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21.
133
22.
Electrovalent bonding
23.
1.
2.
24.
3.
25.
4.
5.
26.
7.
27.
30.
8.
9.
(c)
10.
would be MPO4 .
[PO 4 ] is 3.
11.
32.
33.
34.
(d)
35.
37.
38.
14.
40.
15.
16.
17.
12.
13.
39.
18.
43.
19.
44.
20.
45.
highly
7.
48.
8.
50.
51.
52.
53.
54.
55.
O = C = O, Cl Hg Cl, HC CH
9.
10.
11.
12.
13.
14.
57.
18.
(c)
58.
21.
59.
23.
61.
24.
25.
26.
3d
62.
(b) Co
4s
3d 4 s ,
4s
Ni
3d 4 s ,
64.
66.
67.
68.
Covalent bonding
2.
3.
M (1s 2 2s 2 2 p 5 )
Hence
order
of
BeCl 2 LiCl NaCl .
31.
34.
35.
36.
74
37 pm
2
198
99 pm
2
..
..
.. ..
: M ..M : : M : M :
..
.. ..
..
6.
character
33.
covalent
3 x 8 0, x 5 0 , x 5.
has seven
5.
= 37 + 99 = 136 pm
37.
254
2 mole,
127
80
5 mole so they will form
16
Chemical Bonding
38.
(c)
64.
|
H N
65.
H Cl
39.
41.
Structure is
42.
44.
H
H
..
(b) : N N O : or N N O.
..
(b) The
electronic
configuration
Na (Z 11) is
of
67.
and Cl atoms.
(b) Sulphur has the second highest catenation property
after carbon. Its molecule has eight atom bonded
together (i.e. S8 )
(b) H 2O2 has open book structure.
O
45.
47.
48.
69.
(b) The
7N
51.
52.
electronic
2
1s ,2s ,2 p
configuration
of
nitrogen
..
H N H
.
..
or H N H
|
58.
59.
73.
74.
76.
54.
71.
72.
CO32
become weaker.
60.
(a) Valency of
Na 2 S2 O3 is supposed to be x, then
2 2x ( 6) 0 , 2x 4 0 , x 2 .
||
1.
||
H O S O O S O H (Marshall acid)
61.
(c)
62.
||
63.
(d)
||
Cl
16 S
32
1s ,2s ,2 p ,3s ,3 p .
is
50.
O
H
135
Xe
O
F
F
S
I
I
12.
14.
(c)
H O S O H
3.
(c)
NH 3
O
has lone pair of electron while BF3 is electron
7.
H O N O .
(a) Structure of N 2O5 is O N O N O .
O
9.
10.
planar geometry.
16.
20.
22.
23.
O
(d) Co-ordinate bond is a special type of covalent bond
which is formed by sharing of electrons between two
atoms, where both the electrons of the shared pair are
contributed by one atom. Since this type of sharing of
electrons exits in O3 , SO3 and H 2 SO4 . Therefore all
12.
13.
% of ionic character in
HBr
H O PO H
|
O
|
27.
H
(c) Sulphuric acid contain, covalent and co-ordinate bond.
29.
5.
6.
8.
S
F
10.
31.
32.
F
F
(c)
34.
35.
has
30.
9.
Dipole moment
2.
3.
1.6 10 30
100
1.6 10 19 10 10
25.
1.
15.
1.03
100 16.83% 17%
6.12
Chemical Bonding
2.
(c)
137
(c)
2.
HC
CH
1.
3.
3.
4.
4.
5.
5.
6.
6.
9.
8.
11.
(b) H C C C C
9.
10.
11.
13.
H N
|
14.
15.
C
C
16.
(a)
17.
(c)
S
..
:O
19.
16.
20.
21.
..
:O
..
..
(d) : O S O : 5 atoms has 12 electrons in its outermost
||
O:
..
23.
|
|
18.
H Cl
22.
1 and 2
(b) Ca
O
O
O
P
O
25.
26.
in
Hybridisation
1.
(a)
planar.
27.
H 2O .
2.
(d)
H
|
H C2 O
95.7 pm
sp
(104.5)o
H
4.
(c)
5.
1
[3 3] =0
2
No. of e pair 3 +0
29.
30.
120
28.
H 2O is
120
120
O
H
some value.
No. of atom bonded to the central atom 3
In case of 3, 3 geometry is Trigonal planar.
6.
31.
32.
33.
(d) CH 2 C CH CH 3 1, 2-butadiene.
36.
(b) CCl 4
1/4 s-character.
8.
9.
10.
(d) In
||
13.
(a) In
BeF3 , Be is not
44.
sp 3 hybridised it is
sp 2
hybridised.
17.
