer of electrons take place towards the attacking reagent, the effect is
called +E effect attacking reagent, the effect is called +effect
Ex. Addition of H+ to ethene, H+ + CH2 = CH2 CH3 – CH2
18. When the transfer of electron takes place away from the attacking reagent, the effect is
called –effect.
Ex. The addition of cyanide ion (CN-) to carbonyl group
CN +C=O C–O
|
CN
19. A series of organic compounds which can be represented by a general formula is called
Homologous series.
20. Copper sulphate acts as catalyst
21. Nitro compounds, Azo compounds & compounds containing nitrogen in ring
Ex. Pyridine.
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22. +E effect.
23. Fe2 [Fe(CN)6]3
24. Al2O3(alumina)
25.
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ANSWERS TO TWO MARKS QUESTIONS
1. Ans: Freshly prepared ferrous sulphate solution is added to small portion of SFE &
warmed. Then about 2 to 3 drops of Fecl3 solution are added & acidified with
concentrated Hcl. The appearance of a prussain blue colour indicates the presence
of nitrogen.
Fuse
C, N + Na NaCN
Organic compound
Feso4 + 2NaOH Fe(OH)2 +Na2SO4
6NaCN +Fe(OH)2 Na4 [Fe(CN)6]
Sodium Ferocyanide.
3Na4[Fe(CN)6]+ 4Fecl3 Fe4[Fe(CN)6]3 + 12Nacl
Ferric ferrocyanide(Prussian blue)
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containing distilled water. The contents are crushed & filtered. The filterate is
known as sodium fusion extract.
5. Ans: Silver nitrate test:‐ A small portion of SFE is boiled with dil HNO3, cooled & silver
nitrate is added. A white precipitate soluble in ammonium hydroxide, shows the
presence of chlorine.
A pale yellow precipitate slightly soluble in ammonium hydroxide insoluble in
ammonium hydroxide shows the presence of bromine & yellow precipitate
insoluble in ammonium hydroxide shows the presence of iodine
Note: Nacl +AgNO3 Agcl + NaNO3
White
NaBr +AgNO3 AgBr + NaNO3
Pale yellow
NaI+AgNO3 AgI + NaNO3
Yellow
6. Ans: The energy difference between connonical structure & Resonance hybrid is known as
Resonance energy. The Resonance energy of benzene is 36 k calories or 150kJ/mol
7. Ans: Organic compound containing phosphorous is fused with sodium peroxide. The
phosphorous present in the organic compound is oxidised to phosphate. The fused
mass is extracted with water & filterate. The filterate containing sodium phosphate
is boiled with nitric acid & then treated with ammonium molybdate. A yellow
solution of precipitate indicates the presence of phosphorous.
8. Ans: Inductive effect Mesomeric effect
1) It operates in saturated compound 1) It operates in conjugated
double bond System
2) It involves displacement of sigma electrons 2) It involves displacement of pi
electrons
3) It lasts only for a short distance 3) It last over long distance
4) Partial charges are developed 4) Complete +ve & ‐ve charges
are developed
9. Ans: Inductive effect Electromeric effect
1) It Involves partial displacement of sigma 1) Involves complete transfer of pi
electrons electrons
2) Permanent effect 2) Temporary effect
3) Presence of attacking reagent is not 3) Attacking reagent is required
required
4) Partial charges are developed on atoms 4) Complete charge separation takes
place
10. Ans: 1) All the members can be represented by a general formula
2) Every successive members of the series differ by ‐CH2 group.
3) All the members can be prepared by similar methods
4) All the members will have similar chemical properties
11. Ans:The electron deficient species or positively charged ions which are capable of
accepting an electron from substrate molecule are called electrophiles.
Ex: Positive electrophiles: H+,Cl+, Br+, NO2 etc.
Neutral electrophiles: SO3, BF3, AlCl3 etc.
12. Ans: the a negatively charged ions which are capable of donating an electron pair
Eg. Cl‐, Br‐, OH‐ etc
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13. Ans: Symmetrical breaking of a covalent bond, in which each of the two species contain
one electron of shared electron pair is called hemolytic fission or homolysis.
.
Ex cl – cl + cl.
Chlorine free radicals
14. Ans: Un symmetrical breaking of a covalent bond, in which one the species carry bonded
electron pair is called heterolytic fission or heterolysis.
15. Ans: Free radicals can be defined as an atom or group of atoms having an unpaired
electron.
homolysis
Ex. cl – cl cl. + cl. (Chlorine free radicals)
16. Ans: A reaction intermediate formed by heterolytic fission of a covalent bond which
contains one positively charged carbon is called carbocation.
+
Ex. CH3 – Br CH3+
17. Ans: A reaction intermediate formed by heterolytic fission of a covalent bond which
contains one negatively charged carbon is called carbonion.
