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EVERGREEN
SERIES
HCl (l)
ZZZZZ
X
YZZZZ
Z
CH 3COOH(l) + CH3OH(l)
3. 2,2Dimethylpropan-1-ol
4. CH3CH 2 C CH 2 CH 2 C H
||
||
O
O
5. Antipyretics substances
(Tf) than pure solvent (T 0f ) , because the vapour pressures of solid
water and liquid water become equal at a lower temperature. This
is illustrated in the figure shown.
Vapour Pressure
t
en
olv
s
uid
ion
Liq
lut
So
Solid
t
solven
%T
Tf
Tf
Temperature/K
7. Rate constant is the rate of reaction when the concentration of reactants are unity.
Units for k :
(a) For zero order reaction : mol L1 s1.
(b) For a first order reaction : s1.
8. (a) SbCl3 + H2O SbOCl o
2HCl
Antimony
oxychloride
(White ppt.)
~~~~n S Cl
CH3CN
350K
+ SF4 + 4NaCl
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EVERGREEN
SERIES
C2 H5 OH
Ethanol
2
A
11. (a) E2 value for Cr3+/Cr2+ is negative ( 0.41 V), whereas E2 value for Mn3+/Mn2+ is positive (+1.57V).
Hence, Cr2+ ions can easily undergo oxidation to give Cr3+ ions and, therefore, acts as strong reducing
agent. On the other hand, Mn3+ can easily undergo reduction to give Mn2+ and hence acts as oxidising
agent.
(b) Co(III) has greater tendency to form coordination complexes than Co(II). Hence, in the presence of
ligands, Co(II) changes to Co(III), i.e., is easily oxidized.
(c) The ions with d1 configuration have the tendency to lose the only electron present in d-subshell to acquire
stable d 0 configuration. Hence, they are unstable and undergo oxidation or disproportionation.
12. Two primary alkyl halides having the molecular (formula, C4H9Br are possible. These are CH3CH 2 CH 2CH 2 Br
n Butyl bromide
CH3
|
and CH3 CH CH 2 Br
Isobutyl bromide
Thus, compound (a) is either n-butyl bromide or isobutyl bromide. Since compound (a) when reacted with
Na metal gave a compound (d) with molecular formula C8H18 which is different from the compound obtained
when n-butyl bromide is reacted with Na metal, therefore, (a) must be isobutyl bromide and compound
(d) must be 2,5-dimethylhexane.
CH3
|
CH3 CH CH 2 Br + 2Na
Isobutyl bromide (a) (1)
~~~~~~n
Wurtz reaction
~~~~~~n
Wurtz reaction
CH 3
CH3
|
|
CH3 CH CH 2 CH 2 CH CH3 2NaBr
2,5-Dimethylhexane (d )
Reaction of (a) with alc.KOH (elimination) to give (b) followed by reaction with HBr (addition) to give
(c) is an isomer of (a) is given below.
CH 3
|
CH3 CH CH 2 Br
Isobutyl bromide (a )
~~~~~~n
alc. KOH
KBr, H 2O
CH3
|
CH3 C = CH 2
Isobutylene (b)
~~~~~n
HBr
M.addition
CH3
|
CH3 C CH3
|
Br
tert-Butyl bromide (c )
[Isomer of (a )]
(2)
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EVERGREEN
SERIES
log
Ea 1 1
k2
=
2.303R T1 T2
k1
log
Ea
1
1
10
=
or
or
Ea =
or
Ea =
19.147 t 14
t1
5
or
Ea =
268.058
5
14. (a)
(b)
(c)
15. (a)
(b)
= 53.61 kJ mol1
It is due to the fact that more force of attraction between dispersed phase and dispersion medium exist
in lyophilic colloid than lyophobic colloid.
Fe(OH)3 sol is positively charged which is coagulated by negatively charged Cl present in sodium chloride
solution.
The path of light becomes clearly visible due to scattering of light by colloidal particles i.e., Tyndall effect.
Pig iron is converted into steel by adding carbon and some other elements.
Metallic zinc is obtained from zinc oxide by reduction with coke.
~~~n
Heat
Zn + CO
ZnO + C
(c) Impure titanium is heated from iodine to form volatile complex Til4 which on further heating decomposes
to give pure titanium.
16. Z = 4 for fcc unit cell.
As we know
d =
Z M
N A t a3
Z M
4 t 63.5
N A t d 6.023 t 1023 t 8.93
or
a3 =
or
or
or
a = 3.614 108 cm
= 361.4 pm
Now,
4r =
2a
(3)
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SERIES
or
r=
a
2 2
361.4
2 t 1.414
= 127.7 pm
17. The following data is provided :
Kf = 4.9 K kg mol1, WB = 3.26 g, DTf = 0.112 C, WA = 226 g
We know
DTf = K f t
WB 1000
t
MB
WA
MB =
= 631.084 g mol1
Atomicity of Selenium =
Molecular weight
Atomic weight
631.084
78.8
= 8.00
=
N2+ Cl
NH2
Br
Cu, HBr
NaNO2, HCl
273 K
Aniline
Bromobenzene
NO2
N2+ Cl
NH2
H2, Pt
Nitrobenzene
NaNO2, HCl
OH
H2O
Warm
Aniline
Phenol
HBF 4
NaNO2, HCl
273 K
Aniline
N2+ BF4
N2+ Cl
NH2
NO2
NaNO2
Cu, Heat
Benzene diazonium
chloride
Nitrobenzene
(4)
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EVERGREEN
SERIES
19. (a) Due to extensive network of intermolecular hydrogen bonding. Carboxylic acid exists as dimer structure
in the vapour phase and aprotic solvent.
(b) Aldehydes and ketones are polar molecules. They get associated only due to weak dipole-dipole
interactions. Corresponding acids get associated due to intermolecular hydrogen bonding, which are
comparatively stronger in nature. They usually form the dimer as shown below :
O ........H O
RC
CR
O H ........ O
Dimer
Therefore, boiling points of aldehydes and ketones are lower than those of corresponding carboxylic acids.
(c) In the addition reactions of aldehydes and ketones, the nucleophile attacks the carbonyl carbon atom,
which has a slight positive charge due to more electronegative oxygen.
C+ O
Due to the positive charge on carbon nucleophilic addition reactions with HCN, NaHSO3, Grignard reagent,
alcohol, ammonia and its derivatives take place.
20. (a) Two good sources of Vitamin E are wheat and Green vegetables, oil.
(b) Nucleotides are the monomer units of nucleic acid present in the nucleus of living cells.
(c) Vitamin C is essential for us as it is needful for healthy gums and teeth. Its deficiency causes scurvy.
It cannot stored in body.
Sources of Vitamin C Citrus fruits, green leafy vegetables.
21.
Polymer
Monomer
Polystyrene
Styrene
Urea formal-
1. Urea
dehyde
2. Formaldehyde
High density
polythene
Ethylene
Structure
C 6 H5
|
( CH 2 CH
)n
Uses
As insulator, wraping
material, manufacture of toys,
radio and television cabinets
( NH CO NH CH 2
)n
( CH 2 CH 2
)n
Manufacturing of buckets,
dustbins, bottles.
22. (a) Bithional is used in the soap to reduce the odours produced by the bacterial decomposition of organic
matter.
(b) Paracetamol is used to bring down body temperature.
(c) Streptomycin is used for curing tuberculosis.
23. (a) Iron is present in +3 oxidation state as Fe(III).
(b) Fe(III)EDTA complex.
(c) Fe(III)EDTA complex is readily absorbed by the soil as it is water soluble while Fe(OH)3 is insoluble
in water and is therefore, not assimilated in the soil.
(d) Use of chemistry knowledge for higher yield, helps to others.
(5)
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EVERGREEN
SERIES
24. Using the following relations and substituting the values, we get
-cm
-cm
a =
k t 1000
Molarity
-cm 32.76
-0m 390.5
= 8.4 102
Degree of dissociation may be obtained as under :
Ka =
CB 2
1 B
0.00241 t (8.4 t 102 ) 2
1 0.084
= 1.86 105
25. The order of change of the property under different serial numbers are given below :
(a) MF > MCl > M Br > MI (Decreasing ionic character)
(b) Ga2O3 < GeO2 < As2O3 < ClO2 (Increasing acidity)
(c) H2O < H2S < H2Se < H2Te (Increasing acid strength)
(d) HOCl < HOClO < HOClO2 < HOClO3 (Increasing acid strength)
(e) HOI < HOBr < HOCl (Increasing acid strength)
CH3 O
|
||
26.(a) (i) CH CH C Cl H
3
2
(A)
~~~~~n
Pd/BaSO4
CH3
|
(ii) 2CH3 C C CH3 NaOI
|
||
CH3 O
CH 3 O
|
||
CH3 CH C H + HCl
~~~~n
NaOH
CH3
|
2CH3 C C ONa 2CHI3
|
||
(C)
CH3 O
(B)
~~~~n CH
NaOH
3 CHCH 2 CHO
|
OH
~~~~n CH CH CH
LiAlH 4
~~~~n
LiAIH 4
CH 3 CH CH 3
|
OH
~~~~
n CH
%
H 2SO4
ooooo
(6)
|
OH
2 CH 2
|
OH
3 CH = CH 2
Propene
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EVERGREEN
SERIES
1. 4
1
H2O H 2 + O2
2
1
O 2 2e
2
O2
i.e.,
\
1
Fe O
2 2 3
i.e., Fe2+ Fe 3+ + e
\ Quantity of electricity required = 1F
= 96500 C.
