P Block Elements
P Block Elements
CHAPTER > 11
p-Block Elements
KEY NOTES
Reactions Properties
Reaction with oxygen l
Crystalline boron is unreactive.
∆
4 E (s) + 3O2 (g ) → 2E2O3 (s) l
Tl forms thallium (I) oxide, Tl 2O more stable than Tl 2O 3.
For thallium, 4Tl (s) + O2 (g ) → 2 Tl 2O(s)
l
B 2O 3 is acidic, Al and Ga oxide are amphoteric and those of In and Tl are
basic.
(Exception boron)
layer on surface.
Anomalous Properties and Borax bead test The metaborates of many transition metals have
Important Compounds of Boron characteristic colours and thus, borax bead test can be used to
B due to its small size, high charge density and identify them.
∆ ∆
non-availability of d-electrons, shows anomalous Na 2 B4 O7 ⋅ 10H2 O → Na 2 B4 O7 → 2NaBO2 + B2 O3
behaviour, i.e. it has high melting and boiling points, Sodium metaborate Boric
forms covalent compounds, shows allotropism and anhydride
behaves as a typical non-metal.
Orthoboric Acid (H 3BO 3 )
Some Important Compounds It is a white crystalline solid with soapy touch. It is sparingly soluble
of Boron in water, but highly soluble is hot water.
Chemical Reactions
Important reactions of group 14 are given below :
Reactions Properties
Reaction with oxygen l
Forms two types of oxides, i.e. monoxide and dioxide.
1 Nature of monoxide is CO-neutral, GeO-acidic, SnO and
M (s) + O2 (g ) → MO
l
(Limited supply)
2 PbO-amphoteric
M (s) + O2 (g ) → MO2 (Excess) l
Nature of dioxides is CO2 , SiO2 , GeO2, SnO2 , and PbO2
144 42444 3 1442443
Acidic Amphoteric
Reactions Properties
Reaction with water l
C, Si, Ge are not affected by water.
∆
M (s) + 2H2O(l ) → MO2 + 2H2 (g ) (Exception-Pb) l
Sn decomposes steam to form dioxide and H 2 gas.
l
Pb is unaffected by H2O due to the formation of oxide film.
Reaction with halogen l
MX 4 are covalent in nature (exception SnF4 and PbF4).
M + X 2 → MX 2 l
Stability of dihalides increases down the group.
M + 2 X 2 → MX 4 (Exception-PbI 4 (does not exist ) l
The order of thermal stability of halides is
CX 4 > SiX 4 > GeX 4 > SnX 4 > PbX 4
l
Except CCl 4, other tetrachlorides are easily hydrolysed by water.
Mastering NCERT
MULTIPLE CHOICE QUESTIONS
TOPIC 1 ~ Introduction
1 The characteristic valence shell configurations of 4 The compounds formed by the highly reactive
group-13 and 14 elements are respectively non-metals with highly reactive metals and the
(a) ns2 np1 and ns2 np 2 (b) ns2 np 2 and ns2 np 3 non-metals are respectively
(a) covalent and ionic (b) ionic and covalent
(c) ns2 np 3 and ns2 np 4 (d) ns2 np 4 and ns2 np 5
(c) metallic and ionic (d) metallic and covalent
2 The number of possible oxidation states of p-block 5 The second period elements of p-block starting from
elements boron, are restricted to a maximum covalency of
(a) decreases towards the right of the periodic table (a) four (using 1s, 2s and two 2 p orbitals)
(b) increases towards the right of the periodic table (b) six (using 1s and 2s -orbitals)
(c) first increases then decreases down the group (c) four (using one 2s and three 2 p orbitals)
(d) first decreases then increases down the group (d) six (using 1s and three 2 p orbitals)
3 In boron and carbon families, the group oxidation 6 The third period elements of p-block with the
state is most stable for
electronic configuration 3s 2 3 p n have the vacant
(a) heavier elements in the group
3d orbitals lying between the
(b) lighter elements in the group
(a) 3p and 4s levels of energy (b) 3s and 3p levels of energy
(c) middle element in the group
(c) 3s and 4s levels of energy (d) 2p and 3s levels of energy
(d) last element in the group
7 Which orbitals are used by third period of p-block 9 The element that shows greater ability to form pπ- pπ
elements in order to expand their covalency beyond four? multiple bonds, is JEE Main 2019
(a) 3d (b) 4s (c) 3p (d) 4d (a) Ge
8 Boron forms only [ BF4 ]− which one of the following (b) Si
is formed by aluminium? (c) Sn
(d) C
(a) [AlF 4 ] − (b) [AlF 6 ] 3− (c) [AlF 4 ] 3− (d) [AlF 6 ] −
154 pm (a) Diamond (b) Fullerene (c) Graphite (d) None of these
60 C 60 an allotrope of carbon contains JEE Main 2019
(a) 16 hexagons and 16 pentagons
(b) 20 hexagons and 12 pentagons
(c) 12 hexagons and 20 pentagons
(d) 18 hexagons and 14 pentagons
61 Which of the following is obtained by burning
(A ) (B) hydrocarbons in a limited supply of air?