Ex. CH3 – MgI + I
18. Ans: These are saturated hydrocarbons joined by covalent bond to form ring structure.
Ex. , etc.
19. Ans: These are the compounds containing one benzene ring
Ex. Benzene, Napthalene etc.
20. Ans: These are the compounds containing ring structure in which one or more carbon
atoms are replaced by hetero atoms such as N, S, O etc.
21. Ans: It is done so as to decompose NaCN to HCN & Na2S to H2S
22. Ans: a) 2,2,4‐trimethylhexane b) 6‐chloro‐3‐methyl ‐ 2 hexanone
CH3
|
23. Ans: a) H3C – C – CH – CH2 – CH3 b) cl – H2C – C = CH – CH2 ‐ OH
| | |
CH3 CH3 CH3
24. Ans: A functional group is an atom or group of atoms present in a molecule which
determines the properties of the organic compounds.
Ex: C2H5 – OH, ‐OH is F.G present in ethyl alcohol
CH3COOH, ‐ COOH is F.G. present in Acetic acid.
25. Ans: Two or more compounds having same molecular formula but differ in position of
the same functional group
Ex: CH3 – CH2‐CH2‐OH & CH3 – CH – CH3
|
1 ‐ propanol OH
2 – propanol
26. Ans: Two or more compounds having same molecular formula but differ in the
functional group
Ex. Alcohol and ether
CH3 – O – CH3 CH3 – O – C3H7
Dimethyl ether methyl propyl ether.
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27. Ans:The reaction in which one group replaces another.
Uv
CH4 +Cl2 CH3cl + Hcl
28.Ans: The reaction in which the reagent adds up to the substrate molecule without
elimination of any molecule is called addition reaction
Ni
Ex. CH2 = CH2 + H2 CH3 – CH3
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ANSWERS TO FIVE MARKS QUESTIONS
1. Ans: Principle : A known mass of Organic substance is heated with excess oxygen. The
Carbon and Hydrogen present in the substance are oxidized to Carbon dioxide and water. The
masses fo CO2 and H2O are determined. From which the percentage of Carbon and Hydrogen
can be determined.
Method:
1. The apparatus is arranged as shown in the diagram.
2. It contains a combustion tube connected to a ‘U’ shaped tube containing anhydrous
calcium chloride and a glass bottle containing Potassium hydroxide solution in series [Which
is then connected to guard tube containing anhydrous Calcium chloride to avoid the entry of
moisture and CO2 into the apparatus.]
3. A known mass of organic compound is mixed with cupric oxide and placed in the
combustion tube which is heated strongly.
4. Carbon present in organic compound is oxidized to carbon dioxide and absorbed in
potassium hydroxide solution.
5. Hydrogen present in the organic compound is oxidized to water and absorbed in anhydrous
calcium chloride.
6. The ‘U’ tube and glass bottle are weighted before and after the experiment.
Calculation:
I. Estimation of hydrogen :
a) Mass of organic compound = Wg
b) Mass of ‘U’ tube before experiment = m1g.
c) Mass of ‘U’ tube after experiment = m2g
d) Increase in mass of CaCl2 = Mass of water = (m2-m1g)
e) 18 grams of water contains 2 grams of hydrogen
(m2 – m1)g of water contains
= 0.1111(m2-m1)grams
f) W grams of organic compound contains 0.1111(m2-m1)g of hydrogen
.
100 grams of organic compound contains
.
percentage of hydrogen =
II. Estimation of Carbon:
a) Mass of organic Compound = Wg
b) Mass of glass bottle before experiment = m1g
c) Mass of glass bottle after experiment = m2g
d) Increase in mass of KOH = Mass CO2 = (m2-m1) grams.
e) 44g of CO2 contains 12g of Carbon.
(m2-m1)g of CO2 contains = g of carbon
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= 0.2727(m2-m1)g of carbon
f) W grams of organic compound contains 0.2727(m2-m1)grams of carbon
.
100 grams of organic compound contains
.
percentage of Carbon=
2. Ans: Principle: A known mass of organic compound is heated with concentrated sulphuric
acid. Nitrogen is converted into ammonium sulphate. Which is treated with sodium hydroxide
solution to liberate ammonia. This ammonia is absorbed in excess of standard sulphuric acid.
The unreacted acid is estimated by titration with standard alkali. From which the amount of
ammonia is determined and the percentage of nitrogen in the compound is calculated.
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Percentage of Nitrogen =
3. Ans: Principle: The organic compound containing nitrogen when heated with excess of
copper oxide in the atmosphere of carbon dioxide, gives nitrogen in addition to carbon
dioxide and water.
Traces of nitrogen oxides formed during combustion of organic compound are reduced to
nitrogen by passing the gaseous mixture over a heated copper gauze. The percentage of
nitrogen present in a given organic compound is calculated from the volume of nitrogen
collected over potassium hydroxide solution from a known mass of organic compound.