P
8. (a) P 4
Lone pair
(b)
N
P
F
F
F
P
Tetrahedral
Pyramidal
(7)
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EVERGREEN
SERIES
9 (a) (i)
(ii)
(iii)
(b) (i)
(ii)
(iii)
10. (a) Add Fehling's solution to each of them separately. Acetaldehyde gives brick red precipitate whereas /
acetophenone does not.
Alternatively, add I2 and NaOH to each of them separately. Acetaldehyde gives yellow precipitate of
iodoform whereas acetophenone does not.
(b) Add NaHCO3 to each of them separately. Phenol does not react whereas acetic acid gives brisk
effervescence due to formation of CO2.
Alternatively, add neutral ferric chloride. Phenol gives violet colour whereas acetic acid does not give
violet colour.
11. For fcc structure Z = 2, d = 8 g cm3
a = 250 pm = 250 1010 cm,
M = ?,
Apply the following relation :
d =
ZtM
N A t a3
12. (a)
d t N A t a3
Z
75.28
= 37.64 g mol1
2
Vapour Pressure
Vapour pressure
of solution
p1
p2
X1= 0
X2= 1
Mole fraction
X1
X2
X1= 1
X2= 0
(8)
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EVERGREEN
SERIES
(b) This is due to the force of attraction between the two components (say A and B) is more than the
attractions A A and B B. So, fewer molecules leave the surface and go to the vapour phase.
(c) Examples : Phenol aniline, chloroform acetone.
13.
...(i)
...(ii)
...(iii)
-pm NH 4 OH
= Mpm NH +4 Mpm OH
=
Substituting the values, we get
-pm NH 4 OH
-cm
-em
a =
9.33Scm2 mol 1
238.3Scm2 mol 1
= 0.039
or a = 3.9%
14. (a) Adsorption arises because of the unbalanced forces on the surface of the solids and liquids. These
molecules remain only on the surface and do not penetrate into the bulk. Therefore, adsorption is a surface
phenomenon.
(b) (i) In Tyndall effect, a beam of light is passed through a colloidal solution, the path becomes illuminated
as bluish light. This is due to the scattering of light by the colloidal particles.
(ii) In electrophoresis, the colloidal particles move towards oppositely charged electrodes under in influence
of electrical field.
15. Chemical equations for the processes are given as under :
(a) 6NaOH + 3Cl2 5NaCl +
NaClO3
Sodium chlorate
3H 2 O
(b) Orthophosphorus acid on heating disproportionates into orthophosphoric acid and phosphine.
4H3PO3
~~~n
Heat
3H 3PO4
Orthophosphoric
acid
PH3
Phosphine
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EVERGREEN
SERIES
16. (a) Bidentate ligand has two donor atoms and can form two bonds whereas monodentate ligand has only
one donor atom and can form only one bond with the metal ion.
(b) Diamminedichloridoplatinum(IV) chloride.
(c) Structures of geometrical isomers are given below :
+
NH3
H3N
Cl
H3N
Cl
Co
NH3
Co
H3N
Cl
H3N
NH3
Cl
NH3
cis-tetraamminedichloridocobalt(III) ion
trans-tetraamminedi-chlorido
cobalt(III) ion
17. (a) Addition of H2O to Ethenylbenzene in presence of dil. H2SO4 gives 1-Phenylethanol.
CH = CH2
+ H OH
Ethenylbenzene
CHCH3
|
OH
Dil. H2SO4
Markovnikov
addition
1-Phenylethanol
+ NaOH
Cyclohexylmethyl
bromide
CH2OH
+ NaBr
Hydrolysis
Cyclohexylmethanol
1-Bromopentane
CH3 CH 2 CH 2 CH 2 CH 2 OH NaBr
Pentan-1-ol
18. (i) The organic compound (A) with molecular formula C8H16O2 upon hydrolysis with dil.H2SO4 gives
carboxylic acid (B) and the alcohol (C), therefore (A) must be an ester. Further, oxidation of (C) with
chromic acid produces the acid (B), therefore, both the carboxylic acid (B) and the alcohol (C) must
contain the same number of carbon atoms.
(ii) Since ester (A) contains eight carbon atoms, therefore, the carboxylic acid (B) and the alcohol (C) must
contain four carbon atoms each.
(iii) Since the alcohol (C) on dehydration gives but-1-ene, (C) must be a straight chain alcohol, i.e.,
butan-1-ol.
(10)
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SERIES
(iv) If (C) is butan-1-ol, then the acid (B) which it gives oxidation must be butanoic acid and the ester (A)
must be butyl butanoate.
(v) The reactions can now be explained as follows :
O
||
CH3CH 2 CH 2 C OCH 2 CH 2 CH 2CH 3
Butylbutanoate (A)
(Molecular formula = C8H16 O2 )
~~~~~n
Dil.H 2SO 4
Hydrolysis
O
||
CH3CH2CH2 C OH + CH3CH 2 CH 2 CH 2 OH
Butan-1-ol(C)
CH3 CH 2 CH = CH 2
But-1-ene
l~~~~~
Oxidation
NH2
Sn/HCl
Nitrobenzene
Aniline
CH3COOH
Ethanoic acid
Br2 / KOH
3
2
Ethanamide
CH3 NH 2
Methanamine
O
NH C CH3
NH2
(CH 3CO) 2O
(c)
Aniline
N-Phenylethanamide
Fibrous protein
1.
Globular protein
of protein.
protein.
2.
3.
Water insoluble.
3. Water soluble.
n
21. (a) nCH 2 CH 2 ~~~~~~
0.1% oxygen
( CH 2 CH 2
)n
ethylene
CH = CH2
( CH
polyethylene
)n
CH2
(C6H5)2 O
(b) n
Styrene
Polystyrene
(11)
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EVERGREEN
SERIES
~~~~~n
Al(C2H 5 )3
TiCl4
(c) nCH3 CH = CH 2
Propylene
CH3
|
( CH CH 2
)n
Polypropylene
+
22. (a) CH3 [CH 2 ]10 CH 2 O SO3 Na
Hydrophobic part
Hydrophilic part
(b)
(c)
Hydrophilic
part
Hydrophilic
part
23. (a)
(b)
(c)
(d)
24. (a)
(b)
(c)
(d)
(e)
Ea
RT
Ea
RT
log k = log A
Ea
2.303RT
log A = log k +
Ea
2.303RT
(12)
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EVERGREEN
SERIES
5
log A = log (1.8) t 10 +
94140
2.303 t 8.314 t 313
26. (a)
S N1 Mechanism
the nucleophile.
nucleophile.
6. The order of reactivity in alkyl halide is : The order of reactivity is the reverse. It is :
Primary > Secondary > Tertiary
S N 2 mechanism.
~~~~~n
Hetrolytic
Fission
CH 3 + Cl
Step I :
CH3Cl
Step II :
CH 3 OH CH3OH
~~~~~~n
....
.
HO ......... C......... Cl
~~~~~n
Step II
Fast reaction
CH3OH + Cl
..
....
....
.
Step I
Slow reaction
....
...
OH
H..
..
Intermediate
complex
(13)
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EVERGREEN
SERIES
(b) (i)
Propene to 1-nitropropane
CH3CH = CH2
AgNO
~~~~n CH3CH2CH2Br ~~~~
n
HBr
organic
peroxide
(ii)
(iii)
SOCl 2
C2H5Cl
C2H5OH
Benzene to diphenyl
~~~~n
~~~n C H F
Br2
FeBr3
Br
AgF
CH3CH2CH2NO2
2 5
2Na
Dry ether
wurtz reaction
+ 2NaBr
ooooo
(14)
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SERIES
1. It is defined as the ratio of the experimental value of the colligative property to the calculated value of
the colligative property.
2. Coordination isomerism.
3.
CH2 CH CH3
OH
Strong electrolyte
Thermoplastic Polyethylene
6. Molar conductivity increases sharply for weak electrolyte
with decrease in concentration as shown in diagram because
both number of ions as well as mobility of ions increases
with dilution, i.e., decrease in concentration. In case of
strong electrolyte,
-m
Weak electrolyte
dx
= k[A]x [B]y
dt
From experiments (1) and (2)
2.1 103 = k[0.10]x [1.00]y
8.4
103
k[0.20]x
...(i)
[1.00]y
...(ii)
1
=
4
or
1
2
or x = 2
103
k[0.20]2[1.00]y
...(i)
...(ii)
1
1
= y or 2 y 20 or y = 0
1
2
The overall order of reaction is 2 + 0 = 2.
(15)
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EVERGREEN
SERIES
Cl + 2Na + Cl
Chlorobenzene
+ 2NaBr
Diphenyl
Br
OH
+ NaOH
623 K
300 atm
OH
+ dil. HNO 3
Phenol
bromobenzene
NO2
p-Nitrophenol
11. Applying the following relation and substituting the values; we get
d =
7.80 =
Z=
ZM
a t NA
3
Z56
(290) t 10
3
30
114.52
56
= 2.04 2.00
=
n =2
2
Ecell = E cell
0.0591
[Mg 2+ ]
log
2
[Ag + ]2
(16)
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EVERGREEN
SERIES
2
= (E
Ag + / Ag
0.80
E2
Mg 2+ / Mg
)
V ( 2.37 V)
0.0591
0.2
log
2
(10 3 ) 2
0.0591
log (2 t 105 )
2
= 3.17 V
0.0591
[log 2 + log 105 ]
2
= 3.17 V
0.0591
t 5.3010
2
2.466 102 =
2.303
a
log
t
ax
2.303
1
log
10
(a x )
log (a x) = 0.1071
(a x) = Antilog 1.8929
= 0.7814 mg.
