Electrochemistry JM Questions
Electrochemistry JM Questions
Electrochemistry JM Questions
6. Number of electrons involved in the electrodeposition of 63.5 g of Cu from a solution of CuSO4 is:
(NA = 6.02 × 1023)(atomic wt. of Cu = 63.5g)
(1) 6.02 × 1023
(2) 3.01 × 1023
(3) 12.04 × 1023
(4) 6.02 × 1022
7. When one coulomb of electricity is passed through an electrolytic solution the mass deposited
on the electrode is equal to :
(1) equivalent weight
(2) molecular weight
(3) electrochemical equivalent
(4) one gram
8. A current of 9.65 amp. passing for 16 minute 40 sec through a molten tin salt deposits 5.95 g of
tin. The oxidation state of the tin in the salt is : (at. wt of Sn = 119)
(1) +4
(2) +3
(3) +2
(4) +1
9. The time required for a current of 3 amp. to decompose electrolytically 18 g of H2O is:
(1) 18 hour
(2) 36 hour
(3) 9 hour
(4) 18 seconds
10. An ion is reduced to the element when it absorbs 6 × 1020 electrons. The number of gm equivalents
of the ion is :
(1) 0.10
(2) 0.01
(3) 0.001
(4) 0.0001
11. How many coulombs of electric charge are required for the oxidation of 1 mole of H2O to O2 ?
(1) 9.65 × 104 C
(2) 4.825 × 105 C
(3) 1.93 × 105 C
(4) 1.93 × 104 C
12. The time required to coat a metal surface of 80 cm2 with 5 × 10–3 cm thick layer of silver (density
1.08 g cm–3) with the passage of 9.65A current through a silver nitrate solution is :
(1) 10 sec.
(2) 40 sec.
(3) 30 sec.
(4) 20 sec.
16. The equivalent conductivity (in –1 cm2 eq–1) of 1.0 M – H2SO4 solution of specific conductance
2.6 × 10–1 cm–1, is
(1) 1.3 × 102
(2) 6.5 × 101
(3) 1.3 × 10–1
(4) 2.6 × 102
17. The molar conductance of a 0.01 M solution of acetic acid was found to be 16.30 –1 cm2 mol–1
at 25°C. The ionic conductance of hydrogen and acetate ions at infinite dilution are 349.8 and
40.9 –1 cm2 mol–1, respectively, at the same temperature. What percentage of acetic acid is
dissociated at this concentration ?
(1) 0.04172%
(2) 4.172%
(3) 41.72%
(4) 0.4172%
18. The distance between two electrodes of a cell 2.5 cm and area of each electrode is 5 cm2. The cell
constant is
(1) 0.5 m–1
(2) 12.5 cm3
(3) 2.0 cm
(4) 50 m–1
19. Calculate the ionic product of water at 25° C from the following data :
Conductivity of water = 5.5 × 10–6 mho m–1
°H+ = 0.035 mho m2 mol–1
°OH– = 0.020 mho m2 mol–1
(1) 2 × 10–14 M2
(2) 1 × 10–7 M2
(3) 1 × 10–8 M2
(4) 1 × 10–14 M2
20. Calculate Ka of acetic acid if its 0.05 M solution has molar conductivity of 7.814 × 10–4 –1 m2
mol–1 at 25°C. Given: °m for CH3COOH = 3.907 × 10–2 –1 m2 mol–1.
(1) 2 × 10–5
(2) 1.8 × 10–5
(3) 4 × 10–4
(4) 0.02
3. If Eo
Fe2+ |Fe
= – 0.44 V, Eo
Fe3+ |Fe2+
= 0.77 V. Calculate Eo
Fe3+ |Fe
( −3) .
4. The reduction potential of hydrogen electrode when placed in a buffer solution is found to be
– 0.413V. The pH of the buffer is -
7. If 0.224 litre of H2 gas is formed at the cathode, how much O2 gas is formed at the anode under
identical conditions?
9. The conductivity of pure water in a conductivity cell with electrodes of cross-sectional area 4
cm2 and 2 cm apart is 8 × 10–7 S cm–1.
The value of current that would flow through the cell under an applied potential difference of 1
volt is 1.6 × 10–X amp. The correct value of X is :
10. The value of m for HCl, NaCl and CH3CO2Na are 425, 125 and 100 S cm2 mol–1 respectively. If
the equivalent conductivity of the given acetic acid is 48 at 25° C, calculate its percentage of
dissociation.