Procedure: The apparatus used for the estimation of nitrogen by this method is shown in the
figure.
A known mass of organic compound is mixed with copper oxide and placed in the
combustion tube. The carbon dioxide gas is passed through the combustion tube to displace
air present in the tube. The combustion tube is now heated in the furnace. The nitrogen
evolved collects in the nitrometer. The volume of the nitrogen collected is recorded after
adjusting the levels of potassium hydroxide solution in the two limbs are equal. Room
temperature and atmosphere pressure are recoded.
Calculation: Mass of organic Compound = mg
3
Volume of nitrogen in nitrometer = V cm
Room temperature = toC = (273 + t)K
Atmosphere pressure = P1mm
'
Aqueous tension at room temperature = P mm
Pressure of dry nitrogen gas formed = P = (P-P')mm .
Volume of nitrogen at STP (V0) = cm3
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nitric acid does not enter the weighing tube. The Carius tube is now sealed and heated in a
furnace at 3000 C for about six hours.
The tube is than cooled and its narrow end is cut off and the contents are completely
transferred to a beaker by washing with water. The precipitate of silver halide formed is
filtered through a weighed sintered glass crucible. It is washed, dried and weighed.
Observation and calcualteion:
i) Mass of organic compound taken = W 1g
ii) Mass of silver halide obtained = W2g
a) For chlorine: AgCl Cl
143.5g 35.5g
143.5g of AgCl contains 35.5g of chlorine
.
w2g of AgCl will contain g of chlorine
.
= ‘a’ grams (say)
This amount of chlorine was present in w1g of the compound.
.
%Cl2 = X
.
b) For bromine: AgBr Br
188g 80g
188g of AgBr contains 80 g of bromine
g of AgBr will contain g of bromine.
%Br2 = X
c) For Iodine: Agl I
235g 127g
235g of Agl contains 127g of iodine
w2g of Agl will contain g of Iodine
%I2 = X
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CHEMISTRY
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4. How will you prepare benzene from sodium benzoate?
5. What happens when benzene reacts with acetyl chloride in presence of AlCl3.
Represent in form of chemical reaction .
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3) Why is Wurtz reaction not preferred for the preparation of alkanes containing
odd number of carbon atoms? Illustrate your answer by taking one example.
4) State Huckel’s rule. Draw the structure of Pyridine and Furan. Are these
aromatic?
5) Explain the mechanism involved in the chlorination of methane.
(i)
(ii)
(iii)
(iv)
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CHEMISTRY
1) Chain isomerism
2) Sodium
3) 2,3-dimethyl butane
4) Free radical mechanism
5) Staggered conformation
6) No
7) Due to the presence of pi bond in carbon to carbon double bond
8) sp2 hybridisation
9) CHCl = CHCl
10) Bromine
11) No. Free radical is not formed due to high bond dissociation energy of HCl
12) Dilute alkaline potassium permanganate solution.
13) Pd supported over barium sulphate or calcium carbonate poisoned with
quinoline or sulphur.
14) Ozonolysis
15) a. Bayer’s test
b. Bromination
16) As they are linear in nature.
17) Ethanal is formed.
18) 1,1-dichloroethane
19) Trans-2-butene
20) Benzene.
21) Planar
22) Due to delocalization of pi electron charge.
23) Anhydrous aluminium chloride
24) Ortho directing groups -- OH, NH2
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Meta directing groups --- CHO, NO2
25) Electrophilic substitution
26) Kekule
27) Nitronium ion
28) Liquefied natural gas
29) Methane.
1) The decomposition of higher alkane into a mixture of lower alkanes , alkenes etc
by the application of heat is called pyrolysis / cracking.
2) When unbranched alkanes are heated with anhydrous aluminium chloride and
hydrogen chloride isomeric branched alkanes are formed. This process is called
isomerization
3) X is Cis-but-2-ene ; Y is trans-but-2-ene
4)
5)
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6) Conditions necessary for geometrical isomerism:
All compounds containing carbon-carbon double bonds do not show geometrical
isomerism.
The molecules must contain a double bond.
Each of the two carbon atoms of the double bond must have different substituents
which may be same or different.
7)
Due to the occurrence of both methyl groups on the same side of the C=C
bond, the combined effect of the two polar bonds makes cis-but-2-ene
much more polar than trans-but-2-ene.
8)
9)
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It is used to test for unsaturation.
11) Ketone
12) Markovnikov's rule states that, negative part of the addendum (adding molecule)
gets attached to that carbon atom which possesses lesser number of hydrogen
atoms.
13) Sodium salt of butanoic acid is required for the preparation of propane.
14) Alkyl halides on treatment with sodium metal in dry ether solution give
higher alkanes. This reaction is known as Wurtz reaction.
This reaction is used for the preparation of higher alkanes containing even number
of carbon atoms.