14. (a) Role of NaCN in the extraction of silver is to do the leaching of silver ore in the presence of air from
which the silver is obtained later by replacement.
4Ag(s) + 8CN (aq) + 2H2O + O2(g) 4[Ag(CN)2] (aq) + 4OH
[Ag(CN)2] (aq) + Zn(s) [Zn(CN)4]2 (aq) + Ag(s)
(b) Iodine is heated with titanium to form a volatile compound which on further heating decompose to give
pure titanium as shown :
Ti(impure) + 2I2 TiI4
TiI4 Ti(pure) + 2I2
(c) Cryolite lowers the melting point of mixture of alumina in the extraction of aluminium as well as increase
the conductivity of mixture.
15. (a) The process is known as electrolytic reduction.
(b) The function of adding Na3AIF6 is to lower the melting point and to increase conductivity.
(c) 2Al2O3 + 3C 4Al + 3CO2
(17)
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EVERGREEN
SERIES
~~n Cr O H O
2
2 7
III
IV
IV shows maximum reactivity because the carbocation is stabilised by resonance (conjugation from double
bond). I is least reactive because the carbocation is least stable, being linked to double bond directly.
(b) CH2=CHBr < CH3CH2Br < CH3 CH CH 3 CH 2 CH CH CH3
|
|
Br
Br
This is again based upon the stability of the carbocation.
Cl
|
(c) CH3CH2CH2Cl < (CH3)2CHCl < (CH3)3CCl < C6 H5 C CH3
|
CH3
B
Butan-2-ol
~~~~~n
ZnCl2
Conc. HCl
Cl
|
CH3 CH CH 2 CH3
CH3 CH == CH CH3
A
But-2-ene
C
2-Chlorobutane
Dehydrohalogenation
l~~~~~~~
~
C H ONa
2
A = But-2-ene
B = Butan-2-ol
C = 2-Chlorobutane.
(18)
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EVERGREEN
SERIES
NH3 (excess)
NH 4Cl
3
Ethanoyl
Chloride
CH3CONH 2
Ethanamide
~~~~~~~~~n
Br2 /KOH
(Hoffman bromoamide
reaction)
CH3 NH 2
Methanamine
~~~~~n
H + /H 2O
Hydrolysis
~~~~~n
SOCl2
SO2 HCl
2 4
Br2 / KOH
CH3 (CH 2 )4 NH 2
1 Aminopentane
21. (a)
(b)
(c)
~~~~n CH Cl ~~~~~n
PCl5
POCl3
KCN(alc.)
CH3CN
Ethanenitrile
~~~~~n CH COOH
H+ / H2O
(Hydrolysis)
3
Ethanoic acid
a-Helix Structure
Primary Structure
Secondary Structure
Enzymes
Coenzymes
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EVERGREEN
SERIES
C-Hydroxybutyric acid
(3-Hydroxybutanoic acid)
O CH CH 2 C O CH CH 2 C
|
CH3
|
||
CH 2 CH3 O n
||
O
PHBV
(i) LiAlH4/H3O+
(ii) PCC
(iii) PCC
(b)
(iv) Sodalime
(i) Butanone < Propanone < Propanal < Ethanal < Methanal
(ii) Acetone < Acetaldehyde < Formaldehyde
(iii) Acetophenone < p-Tolualdehyde < Benzaldehyde < p-Nitrobenzaldehyde.
25. (a)
(Given : p = 8.21 atm,V = 1 litre, M B = 180 g mol1 , R = 0.0821 litre atm K1 mol 1 and
T = 37 + 273 = 310 K)
pV = nRT
=
26. (a)
or
wB =
wB =
wB
RT
mB
QVmB
RT
8.21 t1 t 180
0.0821 t 310
= 58.06 g
(i) Benzene to o-nitrochlorobenzene
Cl
Cl
Anhy.AlCl3
Benzene
Chlorobenzene
NO2
o-nitrochlorobenzene
(20)
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EVERGREEN
SERIES
NO 2
Anhy. AlCl3
Benzene
Nitrobenzene
NO2
Cl
m-nitrochlorobenzene
(b)
(i) By unpairing of one paired orbital, two singly occupied orbital come into existence. Thus, either
two or four or six singly occupied orbitals can be formed instead of one, three or five singly occupied
orbitals. Hence XeF, XeF3 or XeF5 are not formed.
(ii) Noble gases have very low boiling points due to weak dispersion forces.
(iii) In OF2, fluorine is more electronegative so it is called oxygen fluoride; while in Cl2O, oxygen is
more electronegative so it is called chlorine oxide.
ooo
(21)
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EVERGREEN
SERIES
1 d [H 2 ]
1 d[NH3 ]
=
.
3 dt
2
dt
(ii ) H
(i) NaOH
Fuming, H2 SO4
4.
OH
Benzene
Phenol
5. Pencillin
6. (a) Frenkel defect
(b) Frenkel and Schottky defect
7. (a) The reactions are described with the help of the following ionic compounds :
Cr2 O72 + 2OH
higher pH
Orange
yellow
When pH is increased, i.e., solution is more basic, orange coloured dichromate ion changes to yellow
coloured chromate ion.
(b)
MnO 24
o
MnO4 + e
electrolysis
purple
When potassium manganate is electrochemically oxidised, i.e., it undergoes, electrolytic oxidation, it forms
purple colour KMnO4.
2 %t
5
%t
Energy
3 %t
5
[
dx y , dz
9.
dx
= k [A] [B]2. Let [A] = a and [B] = b.
dt
Thus dx = k ab2.
dt
8.
d-orbital
free ion
Avg. energy
of the d -orbitals in
spherical crystal
field
(22)
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10. (a)
Benzophenone (C6H5COC6H5)
Acetophenone (C6H5COCH3)
Iodoform test
C6H5COCH3 + 3NaOI
CHI3
Iodoform
C6H5COC6H5 + 3NaOI
No yellow ppt. of CHI3
+C6H5COONa + 2NaOH
(Yellow ppt)
(b)
Ethanol (CH3CH2OH)
Propanal (CH3CH2CHO)
Iodoform test
CH3CH2OH + 4I2 + 3Na2CO3
CHI3 o
Iodoform
(Yellow ppt)
11.
Iodoform test
CH3CH2CHO + 4I2 + 3Na2CO3
No Yellow ppt. of CHI3
WB 1000
t
MB WA
MB =
K b t WB t 1000
%Tb .WA
MB =
= 128.5 g mol1
12. Electrode reactions may be represented as under
Fe(s) Fe2+ (aq) + 2e
2Ag+ (aq) + 2e Ag(s)
Fe(s) + 2Ag+(aq) Fe2+ (aq) + 2Ag(s)
Thus, n = 2
Applying Nernst equation and substituting the values, we get
Ecell = E2
cell
= (E 4
0.0591
[Fe 2+ ]
log
2
[Ag ]2
Ag / Ag
E4 2
Fe
/ Fe
0.0591
0.1
log
2
(Ag )2
= [ + 0.80 V ( 0.44 V)
(23)
0.0591
0.1
log
2
(0.1)2
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= 1.24 V
0.0591
1
2
= 1.240 V 0.0295 V
= 1.2105 V
13. Applying Arrhenius equation
log
k2
E a T2 T1
k1 = 2.303 R T1 T2
k2
6 u 104
3.05 u 103
3050
=
19.147 u 93
1780.671
= 1.7128
or
14.
15.
16.
17.
18.
k2
6 u 104
= Antilog 1.7128
= 51.62
or
k 2 = 51.62 6 104
or
k 2 = 3.097 102 s1.
(a) The process of settling of colloidal particles is called coagulation.
(b) The process of converting a precipitate into colloidal sol by shaking it with dispersion medium in the presence
of a small electrolyte is called peptization.
(c) The sols that can be made again by simply remixing with the dispersion medium.
(a) Electronic configuration : The general electronic configuration of lanthanoids is [Xe] 4f1 14 5d0 1 6s2
whereas that of actinoids is [Rn] 5f114 6d0 1 7s2. Thus, lanthanoids belong to 4f- series whereas actinoids
belong to 5f-series.
(b) Oxidation state : Lanthanoids show limited oxidation states ( + 2, + 3, + 4) out of which + 3 is most
common. This is because of large energy gap between 4f, 5d and 6s subshells. On the other hand, actinoids
show a large number of oxidation states because of small energy gap between 5f, 6d and 7s subshells.
(c) Atomic and ionic sizes : Both lanthanoids and actinoids show decrease in size of their atoms or ions in
+ 3 oxidation state. In lanthanoids, the decrease is called lanthanoid contraction whereas in actinoids, it is
called actinoid contraction. However,the contraction is greater from element to element in actinoids due
to poorer shielding by 5f electrons.
Advantage of fuel cells
(i) A fuel cell can work continuously as long as the oxidising agent (O2) and reducing agent (H2, CH3OH)
are supplied at the electrodes.