18.
19.
20.
46.
47.
H H H
56.
25.
hybridised.
.. ..
(a) : Cl Cl : is the correct electronic formula of
.. ..
Cl 2 molecule because each chlorine has 7 electrons in
(d) H C C C H
H H H
will be tetrahedral.
24.
shape.
is the largest.
sp 3
is
sp 3
11.
23.
sp 2
120o .
21.
sp
approximately 109o .
40.
H CC O H
*
sp 2
Hb
Ht
Ht
61.
(b) PF5
involves
Ht
Ht
Hb
3
sp d
Chemical Bonding
62.
(c) s-character in sp
89.
1
100 50%
2
s-character in sp 2
63.
1
100 33.3%
3
s-character
PCl 5
has
(a) Alkene does not show linear structure but it has planar
structure due to sp 2 hybridisation.
90.
1
s-character in sp 3 100 25%
4
Hence, maximum
hybridisation.
92.
is
found
sp 3 d
in
(c) Atom/Ion
sp-
hybridisation,
65.
PF6
sp 3 d 2
95.
(c) Generally
68.
(b) In
C2 H 2
each
carbon
has
sp
sp
1
, bond angle - 180o
2
In sp 2 - p-character
2
, bond angle - 120o
3
pair
of
electron
hence
it
sp3
shows
hybridization.
octahedral
compound
show
sp 3 d 2
hybridization.
96.
sp -hybridization
H C C H
97.
98.
99.
3
In sp - p-character , bond angle - 109o
4
75.
94.
67.
74.
SF4
72.
sp
93.
66.
71.
Hybridisation
NO 2
70.
139
in BCl 3 is sp 2 .
103. (d) NH 4 and SO42 both show sp 3 hybridization and
tetrahedral structure.
104. (a) It is shows sp 3 d 3 hybridization. Hence the bond angle
is about 72o .
107. (a) s-character increases with increase in bond angle.
Hybridization
s%
Angle
78.
sp
50
180o
79.
sp 2
33.3
120o
sp 3
25
109.28 o
sp 3 d1
20
90 o and 120o
84.
109
120
180
tetrahedral.
86.
88.
square
planar
geometry
y2
hybridization
is
orbital.
92.6
S
H
structure.
117. (c)
N
H 107
109 28'
120
structure.
( sp )
130. (a)
100
100
25 , C2 H 4
33 ,
2
3
4
( sp )
C2 H 2
NC
CN
CN
Square planar
F
Regular tetrahedral
123. (a) In
and
H 2CO3
BF3
central
atom
are
in
that of NH 3 .
H
sp
B
sp2
H3
O
sp
X
X
Cl
107 Cl
Cl
structure.
126. (c) In octahedral molecule six hybrid orbitals directed
towards the corner of a regular octahedron with a bond
angle of 90.
F
Square planar
Xe
NC
Ni
100
50
2
Si
CH 4
92.5
orbitals
two
sp 3 hybridization respectively. In
and
and npz ]
128. (c) In
the
formation
of
d 2 sp 3 hybrid
(n 1) dz
d 2 sp 3 hybrid orbitals.
sp 3 and sp hybridization.
H 2S
and
BeCl 2
Chemical Bonding
134. (c)
1 1
1 1 1
Cground state 2s 2 ,2 px py ; Cexcited state 2s1,2 px py pz
pentagonal bipyramidal.
141. (a)
sp p
bonded
Carbon atom in
excited state
141
p p
p p
sp p
bonded
Oxygen atom in
ground state
H H
4 Be
1s 2 ,2s 2 ,2 p0
Be in ground state
1s
B in ground state
2s
2p
Be in excited state
1s
2s
2p
1s
2s
2p
BeCl2
B in excited state
Cl
Cl
sp hybridisation
(Linear diagonal hybridization)
In BCl3 state
1s
2s
2p
Cl
Cl
Cl
144. (a) Except CO3 other choice CO2,CS2 and BeCl 2 have
sp2hybridisation
S
O
or
Cl
I [ Xe] 5s 2 ,5 p5 hence
5p
5s
Cl
5d
I in ground state
5p
5s
5d
I in excited state
MX3
show
the
sp 2
hybridization
and I F7 in excited
state
trigonal
Cl
Cl
P
Cl Cl Cl
exhibit
sp 3d hybridization
in
which
I
sp3d3
10.
(a)
11.
Xe double excitation
1.
2.
5.
OH
|
7.
(a)
8.
9.
11.
(I)
(II)
(abcd) It has all the characteristics.
15.
(c)
NH 3 (107 )
17.
has 32 electrons.
(c) Molecular oxygen contains unpaired electron so it is
paramagnetic (according to MOT).