(a) Charcoal (b) Carbon black
(a) A → Graphite; B → Diamond (c) Coke (d) None of these
(b) A → Diamond; B → Graphite
(c) It forms carbonic acid on reaction with water 82 The basic structural unit of feldspar, zeolites, mica and
(d) None of the above asbestos is JEE Main 2019
70 H 2CO 3 / HCO 3– buffer system helps to maintain the (a) ( SiO3 )2− (b) SiO2
pH of blood between R
(a) 7.26 to 7.42 (b) 3.26 to 7.42
(c) (SiO4 )4 − (d) ( Si O)
n ( R = Me )
(c) 7.26 to 8.00 (d) 7.42 to 7.96
71 0.03% of carbon dioxide present in the atmosphere R
can be removed by 83 Name the type of the structure of silicate in which one
(a) conversion of CO2 to glucose oxygen atom of [SiO 4 ]4− is shared? CBSE AIPMT 2011
(b) photosynthesis (a) Three dimensional (b) Linear chain silicate
(c) chemical change of CO2 to carbohydrate (c) Sheet silicate (d) Pyrosilicate
(d) All of the above
84 Which of the following is used to convert alcohol to
72 What is the hybridisation of C-atom in CO 2 petroleum directly?
molecule? (a) ZSM-5 (b) Fe2 O3 (c) Cr2 O3 / Al 2 O3 (d) Feldspar
(a) sp 2 (b) sp (c) sp 3 (d) None of these 85 Two elements P and Q react separately with highly
73 95% of earth crust is made up of silica and silicates. electropositive metal to form binary compounds,
Silicon dioxide, commonly known as which upon hydrolysis yield mixture of boranes and
(a) silicate (b) silicon silanes? P and Q respectively are
(c) silica (d) All of these (a) B and Al (b) Si and B (c) B and Si (d) Al and B
CHAPTER 11 > p-Block Elements 305
Answers
> Master NCERT With MCQs
1 (a) 2 (b) 3 (b) 4 (b) 5 (c) 6 (a) 7 (a) 8 (b) 9 (d) 10 (c)
11 (a) 12 (d) 13 (d) 14 (c) 15 (d) 16 (d) 17 (c) 18 (b) 19 (b) 20 (b)
21 (b) 22 (d) 23 (a) 24 (c) 25 (a) 26 (c) 27 (a) 28 (a) 29 (b) 30 (a)
31 (d) 32 (a) 33 (b) 34 (b) 35 (a) 36 (b) 37 (b) 38 (d) 39 (a) 40 (b)
41 (d) 42 (c) 43 (b) 44 (b) 45 (b) 46 (b) 47 (c) 48 (b) 49 (c) 50 (a)
51 (a) 52 (d) 53 (c) 54 (c) 55 (a) 56 (b) 57 (a) 58 (c) 59 (b) 60 (b)
61 (b) 62 (d) 63 (c) 64 (c) 65 (c) 66 (d) 67 (b) 68 (a) 69 (b) 70 (a)
71 (d) 72 (b) 73 (c) 74 (a) 75 (b) 76 (d) 77 (a) 78 (c) 79 (a) 80 (c)
81 (b) 82 (c) 83 (d) 84 (a) 85 (c)
covalency above four. 40 (b) The correct structure of diborane is given in option
Therefore, boron (B) is unable to form MF63 − ion. The (b). The four terminal hydrogen atoms and the two boron
elements like aluminium (Al), gallium (Ga) and indium atoms lie in one plane. Above and below this plane,
(In) have vacant 3d-orbitals, thus they can increase their there are two bridging hydrogen atoms.
covalence above four and form MF63 − ion. 41 (d) Boron forms a series of hydridoborates; the most
important one is the tetrahedral [BH4 ] − ion.
