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Q4 (C) Q14 (C) Q1 The volume occupied by 4.4 g of CO2 at STP Mass of one atom of an element is 8 × 10−24 g
Q5 (C) Q15 (C) is (Gram atomic mass of O = 16 g and C = 12 g) This is equal to
(A) 22.4 L (A) 4.8u
Q6 (D) Q16 (A)
(B) 2.24 L (B) 48u
Q7 (D) Q17 (B) (C) 0.224 L (C) 0.048u
(D) 0.1 L (D) 0.48u
Q8 (B) Q18 (A)
Q12 Number of atoms present in 49 g of H2 SO4 ? Q18 The number of atoms present in 16 g of oxygen
(Gram atomic mass of S = 32 g, O = 16 g and H = gas is: (Gram atomic mass of O = 16 g)
Answer Key
1 g) (A) 6. 02 × 1011.5
Q1 (B) Q12 (C)
(A) NA /7 (B) 3. 01 × 1023
(B) 7NA (C) 3. 01 × 10 11.5 Q2 (D) Q13 (A)
23
(C) 7NA /2 (D) 6. 02 × 10 Q3 (B) Q14 (C)
(D) 14NA
Q19 Number of atoms in 560 g of Fe ( atomic mass Q4 (D) Q15 (B)
Q13 Calculate number of oxygen atoms in 126 g of 56 g mol−1 ) is Q5 (D) Q16 (B)
HNO3 ? (A) Twice that of 70 g N2
Q6 (A) Q17 (B)
(A) 6 NA (B) Half that of 20 gH2
(B) 12 NA (C) Both are correct Q7 (D) Q18 (D)
(C) 3 NA (D) None of these
Q8 (B) Q19 (C)
(D) 14 NA
Q20 How many H -atoms are present in 0.046 g of Q9 (A) Q20 (D)
Q14 Calculate total number of electrons in ethanol?
Q10 (A) Q21 (C)
88 g of CO2 ? (A) 6 × 1020
(Gram atomic mass of C = 12g, O = 16g and (B) 1.2 × 1021 Q11 (B)
atomic number of C=6 , O =8) (C) 3 × 1021
(A) NA (D) 3.6 × 1021
(B) 32 NA Android App | iOS App | PW Website
Q21 Number of atoms of oxygen present in 10.6 g of
(C) 44 NA
Na2 CO3 will be
(D) 22 NA
(A) 6.02 × 1023
Q15 Calculate total number of valence electrons in (B) 12.04 × 1022
2.8 g of N3− ion (C) 1.806 × 1023
(A) 2.6 NA (D) 31.80 × 1028
(B) 1.6 NA
(C) 7.8 NA
(D) 0.8 NA
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Q4 (C) Q16 (A) Q1 The law of conservation of mass is valid for all Q6 The percentage of hydrogen in water and
Q5 (A) Q17 (C) the following, except hydrogen peroxide is 11.1 and 5.9 respectively.
(A) All chemical reactions These figures illustrate
Q6 (A) Q18 (B)
(B) Nuclear reactions (A) Law of multiple proportions
Q7 (D) Q19 (B) (C) Endothermic reactions (B) Law of conservation of mass
(D) Exothermic reactions (C) Law of constant proportions
Q8 (C) Q20 (A)
(D) Law of combining volumes
Q9 (B) Q21 (A) Q2 After a chemical reaction, the total mass of
reactants and products Q7 The law of definite proportions is not applicable
Q10 (D) Q22 (A)
(A) Is always increased to nitrogen oxide because
Q11 (D) Q23 (A) (B) Is always decreased (A) Nitrogen atomic weight is not constant
Q12 (A) (C) Is not changed (B) Nitrogen molecular weight is variable
(D) Is always less or more (C) Nitrogen equivalent weight is variable
(D) Oxygen atomic weight is variable
Q3 A sample of pure carbon dioxide, irrespective of
its source contains 27.27% carbon and Q8 The percentage of copper and oxygen in
Android App | iOS App | PW Website 72.73% oxygen. The data support samples of CuO obtained by different methods
(A) Law of constant composition were found to be the same. This illustrates the
(B) Law of conservation of mass law of
(C) Law of reciprocal proportions (A) Constant proportions
(D) Law of multiple proportions (B) Conservation of mass
(C) Multiple proportions
Q4 ng of substance X reacts with mg of substance
(D) Reciprocal proportions
Y to form pg of substance R and qg of
substance S . This reaction can be represented Q9 How A sample of calcium carbonate (CaCO 3)
as X + Y = R + S. The relation which can be has the following percentage composition:
established in the amounts of the reactants Ca = 40%; C = 12%; O = 48%
and the products will be If the law of constant proportions is true, then
(A) n − m = p − q the weight of calcium in 4g of a sample of
(B) n + m = p + q calcium carbonate obtained from another
(C) n = m source will be (Gram atomic mass of Ca = 40 g,
(D) p = q O = 16 g and C = 12 g)
(A) 0.016 g
Q5 Chemical equation is balanced according to
(B) 0.16 g
the law of
(C) 1.6 g
(A) Multiple proportion
(D) 16 g
(B) Reciprocal proportion
(C) Conservation of mass Q10 Cu forms two oxides cuprous and cupric
(D) Definite proportions oxides, which law can be proved by the weights
of Cu and O ? Q16 Which of the following pairs of substances contain equal number of molecules
(A) Constant composition illustrate the law of multiple proportions (C) Equal volumes of all gases under same
(B) Multiple proportions (A) CO and CO2 conditions of temperature and pressure
(C) Reciprocal proportions (B) H2 O and D2 O contain equal number of atoms
(D) Definite proportions (C) NaCl and NaBr (D) The rates of diffusion of gases are inversely
(D) MgO and Mg(OH)2 proportional to the square root of their
Q11 Which of the following pairs of compound
densities
illustrate law of multiple proportions? Q17 1.0 g of an oxide of A contained 0.5 g of
(A) KOH, CsOH A. 4.0 g of another oxide of A contained 1.6 g Q22 Which one of the following pairs of gases
(B) H2 O, D2 O of A . The data indicate the law of contains the same of molecules? (Gram atomic
(C) Ethane, benzene (A) Reciprocal proportions mass of N = 14 g, C = 12 g, O = 16 g, H = 1 g)
(D) KCI, KBr (B) Constant proportions (A) 16 g of O2 and 14 g of N2
(C) Conservation of energy (B) 8g of O2 and 22 g of C O2
Q12 Element X forms five stable oxides with oxygen
(D) Multiple proportions (C) 28 g of N2 and 22 g of CO2
of formula X2 O, XO, X2 O3 , X2 O4 , X2 O5 . The
(D) 32 g of O2 and 32 g of N2
formation of these oxides explains Q18 2 g of hydrogen combine with 16 g of oxygen to
(A) Law of definite proportions form water and with 6 g of carbon to form Q23 Volume occupied by one molecule of water
(B) Law of partial pressures methane. In carbon dioxide 12 g of carbon are (density = 1 g cm−3 ) is
(C) Law of multiple proportions combined with 32 g of oxygen. These figures (A) 9.0 × 10−23 cm3
(D) Law of reciprocal proportions illustrate the law of (B) 6.023 × 10−23 cm3
(A) Multiple proportions (C) 3.0 × 10−23 cm3
Q13 Two samples of lead oxide were separately
(B) Constant proportions (D) 5.5 × 10−23 cm3
reduced to metallic lead by heating in a current
(C) Reciprocal proportions
of hydrogen. The weight of lead from one oxide Q24 How many years it would take to spend one
(D) Conservation of mass
was half the weight of lead obtained from the Avogadro's number of rupees at a rate of 10
other oxide. The data illustrates Q19 Equal volume of different gases at any definite lakh of rupees in one second?
(A) Law of reciprocal proportions temperature and pressure have (A) 1.90 × 109
(B) Law of constant proportions (A) Equal atoms (B) 1.90 × 1010
(C) Law of multiple proportions (B) Equal masses (C) 1.90 × 1011
(D) Law of equivalent proportions (C) Equal densities (D) 1.90 × 1012
(D) Equal molecules
Q14 Different proportions of oxygen in the various
oxides of nitrogen prove the Q20 Gay Lussac's law is not valid in the
(A) Equivalent proportion chemical reaction:
(B) Multiple proportion (A) H2 ( g) + Cl2 ( g) → 2HCl(g)
(C) Constant proportion (B) 3H2 ( g) + N2 ( g) → 2NH3 ( g)
(D) Conservation of matter (C) 2SO2 ( g) + O2 ( g) → 2SO3 ( g)
Δ
(D) CaCO ( s) →
Q15 Among the following pairs of compounds, the 3 CaO(s) + CO2 ( g)
one that illustrates the law of multiple Q21 Which of the following represents Avogadro's
proportions is hypothesis?
(A) NH3 and NCl3 (A) Gases react together in volumes which bear
(B) H2 S and SO2 a simple ratio to one another
(C) CuO and Cu2 O (B) Equal volumes of all gases under same
(D) CS2 and FeSO4 conditions of temperature and pressure
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Q4 (B) Q16 (A) Q1 How many moles of electron weigh one Q7 The empirical formula of a compound is CH2 O.
Q5 (C) Q17 (D) kilogram? 0.0835 moles of the compound contains 1.0 g
(A) 6.023 × 1023 of hydrogen. The molecular formula of the
Q6 (A) Q18 (C) 1
(B) 9.108 × 1031 compound is
6.023
Q7 (C) Q19 (D) (C) 9.108 × 1054 (A) C6 H12 O6
1
Q8 (A) Q20 (D) (D) 9.108×6.023 × 108 (B) C5 H10 O5
(C) C4 H8 O4
Q9 (C) Q21 (B) Q2 The number of electrons in 3. 1mg of N O3 is (D) C3 H6 O3
(A) 32
Q10 (B) Q22 (A)
(B) 1.6 × 10−3 Q8 A compound (80 g) on analysis gave C =
Q11 (C) Q23 (C) (C) 9.6 × 1020 24 g, H = 4 g, O = 32 g. Its empirical formula
Q12 (C) Q24 (B) (D) 9.6 × 1023 is (Gram atomic mass of C = 12 g, O = 16 g, H = 1
g)
Q3 The total number of protons in 10 g of calcium (A) C2 H2 O2
carbonate is (N0 = 6.023 × 1023 ) (B) C2 H2 O
Android App | iOS App | PW Website (A) 1.5057 × 1024 (C) CH2 O2
(B) 2.0478 × 1024 (D) CH2 O
(C) 3.0115 × 1024
(D) 4.0956 × 1024 Q9 2.2 g of a compound of phosphorous and
Sulphur has 1.24 g of ' P ' in it. Its empirical
Q4 The number of moles of sodium oxide in 620 g formula is
of its is (A) P2 S3
(A) 1 mol (B) P3 S2
(B) 10 moles (C) P3 S4
(C) 18 moles (D) P4 S3
(D) 100 moles
Q10 An organic compound contains carbon,
Q5 1021 molecules are removed from 200mg of hydrogen and oxygen. Its elemental analysis
CO2 . The mole of CO2 left are gave C, 38.71% and H, 9.67% . The empirical
(A) 2.88 × 10−2 formula of the compound would be
(B) 28.2 × 10−3 (A) CH4 O
(C) 2.88 × 10−3 (B) CH3 O
(D) 28.8 × 103 (C) CH2 O
(D) CHO
Q6 The percentage of nitrogen in urea is about
(A) 46 (B) 85 Q11 An organic compound containing C, H and N
(C) 18 (D) 28 gave the following analysis C=
40%, H = 13.33%, N = 46.67% . Its empirical
hydrochloric acid according to the balanced Q17 The mass of carbon anode consumed (giving
Yakeen NEET 2.0 (Alpha) equation below. only carbon-dioxide) in the production of
2Al + 6HCl → 2AlCl3 + 3H2 270Kg of aluminium metal from bauxite by the
Physical Chemistry (A) 1.5 g Hall process is
DPP: 6
(B) 2.0 g (A) 180 kg
Some Basic Concept of Chemistry
(C) 3.0 g (B) 270 kg
(D) 6.0 g (C) 240 kg
Q1 When 200 g of lime stone is strongly heated, it (C) 22.4 litre (D) 11.2 litre
(D) 90 kg
undergoes thermal decomposition to form Q11 What is the total mass of products formed
Q6 What is the weight of oxygen required for
112 g of lime an unknown mass of carbon when 16 grams of CH4 is burned with excess
the complete combustion of 2.8 kg of
dioxide gas as CaCO 3 → CaO + CO2 What oxygen?