Answer Key
Q. 1 2 3 4 5 6 7 8 9 10
A. 3 1 1 4 1 3 3 3 1 3
Section-A
Q. 11 12 13 14 15 16 17 18 19 20
A. 3 2 2 1 3 1 2 4 2 1
Q. 1 2 3 4 5 6 7 8 9 10
Section-B 1.61 1.35 0.11 7 0.0295 4 0.112 1.83 6 12
A.
Solutions
SECTION-A
1. Ans. 3
0.0591 [Sn+2 ]
E = E0 − log
n [Ag + ]2
Cell potential E will increase if [Sn+2] decrease or [Ag+] increase.
2. Ans. 1
0.059 [Zn +2 ]
E = E0 − log
2 [Cu+2 ]
0.059 0.1
E = 1.10 − log
2 0.1
E = 1.10 volt
3. Ans. 1
+2
0.059 [Zn ]PH2
Ecell = E −
0
log
2 [H+ ]2
As [H+] increases, Ecell will also increase and equilibrium will shift in forward direction.
4. Ans. 4
G = +966 × 1000
966000 = – nFE
966000 = –4 × 96500 × E
E = –2.5 volt
So, minimum 2.5 volt battery will be required.
5. Ans. 1
W = ZQ
W = ZIt
So, amount of ion discharge will be not proportional to it’s resistance.
6. Ans. 3
Eq.(Cu) = mole of e
63.5
2 = mole of e
63.5
Mole of e = 2 mol
Number of e = 2 × 6 × 1023
= 12 × 1023
7. Ans. 3
W = ZQ
Q = 1 coulomb
Then W = Z
Here Z is electrochemical equivalent.
8. Ans. 3
Sn + n ( aq ) ⎯⎯
→ Sn ( s )
M i t
W=
n 96500
5.95 9.65 1000
n =
119 96500
n=2
9. Ans. 1
Eq. (H2O) = no. of faraday
18 3 t
2 =
18 96500
t = 64333.33 second
t = 17.87 hour
10. Ans. 3
gm equivalents = number of faradays
6 1020
gm equivalents =
6 1023
gm equivalents = 0.001
11. Ans. 3
Eq. (H2O) = no. of faraday
1 × 2 = no. of faraday
So, charge in coulomb = 2 × 96500
= 193000
= 1.93 × 105 coloumb
12. Ans. 2
Volume of silver plate = 5 × 10–3 × 80
= 0.4 cm3
Mass of silver plate = (0.4 × 1.08) gm
It
Eq. (Ag) =
96500
0.4 1.08 9.65 t
1 =
108 96500
t = 40 sec
13. Ans. 2
On dilution, specific conductance decreases and hence resistance increase.
14. Ans. 1
Increases with increase of temperature.
15. Ans. 3
Liquid HCl does not dissociate into ions.
16. Ans. 1
2.6 10−1
eq = = = 1.3 × 102 ohm–1 cm2 eq–1
C (1 2) 10−3
17. Ans. 2
16.30
= 0m = = 0.04172 or 4.172%
m (349.8 + 40.9)
18. Ans. 4
2.5
Cell constant C = = = 0.5 cm–1 = 5× 10–3 m–1
A 5
19. Ans. 2
0m(H2O) = 0m(H+ ) + 0m(OH− ) = 0.035 + 0.020
= 0.055 mho m2 mol–1
5.5 10−6
Now, m = 0.055 =
C C
C = 10–4 mol m–3 = 10–7M KW = C2 = 10–14M2
20. Ans. 1
m 7.814 10−4
= 0 = = 0.02
m 3.907 10−2
2 .C
Now, K a = 2 .C = (0.02)2 0.05
1−
= 2 × 10–5
SECTION-B
1. Ans. 1.61
E0cell = E0 4+ + ECO
0
CO2+
Ce Ce3+
1.89 = E0 4+ + 0.28
Ce Ce3+
E0 4+ = 1.61 volt
Ce Ce3+
2. Ans. 1.35
E0cell = E0Cl− /Cl + E0Pt2+ /Pt
2
−0.15 = −ECl 0
− + 1.20
2 /Cl
E0Cl = 1.35
2 Cl
3. Ans. 0.11
2e + Fe+2(aq) ⎯→ Fe (s) E10 = −0.44
4. Ans. 7
e + H(aq) ⎯→ 1 H2(g )
+
0.059 PH1/2
E =0− log 2+
1 [H ]
1
E = 0 − 0.059log
[H+ ]
−0.413 = −0.059pH
pH = 7
5. Ans. 0.0295
Zn (s) ⎯→ Zn+2 (aq)+ 2e–
2e– + Zn+2 (aq) ⎯→ Zn (s)
E = 0 – 0.059 log 0.01