31 (d) Boron forms acidic hydroxide B(OH) 3 , while Al Tetrahydridoborates of several metals are known.
forms amphoteric hydroxide Al(OH) 3 . Lithium and sodium tetrahydridoborates are also known
32 (a) The complete reaction is shown below : as borohydrides.
Na 2 B4 O7 + 7H2 O → 2NaOH + 4H3 BO3 43 (b) Nihonium (Z = 113) and flerovium (Z = 114) are
Borax Orthoboric acid prepared only in small amounts. Their half-life is short
(A ) and their chemistry has not been established yet.
So, A is orthoboric acid. 44 (b) There is a considerable increase in covalent radius
33 (b) On heating borax, it first loses water molecules and from C to Si, thereafter from Si to Pb a small increase in
swells up. On further heating, it turns into a transparent radius is observed. This is due to the presence of
liquid, which solidifies into glass like material known as completely filled d and f -orbitals in heavier members.
borax bead. 45 (b) There is a small decrease in ∆ i H from Si to Ge to Sn
The corresponding reaction is given below : and slight increase in ∆ i H from Sn to Pb. This is the
∆ ∆ consequence of poor shielding effect of intervening
Na 2 B4 O7 ⋅ 10H2 O → Na 2 B4 O7 → 2NaBO2 + B2 O3
Sodium d and f -orbitals and an increase in size of the atom.
metaborate Boric
anhydride 46 (b) The tendency of Ge, Sn and Pb to show +2 oxidation
34 (b) The borax bead test can be used to identify transition state increases on moving from Ge to Pb. Thus, the
metals as their metaborates have characteristic colours. correct sequence is Ge < Sn < Pb. It is because of inert
When borax is heated in a bunsen burner flame with pair effect, due to which ns2 electrons of valence shell
CoO(X) on a loop of platinum wire, a blue coloured are unable to participate in bonding.
Co(BO 2 ) 2 (Y) bead is formed. 47 (c) [SiCl 6 ] 2− is not stable and does not exist because
Therefore, X and Y are CoO and Co(BO 2 ) 2 respectively (i) six large chloride ions cannot be accommodated
and the correct option is (b). around Si 4+ due to limitation of its size.
35 (a) The complete reaction is shown below : (ii) interaction between lone pair of chloride ion and
Na 2 B4 O7 + 2HCl + 5H2 O → 2NaCl + 4B(OH)3 Si 4+ is not very strong.
‘X ’ ‘Y ’
On the other hand, due to presence of d-orbital in Si,
So, X is HCl. Ge and Sn they form species like [SiF 6 ] 2− , [ GeCl 6 ]2−
36 (b) On heating, orthoboric acid above 370 K forms and [ Sn ( OH )6 ]2− . Hence, option (c) is correct.
metaboric acid, HBO2 which on further heating yields 50 (a) PbI4 does not exist because Pb—I bond, initially
boric oxide, B2 O3 . formed during the reaction, does not release enough
∆ ∆ energy to unpair 6s2 electrons and excite one of them to
H3 BO3 → HBO2 → B2 O3
Metaboric acid Boric oxide higher orbital to have four unpaired electrons around
(X ) (Y ) lead (Pb) atom.
37 (b) The industrial scale production of diborane involves 51 (a) The complete reaction is given below :
the reaction of BF3 with sodium hydride as shown below : Cl Cl
450 K –HCl
2BF3 + 6NaH → B2 H6 + 6NaF Si + O Si
Cl Cl H H Cl OH
39 (a) Diborane ( B2 H6 ) reacts independently with O2 and
Cl Cl
H2 O to produce B2 O3 and H3 BO3 respectively. Diborane OH
is a colourless, highly toxic gas, having boiling point +3H2O(A)
180 K. Because of its inflammable nature. It catches fire Si
HO OH –3HCl (B)
spontaneously when exposed to air and burns in oxygen
releasing an enormous amount of energy as : OH
Silicic acid (C )
B2 H6 + 3O2 → B2 O3 + 3H2 O + 1976 kJ/mol
Hence, A is 3H2 O, B is 3HCl and C is silicic acid.