200 g 112 g ethylene?
(A) 32 g
will be the mass of CO2 formed? (A) 2.8 kg
(B) 36 g
(A) 88 g (B) 6.4 kg
(C) 44 g
(B) 24 g (C) 9.6 kg
(D) 80 g
(C) 64 g (D) 96 kg
(D) 40 g Q12 The volume of oxygen required for
Q7 How many grams of H2 are required to
complete combustion of 20ml of ethene is
Q2 How many grams of calcium oxide is obtained consume 2 mol of CO ?
(A) 30ml
on heating 100 g of CaCO 3( s) ? (Gram atomic mass of H = 1 g, C = 12 gand O =
(B) 60ml
(A) 50 g 16 g)
(C) 40ml
(B) 40 g CO(g) + 2H2 ( g) → CH3 OH(g)
(D) 50ml
(C) 56 g (A) 2 g
(D) 44 g (B) 4 g Q13 Volume of CO2 obtained at STP by the
(C) 8g complete decomposition of 9.85 g . The volume
Q3 The volume CO2 gas evolved at STP on
(D) 16 g of BaCO3 is
heating 50 g CaCO 3 : (Gram atomic mass of
(A) 2.24 lit (B) 1.12 lit
Ca = 40 g, C = 12 g and O = 16 g) Q8 When a certain amount of octane,C8 H18 , is
(C) 0.84 lit (D) 0.56 lit
Δ
CaCO3(s) → CaO(s) + CO2 (g) burnt completely, 7. 04 gCO2 is formed. What
(A) 11.2 litre (B) 22.4 litre is the mass of H2 O formed simultaneously? Q14 The volume of gas at STP produced by 100 g of
(C) 5.6 litre (D) 2.42 litre (A) 1. 62 g (B) 6. 48 g CaC2 with water
(C) 3. 24 g (D) 2. 28 g (A) 70 litre (B) 35 litre
Q4 What is the mass of glucose required to (C) 17.5 litre (D) 22.4 litre
produce 44 g of CO2 on complete Q9 The amount of zinc required to produce
combustion? 224 mL of H2 at STP on treatment with dilute Q15 How many grams of SO3 are produced from
(A) 30 g H2 SO4 will be 1 mol of S8 ?
(B) 45 g (Gram atomic mass of H = 1 g, O = 16 g, S = 32 (A) 1280.0 (B) 640.0
(C) 60 g g,and Zn = 65 g) (C) 960.0 (D) 320.0
(D) 22 g Zn(s) + H2 SO4 (aq) → ZnSO4 (aq) + H2 ( g)
Q16 If 1/2 moles of oxygen combine with aluminium
(A) 65 g
Q5 The volume of O2 at STP required for the to form Al2 O3 then weight of Aluminium metal
(B) 0.065 g
complete combustion of 4 g CH4 is used in the reaction is (Al = 27)
(C) 0.65 g
(Gram atomic mass of H = 1 g, C = 12 g and O = (A) 27 g
(D) 6.5 g
16 g ) (B) 18 g
CH4 ( g) + 2O2 ( g) ⟶ CO2 ( g) + 2H2 O(g) Q10 Calculate the mass of hydrogen formed when (C) 54 g
(A) 5.6 litre (B) 2.88 litre 27 g of aluminum reacts with excess (D) 40.5 g
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Q4 (A) Q13 (B) Q1 10 g of MnO2 on reaction with HCl forms (C) 1.7 g
Q5 (D) Q14 (B) 2.24 L of Cl2 ( g) at NTP , the percentage (D) 17.0 g
impurity of MnO2 is
Q6 (C) Q15 (B) Q5 The minimum mass of water needed to slake
MnO2 + 4HCl → MnCl2 + Cl2 + 2H2 O
1 kg of quicklime, assuming no loss by
Q7 (C) Q16 (B) (A) 87% (B) 25%
evaporation, is
(C) 33.3% (D) 13%
Q8 (C) Q17 (D) (A) 243.2 g
Q9 (C) Q2 According to the following reaction the (B) 642.8 g
minimum quantity in gm of H2 S needed to (C) 160.7 g
2+
precipitate 63.5gm of Cu ions will be (D) 321.4 g
nearly?
Android App | iOS App | PW Website Q6 What volume at STP of CO is required to
(Gram atomic mass of H = 1 g, Cu = 63.5 g and S
reduce one mole of Fe2 O3 in the following
=32 g)
+2 + reaction
Cu + H2 S → CuS + 2H
Fe2 O3 + CO → Fe + CO2
(A) 63.5 g
(Gram atomic mass of C = 12 g, O = 16 g, and Fe
(B) 31.75gm
=56 g)
(C) 34gm
(A) 11200 cm3
(D) 20gm
(B) 22400 cm3
Q3 A quantity of 2.76 g of silver carbonate on (C) 67200 cm3
being strongly heated yields a residue weighing (D) 33600 cm3
(Ag = 108)
Δ Q7 A gas is found to contain 2.34 grams of
Ag2 CO3 (s) → 2 Ag (s) + CO2 (g) nitrogen and 5.34 grams of oxygen. Simplest
+ 12 O2 (g) formula of the compound is:
(A) N2 O
(A) 2.16 g (B) NO
(B) 2.48 g (C) N2 O3
(C) 2.32 g (D) NO2
(D) 2.64 g
Q8 The weight of lime obtained by heating 200 kg
Q4 The minimum mass of sulphuric acid needed of 95% pure lime stone is
for dissolving 3 g of magnesium carbonate is (A) 98.4 kg
(Gramatomic mass of H = 1 g, C = 12 g, O = 16 g, (B) 106.4 kg
Mg =24 g and S = 32 g) (C) 112.8 kg
MgCO3 ( s) + H2 SO4 (aq) → MgSO4 (aq) (D) 122.6 kg
+ H2 O(l) + CO2 ( g)
Q9 The number of water molecules present in a
(A) 3.5 g
drop of water weighing 0.018 g is
(B) 7.0 g
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Q4 (C) Q16 (B) Q1 Vanadium metal is added to steel to impart Q7 The multiple 5 × 0.2 after rounding off will be
Q5 (D) Q17 (A) strength. The density of vanadium is (A) 1 (B) 1.0
5.96 g/cm3 . Express this in the SI unit. (C) 1.00 (D) 1.000
Q6 (C) Q18 (A)
(A) 5.96 × 103
Q8 Add (0.001 + 0.02) upto the correct number of
Q7 (A) Q19 (B) (B) 59.6 × 103
significant figures
(C) 596 × 103
Q8 (B) Q20 (A) (A) 0.021 (B) 0.02
(D) 0.596 × 103
Q9 (B) Q21 (B) (C) 0.003 (D) 0.001
Q2 Convert 25365 mg to S.I. unit
Q10 (A) Q22 (A) Q9 One fermi is
(A) 253.65 g
Q11 (B) Q23 (C) −3 (A) 10−13 cm
(B) 25.365 × 10 kg
(B) 10−15 cm
Q12 (A) (C) 25.365 kg
(C) 10−10 cm
(D) 253.65 kg
(D) 10−12 cm
Q3 Convert 15.15 pm to basic unit
Q10 A picometre is written as
Android App | iOS App | PW Website (A) 15.15 × 10−13 m
(A) 10−9 m
(B) 1.515 × 10−12 m
−12 (B) 10−10 m
(C) 15.15 × 10 m
(C) 10−11 m
(D) 1.515 × 10−13 m
(D) 10−12 m
Q4 Pressure is determined as force per unit area of
Q11 Significant figures in 0.00051 are
the surface. The SI unit of pressure, pascal is as
(A) 5 (B) 3
shown below:
(C) 2 (D) 4
1 Pa = 1 N m−2
Q12 1 m3 in equal to
−2
If mass of air at sea level is 1034 g cm , (A) 100 litre (B) 10000 litre
calculate the pressure in pascal. (C) 10 litre (D) 1000 litre
(A) 1.01332 × 104 Pa
Q13 NX is produced by the following step of
(B) 1.01332 × 105 Pa
5 reactions:
(C) 10.01332 × 10 Pa
6
(D) 1.01332 × 10 Pa. M + X2 ⟶ MX2
3MX2 + X2 ⟶ M3 X8
Q5 How many significant figures are in 0. 0008 ?