(b) Structure of H 2 O is a bent structure due to repulsion
18.
16.
22.
23.
5.
6.
7.
8.
(c)
9.
F
F
24.
(d)
and
It
4.
in
5d
(III)
5p
than
5s
13.
3.
(104 .5 )
5d
5p
5s
12.
VSEPR Theory
2.
5d
sp 3 d 2 - hybridization
Resonance
CH 3 C CH 2
5p
XeF4
5s
sp 3 d 3
26.
F
.S.
..
F
Xe
..
28.
31.
32.
(c)
Chemical Bonding
34.
35.
(c)
36.
(b)
45.
(d)
Br
..
(l p bp ) repulsion = 4 and
(bp bp ) repulsion =2
37.
Be
3.
2.5 .
2
2
(b) One bonding M.O. and one anti-bonding M.O.
4.
5.
2.
(c)
(d) BCl 3 , BBr3 and BF3 , all of these have same structure
6.
10.
39.
105
107
..
..
P
As
H
H
Less than
107
11.
42.
13.
smallest.
(c) Oxygen is paramagnetic due to the presence of two
unpaired electron :
O2 (1s)2 (1s)2 (2s)2 (2s)2
18.
(b)
(1s)
increases from F to I.
43.
44.
remaining
the
12.
All
CN (6 7 1 14) diamagnetic
..
:O :
H
hence it is paramagnetic.
molecules/ions, i.e.,
B.O.
and of O22 is 1.
38.
40.
..
143
(1s)
B.O.
Magnetic
nature
He 2
H2
H 2
H 2
1
2
1
2
1
2
P
(P = Paramagnetic, D = Diamagnetic)
19.
20.
B.O. ( 8 2) / 2 3.
24.
25.
1
, it has only one electron so
2
49.
(c)
it will be paramagnetic.
(c) When bond forms between two atom then their energy
get lower than that of separate atoms because bond
formation is an exothermic process.
(b) Valency of A is 3 while that of B is 2 so according to
Criss Cross rule the formula of the compound between
these two will be A2 B3 .
50.
diamagnetic.
(a) O22 consist of four antibonding electron pair [1s and
26.
27.
30.
31.
(d) Molecules
having
unpaired
paramagnetism.
(b) NO 2 has unpaired electrons
electrons
it
55.
would
56.
57.
O
O
P
59.
P
O
O
38.
53.
54.
37.
52.
2.
(c) B.O. of carbon b
2
2
N N a 10 4
3.
(a) B.O. b
2
2
N Na 8 3 5
2.5 .
(b) B.O. b
2
2
2
(a) Electronic configuration of O2 is
60.
61.
2 1 1
0.5 .
2
2
(b) ClO 2 has all paired electrons hence it does not show
paramagnetism.
1
(a) B.O. [ N b N a ]
2
1
6
1
6
N 2 [10 4] 3 ; O22 [10 4] 3.
2
2
2
2
1
1
5
(a) B.O. for N 2 = [ N b N a ] = [9 4] 2.5 .
2
2
2
(a) H 2 O2 contain bond angle between two O H planes
about 90 o .
(c) Nitrogen molecule has highest bond energy due to
presence of triple bond.
(c) Cu 2 [ Ar18 ] 3d 9 4 s 0 it has one unpaired electron so
it is paramagnetic.
(a) CN 14 electrons ; CO =14 electrons
1
6
B.O. = [10 4] 3 .
2
2
1
5
(a) B.O. = [10 5] 2.5 , paramagnetic
2
2
P
(a) P
P
P
64.
2pz* 2py*
(2 pz )2 (2 py )1 (2pz )1
Px Py Pz
Px Py Pz
40.
42.
43.
have two
be
34.
51.
show
33.
paramagnetic.
(c) Helium molecule does not exist as bond order of
He 2 0 .
(c) Structure of P4 O10 is
so
2Px bonding
O2 O2 O22
44.
45.
46.
47.
145
Chemical Bonding
66.
Bond order
67.
73.
O
C O
CO
(b) Higher the bond order, shorter will be the bond length,
thus NO having the higher bond order that is 3 as
compared to NO having bond order 2 so NO has
shorter bond length.
O
C=O
72.
75.
( 2 py )2 ( 2 pz )2 ( * 2 py )1 ( * 2 pz )0
Hence, bond order
B2 1s 2 * 1s 2 , 2s 2 * 2s 2 , 2 px 2 py
1
(10 5) 2.5
2
(2 unpaired electron)
* 2 py 2 , * 2 pz 2
paramagnetism.
76.