54 (c) Diamond, graphite and fullerene are crystalline 73 (c) Silica (SiO2 ) is a major constituent present in earth
allotropes of carbon. Whereas, soot is not an allotrope of crust and it occurs in many crystallographic forms such
carbon. as quartz, cristobalite, tridymite etc.
55 (a) Diamond has a crystalline lattice. In diamond, each 74 (a) The complete reactions are given below :
carbon atom undergoes sp 3 -hybridisation and linked to
2NaOH
four other carbon atoms by using hybridised orbitals in Na2SiO3 + H2O
tetrahedral fashion. The structure extends in space and SiO2 A
4HF
produces a rigid three dimensional network of carbon atoms. (Silica) SiF4 + 2H2O
B
56 (b) The figures A and B represent diamond and graphite
respectively. Hence, A and B are Na 2 SiO3 and SiF4 respectively.
60 (b) C60 is aromatic allotrope of carbon containing 12 75 (b) Silica occurs in nature in several amorphous and
crystalline forms. Kieselguhr is the amorphous form of
pentagons and 20 hexagons. It is a fullerene having a
silica. Quartz, tridymite and cristobalite are crystalline
shape like soccer ball and called Buckminster fullerene.
forms of silica.
62 (d) On small scale, pure CO is prepared by dehydration
76 (d) Quartz is used as piezoelectric material which is
of formic acid with conc. H 2 SO 4 at 373 K. Concentrated
used in making clock, modern radio etc.
H2 SO4 is a dehydrating agent. So, it removes water from
HCOOH as shown below : 77 (a) Silica gel is used as dehydrating agent as it removes
373 K
moisture from the atmosphere.
HCOOH → H2 O + CO
Formic acid Conc. H 2SO 4 78 (c) Me 3 SiCl is not a monomer for a high molecular mass
64 (c) Mixture of CO and N2 is known as producer gas silicone polymer because it generates Me3 SiOH when
subjected to hydrolysis which contains only one
which can be prepared as follows : reacting site.
1273 K
2C( s ) + O2 ( g ) + 4 N2 ( g ) → 2CO( g ) + 4 N2 ( g ) Hence, the polymerisation reaction stops just after first
Producer gas step as shown below :
65 (c) CO reduces all metal oxides except Al 2 O3 , alkali and Me Me
alkaline earth metal oxides. A few reduction reactions
are given below : Me Si OH + HO Si Me →
− H 2O
Fe2 O3 ( s ) + 3CO ( g ) → 2Fe ( s ) + 3CO2 ( g )
Me Me
∆
ZnO( s ) + CO ( g ) → Zn ( s ) + CO2 ( g ) Me Me
66 (d) The reaction of CO with H2 O is as follows : Me Si O Si Me [Final product (dimer)]
CO + H2 O → CO2 + H2
Me Me
So, the products obtained are carbon dioxide and
hydrogen. 79 (a) The reaction of hydrolysis of dimethyl dichloro
silicone followed by condensation polymerisation is
68 (a) In laboratory, CO2 can be prepared by the reaction
given below :
of dil. HCl and CaCO3 as shown below : CH3
H3 C Cl 2H O
CaCO3 ( s ) + dil.2HCl ( aq ) → CaCl 2 ( aq ) + CO2 ( g ) Si → HO — Si — OH
2
(B ) ( A)
+ H2 O( l ) H3 C Cl
71 (d) 0.03% of carbon dioxide present in atmosphere can CH3
be removed by photosynthesis, which is a process of
conversion of atmospheric CO2 to carbohydrate like Polymerisation
↓
glucose.
CH3 CH3
The overall chemical change can be expressed as shown
below :
— O ——
Si — O — Si —
hν
6CO2 + 12H2 O → C6 H12 O6 + 6O2 + 6H2 O
Chlorophyll
CH3 n CH3
72 (b) The CO2 molecule is shown below : Silicone (straight chain polymer)
π π 80 (c) Silicones are synthetic organosilicon polymers
O == C == O
containing repeated R2 SiO units. It is used in surgical and
The C atom in CO2 possesses sp-hybridisation due to the cosmetic implants. They are also used as low temperature
presence of 2π bonds. (Q 2π bonds) lubricants, in making waterproof clothes and paper, etc.
81 (b) The basic structural unit of all silicates is the (c) Boron is a hard non-metal.
tetrahedral SiO44− . (d) Melting point of Ga is unusually low (i.e. 303 K).