(ii) Do not cause any pollution.
(iii) The efficiency of a fuel cell as pointed earlier is about 60 to 70 per cent.
(a) Hexaaminecobalt (III) chloride
(b) Potassium tetrachloridopalladate (II)
(c) Potassium hexacyanoferrate (III)
Mechanism
Ethene does not react with water. The reaction is carried to the presence of H2SO4. The acid provides (H+)
for the initial electrophilic attack.
H2SO4 H+ + HSO 4
(24)
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Step II. Nucleophilic attack of water on carbocation. CH3 CH 2 + H2O CH3 CH2 OH2
NH2
OH
(B)
CH 3
CH 3
[C]
CH 3
|
o
ZnCl2 (Anhy.)
CH 3
|
CH3 C CH 3 + H2O
|
OH
Cl
[C]
C is resistent to oxidation, because tertiary alcohol do not undergo oxidation. It gives turbidity immediately
with Lucas reagent. D respond to Lucas reagent test within 5 minutes because it is a secondary alcohol and
turbidity appears after 5 minutes.
CH3 CH CH 2 CH3 + HCl
|
~~~~~~~~n CH
ZnCl2 (Anhydrous)
CH CH 2 CH3
|
~~~~~
n
I2 NaOH
Cl
OH
Butane-2-ol
CH3NH 2 + H OH CH3 N H3 + OH
These OH ions combine with Fe3+ ions present in H2O to form brown ppt. of hydrated ferric oxide.
FeCl3 Fe3+ + 3Cl
2Fe3+ + 6OH 2Fe(OH)3 or Fe2 O3 . 3H 2 O
Hydrated ferric oxide (Brown ppt.)
(c) Aniline being a Lewis base react with Lewis acid AlCl3 to form a salt. As a result, aniline does not undergo
Friedel crafts reactions.
NH 2 AlCl 3
NH2
+ AlCl3
(25)
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EVERGREEN
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21. In transition elements d-orbitals are progressively filled whereas in inner transition elements f-orbitals are
progressively filled.
(a) Atomic size : In 3d-transition series, atomic size first decreases, then remains the same. Thus, copper
has bigger atomic size than Ni. It is because the number of unpaired electrons increases from 21 to 25,
therefore, effective nuclear charge increases and atomic size decreases. Fe, Co, Ni have almost same
size because pairing of electrons in d-orbitals starts and effective nuclear charge almost remains the same.
Cu has bigger size due to repulsion between electrons in d-orbitals.
(b) Oxidation states : Oxidation states of elements increases from 21 to 25 and then decreases because
number of valence electrons decreases. Thus, Se shows +3, Ti shows +4, Vanadium +5, Chromium +3,
Manganese +7 and Iron +3.
(c) Coloured ions : Transition metals form coloured ions due to presence of unpaired electrons and empty
d-orbitals. They absorb light from visible region, undergo d-d transitions and radiate complementary colour.
Thus, Cr3+ is green, Fe2+ is pale green, Co2+ is blue, Ni2+ is green and Cu2+ in blue.
22. (a) Morphine (an alkaloid) is a narcotic which is used as an analgesic i.e., to reduce pain.
Antiseptics
(b)
Disinfectants
(26)
Strong electrolyte
m
Weak electrolyte
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Thus n = 2
0.591
[Cu 2 ]
log
2
[Ag ]2
= 0.46
0.0591
0.1
log
2
(0.001)2
(ii)
Cl
OH
OH
OH
(b)
Pd / BaSO4
(ii) CH3C (CH3)2 C CH3 + NaOI CH3 C(CH3)2 COONa + CHI3 + 2NaOH
||
(b)
~~~~~~n
Aldol
Condensation
OH
o
OH
OH
|
|
CH3 CH CH 2 CH 2
CH3 C CH3
Acetone
o
LiAlH 4
Ether
OH
|
CH3 CH CH3
o CH3 CH = CH2
H 2SO4
H 2O
CHO
+ CO + HCl Anhy. AlCl3
(iii)
Benzene
Benzaldehyde
ooooo
(27)
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4.
Fe
Dark
+ Cl2
Benzene
Chlorobenzene
... (i)
p A = xB pqB
... (ii)
O
P
HO
Xe
H
H
H3PO2
F
XeOF4
(28)
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9. (a) Ni shows + 2 oxidation state because of lower (IE1 + IE2). Pt shows + 4 oxidation state because extra
energy IE3 + IE4 is balanced by hydration energy.
(b) Pt can form compounds in + 4 oxidation state more easily because energy required to remove four electrons
is less in case of Pt than Ni.
10. (a) Acetaldehyde (CH3CHO) and Benzaldehyde (C6H5CHO) : Acetaldehyde contains CH3COgroup,
hence it will respond to iodoform test whereas benzaldehyde will not.
CH 3CHO + 3NaOI
o
I2 / NaOH
Acetaldehyde
C6 H5CHO
HCOONa
Sodium formate
+ 2NaOH +
CHI3
Iodoform
(yellow ppt.)
o No reaction
I 2 / NaOH
NaOH
Benzaldehyde
(b) Propanone (CH3COCH3) and Propanal CH3CH2CHO : Propanone is a methyl ketone, it gives
iodoform test whereas propanal does not.
CH 3COCH3 + 3NaOI CH3COONa + 2NaOH +
Propanone
CHI3
Iodoform
(yellow ppt.)
2a
r = 125 1012 m
a =
4r
2
r u 2 2 125 u 10 12 u 2 2
Total volume
106 m3
=
Volume of one unit cell
44.21 u 1030 m3
1000
DTf = Kf m = Kf B t
M B WA
2.3 K = 5.1
1 1000
u
or MB = 5.1 u 50 110.86
MB
20
2.3
1.3 K = 5.1
1 1000
5.1 u 50
u
or MB =
MB
20
1.3
255
= 196.15
1.3
... (i)
...(ii)
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log
k2
Ea 1
=
k1
2.303 R T1
4.5 u 107 s 1
7 1
1.5 u 10 s
log 3 =
1
T2
Ea
1
1
1100579.725
= 22011.595 J mol1
50
or
Ea = 22.01 kJ mol1
14. (a) Differences between Lyophilic sols and Lyophobic sols :
Lyophilic sols
Lyophobic sols
(b)
Absorption
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(b) Oxidation states : Oxidation states of elements increases from 21 to 25 and then decreases because
number of valence electrons decreases.
Thus, Sc shows + 3, Ti shows + 4, Vandium + 5, Chromium +6, Manganese + 7 and Iron + 3.
(c) Coloured ions : Transition metals form coloured ions due to presence of unpaired electrons and empty
d-orbitals. They absorb light from visible region, undergo d-d transitions and radiate complementary colour.
Thus, Cr3+ is green, Fe2+ is pale green, Co2+ is blue, Ni2+ is green and Cu2+ is blue.
17. (a) Oxidation number of Iron [Fe(en)2Cl2]Cl
x + 2 0 + (1) 2 1 = 0
x =3
(b) d2sp3, octaheadral
(c) Paramagnetic behaviour
Cl
18. (a)
Cl
Cl
Cl
Cl
UV
+ 3Cl2
light
Benzene
Cl
Benzene hexachloride
~~~~~~~~~~~n
Benzoyl
Peroxide
(Anti Markovnikov addition)
Propene
Cl
CH 3CH 2 CH 2 Br
1-Bromopropane
OH
(c)
+ NaOH
623 K
high pressure
+ NaCl
CH3 C CH3
Propanone
o
NaBH 4
OH
|
CH3 CH CH 3
Propan-2-ol
o
conc. H2SO 4
443 K
CH3 CH CH 2
Propene
COOH
COCl
SOCl2
SO2O HCl
Benzoic acid
CHO
H2/PdBaSO4
Benzoyl
chloride
Rosenmunds
reduction
Benzaldehyde
CH3CH 2OH
Ethanol
3
Acetaldehyde
Aldol
condensation
(31)
OH
|
CH3 C H CH 2 CHO
3-hydroxy butanal
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20.
21. (a)
(b)
(c)
22. (a)
(b)
23. (a)
(b) Cl
Cl
C C
Cl H
Cl
(c) DDT is non-biodegradable and not metabolised very rapidly by animals rather it gets deposited and stored
in fatty tissues and its long term effects could be dangerous.
(d) Human welfare and Environmental concerns.
24. (a) (i) Frenkel defect is shown by ionic solids, in which a cation is dislocated from its normal site to an
interstitial site. This defect is shown by ZnS, AgCl and AgI. It does not change the density of solid
substances.
(ii) F-centres are the anionic sites occupied by electrons, they impart colour to the crystal lattice.
(b) We know that for a cubic unit cell,
d =
M
NA
a
d
z
\
zM
10
30
NA u a
g cm 3
(where a is in pm units)
z =
=
d u 1030 u N A a3
M
7.86 u 1030 u 6.02 u 1023 u (286)3
56
= 1.97 | 2
As the number of atoms per unit cell is 2, the iron crystal has bcc structure.