15) Sodium salts of carboxylic acids on heating with soda lime (mixture of sodium
hydroxide and calcium oxide) give alkanes containing one carbon atom less than
the carboxylic acid. This elimination of carbon dioxide from a carboxylic acid is
known as decarboxylation.
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16) Alkanes undergo free radical substitution. The examples of this category are
halogenation, nitration and sulphonation.
17) The spatial arrangements, which are obtained by free rotation around sigma
bonds, are called conformation or conformational isomers.
20)
22) Benzene is a planar molecule having delocalized electrons above and below the
plane of ring. Hence, it is electron-rich. As a result, it is highly attractive to electron
deficient species i.e., electrophiles. Therefore, it undergoes electrophilic substitution
reactions very easily. Nucleophiles are electron-rich. Hence, they are repelled by
benzene. Hence, benzene undergoes nucleophilic substitutions with difficulty.
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23) Any Lewis acid like anhydrous FeCl3, SnCl4, BF3 etc. can be used during the
ethylation of benzene.
24) Organic compounds containing only hydrogen and carbons are called
hydrocarbons.
25) The repulsive interaction between the electron clouds, which affects stability of a
conformation, is called torsional strain. Magnitude of torsional strain depends upon
the angle of rotation about C-C bond. This angle is called dihedral angle or torsional
angle. Of all the conformations of ethane, the staggered form has the least torsional
strain and the eclipsed form has the maximum torsional strain.
26)
a) Unusual stability of benzene.
b) According to Kekule, two ortho disubstituted products are possible. But in
practice only one ortho disubstituted product is known.
c) Heat of hydrogenation of benzene is 49.8 kcal/mole, whereas theoretical value of
heat of hydrogenation of benzene is 85.8 kcal/mole. It means resonance energy is
36 kcal/mole.
d) C - C bond length in benzene are equal, (although it contains 3 double bonds and
3 single bonds) and are 1.39 Å.
27)
H
H
H
H H
H H
H H H
H
H
Eclipsed Staggered
28)
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As the s–character increases, the electronegativity of carbon increases and the
electrons of C–H bond pair lie closer to the carbon atom. As a result, partial
positive charge of H–atom increases and H+ ions are set free. The s–character
increases in the order: sp3 < sp2 < sp. Hence, the decreasing order of acidic
behaviour is Ethyne > Benzene > Hexane.
This ozonide is formed as an addition of ozone to ‘A’. The desired structure of ‘A’ can be
obtained by the removal of ozone from the ozonide. Hence, the structural formula of ‘A’
is:
10
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where an electron-rich species is attacked by a nitronium ion (NO2+). Now, CH3–
group is electron donating and NO2– is electron withdrawing. Therefore, toluene will
have the maximum electron density among the three compounds followed by
benzene. On the other hand, m– dinitrobenzene will have the least electron density.
Hence, it will undergo nitration with difficulty.
3) Wurtz reaction cannot be used for the preparation of unsymmetrical alkanes because if
two dissimilar alkyl halides are taken as the reactants, then a mixture of alkanes is
obtained as the products. Since the reaction involves free radical species, a side reaction
also occurs to produce an alkene. For example, the reaction of bromomethane and
iodoethane gives a mixture of alkanes.
The boiling points of alkanes (obtained in the mixture) are very close. Hence, it becomes
difficult to separate them.
4) Huckel’s rule states that, compounds that have (4n + 2) -electrons, are said to
be Aromatic compounds, where n = 1,2,3,4….etc.
Pyridine is aromatic because it folllows Huckel's rule and has 6 pi electrons where n=1.
Furan is also aromatic compound because one of the lone pair of electrons at the oxygen
delocalise towards benzene ring and then it follows Huckel's rule where n=1.
5) Chlorination of methane proceeds via a free radical chain mechanism. The whole
reaction takes place in the given three steps.
11
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Step 1: Initiation:
Step 2: Propagation:
In the second step, chlorine free radicals attack methane molecules and break down the
C–H bond to generate methyl radicals as:
These methyl radicals react with other chlorine free radicals to form methyl chloride
along with the liberation of a chlorine free radical.
Hence, methyl free radicals and chlorine free radicals set up a chain reaction. While HCl
and CH3Cl are the major products formed, other higher halogenated compounds are also
formed as:
Step 3: Termination:
12
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6) (i)
For the given compound, the number of π-electrons is 6.By Huckel’s rule,
4n + 2 = 6; 4n = 4; n = 1
(ii)
By Huckel’s rule, 4n + 2 = 4; 4n = 2 ;
(iii)
By Huckel’s rule, 4n + 2 = 8; 4n = 6;
7) (i) Pen-1-ene-3-yne
(ii) Buta-1,3-diene
13
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(iv) 2-Methyl phenol
8)
This reaction follows Markovnikov’s rule where the negative part of the addendum is
attached to the carbon atom having a lesser number of hydrogen atoms.