It is represented as shown below : 93 (d) Statement (d) is incorrect. It’s correct form is as
follows :
O– O–
–
O
– Aluminium forms a very thin oxide layer on its surface
O which protects the metal from further attack by oxygen.
Si O –
– Rest other statements are correct.
O –
O=O
O O– = Si 94 (a) Statement (a) is correct, while the other statements
Structure of SiO4 ion
4– are incorrect. Corrected form are as follows :
(b) Aluminium vessel cannot be used to store NaOH.
82 (c) The basic structural unit of feldspar, zeolites, mica
NaOH reacts with Al as follows :
and asbestos is ( SiO4 )4− . These all are silicates. All
2NaOH + 3Al → 2NaAlO 2 + 3H 2 + 2H 2 O
silicates involve two types of Si—O bonds.
Thus, NaOH cannot be stored in a vessel made of Al.
(i) Terminal Si—O bonds in which oxygen is bonded to
(c) Aluminium chloride dissociates in water.
a silicon and not other atom.
(d) AlF 3 is insoluble in anhydrous HF.
(ii) Bridging Si—O—Si bonds in which oxygen is
bonded to two silicon atoms. 95 (b) Statements II, III and IV are correct, while statement
σ I is incorrect. It’s correct form is as follows :
O–
The structure of Al 2 Cl 6 is shown below :
Si Cl Cl Cl
O–
20
22
6
1
101°
pm
pm
O– O– σ σ Al Al 118°
°
79
2–
Tetrahedral structure of SiO 4 anion Cl Cl Cl
In SiO4−
4 ion, each Si atom is bonded to four oxygen The six Al—Cl bonds are not of the same length.
atoms tetrahedrally. 96 (d) Statement III is incorrect.
83 (d) In pyrosilicates, two SiO4−
4 tetrahedrons share a It’s correct form is as follows :
corner oxygen atom as shown below : The compounds of group-13 elements in +1 oxidation
–O O– state, as expected from energy considerations, are more
ionic than those in +3 oxidation state.
–O O O–
O = (oxygen atom) Rest other statements are correct.
–O O–
= Si (silicon) 97 (a) Statement (a) is incorrect.
–
Si2 O6 anion of pyrosilicate It’s correct form is as follows :
7
Tl 3+ is a powerful oxidising agent.
84 (a) The zeolite ZSM-5 is used to convert alcohols
Thus, Tl + is more stable in solution than Tl 3+ .
directly into gasoline.
Rest other statements are correct.
85 (c) P and Q are boron and silicon, as they yield boranes
and silicanes respectively. 99 (d) Statement (d) is correct, while other statements are
incorrect. Corrected form are as follows :
86 (b) The electrons in d-orbitals cannot screen the nucleus
(a) The four terminal hydrogen atoms and the two boron
effectively and hence effective nuclear charge of Ga (It
atoms lie in one plane. Above and below this plane,
contains 10 electrons) is greater in magnitude than that
there are two bridging hydrogen atoms.
of Al. So, electrons of Ga experience greater force of
attraction than Al and hence atomic radius of Ga is lesser (b) The four terminal B H bonds are regular
than that of Al. 2-centre-2-electron bonds.
(c) The two bridged (B H B) bonds are different and
90 (a) Statement I is correct regarding the properties of
can be described in terms of 3-centre-2-electron bonds.
boron, while the statements II and III are incorrect.
Corrected form are as follows : 100 (b) Statement II is correct, while statement I is incorrect.
It’s correct form is as follows :
II. Boron has high melting point and low density.
LiBH4 is used as reducing agent in organic synthesis.
III. Boron shows low electrical conductivity.
102 (c) Statements III and IV are incorrect.
92 (b) Statement (b) is correct, while other statements are
It’s correct form are as follows :
incorrect. Corrected form are as follows :
III. Borazine is more reactive than boron.
(a) Density of the group-13 elements increases down the
IV. Aluminium is stable in air and water.
group from boron to thallium.
Rest other statements are correct.
103 (b) Statement (b) is incorrect. Silicones have many useful properties :
It’s correct form is as follows : (i) They repel water and form watertight seals.
Carbon and silicon are non-metals, germanium is (ii) They are heat resistant because of constancy of
metalloid, whereas tin and lead are soft metals with low properties over a wide range of temperature (−100°
melting points. to 250° C).