2 0.1
0.059
E= = 0.0295
2
6. Ans. 4
½ H2(g) ⎯→ H+(aq) + e–
e– + H+(aq) ⎯→ ½ H2(g)
0.059 x
E=0– log
1 1
0.2364 = –0.059 logx
x = 10–4
pH = –log [H+] = –log 10–4 = 4
7. Ans. 0.112
Eq. H2 = Eq. O2
P(0.224) P
2 = (VO ) 4
RT RT 2
VO2 = 0.112 litre
8. Ans. 1.83
It
Equivalent of Ni =
96500
5 20 60
nNi 2 =
96500
nNi 2 = 0.03108 mol
Mass of Ni = 0.03108 × 58.8
= 1.827 gm
1.83 gm
9. Ans. 6
1
= .
R A
1 2
8 10−7 = .
R 4
107
R= = 6.25 105
16
V 1
I= = 7 = 1.6 10−6 amp
R 10 /16
10. Ans. 12
m (CH3COOH) = m (CH3COONa ) + m (HCl) − m ( NaCl )
= 100 + 425 – 125
= 400 Scm2mol–1
eq nfactor = m
48 × 1 = m
48
= = 12 10−2 = 0.12
100
Dissociation percentage is 12.
3. The standard reduction potentials for Zn2+ | Zn, Ni2+ | Ni and Fe2+ | Fe are – 0.76 V, – 0.23V and
– 0.44 V respectively. The reaction X + Y+2 → X2+ + Y will be spontaneous when
(1) X = Zn, Y = Ni
(2) X = Ni, Y = Fe
(3) X = Ni, Y = Zn
(4) X = Fe, Y = Zn
[AIEEE 2012 (+4 /–1)]
4. Given :
E0 3+ = − 0.74V ; E0 − /Mn2+ = 1.51 V
Cr /Cr MnO4
5. The equivalent conductance of NaCl at concentration C and at infinite dilution are C and ,
respectively. The correct relationship between C and is given as :
(where the constant B is positive)
(1) C = – B C
(2) C = + B C
(3) C = + BC
(4) C = – BC
[JEE (Mains) 2014 (+4 /–1)]
7. At 298 K, the standard reduction potentials are 1.51 V for MnO–4|Mn2+, 1.36 V for Cl2|Cl–, 1.07 V
for Br2 | Br–, and 0.54 V for I2|I–. At pH = 3, permanganate is expected to oxidize
RT
F = 0.059V : −
(1) Cl– and Br–
(2) Cl–, Br– and I–
(3) Br– and I–
(4) I– only
[JEE (Mains) 2015 (+4 /–1)]
9. Two Faraday of electricity is passed through a solution of CuSO4. The mass of copper deposited
at the cathode is : (at. mass of Cu = 63.5 amu)
(1) 2g
(2) 127 g
(3) 0 g
(4) 63.5 g
[JEE (Mains) 2015 (+4 /–1)]
10. What will occur if a block of copper metal is dropped into a beaker containing a solution of 1M ZnSO4
(1) The copper metal will dissolve and zinc metal will be deposited
(2) No reaction will occur
(3) The copper metal will dissolve with evolution of oxygen gas
(4) The copper metal will dissolve with evolution of hydrogen gas
[JEE (Mains) 2016 (+4 /–1)]
11. Oxidation of succinate ion produces ethylene and carbon dioxide gases. On passing
0.2 Faraday electricity through the aqueous solution of potassium succinate, the total volume of
gases (at both cathode and anode) at 1 atm and 273 K is :
(1) 8.96 L
(2) 2.24 L
(3) 4.48 L
(4) 6.72 L
[JEE (Mains) 2016 (+4 /–1)]
(1) +0.30 V
(2) +0.057 V
(3) –0.057 V
(4) –0.30 V
[JEE (Mains) 2017 (+4 /–1)]
14. To find the standard potential of M3+|M electrode, the following cell is constituted: Pt|M|M3+
(0.001 mol L–1)//Ag+(0.01 mol L–1)|Ag.