(32)
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Percentage
At. Mass
Relative number
of atoms
Divide by
the least
Simplest
ratio
69.77
12
69.77
= 5.81
12
5.81
=5
1.16
11.63
11.63
= 11.63
1
11.63
= 10
1.16
10
18.60
16
18.60
= 1.16
16
1.16
=1
1.16
Molecular mass
86
=
=1
86
Empirical formula mass
CH3 C CH 2 CH 2 CH3 or CH 3 C CH CH 3
||
O CH 3
CH3 C CH 2 CH 2 CH3
Pentan-2-one
o
K 2Cr2O7
Conc. H 2SO4 , heat
ooooo
(33)
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OH
OH OH
5. Geometrical isomerism.
6. (a) The value of colligative property decreases.
(b) The value of colligative property increases.
7. (a) For a weak electrolyte, there is a very large increase in the conductance with dilution because as the
conc. of a weak electrolyte is reduced, more it undergoes ionization.
(b)
2
PbSO4(s) + 2e Pb (s) + SO4 (aq)
2
PbSO4(s) + 2H2O PbO2(s) + SO4 (aq) + 4H+ (aq) + 2e
2PbSO4 (s) + 2H2O Pb(s) + PbO2 (s) + 4H+ (aq) + 2 SO24 (aq)
8. (a) Cr2+ is a stronger reducing agent than Fe2+ because it undergoes a change from d4 to d3 stable state as
compared to Fe2+.
(b) Copper ions are not stable in aqueous solution because in aqueous state they form Cu2+ and Cu+ ions
disproportionately.
9. (a) Atomic number of Ti = 22
Ti3+ = 3d 1.
With an unpair electron present in d-orbital, so it shows colour. Its colour is purple
(b) Triammine triaquachromium (III) chloride.
o
NaOH
OH
|
C6 H5 CH CH CHO
|
CH3
~~~~~n
KMnO /H
4
(b) CH3CH2CH2CH2OH
CH3CH2CH2COOH
11. (a) Those polymers which can be decomposed by the action of microorganism, bacteria is called
biodegradable polymers. For example : PHBV and halon-2-nylon-6.
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O
C
H2 C
CH2
H 2C
CH2
Caprolactum
CH3
12. (a)
CHCl2
CHO
H2O/Heat
Cl2/hv
373 K
Benzaldehyde
Toluene
o C6H5COCH2CH3 + Mg
H 2O
Br
OH
13. (a) Ethyl alcohol has intermolecular hydrogen bonding whereas no hydrogen bonding is present in dimethyl
ether.
(b) The oxygen atoms in ethers have two unshared electron pairs and therefore, the oxonium salts are formed
with acids. Therefore, ethers have high solubility in conc. H2SO4 than water.
(c) Due to formation of hydrogen bonding.
14. (a) Glucose despite the presence of aldehyde group does not react or form any product with NaHSO3.
(b) Essential amino acid : Valine.
Non-essential amino acid : Glycine
(c) Keratin serves as functional protein in hairs and nails while insulin as globular protein helps in glucose
metabolism.
15. (a) In KCN, C acts as nucleophile while in AgCN, N acts as nucleophile, hence both gives different products
with chloromethane.
(b) The population of birds who feed on fishes declined sharply because of DDT which was used as pesticide.
Hence, to cut down this loss, US had banned use of DDT in 1972.
(c) Because of high stability of benzyl carbocation as a result of resonance.
16. (a) Henrys law states that the solubility of a gas is directly proportional to the pressure of gas at constant
temperature.
Applications :
(i) The law has been used in producing fizzy drinks where CO2 is dissolved in water under pressure.
(ii) To minimise the painful effects (bends) accompanying the decompression of deep sea divers, diluted
oxygen with less soluble helium gas is used as breathing gas.
(35)
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(b) 0.1 M NaCl has higher boiling point than 0.1 M glucose because NaCl being an electrovalent compound
dissociates immediately when dissolved in water but not glucose.
17. (a) Oxidation :
Reduction :
(b) The froth floatation involves the use of heavy oils like pine oil. When the sulphide ores particles are agitated
with oil and water, they with their affinity to heavy oils bind with them.
18.
d =
a3 =
Putting,
ZM
a t NA
3
Z M
4 u 0.027 kg mol1
=
d t NA
2700 kg m 3 u 6.02 u 1023 mol1
= 66.4 1030 m3
a = (66.4)1/3 1010 m
(66.4)1/3 = n
1
1.8222
log 66.4 =
= 0.6074
3
3
n = 4.050
a = 4.05 1010 m
For, fcc
r =
a
2 2
4.05 u 1010 m
= 1.43 1010 m.
2 u 1.414
19. (a) This difference in oxidising power is because of the increasing stability of the members down the series.
(b) Actinoid contraction is greater for element than lanthanoid contraction because of shielding effect of
electrons that elements of actinoids series possess.
(c) Oxanions of metals show higher oxidation states due to the combination of the metal with oxygen, which
is highly electronegative and oxidising element.
20. (a) Pentaamminechloride cobalt (III) chloride
Oxidation state of Co in [Co(NH3)5 Cl] Cl2 :
x+0 1 =+2
x =+3
3+
Electronic configuration of Co = 3d 6.
(b) Trichloridopyridine chromium (III)
Oxidation state of Cr in [CrCl3(Py)3]
x3+0 =0
x =+3
3+
Electronic configuration of Cr = 3d3
(36)
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NH2
N 2Cl
NaNO2/HCl
0-5C
aniline
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SERIES
25. (a) (i) Bond enthalpy of F2 is lower than that of Cl2 because of its smaller size and higher electronegativity
(ii) PH3 has lower boiling point than NH3 because in NH3 the electron density is maximum on nitrogen
owing to its smaller size than in PH3 which has compraratively lower electron density. NH3 also
formed hydrogen bonding
F
(b) (i) BrF3 =
Br
F
O
(ii) (HPO3)3 =
O
P
OH
HO
O
O
P
OH
O
F
(iii) XeF4 =
Xe
F
26. (a) (i)
CH 3 Br
Methyl bromide
F
+ NaCN
CH3 CN + 4[H]
o
Ethanol
Water
Methylcyanide
o
C2 H5OH
CH 3 CH 2 NH 2
Ethyl amine
OH
NH2
HONO2
(ii)
CH 3 CN NaBr
Warm
NH 2
N2+H2O
NHCOCH 3
NHCOCH 3
NH
Br
(iii)
CH3COCl
CH3
Br2
Base
OH
Br
Hydrolysis
CH3
CH3
CH3
2 bromo 4 Methyl aniline
(b) HNO3 acts as a base in the nitrating mixture used for nitration of benzene and provides the electrophile,
NO2 (nitronium ion).
ooooo
(38)
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SERIES
CH3 Br
Buta-1, 3-diene
Buta-1, 3-diene
COOH
Ethylene glycol
Terephthalic acid
O
O
C2H 5 C Cl
12. (a)
Benzene
C C 2H 5
Anhyd. AlCl3
CS2
Propanylchloride
Ethylphenyl ketone
O
||
(c) CH3 C CH
Ethanoyl chloride
o 2CH
o
Hg 2 / H 2SO 4
Dry ether
O
||
3 C CH 2 C6 H5
Benzyl methyl ketone
+ CdCl2
OH
|
CH3 C CH 2
(39)
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HO H
HOH+H
H
H2C
CH2 + H O+ H
H2C CH3 + H2 O
Carbocation
ethene
CH3 CH2 + O H
Ethyl
carbocation
CH3 CH2 O H
H
Protonated alcohol
CH3 CH2 O H + O H
H
CH 3 CH 2 OH + H3O
14. (a) Vitamin C is water soluble and hence excess of it is readily excreted in urine, so it cant be stored in our
body and hence, it should be regularly supplied in diet.
(b) On hydrolysis, sucrose gives equimolar amounts of glucose and fructose. Since laevorotatory of fructose
is much more than the dextrorotatory of glucose, therefore, the mixture is laevorotatory.
(c) Lactose.
15. (a) This is done to avoid the reaction of magnesium with water and also to prevent the substitution of halide
group by the hydroxyl group during course of its synthesis.
Cl
(b) in
(c) Haloalkanes are more reactive towards nucleophilic substitution reactions than haloarenes because
(C X) bond is the more polar in haloalkanes than haloarenes.
16. DTb = 36.86 35.60 = 1.26C
Given,
Kb = 2.02, WA = 8, WB = 100, MB = ?
DTb = Kb m
WB t 1000
DTb = Kb M t W
B
B
DTb = 2.02 t
8 t 1000
M B t 100
1.26 = 2.02 t
8 t 1000
M B t 100
2.02 u 8 u 10
1.26
161.6
MB =
1.26
MB =
= 128.25 g mol1
(40)
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17. (a)
18.
4r =
2a
2
ta
4
1.414 t 409 pm
=
4
= 144.58 pm
The catalytic properties of the transition elements are probably due to presence of unpaired electrons in
their incompleted d-orbitals and hence possess the capacity to absorb and emit wide range of energies.
Due to lanthanoid contraction.
Actinoids show large energy gap between 4f, 5d and 6s subshells.
Crystal field splitting : In a free transition metal ion all the 5d-orbitals degenerate but when it is involved
in a complex formation, the degeneracy is split.
Linkage isomerism : Isomerism of this type occurs in compounds containing ambidentate ligands.
Ambidentate ligand : Any ligand which has two or more donor atoms but only one donor atom is attached
to the metal ion at a time during complex formation.