Rest other statements are correct. (iii) Silicones are non-toxic.
104 (c) Statement (c) is incorrect. (iv) Silicones are biocompatible because these do not
It’s correct form is as follows : support microbiological growth and these have high
Most of the tetrahalides are covalent in nature. gas permeability at room temperature.
Rest other statements are correct. (v) They are resistant to O2 , O3 and UV-radiation.
105 (b) Statement II is correct, while statements I and III are (vi) Silicones are formulated to be electrically insulative.
incorrect. Corrected form are as follows : (vii) Silicone grease is typically used as a lubricant for
I. Sn in +2 oxidation state is a reducing agent. brake components in automobiles, since it is stable at
high temperature, is not water soluble and is a
III. Pb compounds act as oxidising agent in +4 state. odourless viscous liquid.
106 (a) Statements I and IV are correct, while II and III are
120 (a) The heaviest element in each p-block group is the
incorrect. Corrected form are as follows : most metallic in nature as the non-metallic character
II. Because of sp 2 -hybridisation trisilyl amine is planar. decreases down the group.
III. SnCl 2 is more stable than SnCl 4 due to inert pair effect. Thus, both A and R are correct and R is the correct
108 (a) The major difference between diamond and graphite explanation of A.
is due to the crystal structure of diamond which is 121 (c) Boron always forms covalent bond because of its
different from that of graphite. small size. B never forms B3+ ion.
111 (a) Statements I and III are correct while statement II is Thus, A is correct but R is incorrect.
incorrect. It’s correct form is as follows : 123 (a) On moving down the group, due to poor shielding
Fullerene are the only pure form of carbon because they effect of intervening d and f-orbitals, the increased
have smooth structure without having ‘dangling’ bonds. effective nuclear charge holds electrons tightly
113 (c) Statement I, II and IV are correct, while statement (responsible for inert pair effect) and thereby, restricting
III is incorrect. It’s correct form is as follows : their participation in bonding. As a result of this, only
p-orbital electron may be involved in bonding. So, inert
Spherical fullerenes are also called bucky balls in short. pair effect increases on going down the group 13.
114 (c) Statements, I, III and IV are correct while statement Thus, both A and R are correct and R is the correct
II is incorrect. It’s correct form is as follows : explanation of A.
CO is water insoluble. 124 (c) Aluminium dissolves in mineral acids and aqueous
115 (a) Statements I, II and III are correct, while IV is alkalies. Thus, Al shows amphoteric character.
incorrect. It’s correct form is as follows : Thus, A is correct and R is incorrect.
CO reacts with certain metals when heated to form metal 125 (a) Since, d-orbitals are available in Al the maximum
carbonyls. covalence can be expected beyond 4. Thus, AlCl 3 is
116 (c) Statements I and IV are correct while statements II dimerised through bridged halogen, to form Al 2 Cl 6 .
and III are incorrect. Corrected form are as follows : Al completes its octet by accepting electrons from
II. Increase in combustion of fossil fuels and halogens present at bridge.
decomposition of limestone for cement manufacture Thus, both A and R are correct and R is the correct
increases CO 2 content of the atmosphere. This may explanation of A.
lead to increase in greenhouse effect.
126 (d) In trivalent state most of the halides of group 13 are
IV. In CO 2 molecule, carbon atom undergoes hydrolysed in water as they are covalent in nature.
sp-hybridisation. Two sp-hybridised orbitals of
carbon atom overlap with two p-orbitals of oxygen Thus, A is incorrect but R is correct.
atoms to make two sigma bonds while other two 127 (a) White fumes appear around the bottle of anhydrous
electrons of carbon atom are involved in pπ- pπ aluminium chloride because anhydrous aluminium
bonding with oxygen atom. This results in its linear chloride is partially hydrolysed with atmospheric moisture
shape with no dipole moment. to liberate HCl gas. Moist HCl appears white in colour.
119 (d) Silicones are polysiloxanes with general chemical Thus, both A and R are correct and R is the correct
formula, [ R2 SiO]n , where R is an organic group such as : explanation of A.
CH3 , C2 H5 , C6 H5 etc.