The emf of the cell is found to be 0.421 volt at 298 K. The standard potential of half reaction
M3+(aq) + 3e– → M(s) at 298 K will be : (Given E + at 298 K = 0.80 Volt)
Ag / Ag
(1) +0.32 V
(2) +0.057 V
(3) –0.057 V
(4) –0.32 V
[JEE (Mains) 2017 (+4 /–1)]
15. How long (approximate) should water be electrolysed by passing through 100 amperes current
so that the oxygen released can completely burn 27.6 g of diborane ?
(Atomic weight of B = 10.8 u)
(1) 0.8 hours
(2) 3.2 hours
(3) 1.6 hours
(4) 6.4 hours
[JEE (Mains) 2017 (+4 /–1)]
16. When an electric current is passed through acidified water, 112 mL of hydrogen gas at N.T.P. was
collected at the cathode in 965 seconds. The current passed, in ampere, is :
(1) 2.0
(2) 1.0
(3) 0.1
(4) 0.5
[JEE (Mains) 2018 (+4 /–1)]
17. When 9.65 ampere current was passed for 1.0 hour into nitrobenzene in acidic medium, the
amount of p-aminophenol produced is :-
(1) 10.9 g
(2) 98.1 g
(3) 109.0 g
(4) 9.81 g
[JEE (Mains) 2018 (+4 /–1)]
18. For the cell Zn(s) | Zn2+(aq) || Mx+ (aq) | M(s), different half cells and their standard electrode
potentials are given below :
Mx+(aq)/M(s) Au3+(aq)/Au(s) Ag+(aq)/Ag(s) Fe3+(aq)/Fe2+(aq) Fe2+(aq)/Fe(s)
Eo x + (v) 1.40 0.80 0.77 –0.44
M /M
o
If Eo = −0.76V , which cathode will give a maximum value of Ecell per electron transferred ?
Zn2+ /Zn
19. If the standard electrode potential for a cell is 2 V at 300 K, the equilibrium constant (K) for the
reaction
Zn(s) + Cu2+(aq) Zn2+(aq) + Cu(s)
at 300 K is approximately. (R = 8 JK–1 mol–1, F = 96000 C mol–1)
(1) e160
(2) e320
(3) e–160
(4) e–80
[JEE (Mains) 2019 (+4 /–1)]
dE0
21. The standard electrode potential E0 and its temperature coefficient for a cell are 2V and
dT
–5 × 10–4 VK–1 at 300 K respectively. The cell reaction is
Zn(s) + Cu2+ (aq) → Zn2+(aq) + Cu(s)
( )
The standard reaction enthalpy r H0 at 300 K in kJ mol–1 is,
[Use : R = 8 JK–1 mol–1 and F = 96,000 Cmol–1]
(1) –412.8
(2) –384.0
(3) 206.4
(4) 192.0
[JEE (Mains) 2019 (+4 /–1)]
22. m for NaCl, HCl and NaA are 126.4, 425.9 and 100.5 S cm2mol–1, respectively. If the conductivity
of 0.001 M HA is 5×10–5 S cm–1, degree of dissociation of HA is :
(1) 0.75
(2) 0.125
(3) 0.25
(4) 0.50
[JEE (Mains) 2019 (+4 /–1)]
25. The anodic half-cell of lead-acid battery is recharged using electricity of 0.05 Faraday. The
amount of PbSO4 electrolyzed (in g) during the process is : (Molar mass of PbSO4 = 303 g mol–1)
(1) 22.8
(2) 15.2
(3) 7.6
(4) 11.4
[JEE (Mains) 2019 (+4 /–1)]
26. Given that the standard potentials (E°) of Cu2+/Cu and Cu+/Cu are 0.34 V and 0.522 V
respectively, the E° of Cu2+/Cu+ is :
(1) +0.158 V
(2) 0.182 V
(3) –0.182 V
(4) –0.158 V
[JEE (Mains) 2020 (+4 /–1)]
28. What would be the electrode potential for the given half cell reaction at pH = 5
2H2O → O2 + 4H + 4e– ; E0red = 1.23 V
(R = 8.314 J mol–1 K–1 ; Temperature = 298 K; oxygen under pressure of 1 bar)
[JEE (Mains) 2020 (+4 /–1)]
30. 108 g of silver (molar mass 108 g mol–1) is deposited at cathode from AgNO3(aq) solution by a
certain quantity of electricity. The volume (in L) of oxygen gas produced at 273 K and 1 bar
pressure from water by the same quantity of electricity is _______.