M3 X8 + N2 CO3 ⟶ NX + CO2 + M3 O4
(A) 1 (B) 2
(C) 3 (D) 4 How much M (metal) is consumed to produces
206 gm of NX? (Take at. Wt. of
Q6 Round off 0.1525 upto three significant figures
M = 56, N = 23, X = 80)
(A) 0.153 (B) 0.152
(A) 42 gm
(C) 0.16 (D) 0.15
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NEET NEET
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Q15 (D)
Q11 O2 is bubbled through water at 293 K . Assume Q16 Vapour pressure is achieved in
Yakeen NEET 2.0 2025 (Alpha) that O2 exerts a partial pressure of 0.98 bar, (A) open container
find the solubility of O2 in gL−1 . The value of (B) closed container
Physical Chemistry Henry's law constant KH for O2 is 34.84k bar. (C) both a & b
DPP: 4
(A) 0.05 (B) 0.08 (D) none of these
Solutions
(C) 0.07 (D) 0.01
Q17 At vapour pressure
Q1 The gas for which Henry's law is not applicable Q6 The factor which decreases the solubility of gas Q12 Gases with their Henry's constant values are (A) forward change is favoured
in aqueous solution is in liquid is given.The gas having maximum solubility will be (B) backward change is favoured
(A) HCl (A) low temperature Gas A − KH = 21.2 k bar (C) both forward & backward changes are
(B) N2 (B) interaction between molecules of gas & Gas B − KH = 11.2 k bar favoured but with equal rate
(C) Xe liquid Gas C − KH = 5.6 k bar (D) none of these
(D) He (C) high temperature Gas D − KH = 2.4 k bar
(D) high pressure (A) A
Q2 Unit of Henrys constant KH is same as that of
(B) B
(A) Volume (B) Temperature Q7 The gas dissolved in carbonated drinks escapes
(C) C
(C) Energy (D) Pressure an opening the bottle due to
(D) D
(A) increase in temperature
Q3 If partial pressure of Gas A = 0.4 bar, Gas
(B) increase in pressure Q13 The gas which is expected to have maximum
B = 0.2 bar and Gas C = 0.5 bar, then the
(C) decrease in pressure over gas value of KH will be
gas having maximum solubility (neglecting
(D) Increase in molecular interaction (A) BH3
other factors) is:
(B) CO2
(A) A Q8 A person feels more fatigue at high altitudes
(C) H2 S
(B) B due to
(D) He
(C) C (A) low pressure of oxygen
(D) All are equal soluble (B) low temperature Q14 An unopened soda has an aqueous
(C) nausea concentration of CO2 at 25∘ C equal to 0.05
Q4 Which law states that the amount of gas that is
(D) contraction of body mole kg−1 . The pressure of CO2 gas in the can
soluble in a liquid is directly proportional to the
is (KH = 0.34 mole /kg bar )
partial pressure of that gas above the liquid Q9 Henry's law is not applicable for aqueous
when the temperature is kept constant? solution of
(A) 0.671 bar
(A) Raoult's Law (B) Henry's Law (A) O2
(B) 1.49bar
(C) Coloumb's Law (D) Dalton's Law (B) N2
(C) 0.147 bar
(C) SO3
Q5 The value of Henry's constant (KH ) depends (D) 1.71bar
(D) He
on
Q15 At vapour pressure
(A) nature of the gas Q10 Henry’s law is not applicable at
(A) ( rate )evaporation = ( rate )condensation
(B) nature of the solvent (A) low pressure
(B) (rate )evaporation > ( rate )condensation
(C) temperature and pressure (B) high pressure
(C) (rate )evaporation < ( rate )condensation
(D) all of these (C) gas does not react with liquid
(D) None of the above
(D) high temperature
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Android App | iOS App | PW Website Q3 A solution which is ideal in nature follows.
(A) Graham's Law
(B) Ostwald Law
(C) Fleming's Law
(D) Raoult's Law
(D)
Q4 A container having liquid in equilibrium with its
vapour has volume of 10 L . If the volume of
container is reduced to 5 L, the vapour
pressure (consider constant temperature):
(A) is reduced by 50%
(B) is increased by 50%
(C) remain constant Q7 According to Raoult's law, vapour pressure of
(D) None of these a solution containing non-volatile solute, is
directly proportional to mole fraction of
Q5 If vapour pressure of 10 gram of a liquid solution
(A) solute
is P , then what is the vapour pressure of 5
(B) solvent
gram of same liquid solution?
(C) both solute and solvent
(A) P
(D) none of these
(B) 2P
(C) P/2 Q8 If P∘ → vapour pressure of solvent and
(D) none of these P → vapour pressure of solution then
(assume the solute used is non-volatile)
Q6 The correct relationship of vapour pressure
(A) P∘ > P
and temperature is given by
(B) P ∘ < P
(A)
(C) P∘ = P
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Q4 (C) Q14 (B) Q1 Which of the following solution has least value Q5 A solution consists of two components X and Y.
Q5 (A) Q15 (A) of vapour pressure? Which of the following relation of interaction
(A) HCl + H2 O between molecules is true for ideal solution of X
Q6 (A) Q16 (A)
(B) NaOH + H2 O and Y ?
Q7 (B) Q17 (C) (C) R − OH + H2 O (A) X − X =Y−Y≠X−Y
(D) CH3 − Cl + H2 O (B) X − X ≠Y−Y=X−Y
Q8 (A) Q18 (D)
(C) X − X ≠ Y − Y ≠ X − Y
Q9 (D) Q19 (A) Q2 Solutions in which both the component has
(D) X − X = Y − Y = X − Y
nearly same polar nature as well as molecular
Q10 (A)
size will form. Q6 A solution which boils at constant temperature is
(A) ideal solution called
(B) non-ideal solution (A) Azeotrope
Android App | iOS App | PW Website (C) Both (A) & (B) (B) Ideal solution
(D) None of these (C) Saline water
(D) Alkaline solution
Q3 The diagram given below is a vapor pressure
composition diagram for a binary solution of A Q7 A mixture of water and benzene is a/an
and B In the solution, A − B interactions are (A) ideal solution
(B) non-ideal solution with positive deviation
(C) non-ideal solution with negative deviation
(D) none of these
(C) non-ideal solution with negative deviation 40 g of CH3 OH. Total vapour pressure of the
(D) none of the above solution is approximately-
Answer Key
(A) 67 mmHg
Q11 A non-ideal solution with negative deviation are Q1 (C) Q10 (C)
(B) 35 mmHg
called Q2 (A) Q11 (A)
(C) 105 mmHg
(A) maximum boiling azeotropes
(D) 27 mmHg Q3 (C) Q12 (A)
(B) minimum boiling azeotropes
(C) both (A) & (B) Q17 Mixture of volatile components A and B has Q4 (A) Q13 (C)
(D) none of these total vapour pressure (in torr) Q5 (D) Q14 (C)
P = 254 − 119XA Where XA is mole fraction
Q12 Which of the following is a characteristic of non- Q6 (A) Q15 (B)
of A in mixture. The values of p0A and p0B (in torr)
ideal solution with negative deviation?
are Q7 (B) Q16 (A)
(A) ΔVmix < 0
(A) 254,119 (B) 119,254
(B) ΔHmix > 0 Q8 (D) Q17 (C)
(C) 135,254 (D) 154,119
(C) ΔSmix < 0 Q9 (C) Q18 (A)
(D) ΔGmix > 0 Q18 At 25∘ C , the vapour pressure of pure liquid A
(mol. mass = 40 ) is 100 torr, while that of pure
Q13 The correct expression for vapour pressure of a
liquid B is 40 torr, (mol. mass = 80 ). The vapour
solution containing volatile solute A and solvent Android App | iOS App | PW Website
pressure at 25∘ C of a solution containing 20 g
B is
of each A and B is
(A) P = P∘A XA − P∘B XB
(A) 80 torr (B) 59.8 torr
(B) P = P∘A + (P∘B × P∘A )XB
(C) 68 torr (D) 48 torr
(C) P = P∘B + (P∘A − P∘B )XA
(D) None of these
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Q4 (D) Q13 (A) Q1 Correct expression for Van't Hoff factor in case of molarity of solution of substance is
Q13 Correct expression for degree of dissociation ' α ' Q6 (A) Q13 (A)
of electrolyte Ax By is given by
i−1
Q7 (D)
(A) α = x+y−1
i−1
(B) α = (1+y+1)
1−i
(C) α = 1−x−y Android App | iOS App | PW Website
(D) α (1+y+1)
= i−1
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Q8 (C) Q18 (C) Q2 Intensive property is Q10 The intensive property among these quantities is
Q9 (A) Q19 (A) (A) Moles (B) Volume (A) Enthalpy (B) Mass/volume
(C) Mass (D) Temperature (C) Mass (D) Volume
Q10 (D)
Q3 Which of the following is not a state function? Q11 In thermodynamics which one of the following is
(A) Pressure (B) Volume not an intensive property?
Android App | iOS App | PW Website (C) Temperature (D) Heat (A) Pressure (B) Density
(C) Volume (D) Temperature
Q4 Extensive property is
(A) Enthalpy (B) Density Q12 If in a container neither mass and nor heat
(C) Pressure (D) Temperature exchange occurs then it constitutes a
(A) Closed system
Q5 A refrigerator is an example of
(B) Open system
(A) Open system
(C) Isolated system
(B) Closed system
(D) Imaginary system
(C) Isolated system
(D) Non thermodynamic system Q13 Which of the following is not a state function?
(A) ΔS
Q6 Out of E, H, q, W and S which are state function?
(B) ΔG
(A) E, H, W (B) E, S, H, W
(C) ΔH
(C) E, H, S (D) E, H, q, W, S
(D) △Q
Q7 Which of the following statements are false?
Q14 Which of the following is not a state function
(A) Work is a state function
(A) Internal energy
(B) Temperature is a state function
(B) Enthalpy
(C) Change in state is completely defined when
(C) Work
initial and final state are specified
(D) Entropy
(D) Work appears at the boundary of the system
Q15 Which among the following is an extensive
Q8 Both q and w are_____________ function and
property of the system?
q + w is a_______________ function.
(A) Temperature
(A) State, State (B) State, path
(B) Volume
(C) Path, state (D) Path, path
(C) Refractive index
(D) Viscosity Q21 A tightly closed thermo flask contains some ice
cubes. This constitutes
Answer Key
Q16 Which of the following is not a state function?
(A) Closed system
(A) Heat Q1 (B) Q13 (D)
(B) Open system
(B) Internal energy Q2 (D) Q14 (C)
(C) Isolated system
(C) Enthalpy
(D) Non-thermodynamic system Q3 (D) Q15 (B)
(D) Entropy
Q22 Choose the correct answer- A thermodynamic Q4 (A) Q16 (A)
Q17 Which of the following quantities is not a
state function is a quantity Q5 (B) Q17 (D)
state function?
(A) Used to determine heat changes
(A) Temperature (B) Entropy Q6 (C) Q18 (A)
(B) Whose value is independent of path
(C) Enthalpy (D) Work
(C) Used to determine pressure volume work Q7 (A) Q19 (A)
Q18 Which of the following is not an intensive (D) Whose value depends on temperature only
Q8 (C) Q20 (C)
property?
Q23 A thermodynamic quantity is that: Q9 (B) Q21 (C)
(A) Entropy (B) Pressure
(A) Which is used in thermochemistry
(C) Temperature (D) Molar volume Q10 (B) Q22 (B)
(B) Which obeys all the laws of thermodynamics
(C) Quantity which depends only on the state of Q11 (C) Q23 (C)
Q19 Which of the following is a state function and
also an extensive property? the system Q12 (C) Q24 (D)
(A) Internal energy (D) Quantity which is used in measuring thermal
(B) Pressure change
(C) Molar heat capacity
Q24 Which is not characteristic of thermo-chemical Android App | iOS App | PW Website
(D) Temperature
equation?