128 (a) The boron-10 (10 B) isotope has high ability to 146 (c) Borax is a salt of strong base (NaOH) and weak acid
absorb neutrons and therefore, metal borides are used in (H3 BO3 ), therefore, its aqueous solution is basic in nature.
nuclear industry as protective shields and control rods. 147 (b) Boric acid is polymeric due to the presence of
Thus, both A and R are correct and R is the correct hydrogen bonds. (as it has polar O H bonds).
explanation of A.
148 (c) In B2 H6 , each boron atom is sp 3 -hybridised.
129 (a) The use of aluminium and its compounds for
domestic purposes is now reduced considerably because 149 (b) Due to inert pair effect, elements of group-14 exhibit
of toxic nature of aluminium and its compounds. oxidation states of + 2 and + 4.
Thus, both A and R are correct and R is the correct 151 (c) In gallium, the crystal structure is different, i.e. each
explanation of A. Ga-atom has one close neighbour at a distance of 2.43 Å
and six more distant neighbours at distance between 2.70
130 (c) Group 14 elements are actually smaller in size than
Å to 2.79 Å suggesting that Ga consists of almost
group 13 elements. Group 14 elements are slightly more
discrete Ga 2 molecule. That’s why, its melting point is
electronegative than the latter.
the lowest. Ga exists as liquid from 30°C upto 2000°C
Thus, A is correct but R is incorrect. and hence, it is used in high temperature thermometry.
131 (d) The common oxidation states exhibited by the 152 (d) On moving from B to Al, the ionisation enthalpies
group-14 elements are +4 and +2. decreases as expected and this decrease is due to an
Thus, A is incorrect but R is correct. increase in atomic size and shielding effect.
132 (a) Except CCl 4 , other tetrachlorides are easily On moving from Al to Ga, the ionisation enthalpy
hydrolysed by water because the central atom can increases slightly, because on moving from Al to Ga,
accommodate the lone pair of electrons from oxygen both nuclear charge and shielding effect increases. Due
atom of water molecule in d -orbital. to poor shielding by d-electrons in Ga, effective nuclear
Thus, both A and R are correct and R is the correct charge on valence electron increases resulting in d-block
explanation of A. contraction, that’s why ionisation enthalpy increases.
133 (d) Heavier elements do not form pπ- pπ bonds because On moving from Ga to In, again there is slight decrease
in ionisation enthalpies due to increased shielding effect
their atomic orbitals are too large and diffuse to have by additional ten 4d electrons, which outweighs the
effective overlapping. effect of increased nuclear charge.
Thus, A is incorrect but R is correct. On moving from ln to Tl, ionisation enthalpy again
134 (a) In graphite, each carbon atom in hexagonal ring increases because fourteen 4f electrons shield valence
undergoes sp 2 -hybridisation and makes three sigma electrons poorly (order of shielding effect s > p > d > f )
bonds with three neighbouring carbon atoms. Fourth and so effective nuclear charge increases, consequently
electron forms π −bond. Due to delocalisation of this ionisation enthalpy increases.
fourth electron, graphite conducts electricity. 153 (a) The lowest atomic number among the given is of boron.
Thus, both A and R are correct and R is the correct Boron has atomic number 5 and does not have vacant
explanation of A. d-orbital. The element M in the complex ion MF63− has a
135 (a) Graphite is thermodynamically most stable allotrope coordination number of six. Boron can show maximum
of carbon and therefore, ∆ f H s of graphite is taken as zero. coordination number of 4 due to absence of d-orbitals.
Thus, B cannot form complex of the type M F63− .
Thus, both A and R are correct and R is the correct
explanation of A. 154 (a) Alkaline earth metals form ionic chloride whereas
136 (b) Buckminster fullerene is a variety of carbon, which aluminium chloride is covalent. Despite of sharing
is abbreviated as C60 . electrons with chlorine, the octet of aluminium is
incomplete. To complete the octet, it needs electrons and
Thus, both A and R are correct and R is not the correct
thus, acts as a Lewis acid as shown below :
explanation of A.
137 (b) Due to layered structure of graphite, graphite fibres 13 Al = 2, 8, 3 and 17 Cl = 2, 8, 7
embedded in plastic material form high strength, light Cl
weight composites. The composites are used in products |
such as tennis rackets, fishing rods, aircrafts and canoes. Cl Al Cl
Thus, both A and R are correct and R is not the correct ↑
Incomplete octet
explanation of A.