14
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Secondary free radicals are more stable than primary radicals. Hence, the former
predominates since it forms at a faster rate. Thus, 1 – bromopropane is obtained as the
major product.
In the presence of peroxide, Br free radical acts as an electrophile. Hence, two different
products are obtained on addition of HBr to propene in the absence and presence of
peroxide.
15
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(ii) Benzene to acetophenone
16
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11) The structure of benzene molecule is best described in terms of molecular orbital
treatment theory. According to this theory, all the C-atoms in benzene are sp2-
hybridized. Two sp2-hybrid orbitals of each C-atom overlap with two sp2-hybrid orbital
of two other C-atoms to form sigma bonds. In this way there are six sigma bonds are
formed between six C-atoms which are 120o apart. Remaining six sp2-orbital of six C-
atoms overlap with 1s orbital of six H-atoms individually to form six sigma bonds. Since
sigma bond results from the overlap of above said planar orbital, all H and C atoms are in
the same plane and their generate a hexagonal ring of C-atoms.
Each C-atom in benzene also has an unhybrid 2pz-orbital containing one electron. These
2pz-orbital are perpendicular to the plane of sigma bonds.
17
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OR
Actually these 2pz-orbital produce a pi-molecular orbital containing six electrons. One
half of this pi- molecular orbital lies above the plane of hexagonal ring and remaining
half below the ring like a sandwich.
18
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CHAPTER‐14
ENVIRONMENTAL CHEMISTRY
I) One mark questions and answers:
1. Name one insecticide?
A. DDT
2. Which acid is not present in acid rain?
HNO3, H2SO4, CH3COOH, H2CO3?
A. CH3COOH
3. Define the term pollution?
A. It is a substance present in the environment in great
proportion than its natural abundance and resulting in
harmful damage effect.
4. Name two gases which are responsible for green house
effect?
A. CO2 and CH4 gases.
5. Which part of the atmosphere contains ozone
layers?
A. Stratosphere contains ozone layers.
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6. What is full form BOD and DDT?
A. BOD‐Biochemical oxygen Demand and DDT‐ Dichchloro
Diphenyl Trichloro ethane.
7. What are PCBs?
A. Poly chlorinated biphenyls (PCBs) are used as cleansing
solvent, detergents and fertilizers cause water pollution
and it is carcinogenic compound.
8. What is PAN?
A. Peroxyacetyl nitrate (PAN) is one of the components of
photo chemical smog and it is powerful eye irritant.
‐
9. What is desirable concentration of F ions and PH of
drinking water?
‐
A. Desirable concentration of F ions is 1ppm or 1mgdm‐3
and PH is 5.5 to 9.5
10. Name the oxides of nitrogen?
A. Nitric oxide (NO) and Nitrogen dioxide (NO2).
11. Which gas caused Bhopal gas tragedy? Give its formula.
A. Methyl isocyanate (MIC) and its molecular formula
CH3N=C =0
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12. Write any two common chemicals of photochemical smog?
A. Acrolein and formaldehyde
13. Which can damage the great historical monument
Tajmahal?
A. Acid rain
(CaCO3 (marble) +H2SO4 Æ CaSO4+H2O+CO2)
14. What is effect of excess of SO42‐ion in drinking water?
A. Excess of SO42‐ ion in drinking water causes laxative effect
(>500ppm)
15. What is the cause of methemeglobinemia?
A. Excess of nitrate ion (>50ppm) in drinking water cause
methemeglobinemia (blue baby syndrome).
16. What is troposphere?
A. The lower regions of atmosphere in which the human beings
along with other organisms live are called troposphere. It
extends up to the high of ~10KM from sea level
17. What is stratosphere?
A. Above the troposphere, between 10 and 50km above sea
level lies is called stratosphere.
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18. Name the harmful radiation emitted from sun?
A. UV radiation
19. Which type of harmful radiations absorbed in ozone
layers?
A. UV radiation
20. Name the types of pollutants cause troposphere pollution?
A. 1. Gaseous air pollutants
2. Particulate pollutants
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23. What type of radiation are absorbed by CO2 in the
atmosphere
A. IR radiations
24. Name the oxide of carbon?
A. CO & CO2
25. What is green house effect?
A. The increase in temperature of atmosphere due to
presence of gases like CH4 , CO2 and water vapours, which
absorb infrared radiation is called green house effect.
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3. Write any two achievement of green chemistry?
A. 1.Development of polystyrene foam sheet packaging
material this Technology allows eliminations CFCS which
contribute to ozone depletion, global warming and ground
level smog.
2. Catalytic hydrogenation of diethanolamine in which
environmental friendly herbicide is produced in less dangerous
ways.