Q20 Warming ammonium chloride with sodium (A) It indicates physical state of reactants and
hydroxide in a test tube is an example of: products
(A) Closed system (B) It indicates whether the reaction is
(B) Isolated system exothermic or endothermic
(C) Open system (C) It indicates allotrope of reactants if present
(D) None of these (D) It indicates whether reaction would occur or
not
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Q12 For isothermal expansion of ideal gas which is Q18 In an adiabatic expansion of an ideal gas
correct? (A) ΔT =0
Answer Key
(A) ΔH =0 (B) W = 0
Q1 (A) Q10 (D)
(B) ΔE =0 (C) q = 0
(C) ΔT = 0 (D) ΔU = 0 Q2 (B) Q11 (B)
(D) All Q3 (A) Q12 (D)
Q13 As per the First Law of thermodynamics, which of Q4 (B) Q13 (D)
the following statement would be appropriate: Q5 (D) Q14 (D)
(A) Energy of the system remains constant
Q6 (C) Q15 (A)
(B) Energy of the surroundings remains constant
(C) Entropy of the universe remains constant Q7 (A) Q16 (B)
(D) Energy of the universe remains constant
Q8 (A) Q17 (C)
Q14 For a particular process q = −10 kJ and Q9 (B) Q18 (C)
w = 25 kJ. Which of the following statements is
true?
(A) Heat flows from the surroundings to the
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system
(B) The system does work on the surroundings
(C) ΔE = −35 kJ
(D) None of the above is true
Q9 Two moles of an ideal monoatomic gases are The work done in an adiabatic process on ideal
Yakeen NEET 2.0 2025 (Alpha) allowed to expand adiabatically and reversibly gas by a constant external pressure would be
from 300 K to 200 K . The work done in the (A) Zero
Physical Chemistry system is (CV = 12.5 J/Kmol) (B) ΔE
DPP: 4
(A) −12.5 kJ (C) ΔH
Thermodynamics and Thermochemistry
(B) −2.5 kJ (D) ΔG
∘
(C) −625 kJ
Q1 One mole of an ideal gas at 25 C expands in Q5 The maximum work done in expanding 16 g Q15 A certain amount of zinc is dissolved in HCl at
(D) 500 kJ
volume from 1.0 L to 4.0 L at constant oxygen at 300 K and occupying a volume of 25∘ C in an open vessel. The type of process and
temperature. What work (in J) is done if the gas 5dm3 isothermally until the volume becomes Q10 Adiabatic expansion of ideal gas into the work done by the system respectively would
expands against vacuum (Pexternal = 0) ? 25dm3 is: vacuum correspond to be
(A) −4.0 × 102 (A) −2.01 × 103 J (A) w = 0 (A) Isothermal, positive
(B) −3.0 × 102 (B) 2.81 × 10−3 J (B) ΔE = 0 (B) Isobaric, negative
(C) −1.0 × 102 (C) 2.01 × 10−6 J (C) ΔH = 0 (C) Isochoric, zero
(D) Zero (D) 2.01 × 10−6 J (D) All of these (D) None
Q2 The maximum work obtained by an Q6 The internal energy change when a system goes Q11 The temperature of 1 mole of a gas is increased Q16 A system absorb 20 kJ heat and does 10 kJ
isothermal reversible expansion of 1 mole of an from state A to B is 40 kJ/mol. If the system by 1∘ C at constant pressure. The work done is: work then internal energy of system will be-
ideal gas at 27∘ C from 2.24 to 22.4 L is (R = 2 goes from A to B by a reversible path and (A) −R (A) Decreases by 10 kJ
−1
cal K mol−1 ) returns to state A by an irreversible path. What (B) 2R (B) Increases by 10 kJ
(A) −1381.8cal would be the change in internal energy? (C) R/2 (C) Increases by 30 kJ
(B) −600cal (A) 40 kJ (D) 3R (D) Decreases by 30 kJ
(C) −138.18cal (B) > 40 kJ
Q12 The relation of internal energy, enthalpy and Q17 5 mol of ideal gas expands isothermally and
(D) −690.9cal (C) < 40 kJ
work done can be represented by irreversibly from a pressure of 10 atm to 1 atm
(D) Zero
Q3 2 mole of an ideal gas at 27∘ C expands (A) ΔE = ΔH + W against constant external pressure of 1 atm work
isothermally and reversibly from a volume of 4 Q7 One mole of oxygen is allowed to expand (B) ΔE = W − ΔH at 300 K will be
litres to 40 litres. The work done (in kJ ) is: isothermally and reversibly from 5 m3 to 10 m3 (C) ΔH = ΔE + W (A) −15.921 kJ
(A) w = −28.72 kJ at 300 K . Calculate work done in expansion of (D) W = ΔE + ΔH (B) −11.224 kJ
(B) w = −11.488 kJ gas. (C) −110.83 kJ
Q13 A gas expands isothermally against a constant
(C) w = −5.736 kJ (A) −172.89 J (D) None of these
external pressure of 1 atm from a volume of
(D) w = −4.988 kJ (B) 1728.98 J 3 3
10 dm to a volume of 20 dm . It absorbs Q18 Match the column:
(C) −1728.98 J
Q4 The work done on the system when one mole of 800 J of thermal energy from its surroundings. Column-I Column-II
(D) 172.89 J
an ideal gas at 500 K is compressed The ΔU is a. Adiabatic process i. q = 0
1
isothermally and reversibly to 10 th of its original Q8 Isothermal free expansion of an ideal gas (A) −312 J b. Isothermal process ii. ΔH = 0
volume (R = 2cal) correspond to (B) +123 J c. Isoenthalpic process iii. ΔT = 0
(A) 500kcal (A) q = 0 (C) −213 J d. Isoentropic process iv. ΔS = 0
(B) 15.1kcal (B) W = 0 (D) +231 J (A) a-i, b-iv, c-ii, d-iii
(C) 25.03kcal (C) None of these (B) a-ii, b-i, c-iv, d-iii
Q14
(D) 2.303kcal (D) Both (A) and (B) (C) a-i, b-iii, c-ii, d-iv
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(D) a-i, b-iii, c-iv, d-ii to be ideal. What is the work for the process C to 4.48 L of an ideal gas at STP requires 12.0
∘
D? calories to raise its temperature by 15 C at
Q19 Which of the following is correct for free
constant volume. The Cp of the gas is:
expansion of ideal gas under isothermal
(A) 3 cal
condition:
(B) 4 cal
(A) q = 0, ΔT < 0, w < 0
(C) 7 cal
(B) q = 0, ΔT = 0, w = 0
(D) 6 cal
(C) q ≠ 0, ΔT = 0, w = 0
(D) q ≠ 0, ΔT = 0, w ≠ 0 (A) 12P1 V1 Q32 Calculate the amount of heat required to raise
(A) −800R ln 2
(B) 6P1 V1 the temperature of 5 g of iron from 25 C to
∘
Q20 An ideal gas receives 10 J of heat in a reversible (B) Zero
(C) 5P1 V1 ∘
75 C . The specific heat capacity of iron is
isothermal expansion. Then the work done by the (C) +200R ln 2
(D) P1 V1 0.45 J/g.
gas: (D) −600R ln 2
(A) 112.1 (B) 112.5
(A) Would be more than 10 J Q24 What is the final temperature of 0.10 mole
Q27 Heat capacity of H2 O at its boiling point is: (C) 112.9 (D) 112
(B) 10 J monoatomic ideal gas that performs 75 cal of
(A) 3calmol−1 K−1
(C) Would be less than 10 J work adiabatically if the initial temperature is Q33 For two mole of an ideal gas
(B) 5calmol−1 K−1
(D) Cannot be determined 227∘ C ? (A) Cv − Cp = R
(C) 7calmol−1 K−1
(use R = 2cal/K − mol ) (B) Cp − Cv = 2R
Q21 Net work done by the system in a cyclic process (A) 250 K (D) Infinite
(C) Cp − Cv = R
is equal to: (B) 300 K
Q28 For monoatomic ideal gas, the exact value of (D) Cv − Cp = 2R
(A) Zero (C) 350 K
the ratio of Cp,m and Cv,m is:
(B) △U (D) 750 K Q34 The heat required to raise the temperature of a
(A) 53
(C) ΔH body by 1 K is called
(D) q Q25 A given mass of gas expands from the state A to (B) 75 (A) Specific heat
the state B by three paths 1,2 and 3 as shown in (C) 97 (B) Thermal capacity
Q22 Heat absorbed by a system in going through a the figure. If w1 , w2 , and w3 respectively be the 9
(D) 11 (C) Water equivalent
cyclic process shown in figure is: magnitudes work done by the gas along three (D) None of these
Q29 Molar heat capacity of water in equilibrium with
paths then:
ice at constant pressure is: Q35 A gas expands adiabatically at constant pressure
(A) Zero 1/2
such that TV The value of (Cp /CV ) of the
(B) Infinity gas will be:
(C) 40.45 kJ K−1 mol−1 (A) 1.30 (B) 1.50
(D) 75.48JK−1 mol−1 (C) 1.70 (D) 2
7
(A) 10 πJ
6
(B) 10 πJ Q30 How many calories are required to heat 40
(C) 102 πJ grams of argon from 40 to 100∘ C at constant
(D) 104 πJ (A) w1 > w2 > w3 (B) w1 < w2 < w3 volume? (R = 2cal/molK)
(C) w1 = w2 = w3 (D) w2 < w3 < w1 (A) 120 (B) 2400
Q23 An ideal gas is taken around the cycle ABCA as
(C) 1200 (D) 180
shown in P − V diagram. The net work done Q26 Two moles of Helium gas undergo a reversible
during the cycle is equal to: cyclic process as shown in figure. Assuming gas Q31
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Q14 When the egg is hard boiled, there is- Q20 Which of the following is true for the reaction
(A) Increase in disorder H2 O(ℓ) ⇌ H2 O(g) at 100∘ C and 1
(B) Decrease in disorder atmosphere
(C) No change in disorder (A) ΔS =0
(D) ΔG is negative (B) ΔH =0
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Answer Key
Q1 (A) Q13 (C)
DPP SOLUTION
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One mole of an ideal gas at 25°C expands in volume from 1.0 L to 4.0 L at constant The maximum work obtained by an isothermal reversible expansion of 1 mole of
temperature. What work (in J) is done if the gas expands against vacuum an ideal gas at 27°C from 2.24 to 22.4 L is (R = 2 cal K–1 mol–1)
(Pexternal = 0)?
1 –1381.8 cal
1 –4.0 × 102
2 –600 cal
2 –3.0 × 102
3 –138.18 cal
3 –1.0 × 102
4 –690.9 cal
4 Zero
Question Question
2 mole of an ideal gas at 27°C expands isothermally and reversibly from a volume The work done on the system when one mole of an ideal gas at 500 K is
of 4 litres to 40 litres. The work done (in kJ) is: compressed isothermally and reversibly to
𝟏 th
of its original volume (R = 2 cal)
𝟏𝟎
1 w = –28.72 kJ
1 500 kcal
2 w = –11.488 kJ
2 15.1 kcal
3 w = –5.736 kJ
3 25.03 kcal
4 w = –4.988 kJ
4 2.303 kcal
Question Question
The maximum work done in expanding 16g oxygen at 300 K and occupying a The internal energy change when a system goes from state A to B is 40 kJ/mol. If
volume of 5 dm3 isothermally until the volume becomes 25 dm3 is: the system goes from A to B by a reversible path and returns to state A by an
irreversible path. What would be the change in internal energy?