Cu Cu2+ + 2e
...(i)
+
Ag + e Ag
...(ii)
+
2+
2Ag + Cu 2Ag + Cu
r =
19. (a)
(b)
(c)
20. (a)
(b)
(c)
21.
E = Epcell
0.0591
[Cu 2+ ]
log
n
[Ag + ]2
o.422 = 0.46
log
0.10
[Ag ]2
0.10
[Ag ]2
0.0591
[0.10]
log
2
[Ag ]2
0.0591
[0.10]
log
2
[Ag ]2
0.0591
[0.10]
log
2
[Ag ]2
= 1.28
= Antilog (1.28)
(41)
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SERIES
0.10
[Ag ]2
= 0.1950 102
[Ag+]2 =
Ag+ =
0.10
19.5
0.10
= 0.071
19.5
k =
[R ]
2.303
log 0
t
[R]
[R 0 ]
2.303
log
70
40
[R 0 ]
100
2.303
10
log
40
7
2.303
log 1.428
40
= 0.0090 min1
t1/2 =
(b) (i)
(ii)
0.693
min1 = 77 min
0.0090
Rate
Rate
Rate
Rate
d [A]
dt
d [B]
dt
[3A]2
=k
[B]
2
= 9k[A] [B]
= 9 Rate
(iii)
= k[2A]2 [2B]
= 8k [A]2 [B]
= 8 Rate
25. (a) (i) NF3 is an endothermic compound but not NCl3 because F F bond has the minimum bond dissociation
energy.
(ii) Fluorine shows only a negative one oxidation state as compared to other halogens down the group
which shows both positive and negative oxidation state.
(42)
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(b) (i)
Cl2 + 3F2
o 2ClF3
473 K
o B o (CC
'
H N)
NH 3
Br2 /KOH
So, the compound C is an amine (NH2) and B must be an amide ( CONH2). Therefore, (C) is
C6H5NH2 (Aniline) and (B) is C6H5CONH2 (Benzamide). Hence, A is C6H5COOH (Benzoic acid)
C6 H5COOH
(A)
~~~n
NH 3
Heat
C6 H5CONH 2
(B)
o C6 H5 NH 2
Br2 / KOH
(C)
oooo
(43)
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EVERGREEN
SERIES
4A
as
a =
1=
i=
i 1
1
1
n
n=4
i 1
1
1
4
1
4
2. Glycogen.
3. Depressant (NaCN) is used to concentrate galena selectively by froth floatation method.
4. K2 [Ni(CN)4]
5. Phosphodiester linkage
6. (a) Schottky defect
(c) NaCl
(d) No effect.
Tf = ?
7.
DTf = iKf m
T fq Tf = iKf
273 Tf = 3 1.86
0.322
0.1
273 Tf = 17.96
Tf = 273 17.96
Tf = 255.04
F
8. (a) XeF4
(b) H2S2O7
Xe
OH
O
OH
9. (a) Zone refining : In this method, an impure metal rod is placed inside a small high frequency induction
furnace. A narrow zone of metal is melted. The furnace is now slowly moved along the rod. The pure
metal recrystalised out of the melt. The end of the rod where the impurities have collected is cut off. The
method is employed for the purification of Ge, Si, Ga etc.
(44)
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EVERGREEN
SERIES
(b) Vapour phase refining : It is based on the principle that impure metal should form a volatile compound
with some reagent and that volatile compound should decompose to form pure metal. It is used for Ni, Ti
etc.
10. (a)
Acetone (CH3COCH3)
Acetaldehyde (CH3CHO)
Fehling solution test
CH3 CHO + 2Cu2+ + 5OH
No Red ppt.
Red ppt.
(b)
Phenol (C6H5OH)
FeCl3 test
C6H5COOH + FeCl3
3C6H5 OH + FeCl3
(C6H5O)3 Fe + 3HCl
No reaction
Violet Colour
(C HOH) 4
|
~~~
n
Heat
HI
CH 2 OH
Glucose
(C HOH) 4
|
o
HNO3
CH 2 OH
(C HOH) 4
|
COOH
Saccharic acid
Glucose
d [A]
dt
=K
d[A] = Kdt
(45)
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EVERGREEN
SERIES
d [A ] =
Kdt
[A]
K dt
d [A] =
0
[A]o
[A]
t
[A]o = K | t |o
[A] [A]o = Kt
[A]o [A] = Kt
t=
15. (a)
[A]o [A]
K
The colloidal solution in which dispersed phase does The colloidal solution in which dispersed phase have
not have affinity for dispersion medium.
a affinity for dispersion medium.
(b)
Chemical catalyst
Enzymes
Chemical catalyst are the catalyst which catalyse Enzymes are those catalysts which catalys
the chemical reaction and may increase their speed biological reaction and may increase their speed
upto 1010 times.
upto 1020 times.
(c)
Multimolecular colloids
Macromolecular colloids
These are those colloidal in which multiple small Macromolecular colloidal are the colloidal in which
particle aggregate themself in dispersion medium to large size particle decompose in dispersion medium
become particle of colloidal range.
to become particles of colloidal range.
16.
DG = nF Eqcell
DG = 2 96500 1.10
DG = 212300
17. (a) 0.2% of phenol acts as an antiseptic and 1% of phenol acts as a disinfectant.
(b) (i) Broad spectrum antibiotics : These are those antibiotics which are used for wide range of diseases
For example : Chloramphenicol.
(ii) Tincture of Iodine : Tincture of iodine can be define as 2-3% solution of iodine in alcohol and
water. It possesses antiseptic property that is applied on wounds, cuts etc.
(46)
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EVERGREEN
SERIES
+ 4KOH + O2
2K 2 MnO 4
Potassium Manganate
(Green)
+ 2H2O
+ Cl2
+
2KMnO 4
Potassium permanganate
(Purple)
2KCl
3d 5
4s
4p
3d
4s
4p
CO CO
CO
CO CO CO
6e pair donated by CO
Hybridisation : d2sp3
Magnetic behaviour : Diamagnetic
20. For a solution of CH2FCOOH in H2O.
Let solute (B) and solvent (A)
vant Hoff factor i = ?
as
DTf = iKf m
= i Kf
19.5 / 24 3 32 14
500 / 1000
1 = i 1.86
1 = i 1.86
19.5 / 78
1/ 2
1 = i 1.86
39
75
i=
1
0.93
(47)
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EVERGREEN
SERIES
21. (a)
Aniline
Benzylamine
NH2
CH 2NH2
NH2
NH2
Br
+ 3Br2
CH2 NH2
Br
H2O
+ 3HBr
+ 3Br2
H2O
No Reaction
Br
(White ppt)
.
(b) (i) Sandmeyers Reaction.
N2+Cl2
NH2
NaNO2 + HCl
Cl
CuCl/HCl
+ N2
273 278K
N2 + Cl + H
OH
OH
OH
N=N
p (Hydroxy azobenzene
(Orange dye)
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EVERGREEN
SERIES
24. (a)
Molecularity
Order of reaction
(b)
SO2Cl2
SO2
Cl2
at initial (t = 0)
0.5 atm
(Pressure at time = t)
0.5 x
at
Total pressure at time t = 0.5 x + x + x
= 0.5 + x
0.6 = 0.5 x
x = 0.1
Pi = 0.5 atm and P(at time 100 sec) = 0.5 x
= 0.5 0.1
= 0.4 atm
As for the first order
t=
100 =
K =
2.303
Initial pressure
log
K
Pressure at time t
2.303
0.5
log
K
0.5 0.1
2.303
0.5
log
100
0.4
2.303 t 0.0969
100
K = 2.23 103 s1
K =
Rate of PTotal
= 0.65 atm
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EVERGREEN
SERIES
~~~~~~n CH
(i ) X 2 / Red P
(ii ) H2 O
CH COOH
|
o
50% NaOH
O3
(b) (i)
O + HCHO
Zn H2O
1, 2 dicyclohexyl ethene
C2H 5
(ii)
CH3OH + HCOONa
Ozonolysis
COOK
COOH
KMnO4
Hydrolysis
KOH/%
Potassium benzoate
(iii) CH3COCH2COOC2H5
Benzoic acid
o
CH3CH(OH) CH2COOC2H5
26. (a) Lanthanoids shows + 2, + 3 and + 4 oxidation state, out of which + 3 is most common. This is because of
a large energy gap between 4f, 5d and 6s sub shells.
NaBH4
ooooo
(50)
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EVERGREEN
SERIES
1. Chloramphenicol.
2. It is due to the fact that alkali metal ions have large size which cannot fit into the interstitial sites.
3. Bi2O3 + 6HNO3 2Bi(NO3)3 + 3H2O
CH3
|
4. CH3 C CH 2OH
|
CH3
5. 2-Chloro-3-methylpentane
6. Sodium chloride depresses the freezing point of water to such an extent that it cannot freeze to form ice.
Hence, it melts off easily at the prevailing temperature.
7. H2O has higher oxidation potential than F ions. Hence, in aqueous solution as compared to F ions, H2O is
more easily oxidised to give O2 gas. Therefore, F2 cannot be obtained by electrolysis of aqueous HF solution.
8. (a) Because the number of unpaired electrons in most of the transition metal ions.
(b) Colour is due to the presence of incomplete d-subshell or unpaired electrons.