2 py 2 * 2 py 1
2 pz 2 * 2 pz 2
2 pz 2 , * 2 py 2 * 2 pz1
2
O2 (16e) 1s 2 * 1s 2 , 2s 2 * 2s 2 , 2 p x , 2py ,
2 pz 2 * 2 py1 * 2 pz1
2
2py 2 * 2py1
2
2
O22 (18e) 1s 2 * 1s 2 , 2s 2 * 2s 2 , 2 px , 2 py ,
2 pz 2 * 2 py 2 * 2 pz 2
2pz 2 * 2pz 1
10 6
2.0
2
79.
10 5
2.5
2
(One unpaired electron in antibonding molecular orbital
so it is paramagnetic)
80.
Bond order
(b) O2 1s , 1s , 2s , 2s , 2 p x
O2 O2 O2 .
Bond order
1
1
Hence bond order N b N a [10 6] 2 .
2
2
(c) Nitrogen form triple bond N N
In which 6 electron take part.
(a) As bond order increase bond length decrease the bond
order of species are
number of bonding electron - Number of a.b. electron
2
10 6
2 ;
For O2
2
10 5
O2
2.5
2
10 7
O2
1.5
2
(b) O2 : 1s 2 , * 1s 2 , 2s 2 , * 2s 2 , 2 p x
71.
F2 s 2 , * 1s 2 , 2s 2 , * 2s 2 , 2 px , 2 py , 2 pz ,
( 2 p x2 2 p y2 ) ( * 2 p1x * 2 p1y )
70.
69.
N 2 1s 2 * 1s 2 , 2s 2 * 2s 2 , 2 px , 2 py 2 pz
1
Hence, bond order (9 4) 2.5 .
2
(a) Electronic configuration of O2 is
*
( 2 py )2 ( 2 p z )1
C2 1s 1s , 2s 2 * 2s 2 , 2 px . 2 py
68.
(c)
H OO H ,O O O,O O
O
O
O
O
b/w O O and O O .
(a) From valency bond theory, bond order in CO, i.e.
15.
22.
23.
25.
28.
(c)
N2 : KK (2s)2 * (2s)2 (2 px )2 (2 py )2 (2 pz )2
does not.
30.
(diamagnetic)
31.
N2 : KK (2s)2 * (2s)2 (2 px )2 (2 py )2 (2 pz )2
(paramagnetic)
34.
35.
* (2 px ) * (2 py ) (diamagnetic)
84.
36.
37.
38.
2.
3.
6.
7.
8.
9.
10.
1
atomic size
Interamolecular H-bonding.
Hydrogen bonding
1.
O
C
H
(diamagnetic)
(c)
39.
40.
41.
43.
45.
46.
47.
48.
49.
2.
11.
3.
12.
4.
14.
Chemical Bonding
9.
10.
12.
13.
14.
16.
NH 4
17.
18.
22.
11.
12.
is angular.
BF3 ] are planar. Hence answer (c) is correct.
13.
(d) CH 2 CH CH 2 CH 2 C CH
14.
increases
17.
H Cl
20.
21.
Fe 3 3d 5 4 s 0
22.
23.
(a) H O : H H O H
|
24.
(d) N 2
paramagnetic.
(a) Each of the species has 14 electron so isoelectronic and
shows bond order 3.
1
1
6
B.O. [ N b N a ] [10 4] 3 .
2
2
2
(d)
S
O
CH 4 0 D,
Trimer of SO3 .
dipole
moment
of
and
H 2 O 1.85D .
27.
(c)
O O
d 2sp 3 hybridization
Unpaired electron
(2p z )2 (2 p x )1 (2py )1 ]
10.
i.e.
8.
decreases
7.
order
O
O
O Cr O Cr O
O
O
6.
bond
3.
the
15.
1.
as
bonds.
23.
(a) H N
|
sp 3
hybridised
sp 2
147
CuSO4 .5H 2 O
has
electrovalent,
coordinate bonds.
Cu
O S O . 5 H 2 O .
covalent
and
19.
20.
21.
(c)
109.5
which
is
but
greater than 90
o
F
109.5o
S
F
(c)
The
diamagnetic
10.
11.
12.
13.
(a)
14.
(e)
15.
(c)
16.
(c)
17.
(c)
18.
22.
(e)
(b)
Lone
pair
in
the
equatorial position (two
L.p b.p repulsion)
F
F B 0
F
H 2 S has two lone pairs on sulphur atom & hence. It
23.
24.
25.
26.
space lattice.
(a) Both assertion & reason are true & reason is the correct
explanation of assertion, because helium molecule is
formed by linking two helium atoms. both have 1s
orbitals. These will combine to form two molecular
orbitals ( 1s ) & * ( 1s ) four available electrons are
accommodated as (1s)2 & * (1s)2 .