1 –2.01 × 103 J
1 40 kJ
2 2.81 × 10–3 J
2 > 40 kJ
3 2.01 × 10–6 J
3 < 40 kJ
4 –2.01 × 10–6 J
4 Zero
Question Question
One mole of oxygen is allowed to expand isothermally and reversibly from 5 m3 to Isothermal free expansion of an ideal gas correspond to
10 m3 at 300 K. Calculate work done in expansion of gas.
1 q=0
1 –172.89 J
2 w=0
2 1728.98 J
3 None of these
3 –1728.98 J
4 Both (1) and (2)
4 172.89 J
Question Question
Two moles of an ideal monoatomic gases are allowed to expand adiabatically and Adiabatic expansion of ideal gas into vacuum correspond to:
reversibly from 300K to 200 K. The work done in the system is (CV = 12.5 J/K mol)
1 w=0
1 –12.5 kJ
2 E = 0
2 –2.5 kJ
3 H = 0
3 –625 kJ
4 All of these
4 500 kJ
Question Question
The temperature of 1 mole of a gas is increased by 1°C at constant pressure. The The relation of internal energy, enthalpy and work done can be represented by
work done is:
1 E = H + W
1 –R
2 E = W – H
2 2R
3 H = E + W
3 R/2
4 W = E + H
4 3R
Question Question
A gas expands isothermally against a constant external pressure of 1 atm from a The work done in adiabatic process on ideal gas by a constant external pressure
volume of 10 dm3 to a volume of 20 dm3. It absorbs 800 J of thermal energy from would be
its surroundings. The U is
1 Zero
1 –312 J
2 E
2 +123 J
3 H
3 –213 J
4 G
4 +231 J
Question Question
A certain amount of zinc is dissolved in HCl at 25oC in an open vessel. The type of A system absorb 20 kJ heat and does 10 kJ work then internal energy of system
process and the work done by the system respectively would be will be–
4 None 4 Decreases by 30 kJ
Question Question
5 mol of ideal gas expands isothermally and irreversibly from a pressure of 10 Match the column:
atm to 1 atm against constant external pressure of 1 atm work at 300 K will be: Column-I Column-II
a. Adiabatic process i. q=0
1 –15.921 kJ b. Isothermal process ii. H = 0
c. Isoenthalpic process iii. T = 0
2 –11.224 kJ d. Isoentropic process iv. S = 0
Which of the following is correct for free expansion of ideal gas under isothermal An ideal gas receives 10 J of heat in a reversible isothermal expansion. Then the
condition: work done by the gas:
2 q = 0, T = 0, w = 0 2 10 J
4 q 0, T = 0, w 0 4 Cannot be determined
Question Question
Net work done by the system in a cyclic process is equal to: Heat absorbed by a system in going through a cyclic process shown in figure is:
1 Zero 1 107 J 30
V (in L)
2 ΔU 2 106 J
10 30
10
3 ΔΗ 3 102 J
P (in kPa)
4 q 4 104 J
Question Question
An ideal gas is taken around the cycle ABCA as shown in P–V diagram. The net What is the final temperature of 0.10 mole monoatomic ideal gas that performs 75
work done during the cycle is equal to: cal of work adiabatically if the initial temperature is 227°C?
(use R = 2 cal/K-mol)
1 12P1V1 B
6P 1
1 250 K
Pressure
2 6P1V1
P1 C
A 2 300 K
3 5P1V1 V1 3V1
Volume 3 350 K
4 P 1 V1
4 750 K
Question Question
A given mass of gas expands from the state A to the state B by three paths 1, 2 Two moles of Helium gas undergo a reversible cyclic process as shown in figure.
and 3 as shown in the figure. If w1, w2, and w3 respectively be the magnitudes Assuming gas to be ideal. What is the work for the process C to D?
work done by the gas along three paths then:
1 –800 Rℓn2
B
1 w1 > w2 > w 3 P 2 atm C
2 Zero
1 atm D
2 w1 < w2 < w 3 A A
3 300 K 400 K
T
2 3 +200 Rℓn2
3 w1 = w2 = w 3 1 B
V 4 –600 Rℓn2
4 w2 < w3 < w 1
Question Question
Heat capacity of H2O at its boiling point is: For monoatomic ideal gas, the exact value of the ratio of Cp, m and Cv, m is:
4 Infinite
4
Question Question
Molar heat capacity of water in equilibrium with ice at constant pressure is: How many calories are required to heat 40 gram of argon from 40 to 100°C at
constant volume?
1 Zero
(R = 2 cal/mol K)
2 Infinity 1 120
4 180
Question Question
4.48 L of an ideal gas at STP requires 12.0 calories to raise its temperature by 15°C Calculate the amount of heat required to raise the temperature of 5 g of iron from
at constant volume. The Cp of the gas is: 25°C to 75°C. The specific heat capacity of iron is 0.45 J/g.
1 3 cal 1 112.1
2 4 cal 2 112.5
3 7 cal 3 112.9
4 6 cal 4 112
Question Question
For two mole of an ideal gas The heat required to raise the temperature of a body by 1 K is called
1 Cv – Cp = R 1 Specific heat
2 Cp – Cv = 2R 2 Thermal capacity
3 Cp – Cv = R 3 Water equivalent
4 Cv – Cp = 2R 4 None of these
Question
A gas expands adiabatically at constant pressure such that TV1/2. The value of
(Cp/Cv) of the gas will be:
1 1.30
2 1.50
3 1.70
4 2
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∘
A(g) + B(g) → C(g) Q15 Which one of the following has ΔS greater
Yakeen NEET 2.0 2025(Alpha) ΔU = −3.0 kcal ΔS = −10.0 cal/K than zero?
(R ≈ 2 calmol−1 K−1 ) (A) CaO(s) + CO2 ( g) ⇌ CaCO3 ( s)
Physical Chemistry (B) NaCl(aq) ⇌ NaCl(s)
DPP: 6
ΔG is (C) NaNO3 ( s) ⇌ Na+ (aq) + NO− 3 (aq)
Thermodynamics and Thermochemistry (A) −600 cal (D) N2 ( g) + 3H2 ( g) ⇌ 2NH3 ( g)
(B) −3600 cal
Q1 5 mole of an ideal gas expand reversibly from (A) Entropy increases Q16 The entropy of vaporization of benzene is
(C) 2400 cal
a volume of 8dm3 to 80dm3 at a temperature (B) Entropy decreases
(D) 3000 cal
85JK−1 mol−1 . When 117 g benzene vaporizes
of 27∘ C . The change in entropy is (C) Entropy increases and then decreases at its normal boiling point, the entropy change of
−1 Q11 Mark the correct statement
(A) 41.57JK (D) Free energy increases surrounding is :
(B) −95.73JK
−1 (A) For a chemical reaction to be feasible, ΔG (A) −85 J/K
Q6 Which of the following is true for the reaction?
(C) 95.73JK−1 should be zero (B) −85 × 1.5 J/K
H2 O(ℓ) ⇌ H2 O(g) at 100∘ C and 1 atm
(D) −41.57JK−1 (B) Entropy is a measure of order in a system (C) 85 × 1.55 J/K
pressure
(C) For a chemical reaction to be feasible, ΔG (D) None of these
Q2 Which of the following conditions is not (A) ΔS=0 should be positive
favourable for the feasibility of a process? (B) ΔH = TΔS
(D) The total energy of an isolated system is
Q17 1 mole of a diatomic ideal gas at 25∘ C is
(A) ΔH = −ve, TΔS = − ve and (C) ΔH = ΔU subjected to expand reversibly and adiabatically
constant
TΔS < ΔH (D) ΔH = 0 to ten times of its initial volume. Calculate the
(B) ΔH = + ve, TΔS = + ve and Q12 Two molecules of an ideal gas expand change in entropy during expansion (in
Q7 For a reaction to be spontaneous at all
TΔS > ΔH spontaneously into a vacuum. The work done is JK−1 mol−1 )
temperatures
(C) ΔH = − ve, TΔS = + ve and (A) 2J (A) R ln 10
(A) ΔG and ΔH should be negative
ΔH > TΔS (B) 4 J (B) −R ln 10
(B) ΔH = ΔG = 0
(D) ΔH = + ve, TΔS = + ve and (C) 8 J (C) 2.5R ln 10
(C) ΔG and ΔH should be positive
ΔH > TΔS (D) Zero (D) zero
(D) ΔH < ΔG
Q3 In which of the following cases, the reaction is Q13 Predict which of the following reaction (s) has a Q18 Three moles of an ideal gas expanded
Q8 For isothermal expansion in case of an ideal gas:
spontaneous at all temperatures? positive entropy change. spontaneously in to vacuum. Then which is
(A) ΔG = ΔS +
(A) ΔH > 0, ΔS > 0 I. Ag (aq) + Cl− (aq) → AgCl(s) correct?
(B) ΔG = ΔH
(B) ΔH < 0, ΔS > 0 II. NH4 Cl(s) → NH3 ( g) + HCl(g) (A) W = 0, ΔG = 0
(C) ΔG = −T. ΔS
(C) ΔH < 0, ΔS < 0 III. 2NH3 ( g) → N2 ( g) + 3H2 ( g) (B) W = 0, ΔG < 0
(D) None of these
(D) ΔH > 0, ΔS < 0 (A) I and II (B) III (C) W = 0, ΔG > 0
Q9 A reaction has ΔH = −33 kJ and (C) II and III (D) II (D) W ≠ 0, ΔG = 0
Q4 For an endothermic reaction, ΔS is positive. The
ΔS = −58 J/K. This reaction would be: Q14 Which of the following reactions is associated
reaction is: Q19 Match the following in List-I with List-II and select
(A) Spontaneous below a certain temperature
(A) Feasible when TΔS > ΔH with negative change in entropy? the correct option:
(B) Non-spontaneous at all temperature
(B) Feasible when ΔH > TΔS (A) 2SO3 ( g) → 2SO2 ( g) + O2 ( g)
(C) Spontaneous above a certain temperature
(C) Feasible at all temperatures (B) C2 H6 ( g) → C2 H4 ( g) + H2 ( g)
(D) Spontaneous at all temperature
(D) Not feasible at all (C) 2C (s , graphite) +O2 ( g) → 2CO(g)
Q10 For the reaction at 300 K. (D) 3C2 H2 ( g) → C6 H6 (l)
Q5 When potassium chloride is dissolved in water
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Answer Key
Q1 (C) Q17 (D)
Q11
Q12
(D)
(D)
Q27
Q28
(A)
(C)
DPP SOLUTION
Q13 (C) Q29 (C)
For a given reaction, H = 40 kJ mol–1 and S = 80 JK–1 mol–1. The reaction is A reaction occur spontaneously. If
spontaneous at (assume that H and S do not vary with temperature)
1 TS = H and both H and S are positive
1 T > 500
Which of the following endothermic process is/are spontaneous? During an adiabatic process:
4 Both (1) and (2) 4 The system changes heat with surroundings
Question Question
The entropy of the universe Which of the following has highest entropy?