9. (a) [Co(NH3)4 (H2O)2] Cl3
(b) Pentaamminechloridocobalt (III) chloride
OCH3
CH3
10. (a)
NOH
(b)
C
H
OCH3
H
11. (a)
C=C
H
F
CH2 = CHCl
Vinyl chloride
(b)
Cl
CF2 = CF2
C=C
F
Tetrafluoroethane
H
(c)
OH and
C=O
H
Phenol
Formaldehyde
12. (a) Cannizaros reaction : This reaction takes place between those aldehydes which having absence of ahydrogen.
2HCHO
o
conc. NaOH
CH3OH + HCOONH
(51)
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EVERGREEN
SERIES
(b) Acetylation :
o
+ HOC2 H5
CH 3COCl
Ethanol
Ethanoyl chloride
CH 3COOC 2 H 5 + HCl
Pyridine
Ethyl ethanoate
(c) Decarboxylation : Phenol is obtained by decarboxylation of sodium salt of salicylic acid with soda-lime
followed by acidification with dil. HCl.
OH
ONa
COONa
+ 2 NaOH
CaO/%
Dil. HCl
Na2CO3, H2O
NaCl
Sod. Salicylate
Sod. phenoxide
Sodium propoxide
O Na +
(b)
o
Heat
Phenol
OCH2CH3
Heat
+ CH3CH2 Br
Sod. phenoxide
OH
+ NaBr
Bromoethane
Ethoxybenzene
14.
o
Heat
CH 3CH 2 O CH 3 + NaBr
1-Methoxyethane
DNA
RNA
15. (a)
E E
E
C = O + R Mg X
H
R
OMgX
H3O+
RCH2OH
Conc. H 2SO4
Conc. H2SO4
H 2O
Heat
(52)
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EVERGREEN
SERIES
3
= 0.75
4
4
= 0.80
5
px = 600 mm
py = 400 mm
18.
M Z
d NA 1030
93 g mol1 t 2
a 3 = 3.61 107
a = 3.304 102 pm = 330.4 pm
For body centred cubic
r =
3
a
4
= 0.433 330.4 pm
r = 143.1 pm
19. (a)
(b)
(c)
+
3MnO2
4 + 4H 2MnO4 + MnO2 + 2H2O
(53)
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EVERGREEN
SERIES
3d
Cr3+
4p
NH3 NH3
NH3
NH3 NH3
(ion) =
[Cr(NH 3)6]3+ =
Shape : Octahedral
Hybridisation =
4s
d2sp3
-m
-pm =
CH3COOH
Initial conc.
390.5 S cm 2 mol1
= 0.1233
CH3COO + H+
Eq. Conc. C Ca = C (1 a)
K=
48.15 S cm 2 mol 1
0
Ca
0
Ca
1
2
CB. CB
CD 2
=
= (0.001028 mol L ) (0.1233)
C (1 B )
1 D
1 0.1233
(54)
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EVERGREEN
SERIES
2.303
a
log
t
ax
x = a/2
2.303
a
log
a
t1/ 2
a
2
2.303
K =
log 2
t1/ 2
0.6931
K =
t1/ 2
K =
1 d H2
dN 2
=
3 dt
dt
dx
d N2
=
K = 2.5 104 M sec1
dt
dt
Rate of reaction,
dN 2
= K = 2.5 104 M/sec.
dt
OH
S
25. (a) (i)
26. (a)
(b)
(c)
(d)
(e)
(ii)
OH
Cl
O
O
O
H2S2O8
HClO4
(i) As, PH3 has less tendency than NH3 to accept a proton, hence NH3 has higher proton affinities
than PH3.
(ii) Due to tendency of pp pp bond formation.
(iii) Due to small size and electronegativity.
In aniline, lone pair of electrons decreases the electron density on nitrogen while in methylamine. +I effect
of CH3 increases the electron density on N-atom. Hence, pKb of aniline is more than that of CH3NH2.
Ethylamine dissolves in water due to intermolecular H-bonding but in aniline, due to the large hydrophobic
part, it is insoluble in water.
Methylamine being more basic than water, accept a proton from OH ions. These ions combine with
Fe3+ ions present in H2O to form brown ppt. of hydrated ferrous oxide.
Due to dispersal of the positive charge on the benzene.
Because this reaction gives pure 1 amines 2 and 3 amine unreactive with phthalamide.
(b)
OH
ooooo
(55)
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EVERGREEN
SERIES
p
- b
(CaSO4) =
M 2+ Mp 2
Ca
SO 4
= 119.0 + 160.0
= 279.0 cm2 mol1
8. The irregularities in the configuration are explained on the basis of the concept that half-filled and completely
filled orbitals are relatively more stable than other configurations.
The irregularities in some elements are explained by factor as :
Nuclear-electron attractions.
Inter-electronic repulsions.
Shielding effect.
O
+ HO NH2
(56)
10. (a)
NOH
+
R CH = CH CH = N NH C NH2
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EVERGREEN
SERIES
(b) CH 2 C CH CH 2
Chloroprene
~~~~n
Peroxide
Cl
|
(CH 2 C CH CH 2
)n
Neoprene
12. (a)
Anhydrous AlCl3
+ C6H 5 COCl
Benzophenone
(i) B2H6, H2O2/OH
(b)
CH2
CHO
(ii) PCC
CH2 CH3
(c)
KMnO4/KOH
Heat
OH
|
CH2Cl
(b) Benzyl chloride to benzyl alcohol
CH2OH
+ KOH (aq)
OH
CHCl3 + NaOH
OH
ONa
ONa
CHO
CHCl2
NaOH
H3 O
CHO
salicyaldehyde
Phenol
14. (a) Amylose is a linear chain of a-D(+) glucose structure while amylopectin is a branch chain of a-D(+)
glucose structure.
(b) Globular protein having spherical shape.
(c) These are liver and adipose tissue.
15. (a) Due to large van der Waals force of attraction.
(b) Because both sulphur dioxide and hydrogen chloride are in the gaseous state. They readily leave the
reaction mixture leaving behind the alkyl chloride.
(c) Since C I bond can cleave more readily than C Br.
16.
10 g
122.5 g mol 1
(57)
EVERGREEN
SERIES
CH3CH2CHClCOO
0
Ca
CH3CH2CHClCOOH
Initial conc.
C mol L1
At equilibrium
C (1 a)
\
Ka =
or
a =
CD . CD
= Ca2
C(1 D )
3
= 1.4 t 10 = 0.065
Ka
C
0.3264
or
H+
0
Ca
H+
0
a
i=
i=
1 D
= 1 + a = 1 + 0.065 = 1.065
1
o
1470 K
Al2O3.xH2O(s)
Al2O3(s) + xH2O(g)
18. Edge length of unit cell a = 4.077 108 cm
r =
a
2 2
4.077 u 10 8
2 2
= 1.441 108 cm
zM
= a3 t N
A
(for fcc z = 4)
(58)
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EVERGREEN
SERIES
4 u 108
= 10.58 g cm3
19. (a) Due to small size and high electronegativity.
(b) Copper has positive reduction potential and this shows that copper is least reactive metal out of the first
transition series. The high energy required to convert Cu(s) to Cu2+ (aq) is not balanced by its hydration
enthalpy.
(c) In the presence of dilute sulphuric acid, K2Cr2O7 liberates nascent oxygen and, therefore, acts as an
oxidising agent.
Cl
NH3
20. (a)
H3N
H3N
Cl
NH3
Pt
Pt
NH3
H3N
Cl
NH 3
Cl
NH3
2H+
= 0.44
Sn +
103
0.0591
log 4
2
10
0.0591
[Fe 2 ]
log 2
2
[H ]
Ecell = 0 ( 0.44)
2H+
Ecell = Eqcell
(c)
[Cu
0.0591
[103 ]
log
2
(1)2
0.0591
u (3) = 0.44 + 0.0887V
2
= 0.523 V
Sn2+ + H2;
: Ecell = Eqcell
n=2
0.0591
[Sn 2 ]
log 2
2
[H ]
(59)
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EVERGREEN
SERIES
= 0 ( 0.14)
0.0591
(0.05)
log
2
(0.02)2
= 0.14
0.0591
log (125)
2
= 0.14
0.0591
(2.0969) = 0.078 V
2
o
Organic
Peroxide
CH3
|
(CH 2 C COOCH 2
)n
PMMA
(d) Rama gives good advise to Jyotsana about the alternate of spectacles.
24. (a) (i) When concentration of A is tripled
Rate = k [3A]2 [B] = 9k [A]2 [B]
i.e., Rate of reaction will become 9 times.
(ii) When concentration of both A and B is doubled
Rate = k [2A]2 [2B] = 8k [A]2 [B]
i.e., Rate of reaction will become 8 times.
(b) For a first order reaction
k =
When t = 40 minutes,
[R]0
2.303
log
t
[R]
[R]0
100
=
100 30
[R]
10
7
k =
2.303
10
log
40
7
k =
2.303
0.1548 = 8.91 103 min1
40
t1/2 =
0.693
k
2.303
log 1.428
40
0.693
8.91 u 103 min 1
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EVERGREEN
SERIES
Cl
Cl
O
Cl
(ii)
Si
O
Cl
Cl
(b) (i) HF does not attack wax but reacts with glass, it dissolves SiO2 in glass present in glass forming
hydrofluorosilicic acid.
SiO2 + 6HF H2SiF6 + 2H2O
(ii) Iodine is covalent in nature, it does not dissolve in water which is polar. In KI solution, iodine reacts
to form KI3 which is ionic in nature.