155 (a) The acidic nature of oxides changes from acidic to
138 (a) Due to inert pair effect, +2 oxidation state of Pb is basic through amphoteric on moving down the group as
more stable than + 4 oxidation state. That is why, PbI4 is shown below :
an unstable compound.
B2 O,3 Al 2 O3 and Ga 2 O3 , In 2 O3 and Tl 2 O3
Thus, both A and R are correct and R is the correct 123 144 42444 3 1442443
explanation of A. Acidic Amphoteric Basic
−
OH (ii) Diborane can be prepared by the reduction of BF3
| with lithium aluminium hydride in diethyl ether.
156 (a) Structure of B(OH)−4 is HO B OH
4BF3 +3LiAlH4 → 2B2 H6 + 3AlF3 + 3LiF
|
(X )
OH 160 (b) The tendency to form long open or closed atom
[B(OH)4 ]− contains four bond pairs and no lone pairs. chains by combination of some atoms among themselves
3
Thus, the hybridisation of central atom is sp and the is known as catenation. The catenation is maximum in
carbon and decreases down the group as shown below :
geometry of the complex is sp 3 .
C > > Si > Ge ≈ Sn > Pb
157 (c) Lewis acids are the substances in which octet is
incomplete and hence, they accept electrons. Boric acid This is due to high bond energy of C — C bonds. Down
is a monobasic weak acid. It does not liberate H+ ion but the group, size increases and electronegativity decreases,
accept electrons from OH− ion, i.e. behaves as Lewis thereby, the tendency to show catenation decreases.
acid as shown below : 161 (d) Reducing agents are those substances, which reduces
H3 BO3 + H2 O → [B(OH)4 ]− + H+ other substances and itself gets oxidised.
In SnCl 2 , Sn exists in +2 oxidation state, thus acts as a
or, B(OH)3 + 2H2 O → [B(OH)4 ]− + H3 O+ strong reducing agent. i.e.
158 (b) In diborane, there are 12 valence electrons, SnCl 2 + 2FeCl 3 → 2FeCl 2 + SnCl 4
three from each boron atoms and six from the six SnCl 2 + 2CuCl 2 → 2CuCl + SnCl 4
hydrogen atoms. The geometry of B2 H6 can be
162 (c) Carbon dioxide can be obtained as a solid in the form
represented as shown below :
of dry ice by allowing the liquefied CO2 to expand rapidly.
H H H
163 (c) Silicon has a strong tendency to form polymers like
silicones. The chain length of silicon polymer can be
B B controlled by adding Me 3 SiCl which blocks the ends as
shown below :
H H H
Bonding in diborane CH3 CH3
The four terminal hydrogen atoms and two boron atoms n HO—Si—OH + HO—Si—CH3
lie in one plane. Above and below the plane, there are
two bridging hydrogen atoms. Each boron atom forms CH3 CH3
four bonds even though it has only three electrons. The –H2O Polymerisation
terminal B H bonds are regular bonds but the bridge
B H bonds are different. Each bridge hydrogen is CH3 CH3
bonded to the two boron atoms only by sharing of two
electrons. Such covalent bond is called —O—Si—O—Si—CH3
3-centre-2-electron bond or a multicentre bond or
CH3 n CH3
banana bond.
Silicone
159 (a)
(i) Reaction of ammonia with diborane gives initially 164 (b) Quartz (crystalline form of silica, SiO2 ) is extensively
B 2 H6 ⋅ 2NH3 , which is formulated as : used as a piezoelectric material as it contains Si.
[BH2 (NH3 )2 ] + [BH4 ] − . On further heating, it gives 165 (b) Cement is a product obtained by combining a
borazine, B 3 N3 H6 as shown by the reaction given material rich in lime. The average composition of
below : Portland cement is given below :
3B2 H6 + 6NH3 → 3[BH2 (NH3 )2 ] + [BH4 ] − CaO (50 – 60%) SiO2 (20 – 25%)
Diborane
(X )
473
K
→ 2B 3 N3 H6 + 12H2 Al 2 O3 (5 – 10%) Fe2 O3 (1 – 2%)
Borazine SO3 (1 – 2%) MgO (2 – 3%).
(Y )
Thus, it contains elements of group 2 (Ca, Mg),
Borazine has cyclic structure and is isoelectronic Group 13 (Al) and group 14 (Si).
with benzene and thus called inorganic benzene.