Which of the following processes is not accompanied by increase of entropy? For a reversible process at equilibrium, the change in entropy may be expressed
as:
1 Dissolution of NH4Cl in water
1 S = Tqrev
2 Burning of rocket fuel
qrev
2 S =
T
3 Sublimation of dry ice
ΔH
3 S =
T
4 Condensing steam
4 S = G
Question Question
Entropy is a measure of When a solid is converted directly into gaseous state, the process is called
sublimation. The entropy change during the process is:
1 Disorder
1 Zero
2 Internal energy
2 Negative
3 Efficiency
3 Positive
4 Useful work done by the system
4 May be negative or zero
Question Question
The enthalpy of vaporisation of a compound AB at its boiling point (127°C) is 6.4 The entropy change for the conversion of 1 mol of -tin (at 13°C, 1 atm) to 1 mol of
kJ mol–1. Its entropy of vaporisation is: -tin (13°C, 1 atm), if enthalpy of transition is 2.095 kJ mol–1 is:
1 2.56 kJ mol–1 1 7.32 J mol–1 K–1
The following data is known about the melting of a compound AB. H = 9.2 kJ 𝟓
When two mole of an ideal gas 𝐂𝐩,𝐦 = 𝐑 heated from 300 K to 600 K at constant
mol–1. S = 0.008 kJ K–1 mo1–1. Its melting point is: 𝟐
pressure. The change in entropy of gas (S) is:
1 736 K
3
1 R𝓁n2
2
2 1050 K
3
2 – R𝓁n2
2
3 1150 K
3 5R𝓁n2
4 1150C
5
4 R𝓁n2
2
Question Question
𝟑
When two mole of an ideal gas 𝐂𝐯 = 𝐑 heated from 300 K to 600 K at constant The entropy change when two moles of ideal monoatomic gas is heated from
𝟐
200°C to 300°C reversibly and isochorically?
volume. The change in entropy of gas (S) is:
1 5Rln2 1
3
2 𝑅𝓁𝑛2 2
2
3 3Rln2
3
4 –3Rln2
4
Question Question
𝟓
If one mole of an ideal gas 𝐂𝐩.𝐦. = 𝐑 is expanded isothermally at 300 K until it's When one mole of an ideal gas is compressed to half of its initial volume and
𝟐
simultaneously heated to twice its initial temperature, the change in entropy of
volume is tripled, then change in entropy of gas is:
gas (S) is:
1 Zero
1 Cp ln2
2 Infinity
2 Cv ln2
5
3 𝑅𝓁𝑛3
2 3 Rln2
Theheat of combustion of ethanol determined in a bomb calorimeter is –670.48 From the reaction P(White) → P(Red);
Kcals mole–1 at 25°C. What is ∆H at 25°C for the reaction: ∆H = –18.4 KJ. It follows that:
4 +670.48 Kcals. 4 White P can be converted into red P and red P is more stable
Question Question
Since the enthalpy of the elements in their standard states is taken to be zero. The Which of the following equations represents standard heat of formation of CH4?
heat of formation (∆Hf ) of compounds:
1 C(diamond) + 2H2(g) → CH4(g)
1 Is always negative
2 C(graphite) + 2H2(g) → CH4(g)
2 Is always positive
3 C(diamond) + 4H2(g) → CH4(g)
3 Is zero
4 C(graphite) + 4H2(g) → CH4(g)
4 May be positive or negative
Question Question
Given enthalpy of formation of CO2(g) and CaO(s) are –94.0 KJ and –152 KJ The enthalpies of combustion of carbon and carbon monoxide are –393.5 KJ and
respectively and the enthalpy of the reaction: –283 KJ, respectively the enthalpy of formation of carbon monoxide is:
CaCO3(s) → CaO(s) + CO2(g) is 42 KJ.
1 –676.5 KJ
The enthalpy of formation of CaCO3(s) is
1 –42 KJ 2 –110.5 KJ
2 –202 KJ 3 110.5 KJ
3 +202 KJ 4 676.5 KJ
4 –288 KJ
Question Question
The heat of combustion of CH4(g), C(s) and H2(g) at 25°C are –212.4 Kcal, –94.0 Standard enthalpy of formation is zero for.
Kcal and –68.4 Kcal respectively, the heat of formation of CH4 will be-
1 Cdiamond
1 +54.4 Kcal
2 Br(g)
2 –18.4 Kcal
3 Cgraphite
3 –375.2 Kcal
4 O3(g)
4 +212.8 Kcal
Question Question
Heat of formation of CO2 is –94.0 Kcal. What would be the quantity of heat If S + O2 → SO2; ∆H = –298.2 kJ mol–1
𝟏
liberated, when 3 g of graphite is burnt in excess of oxygen: SO2 + O2 → SO3; ∆H = –98.7 kJ mol–1
𝟐
1 23.5 Kcals SO3 + H2O → H2SO4; ∆H = –130.2 kJ mol–1
𝟏
H2 + O2 → H2O; ∆H = –287.3 kJ mol–1
𝟐
Then the enthalpy of formation of H2SO4 at 298 K will be–
2 2.35 Kcals
1 –814.4 kJ mol–1
3 94.0 Kcals
2 –650.3 kJ mol–1
4 31.3 Kcals
3 –320.5 kJ mol–1
4 –433.5 kJ mol–1
Question Question
𝟏 𝟏
The heat of reaction for 𝐀 + 𝐎𝟐 → 𝐀𝐎 is –50 kcal/mol and 𝐀𝐎 + 𝐎𝟐 → 𝐀𝐎𝟐 is Which of the reaction defines molar ∆Hf°?
𝟐 𝟐
100 kcal/mol. The heat of reaction (in kcal/mol) for A + O2 → AO2 will be: 1 CaO(s) + CO2(g) → CaCO3(s)
1 –50
1 1
2 Br2 (g) + H2 (g) → HBr(g)
2 2
2 +50
3
3 N2(g) + 2H2 (g) + O2 (g) → NH4 NO3 (s)
2
3 100
4 I2(g) + H2(g) → 2HI(g)
4 150
Question Question
The enthalpy of formation of ammonia is –46.0 kJ mol–1. The enthalpy change for The molar heat of combustion of C6H6 is –3250 kJ mol–1. When 0.39 g of C6H6 is
following reaction is 2NH3 → N2 + 3H2 burnt in excess of oxygen in an open vessel, the amount of heat evolved is:
1 285.7 K
2 N2(g) + 3H2(g) → 2NH3(g)
2 273 K
3 PCl5(g) → PCl3(g) + Cl2(g)
3 450 K
4 SO2(g) + 1/2O2(g) → SO3(g)
4 300 K
Question Question
The following reactions are given : U° of combustion of methane is –X kJ mol–1. The value of H° is:
CH4(g) + 2O2(g) → CO2(g) 2H2O(g); H = –x …(i)
1 –X –596 R
C(s) + O2(g) → CO2(g); H = –y …(ii)
H2(g) + 1/2O2(g) → H2O(g); H = –z ...(iii)
Calculate the heat of formation of CH4? 2 –X + 596 R
1 x+y+z
3 X + 596 R
2 y + 2z – x
4 X – 596 R
3 x – y – 2z
1 +525 kJ
2 +325 kJ
3 –175 kJ
4 –325 kJ
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(D) May be negative or zero Q16 The entropy change when two moles of ideal
Yakeen NEET 2.0 2025(Alpha) monoatomic gas is heated from 200∘ C to
Q11 The enthalpy of vaporisation of a compound AB ∘
300 C reversibly and isochorically?
Physical Chemistry at its boiling point (127
∘
C) is 6.4 kJ mol−1 . Its (A) 32 Rℓn ( 300 )
DPP: 7 entropy of vaporisation is:
200
(B) 52 Rℓn ( 573 )
Thermodynamics and Thermochemistry (A) 2.56 kJ mol−1 273
(C) 3R ln( 573 )
(B) 16 J mol−1 K−1 473
(D) 32 Rℓn ( 573 )
Q1 For a given reaction,ΔH = 40 kJ mol−1 and (B) Tends towards a minimum (C) 16 × 10−3 J mol−1 473
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(D) White P can be converted into red P and red (A) +54.4 Kcal Q30 Which of the reaction defines molar ΔHf ? Q35 The following reactions are given :
P is more stable (B) −18.4Kcal (A) CaO(s) + CO2 ( g) → CaCO3 ( s)
CH4 ( g) + 2O2 ( g) → CO2 ( g)2H2 O(g);
(C) −375.2 Kcal (B) 12 Br2 ( g) + 12 H2 ( g) → HBr(g)
Q21 Since the enthalpy of the elements in their ΔH = −x … (i)
(D) +212.8 Kcal (C) N2 ( g) + 2H2 ( g) + 32 O2 ( g)
standard states is taken to be zero. The heat of C(s) + O2 ( g) → CO2 ( g); ΔH = −y
formation (ΔHf ) of compounds: Q26 Standard enthalpy of formation is zero for
→ NH4 NO3 ( s)
(D) I2 ( g) + H2 ( g) → 2HI(g) … (ii)
(A) Is always negative (A) Cdiamond
H2 ( g) + 1/2O2 ( g) → H2 O(g); ΔH = −z
(B) Is always positive (B) Br(g) Q31 The enthalpy of formation of ammonia is … (iii)
(C) Is zero (C) Cgraphite −46.0 kJ mol−1 . The enthalpy change for
(D) May be positive or negative (D) O3(g) following reaction is 2NH3 → N2 + 3H2 Calculate the heat of formation of CH4 ?
(A) 42.0 kJ mol−1 (A) x + y + z
Q22 Which of the following equations represents Q27 Heat of formation of CO2 is −94.0 K. cal. What
(B) 64.0 kJ mol m−1 (B) y + 2z − x
standard heat of formation of CH4 ? would be the quantity of heat liberated, when
(C) 86.0 kJ mol−1 (C) x − y − 2z
(A) C(diamond) + 2H2 ( g) → CH4 ( g) 3 g of graphite is burnt in excess of oxygen:-
(D) 92.0 kJ mol−1 (D) none of the above
(B) C(graphite) + 2H2 ( g) → CH4 ( g) (A) 23.5 K cals
(C) C(diamond) + 4H2 ( g) → CH4 ( g) (B) 2.35 K cals Q32 The molar heat of combustion of C6 H6 is Q36 ΔU∘ of combustion of methane is
(D) C(graphite) + 4H2 ( g) → CH4 ( g) (C) 94.0 K cals −3250 kJ mol−1 . When 0.39 g of C6 H6 is −XkJmol−1 . The value of ΔH∘ is:
(D) 31.3 K cals burnt in excess of oxygen in an open vessel, the (A) −X − 596R
Q23 Given enthalpy of formation of CO2 ( g) and (B) −X + 596R
−1 amount of heat evolved is:
CaO(s) are −94.0KJ and −152KJ Q28 If S + O2 → SO2 ; ΔH = −298.2 kJ mol
(A) 8.32 kJ (C) X + 596R
respectively and the enthalpy of the reaction: 1
SO2 + O2 → SO3 ; ΔH = (B) 12.36 kJ (D) X − 596R
CaCO3 ( s) → CaO(s) + CO2 ( g) is 42KJ. 2
(C) 16.25 kJ
The enthalpy of formation of CaCO3 ( s) is −98.7 kJ mol−1 Q37 Consider the following process:
SO3 + H2 O → H2 SO4 ; ΔH = (D) 20.74 kJ
(A) −42KJ A → 2 B; ΔH = +150 kJ
(B) −202KJ −130.2 kJ mol−1 Q33 The enthalpy and entropy change for the 3 B → 2C + D; ΔH = −125 kJ
(C) +202KJ 1 G + A → 2D; ΔH = +350 kJ
H2 + O2 → H2 O; ΔH = reaction,Br2 (l) + Cl2 ( g) → 2BrCl(g) are
(D) −288KJ 2 For B + D → G + 2C; ΔH will be
30 kJ mol−1 and 105 Jk−1 mol−1 respectively.