4. Define environmental chemistry?
A. It is the study of chemical and biochemical process occurring
in nature
(OR)
It deals with the study of origin, transport relation, effects and
fates of various chemical species in the environment
5. What do you mean by ozone hole? What are its
Consequences
A. Ozone hole implies distribution of the ozone layer by the
Harmful UV radiations the depletion will virtually result
In creating some sort of holes in the blanket of ozone which
surround us. As a result, the harmful radiations cause skin
cancer, loss of sight and also affect our immune system
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6. What do you mean by Biochemical oxygen demand?
A. Biochemical oxygen demand is the amount of oxygen
required by bacteria to decompose organic matter in a certain
volume of sample of water. Clean water would have BOD value
of less than 5ppm, where as highly polluted water has a BOD of
17ppm or more
7. How does detergent cause water pollution?
A. Tetrachlorothene (Cl2C=CCl2) was used as solvents for dry
cleaning of clothes. This compound is suspected to carcinogenic
and contaminated the suspected to carcinogens for bleaching
cloths in the laundry, hydrogen peroxide (H2O2)is being used
which gives better result and is not harmful detergents produce
pathogens which are diseases causing bacteria and result in
gastrointestinal diseases.
8. Write the methods for management of waste material?
1. Recycling:‐materials are recycled which saves the cast of raw
material and waste disposal.
2. Sewage treatment
3. Burning and Incineration
4. Digesting
5. Dumping
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9. Write the chemical reaction take place during acid rain in
the atmosphere?
A. 1. H2O + CO2 ‐‐‐‐‐‐‐> H2CO3
+ ‐
2. H2CO3 ‐‐‐‐‐‐> H + HCO3
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dissolved oxygen. This is because phytoplanktons are degraded
by bacteria present in water. For their decomposition, they
require a large amount of oxygen. hence, they consume the
oxygen dissolved in water. As a result, the BOD level of water
drops below 6ppm, inhibiting the growth of fish and causing
excessive fish kill.
12. What are harmful effects as depletion of ozone layer?
A. 1) The ozone layer protects the earth from the harmful UV
radiation of the sun, with the depletion of the layer, more
radiation will enter the earth’s atmosphere. UV radiations are
harmful because they lead to the skin cancer and sun burns.
2) They cause death of many phytoplanktons which lead to a
decrease of fish productivity.
3) Increase in UV radiation, decreases the moisture content of
the soil and damages both plants and fibres.
13. What are pathogens? Mention its harmful effect?
A. Pathogens are water pollutants include bacteria and other
organism. They enter water from animal excreta and domestic
sewage.
14. What are harmful effects of acid rain?
A. 1. It is harmful for crops
2. It damages buildings made up of marble.
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14. Write by two harmful effects of oxides of nitrogen?
1. Damage the leaves of plants and retard the rate of
photosynthesis.
2. Nitrogen dioxide is a lung irritant that can lead to an acute
respiratory disease in children.
15. Write any two harmful effects of oxide of sulphur?
1. It causes respiratory diseases e.g. Asthama bronchitis in
human beings
2. It causes irritation to the eyes, resulting in tears and redness.
16. Write the harmful effects of hydrocarbons pollutants?
Mention its sources?
Harmful effects:
1. Hydrocarbons are carcinogenic i.e. they cause cancer
2. They harm plants and shedding of leaves flowers & twinges
Sources: Incomplete combustion of fuel used in automobiles.
17. What are the harmful effects of CO? Mention its sources?
Harmful effects:
1. It is high poisonous to living beings
2. It causes, headache, weak eyesight, nervousness and
cardiovascular disorder
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Sources: 1. incomplete combustion of coal, firewood, petrol
etc….
2. by automobile exhaust
18. Write the harmful effect of CO2 ?mention its sources.
A. Harmful effect:
It causes global warming
Sources: 1. Respiration
2. Burning of fossil fuels for energy
3. By volcanic eruptions
4. Deforestation
5. By decomposition of limestone during the manufacture of
cements.
19. Giving example differentiate b\w viable and non viable
particulate pollutants.
A. 1.viable particulate:‐ They are minute living organisms that
are dispersed in atmosphere.
Ex:‐ Bacteria, fungi, moulds, algae etc….
It may be noted that human being are allergic to some of the
fungi found in air. Fungi can also cause plant diseases
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2. Non viable particulate:‐ They are formed by the
breakdown of larger materials or by condensation of minute
particles and droplets.
Ex. mists, smoke, fumes and dust.
20. During ward war II DDT, was found to be of great use
for which purpose was is used? Why has its use been
banned in India now?
A. It is used to control of malaria and other insect borne
diseases.
After the war, DDT is used in Agriculture to control the
damages caused by insects, weeds and various crop diseases
However, due to adverse effects, its use has been banned
India and it is nonbiodegradable and carcinogenic.
21. Acid rain is known to contain some acids. Name these
acids and where from they come in rain?