KI + I2 KI3
(iii) When sodium sulphite is heated with sulphur, we get sodium thiosulphate which is soluble in water
that is why sulphur disappears.
Na2SO3 + S
'
o Na2S2O3
C 2 H5
(ii) C2H5
C 2 H5
C 2 H5
N + HCl C2 H5
C 2 H5
N HCl
Triethylammonium chloride
Phenyl isocyanide
NHCOCH3
NH2
(iii)
+
Aniline
CH3CO
CH3CO
CH 3COOH
Acetic acid
Acetanilide
ooooo
(61)
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EVERGREEN
SERIES
2. F
F
F
Perfluorobenzene
NH2
3.
N2 Cl
+ NaNO2 + 2HCl
273-278 k
Aniline
Cl
HCl
CuCl
+ N2
Benzenediazonium
chloride
Chlorobenzene
1
1
6u
8
2
5. Electrophoresis : The movement of colloidal particles under the influence of an electric field is called
electrophoresis.
6. Step I : Formation of Carbocation
CH3 C CH 2
|
o
H
CH3
CH3
3q Carbocation
(more stable)
Isobutylene
CH3
1p Carbocation
(less stable)
CH3 C CH3
|
CH3
o
Cl
Cl
|
CH3 C CH3
|
CH3
7. According to Raoults law the partial pressure of each component is directly proportional to the mole fraction.
For example.Ethyl alcohol and water, Acetone and benzene.
(62)
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EVERGREEN
SERIES
Positive deviation : For the solution showing this type of deviation the partial vapour pressure of each component
(A and B) of solution is greater than the vapour pressure as expected according to Raoults law. This type of
deviation is shown by the solution in which solvent-solvent and solute-solute interactions are stronger than
solvent-solute interaction.
= A
+ B
V.P.
A=
B=
1
0
A=
Mole fraction
B=
0
1
B
A
x , p p x
pA pA
A
B
B B
9. (a)
(b)
P
H
Xe
OH
OH
Phosphorus acid or
phosphoric acid
H3PO3 (P = +3)
(Dibasic)
F
XeOF4
10. (a) Oxidation number : Elements show variable oxidation states in all the transition series. For the first
transition series, the lower oxidation states especially + 2 and + 3 are more stable than for the elements
of second and third transition series. For example, in cobalt group, cobalt forms a large number of
(63)
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EVERGREEN
SERIES
complexes in Co(II) and Co(III) states. But on similar complexes of Rh2+ or Rh3+ and Ir2+ or Ir3+
are known. Within a group, the maximum oxidation state increases as we move from element of first
transition series to second and third transition series. For example, in group 8 iron shows common oxidation
states of + 2 and + but rubhenium and osmium in the same group form compounds in + 4, + 6 and + 8
oxidation states.
(b) Atomic size : The atomic size of 4d series are larger than those of 3d series. However, the elements
of 5d series have nearly the same size as those of 4d series because of lanthanoid contraction.
11. (a) HCHO + CH3CH2MgCl
(b)
Methanal
CH 2 CH3
CH3
CH 3
OMgBr
C = O + CH3MgBr
CH3
~~~~~~
n
H , H 2O
Mg (OH) Cl
C
CH3
CH3
H ,H 2O
Mg(OH) Br
CHO
oxidation
(c)
Propan-1 ol
CH3
o
OH
C
CH3
CH3
2-Methyl propan-2-ol
Propanone
CH2OH
CH 3 CH 2 CH 2 OH
COOH
oxidation
Benzyl
alcohol
Benzaldehyde
Benzoic acid
o 2CH3CHO
C4 H8
o C4H9Cl (Addition of HCl has occurred on A. This implies A is an alkene)
12. (A)
Ozonolysis
HCl
(A)
(B)
C4 H9Cl
(B)
CH3 CH CH CH3
(A)
Cl
|
4 4
(C)
~~~n
HCl
o
NH3
to give C)
Cl
|
CH3CH 2 CH CH3
(B)
CH3 CH 2 CH CH3
|
NH 2
(C)
13. (i) Vitamin A is essential for us because its deficiency causes-Xerophthalmia (hardening of cornea of eye)
and night blindness.
(ii) Vitamin C is essential as deficiency will causes scurvy (bleeding gums).
Sources :
Vitamin A : Fish liver oil, carrot, butter and milk.
Vitamin C : Citrus fruit, amla and green leafy vegetables.
(64)
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EVERGREEN
SERIES
Monomer unit/s
Structure
O
||
NH
(CH
)
C
2 5
(a) Nylon-6
Cyclohexane
Condensation polymer
Vinyl Chloride
(b) PVC
(CH 2 CH Cl)
Cl
|
CH 2 CH n
Addition polymer
Propene
(c) Polyprene
(CH 3CH CH 2 )
CH 3
|
CH 2 CH n
Addition polymer
15. (a) Interstitial defect : When some constituent particles, atoms or molecules occupy vacant interstitial
positions, the crystal is said to have interstitial defect.
(b) Doping : The introduction of small amount of impurities like P, As, B into the pure crystal is called doping.
(c) Ferrimagnetism : When the magnetic moments of domains are aligned in parallel and antiparallel directions
in unequal numbers resulting in net magnetic moment we get ferrimagnetism.
16.
Mass of glucose (WB) = 54 g
Molecular mass of glucose (MB) = 180 g mol1
Mass of water (WB) = 250 g
Kf for water = 1.86 K mol1 kg
Applying the formula, DTf =
=
K f t WB t 100
MB t WA
1.86 u 54 u 1000 g kg1
180 g mol 1 u 250 g
= 2.23 K or 2.23 C
Tf = Tf DTf = 0C (2.23C)
Tf = 2.23C
17.
log
E a T2 T1
k2
=
2.303 R T1T2
k1
Ea =
2.303 R T1 T2
log
T2 T2
k2
k1
(65)
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EVERGREEN
SERIES
Ea =
Ea = 18224 kJ mol
18. (a) Demulsification : It is the process of decomposing an emulsion back into its constituent liquids. The
demulsification can be done by centrifugation, filtration, boiling, freezing and some chemical methods.
(b) Adsorption isotherm : Adsorption isotherm represents the variation of the mass of the gas adsorbed
per gram of the adsorbent with pressure at constant temperature.
(c) Aerosol : It is a colloidal dispersion of a liquid in a gas. For example, fog.
19. (a) Electrolytic reduction of Al2O3 :
Ni + 4CO
330 350 K
450 470 K
OX
OX
CO
CO
OX
OX
OX
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EVERGREEN
SERIES
en
en
Cl
Cl
Pt
Pt
Cl
Cl
en
en
(c) Optical isomers
NH3
NH3
NH3
NH3
en
en
Pt
Pt
Cl
Cl
Cl
Cl
22. (a)
(b)
(c)
23. (a)
(b)
(c)
o
KOH(Conc.)
CH 3OH
Methyl alcohol
HCOO K
Potassium formate
o
Zn / Hg
HCl
R CH3 + H2O
Alkane
OH
(b)
(i)
(ii)
Heat
~~~~~
n
CH CH CH CHO ~~~
n
l~~~~
~
Ethanal
CH3CH 2 CH 2CH 2OH o CH CH CH COOH
CH3CHO
dil. NaOH
CrO3 , H 2SO4
Butanol
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CH3CH CHCHO
But-2-enal
2
2
Butanoic acid
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EVERGREEN
SERIES
(iii)
CH2 CH3
COO K
COOH
+
KMnO4 KOH
H3 O
Heat
Ethyl benzene
25. (a)
(b)
Benzoic acid
(i)
XeF4 + SbF5
(ii)
Cl2 + 3F2
[XeF3]+ + [SbF6]
o 2ClF3
537K
(i) N-N single bond is weaker than P-P single bond because of high interelectronic repulsions of nonbonding electrons due to small bond length.
(ii) Due to inert pair effect + 5 oxidation decreases down the group.
(iii) In NO2 there is one electron on N. While in NO+2 there is no electron on N atom and there is a
lone pair of electrons on N atom in NO2 .
+
O=N =O
N
N
O
NO+2 is linear and has bond angle of 180. Because of repulsions by a lone pair of electrons in NO 2 , the
molecule has angular shape and bond angle has been bound to be 115. Hence, the bond angles in NO+2 and
NO 2 are different.
26. (a) (i) Faradays Second Law of Electrolysis : On passing same quantity of electricity through solutions
of different electrolytes the masses of the substances deposited are directly proportional to their
equivalent weights (W1/W2 = E 1/E2).
(ii) Kohlrauschs Law : For an electrolyte Ax By , - pm = x l + y Mp or Leq = M p M p , where Oq
and Oq are limiting ionic conductivities of cation and anion respectively.
(b) (i) Mercury Cell : Anode = Zn container,
Cathode = Carbon rod,
Electrolyte = Paste of HgO + KOH
Cell reaction : Zn + HgO ZnO + Hg
(ii) Faraday Constant : Faraday constant F = 96500 coulombs. It is that quantity of electricity which
deposits one gram equivalent of the substance ore. It is the charge carried by one mole of electrons.
(iii) Primary Batteries : A primary cell is the cell in which the redox reaction occurs only once and the
cell becomes dead after sometime. It cannot used again.
ooooo
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