−287.3 kJ mol−1 (A) +525 kJ
The temperature at which the reaction will be in
Q24 The enthalpies of combustion of carbon and Then the enthalpy of formation of H2 SO4 at (B) +325 kJ
equilibrium is:
carbon monoxide are −393.5KJ and −283KJ , 298 K will be- (C) −175 kJ
(A) 285.7 K
respectively the enthalpy of formation of carbon (A) −814.4 kJ mol − 1 (D) −325 kJ
(B) 273 K
monoxide is (B) −650.3 kJ mol−1
(C) 450 K
(A) −676.5KJ (C) −320.5 kJ mol−1
(D) 300 K
(B) −110.5KJ (D) −433.5 kJ mol−1
(C) 110.5KJ Q34 Assume each reaction is carried in open
Q29 The heat of reaction for A + 12 O2 → AO is
(D) 676.5KJ container. For which reaction ΔH
> ΔE ?
−50kcal/mol and AO + 12 O2 → AO2 is
(A) H2 ( g) + I2 ( g) → 2HI(g)
Q25 The heat of combustion of CH4( g) , C(s) and 100kcal/mol. The heat of reaction (in
(B) N2 ( g) + 3H2 ( g) → 2NH3 ( g)
H2( g) at 25∘ C are −212.4 Kcal, −94.0 Kcal kcal/mol ) for A + O2 → AO2 will be:
(C) PCl5 ( g) → PCl3 ( g) + Cl2 ( g)
and −68.4 Kcal respectively, the heat of (A) -50 (B) +50
(D) SO2 ( g) + 1/2O2 ( g) → SO3 ( g)
formation of CH4 will be- (C) 100 (D) 150
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Q4 (C) Q23 (D) Q1 The heat of combustion of CH4 is ethanol at the same temp. and constant volume
(D) NaOH and HCl Q14 On combustion, carbon forms two oxides CO The standard Gibbs energy of reaction (at At absolute zero temp. the entropy of all
and CO2 . Heat of formation of CO2 is 1000 K ) is −8.1 kJ mol−1 . Value of crystalline substance is taken be zero
Q9 Heat of combustion of a substance:
−393.5 kJ and that of CO is −110.5 kJ . Heat equilibrium constant is- (D) At absolute zero temp. the entropy of a
(A) is always positive
of combustion of CO is: (A) 2.6 (B) 6.2 perfectly crystalline solid is taken to be zero.
(B) is always negative
(A) −393.5 kJ (C) 8.2 (D) 10
(C) is equal to heat of formation
(B) −504.0 kJ
(D) Nothing can be said without reaction Q20 Calculate the Gibbs energy change when 1 mole
(C) −283.0 kJ
of NaCl is dissolved in water at 25∘ C . Lattice
Q10 The heat of formations of CO(g) and CO2 ( g) (D) 2830.0 kJ −1
energy of NaCl = 777.8 kJ mol ; ΔS for
are- 26.4kcal and −94.0kcal respectively. The
Q15 The equilibrium constant for a reaction is 100 dissolution = 0.043 kJmol−1 and hydration
heat of combustion of carbon monoxide will be
what will be the value of ΔG∘ ? energy of NaCl = −774.1 kJ mol−1 .
(A) −67.6kcal
R = 8.314JK−1 mol−1 , T = 300 K : (A) −9.114 kJ mol−1
(B) 36.5kcal
(A) −11488 kJ (B) −11.4 kJ mol−1
(C) −36.5kcal
(B) −11.488 kJ (C) −5.4 kJ mol−1
(D) −46.5kcal
(C) −12 kJ (D) −4.5 kJ mol−1
Q11 Which of the following statement is true? (D) −12000 kJ
Q21 For vaporization of water at 1 atm pressure, the
(A) ΔH is positive for exothermic reactions
Q16 For the reaction: N2 O4 (g)
⇌ 2 NO2 (g) values of ΔH and ΔS are 40.63 kJ mol−1 and
(B) ΔH is negative for endothermic reactions
ΔU = 2. 0 Kcal, Δ S = 50 cal K−1 at 108.8 JK −1
mol −1
respectively. The temp. at
(C) The enthalpy of fusion is negative
300 K which Gibbs energy change (ΔG) for this
(D) The heat of neutralization of strong acid with
Calculate ΔG transformation will be zero is:
strong base is always the same
(A) +12.4 kcal (A) 273.4 K
Q12 Given (B) −12.4 kcal (B) 393.4 K
(C) −6.4 kcal (C) 373.4 K
H2 ( g) + 1/2O2 ( g) → H2 O(g) + q1 (D) +6.4 kcal (D) 293.4 K
H2 ( g) + 1/2O2 ( g) → H2 O(l) + q2
Q17 Which relation is incorrect: Q22 Calculate ΔG∘ for the conversion of oxygen
The enthalpy of vaporization of water is equal to (A) ΔG = −TΔST to ozone, 3/2O2 ( g) ⟶ O3 ( g) at 298 K . If
(A) q1 + q2 (B) ΔG∘ = −2.303 RT log K KP for this conversion is 3 × 10−29 .
(B) q1 − q2 (C) ΔH = ΔU + Δng RT (A) +175.3 kJ mol−1
(C) q2 − q1 (D) Wuseful = ΔH (B) +162.7 kJ mol−1
(D) q1 q2 (C) −162.7 kJ mol−1
Q18 Which is always correct at equilibrium
∘ (D) −140.5 kJ mol−1
Q13 (A) ΔG =0
(B) ΔG = 0 Q23 Identify the correct statement regarding entropy.
(C) ΔSsystem = 0 (A) At 0∘ C , the entropy of a perfectly crystalline
(D) ΔE = 0 substance is taken to be zero.
(A) x + y (B) At absolute zeró temp. the entropy of a
Q19 For the water gas reaction
(B) x−y perfectly crystalline solid is positive.
(C) y − x C(s) + H2 O(g) ⇌ CO(g) + H2 ( g) (C)
(D) x − y/2
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NEET
Answer Key
Q1 (C) Q13 (C)
Q11
Q12
(D)
(C)
Q23 (D)
DPP SOLUTION
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• Subject – Physical Chemistry
Enthalpy of neutralisation of CH3COOH by NaOH is –50.6 kJ/mol and the heat of If heat of dissociation of CHCl2COOH is 0.7 kcal/mol then ∆H for the reaction
neutralisation of a strong acid with NaOH is –55.9 kJ/mol. The value of ∆H for the CHCl2COOH + KOH → CHCl2COOK + H2O
ionisation of CH3COOH is
1 –13 kcal
1 3.5 kJ/mol
2 +13 kcal
2 4.6 kJ/mol
3 –14.4 kcal
3 5.3 kJ/mol
4 –13.7 kcal
4 6.4 kJ/mol
Question Question
The bond dissociation energy of gaseous H2, Cl2 and HCl are 104, 58 and 103 kcal AB, A2 and B2 are diatomic molecules. If the bond enthalpies of A2, AB and B2 are
mol–1 respectively. The enthalpy of formation for HCl gas will be in the ratio 1 : 1 : 0.5 and enthalpy of formation of AB from A2 and B2 is – 100
kJ/mol–1. What is the bond enthalpy of A2?
1 –44.0 kcal
1 400 kJ/mol
2 –22.0 kcal
2 200 kJ/mol
3 22.0 kcal
3 100 kJ/mol
4 44.0 kcal
4 300 kJ/mol
Question Question
Heat of combustion ∆Ho for C(s), H2(g) and CH4(g) are –94, –68 and –213 kcal/mol. If the bond energies of H–H, Br–Br and H–Br are 433, 192 and 364 kJ mol–1
Then, ∆Ho for respectively, then ∆Ho for the reaction H2(g) + Br2(g) → 2HBr(g) is
C(s) + 2H2(g) → CH4(g) is
1 –261 kJ
1 –17 kcal/mol
2 +103 kJ
2 –111 kcal/mol
3 +261 kJ
3 –170 kcal/mol
4 –103 kJ
4 –85 kcal/mol
Question Question
The absolute enthalpy of neutralisation of the reaction, Given C(s) + O2(g) → CO2(g); H = –94.2 kcal
MgO(s) + 2HCl(aq) → MgCl2(aq) + H2O(l) will be H2(g) + 1/2O2(g) → H2O(g); H = –68.3 kcal
CH4(g) + 2O2(g) → CO2(g) + 2H2O(g); H = –210.8 kcal
1 Less than –57.33 kJ mol–1
What will be heat of formation of CH4 in (kcal)?
4 –47.3
Question Question
From the given information, what is the standard enthalpy of formation for Consider the following reactions
Al2O3(s)? C(s) + O2(g) → CO2(g) + X kJ
2Al2O3(s) → 4Al(s) + 3O2(g); H°rxn = 3352 kJ CO(g) + 1/2O2(g) → CO2(g) + Y kJ
The heat of formation of CO(g) is
1 –6704 kJ/mol
1 –(X + Y) kJ/mol
2 –3352 kJ/mol
2 (X – Y) kJ/mol
3 –1676 kJ/mol
3 (Y – X) kJ/mol
4 1676 kJ/mol
4 (Y + X) kJ/mol
Question Question
The enthalpy change for the following reaction is 368 kJ. Calculate the average N2(g) + 2O2(g) → 2NO2(g) + xkJ
O–F bond energy 2NO(g) + O2(g) → 2NO2(g) + ykJ
OF2(g) → O(g) + 2F(g) The enthalpy of formation of NO is
1 184 kJ/mol 1 x – 2y
1
3 536 kJ/mol 3 (y – x)
2
4 736 kJ/mol 4
1
(x – y)
2
Question Question
Consider the reaction: Use the given H°f value to determine enthalpy of reaction of the following
4NO2(g) + O2(g) → 2N2O5(g) rH = –111 kJ. If N2O5(s) is formed instead of N2O5(g) in reaction.
the above reaction the rH value will be (given DH of sublimation of N2O5 is 54 kJ NH3(g) + 3F2(g) → NF3(g) + 3HF(g)
mol–1) H°f (NH3, g) = –46.2 kJ/mol
H°f (NF3, g) = –113.0 kJ/mol
1 –219 kJ
H°f (HF, g) = –269.0 kJ/mol
1 –335.8 kJ/mol
2 –165 kJ
2 –873.8 kJ/mol
3 54 kJ
3 –697.2 kJ/mol
4 218 kJ
4 –890.4 kJ/mol
Question Question
2 moles of an ideal gas is expanded isothermally and reversibly from 1 L to 10 L. When 0.5 g of sulphur is burnt to SO2, 4.6 kJ of heat is liberated. What is the
Find the enthalpy change in kJ mol–1. enthalpy of formation of Sulphur dioxide.