A. The acids commonly present in acid rain are nitric acid,
sulphuric acid and carbonic acid. Nitric acid is formed by
oxidation of nitric oxide present in air to NO2 & NO3, which
dissolve in water also present in air.
Sulphuric acid is formed by the oxidation of SO2 result in air
to SO3 followed by dissolution in water.
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CO2 present in the acid dissolves in water to give carbonic
acid.
III) Three marks questions and answers
1. Explain tropospheric pollution?
A. Troposphere pollution occurs due to the presence of
undesirable gases and the solid particles in the air the major
gaseous and the Particulate pollutants presents in the
troposphere as follows.
1. Gaseous air pollutants: These include mainly oxides of
sulphur (SO2&SO3), oxide of nitrogen (NO&NO2) and oxides of
carbon (CO&CO2) in addition to hydrogen sulphide (H2S),
hydrocarbons and other oxidants.
2. Particulate pollutions: These include dust, mist, fumes,
smoke, smog etc…..
2. What is smog? How is classical smog different from photo
chemical smog?
A. Smog is a mixture of smoke, dust partials and small drops of fog.
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¾ It is a mixture of smoke, It is a mixture of
Fog and sulphurdioxide unsaturated
hydrocarbons and
Oxides of nitrogen
3. Statues and monuments in India are affected by acid rain,
how?
A. The air around the statues and monuments in India contains
fairly high levels of the oxides of sulphur and nitrogen.
This is due to a large number of industries and power plants in
the near by areas.
The problem has been further aggravated due to use of poor
quality of coal, kerosene and fire wood as fuel for domestic
purposes.
The states acid rain affects for marble of these statues and
monuments.
CaCO3+H2SO4 ‐> CaSO4+H2O+CO2
As a result, this away and marble is getting discolored and
lusterless.
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4. Carbon monoxide gas is more dangerous than carbon
dioxide gas. Why? Explain
A. It is highly poisonous to living beings because of its ability to
block the delivery of oxygen to the organs and tissues. It binds
to haemoglobin complex to form carboxyl haemoglobin (COHb)
which is about 300 times more stable than oxy‐hemoglobin
complex. In the blood when the concentration of carbon
haemoglobin reaches about 3‐4 percent, the oxygen carrying
capacity blood is greatly reduced. This oxygen deficiency,
results in to headache, weak eyesight, nervousness and
cardiovascular disorder CO2 does not combine with
haemoglobin and hence is less harmful as pollutant but it is the
main contributor forwards green house effect & global
warming.
5. What are pesticides and herbicides? Give examples
A. Pesticides: These are a mixture of two or more substances.
They are used for killing pests. Pests include insects, plants
pathogens, weeds, mollusks etc…., that destroys the plant crop
and spread diseases
ex: ‐ Aldrin and Dieldrin
Herbicides: These are chemicals specially meant for killing
weeds. Ex:‐Sodium chlorate (NaClO3)
Sodium Arsenite (Na3 AsO3)
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6. Define environmental pollution? Name its types?
A. The addition of any undesirable material to air, water and
soil by a nature source
or
Due to human activity to such a level of concentration warm
adversely affects the quality of environment is called
environmental pollution.
Types
1. Water pollution
2. Soil pollution
3. Air pollution
8. How can domestic waste be used as manure?
A. Depending upon the nature of the waste domestic waste can
be segregated in to two categories. i.e. biodegradable and non
biodegradables. Biodegradables waste such as leaves, rotten
food etc…. should be deposited in land hills, where they get
decomposed aerobically and anaerobically in to manure. Non
biodegradable waste (Which cannot be degraded) such as
plastic, glass, metal scrapes etc…. should be sent for recycling.
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9. Write short note on a).BOD b). Photo chemical smog c).
Ozone hole.
A. BOD: Biochemical oxygen demand is defined as the amount
of oxygen required to oxidise the pollutants presents in water.
Water having BOD less than 5ppm is clean water and greater
than 17ppm is polluted water
Photo chemical smog: It consists of oxides of nitrogen which
absorb light and form free radicals.
It is extremely harmful and is oxidizing in nature.
Ozone hole: ozone layer is depleted near Antarctica and it is
called ozone hole.
10. Define green chemistry? Explain with one example.
Chemistry and chemical process involving the minimum use
and generation of harmful substances is called green chemistry
Ex:‐ Earlier tetrachloroethene themes was used as solvents for
dry cleaning. This compound is carcinogenic; therefore it has
been replaced by liquefied CO2 along with a suitable detergent
which is less harmful.
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11. What are the reactions involves for ozone layer depletion
in the stratosphere?
A. CFC’S (chlorofluorocarbons) that are released in the
atmosphere mix with the other atmospheric gases and when
eventually reach the stratosphere, gets broken down by UV
radiations as fallows
. .