1 0 1 +147.2 kJ
2 11.7 2 –147 kJ
3 –11.7 3 –294.4 kJ
4 25 4 +294.4 kJ
Question Question
The species which by definition has zero standard molar enthalpy of formation at The enthalpies of formation of N2O and NO at 298 K are 82 and 90 kJ mol–1. The
298 K is: enthalpy of the reaction:
Br2(g) N2O(g) + ½O2(g) → 2NO(g)
1
1 –8 kJ
2 Cl2(g)
2 98 kJ
3 H2O(g)
3 –74 kJ
4 CH4(g)
4 8 kJ
Question Question
Calculate the heat required to make 6.4 Kg CaC2 from CaO(s) and C(s) from the The enthalpies of elements in their standard states are taken as zero. Hence the
reaction: enthalpy of formation of a compound
CaO(s) + 3C(s) → CaC2(s) + CO(g) given that fH°(CaO) = –151.6 kcal, fH° Should always be negative
1
(CaC2) = –14.2 kcal.
fH°(CO) = –26.4 kcal.
2 Should always be positive
1 5624 kcal
3 Will be equal to twice the energy of combination
2 1.11 × 104 kcal
4 May be positive or negative
3 86.24 × 103
4 1100 kcal
Question Question
Which of the following equations represents standard heat of formation of For the reaction,
methane? 2H2O(l) → 2H2(g) + O2(g) H = 571.6 KJ
C (diamond) + 2H2(g) → CH4(g) fH° of water is:
1
1 285.8 kJ
2 C (graphite) + 2H2(g) → CH4(g)
2 –285.8 kJ
3 C (diamond) + 4H(g) → CH4(g)
3 1143.2 kJ
4 C (graphite) + 4H(g) → CH4(g)
4 –1143.2 kJ
Question Question
Bond dissociation enthalpy is used to defining enthalpy change of a reaction as In which of the following case carbon-carbon bond dissociation energy is
maximum?
1 ΔHr = Σ(Bond dissociation enthalpy)Reactant – Σ(Bond dissociation enthalpy)Product
1 Ethane
2 ΔHr = Σ(Bond dissociation enthalpy)Product – Σ(Bond dissociation enthalpy)Reactant
2 Ethene
3 ΔHr = Σ(Bond dissociation enthalpy)Product + Σ(Bond dissociation enthalpy)Reactant
3 Butene
4 None of these
4 Ethyne
Question Question
In which of the following case enthalpy of a reaction is just a bond dissociation Calculate ΔHreaction for
enthalpy of reactant? 𝟏 𝟏
H2 + Cl2 → HCl
𝟐 𝟐
1 PCl5 → PCl3 + Cl2 When bond dissociation enthalpy of H2, Cl2 and HCl is given as 433 kJ/mol, 243.5
kJ/mol and +431 kJ/mol respectively
2 H2 → 2H 1 –244.5 kJ/mol
1
3 H2O2 → H2O + O2 2 244.5 kJ/mol
2
4 –93.25 kJ/mol
Question Question
The enthalpy of dissociation of PH3 is 954 kJ/mol and that of P2H4 is 1.485 Which of the following acid has lowest value (magnitude) of heat neutralization?
MJ/mol. What is the bond enthalpy of P–P bond?
1 CH3COOH
1 213 kJ/mol
2 HCl
2 413 kJ/mol
3 HBr
3 200 kJ/mol
4 HI
4 Given data is incorrect
Question Question
The enthalpy of neutralization of any strong acid and strong base is nearly equal The Enthalpy of neutralization of acetic acid and sodium hydroxide is –55.4kJ.
to What is the enthalpy of ionisation of acetic acid?
1 +57.3 kJ/mol 1 –5.54 kJ
Heat of neutralization of strong acid by a strong base is equal to ΔH of In the heat released in neutralization of HCl and NaOH is 13.7 kcal/mol, the heat
released on neutralization of NaOH with CH3COOH is 3.7 kcal/mol. The H° of
1 H+ + OH– ⎯→ H2O
ionization of CH3OOOH is
4 9.5 kcal
Question Question
From the following bond energies:
Given that
H-H bond energy = 420 kJ mol–1
A(s) → A(l) H = x
CoC bond energy = 601 kJ mol–1
A(l) → A(g) H = y
C-C bond energy = 340 kJ mol–1
The heat of sublimation of A will be
C-H bond energy = 425 kJ mol–1
1 x–y Enthalpy for the reaction:
C2H2 + 2H2 → C2H6
2 x+y 1 –599 kJ mol–1
3 x or y 2 –580 kJ mol–1
4 –x + y 3 –625 kJ mol–1
4 –325 kJ mol–1
Question Question
Consider the following reaction: Given that Bond energies of H2 and N2 are 400 kJ mol–1 and 240 kJ mol–1
(a) H+(aq) + Cl–(aq) → HCl(l) ; DH = –X1 kJ mol–1 respectively and Hf of NH3 is –120 kJ mol–1. Calculate the bond energy of N–H
(b) H2(g) + Cl2(g) → 2HCl(l) ; DH = –X2 kJ mol–1 bond:
(c) 1/2H2(g) + 1/2 Cl2(g) → HCl(l);DH = –X3 kJ mol–1
1 300 kJ mol–1
(d) H(g) + Cl(g) → HCl(l) ; DH = –X4 kJ mol–1
Enthalpy of formation of HCl(l) is:
2 250 kJ mol–1
1 –X1 kJ mol–1
3 410 kJ mol–1
2 –X2 kJ mol–1
4 280 kJ mol–1
3 –X3 kJ mol–1
4 –X4 kJ mol–1
Question Question
Standard enthalpy of vapourisation H° for water is 40.66 kJ mol–1. The internal Enthalpy change for the reaction
energy of vapourisation of water will be: 2N (g) + 6H (g) → 2NH3 (g) is – 900 kJ
The dissociation energy of N – H bond is
1 +43.76 kJ mol–1
1 +450 kJ
2 +40.66 kJ mol–1
2 –450 kJ
3 +37.56 kJ mol–1
3 +150 kJ
4 None of these
4 –150 kJ
DPP SOLUTION
• Subject – Physical Chemistry
The heat of combustion of CH3 is –400 kJ mol–1. Calculate the heat transfer when 𝟏
CH4 + O2 → CH3OH; H = –ve
𝟐
40 g of H2 is formed upon combustion:
If enthalpy of combustion of CH4 and CH3OH is –x & –y respectively which relation
1 +444.4 kJ is correct?
1 x>y
2 +888.8 kJ
2 x<y
3 –444.4 kJ
3 x=y
4 –888.8 kJ
4 xy
Question Question
The heat of neutralization of LiOH and H2SO4 at 25°C is –69.6 kJ mol–1. The heat of Na(s) → Na(g), the heat of reaction is called as
ionization of LiOH will be nearly:
1 Heat of vaporisation
1 22.5 kJ mol–1
2 Heat of atomisation
2 90 kJ mol–1
3 Heat of sublimation
3 45 kJ mol–1
Heat of combustion of ethanol at const. pressure and at temp. TK in found to be For the combustion of 1 mole of liquid benzene at 27°C, the heat of reaction at
–q J mol–1. Hence, heat of combustion in (Jmol–1) of ethanol at the same temp. and const. pressure is given by
constant volume will be: C6H6(l) + 15/2O2(g) → 6CO2(g) + 3H2O(l)
H = –78 kcal. What would be heat of reaction at const. volume?
1 RT – q
1 –78.0 kcal
2 –q – RT
2 –78.9 kcal
3 q – RT
3 –77.1 kcal
4 q + RT
4 816.0 kcal
Question Question
Enthalpies of formation of C2H4(g), CO2(g) and H2O at 25°C and 1 atm pressure be In which of the following neutralization reactions, the heat of neutralization will
52, –394 and –286 kJ mol–1 respectively. The enthalpy of combustion of C2H4(g) be the highest?
will be:
1 NH4OH and CH3COOH
1 +1412 kJ mol–1
2 NH4OH and HCl
2 –1412 kJ mol–1
3 NaOH and CH3COOH
3 +141.2 kJ mol–1
4 NaOH and HCl
4 –141.2 kJ mol–1
Question Question
Heat of combustion of a substance: The heat of formations of CO(g) and CO2(g) are –26.4 kcal and –94.0 kcal
respectively.
1 Is always positive
The heat of combustion of carbon monoxide will be
4 –46.5 kcal
Question Question
4 The heat of neutralization of strong acid with strong base is always the same
3 q2 – q1
4 q1q2
Question Question
If CH3COOH + OH– → CH3COO– + H2O + x kJ On combustion, carbon forms two oxides CO and CO2. Heat of formation of CO2 is
H+ + OH– → H2O + y kJ –393.5 kJ and that of CO is –110.5 kJ. Heat of combustion of CO is:
The enthalpy change for the reaction:
1 –393.5 kJ
CH3COOH → CH3COO– + H+ is
1 x+y 2 –504.0 kJ
2 x–y 3 –283.0 kJ
3 y–x 4 2830.0 kJ
4 x – y/2
Question Question
The equilibrium constant for a reaction is 100 what will be the value of G°? For the reaction : N2O4(g) ⇌ 2NO2(g)
R = 8.314 JK–1 mol–1, T = 300 K: U = 2.0 kcal, S = 50 cal K–1 at 300 K calculate G?
1 –11488 kJ 1 +12.4 kcal
1 G = –T ST 1 G° = 0
3 H = U + ngRT 3 Ssystem = 0
4 wuseful = H 4 E = 0
Question Question
For the water gas reaction Calculate the Gibb’s energy change when 1 mole of NaCl is dissolved in water at
C(s) + H2O(g) ⇌ CO(g) + H2(g) 25°C. Lattice energy of NaCl = + 777.8 kJ mol–1; S for dissolution = 0.043 kJ mol–1
The standard Gibb’s energy of reaction (at 1000 K) is –8.1 kJ mol–1. Value of and hydration energy of NaCl = –774.1 kJ mol–1.
equilibrium constant is–
1 –9.114 kJ mol–1
1 2.6
2 –11.4 kJ mol–1
2 6.2
3 –5.4 kJ mol–1
3 8.2
4 –4.5 kJ mol–1
4 10
Question Question
For vaporization of water at 1 atm pressure, the values of H and S are 40.63 kJ Calculate G° for the conversion of oxygen to ozone, 3/2O2(g) → O3(g) at 298 K. If
mol–1 and 108.8 JK–1 mol–1 respectively. The temp. at which Gibbs energy change KP for this conversion is 3 × 10–29.
(G) for this transformation will be zero is:
1 +175.3 kJ mol–1
1 273.4 K
2 +162.7 kJ mol–1
2 393.4 K
3 –162.7 kJ mol–1
3 373.4 K
4 –140.5 kJ mol–1
4 293.4 K
Question
3 At absolute zero temp. the entropy of all crystalline substance is taken be zero