CF2Cl2 ‐‐‐‐‐‐> Cl + CF2Cl
The chlorine radical reacts with ozone and breaks down ozone
molecule as follows
. .
Cl + O3 ‐‐‐‐‐> ClO + O2
.
ClO radical further reacts with atomic oxygen and produces
more chlorine radicals as follows
. .
ClO + O ‐‐‐‐‐‐> Cl + O2
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3. NO(g)+O3(g) ‐‐‐‐‐‐> NO2(g)+O2(g)
Sources: 1. At high attitude when lightning strokes, dinitrogen
and dioxygen combine to form oxides of nitrogen.
2. Burning of fossil fuels in an automobile engine at high
temperature, dinitrogen and dioxygen combine to yield
significant quantities of nitric oxide and nitrogen dioxide.
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.
b) O + O2 ‐‐‐‐‐‐> O3
.
c) N O + O3 ‐‐‐‐‐‐>NO 2 + O 2
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.
2. O (g)+O2(g) ‐>O3(g)
. .
3. O3(g)+N O (g) ‐>NO2(g)+ O (g)
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Control of photochemical smog
1. Use of catalysts converters in automobiles Which prevents
the release of oxides of nitrogen and hydrocarbons to the
atmosphere
2. Certain plants e.g.…pines, Juniparus, quercus pyrus and vitis
can metabolize oxides of nitrogen and therefore, their
plantation could help in this matter.
3. What are the major causes of water pollution? Explain
A. 1. Pathogens: These are water pollutants include bacteria
and other organisms.They enter water from animal excreta
and domestic Sewage. Bacteria presents in human excreta
causes gastrointestinal diseases (Excreta contains, escherichia
Coil and streptococcus faecalis)
2. Organic wastes: These are biodegradable water that pollutes
water as a result run off. The presence of excess of organic
wastes in water decreases the amount of oxygen held by water.
This decrease in the amount of dissolved oxygen inhibits
aquatic life.
3. Chemical pollutants: These are the water soluble chemicals
like heavy metals such as cadmium, mercury, nickel etc…
The presence of these chemicals (above the tolerance
limit) can damage the kidneys, central nervous system
and liver.
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4. What do you mean by green chemistry? How will it help in
decreasing environmental pollution?
A. It is a production process that aims at using the existing
knowledge and principles of chemistry for developing and
implenting chemical products and processes to reduce the use
and generation if substances hazardous to the environment.
The release of different harmful chemicals (particulates, gases,
organic and inorganic wastes) causes environmental pollution.
In green chemistry, the reactants to be used in chemical
reactions are chosen in such way that the yield of the end
products is up to 100%. This prevents or limits chemical
pollutants from being introduced in to the environment
For example, through the efforts of green chemists, H2O2 has
replaced tetrachloromethene and chlorine gas in drying and
bleaching of paper.
CO2 has replaced CFCs as blowing agents in manufacture of
polystyrene foam sheet.
5. Name the pollutants which cause soil pollution?
A.1. Pesticides
2. Insecticides
3. Herbicides
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4. Fungicides
5. Industrial wastes
6. Urban wastes
7. Agriculture pollutants
8. Fertilizers
6. What is green house effect? How does it affect the global
climate?
A. It is the phenomenon in which earth’s atmosphere trap the
heat from the sun and prevent it form escaping in to the outer
space.
Green house gases such as CO2, CH4, ozone, chlorofluorocarbon
compounds and water vapour in the atmosphere result in
climate changes sunlight intense a green house through. The
transparent glass or plastic panes and heats the plants by the
heat emitted by the plants in the form of infrared radiation
cannot puss through the glass or plastic panes. As a result of
inside temperature increases. Increased CO2 levels in the
atmosphere can also cause plants, undergoing photosynthesis,
to take use the gas at a greater rate so that plants in warmer
climate with adequate rainfall would grow faster. An increase in
average global temperature to increase the incidence of
infectious diseases like malaria, sleeping sickness, dengue and
yellow fever CFCs are also damaging ozone layer. The average
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global temperature increase to a level which may lead melting
polar ice caps and flooding of lying areas all over the earth.
There may be less rain fall in temperature zones and more rain
fall in the drier areas of the world. (CO2 in the major contribute
to global warming)
7. What is acid rain? How is it harmful to the environment?
A. When the PH of the rain water below 5.6 due to the
presence of oxides of sulphur & nitrogen and carbon dioxide in
the atmosphere is called acid rain.
Harmful effects of acid rain
1. It is toxic to vegetation and aquatic life
2. It damages building and states and dissolves heavy metals
from soils, rocks and sedimentals. Tajmahal has been
damaged by acid rain.
3. The heavy metal ions such as copper, lead and aluminum,
leached from the soil, enter well water and produced
variety of toxic effects.
4. Acid rain also corrodes water pipes resulting in the
leaching as heavy metals such as iron, lead and copper in
to drinking water.
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