[JEE (Mains) 2020 (+4 /–1)]
Answer Key
1 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
Answer 2 1 1 4 1 3 3 2 4 2 1 1 3 1 2
Question 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Answer 2 4 3 1 2 1 2 2 1 3 1 1 –0.93 2.15 5.67
SOlutions
1. Ans. 2
1 l
= .
R A
1
1.3 = .
50 A
= 65m−1
A
1 l
= .
R A
1
= 65
260
65/ 260
m = = 6.25 × 10–4 Sm2mol–1
1000 0.4
2. Ans. 1
2e + 2H+(aq) ⎯→ H2(g)
0.0591 pH
E =0− log +2 2
2 [H ]
Potential will be negative if pH2 [H+ ]2
That is satisfied by option (1)
3. Ans. 1
X + Y+2 ⎯→ X+2 + Y
For spontaneous reaction
E = EY+2|Y − EX+2|X > O
So, reduction potential Y +2 Y must be greater than reduction potential of X +2 X .
So, option (1) is correct.
4. Ans. 4
Species that have highest value of reduction potential will be have as strongest oxidising agent
i.e. MnO4 .
5. Ans. 1
C = – B C (Debye Huckel Onsager equation)
6. Ans. 3
1
=
RA
1
1.4 = . = 70m−1
50 A A
1 1 1
= . = 70 = Sm−1
R A 280 4
1/4
m = = 5 × 10–4 Sm2 mol–1
1000 0.5
7. Ans. 3
5e + 8H+ + MnO4 ⎯→ Mn+2 + 4H2O
0.059 1
EMnO /Mn+2 = E0MnO /Mn+2 − log + 8
4 4
5 [H ]
0.059 1
EMnO /Mn+2 = 1.51 − log
4
5 (10−3 )8
EMnO /Mn+2 = 1.22 volt
4
8. Ans. 2
If Eext < 1.1V current will flow in natural direction that will be cathode to anode. Since, direction
of flow of electron and conventional current is opposite.
But if Eext > 1.1V then current will flow from anode to cathode.
9. Ans. 4
No. of equivalents of copper deposited = number of Faradays
mCu
2 = 2
63.5
MCu = 63.5 gm
10. Ans. 2
Copper cannot displace Zn+2 as Zn is present above in electrochemical series with respect to
copper.
11. Ans. 1
Potassium succinate
Eq. H2 = Eq. C2H4 = Eq. CO2 = 0.2
12. Ans. 1
Species that has highest value of oxidation potential will be the strongest reducing agent i.e. Cr.
13. Ans. 3
Fe+2 (aq)+ 2e ⎯→ Fe (s) E10 = −0.47
Fe+3 (aq) + e ⎯→ Fe+2 (aq) E02 = +0.77
Fe+3 (aq) + 3e → Fe (s)
n1E10 + n2E20 2( −0.47) + 0.77
E0 = =
n 3
E0 = −0.057 V
14. Ans. 1
M (s) + 3Ag+(aq) ⎯→ M+3(aq) + 3Ag(s)
(
0.421 = E0M/M+3 + 0.8 −) 0.0591
3
log
10−3
(10−2 )3
EM/M+3 = −0.32 V
EM+3 /M = +0.32 V
15. Ans. 2
B2H6 (g) + 3O2 ⎯→ B2O3 (s)+ 3H2O
27.6
moles of B2H6 = =1
27.6
Moles of O2 required = 3 x 1 = 3
It
Equivalent of O2 =
96500
100 t
3 4 = t = 11580 sec (nf of O2 in this reaction is 4)
96500
t = 3.2 hours.
16. Ans. 2
It
Equivalent of H2 =
96500
112 I 965
2 = I = 1 amp
22400 96500
17. Ans. 4
It
Eq. (p-aminophenol) =
96500
m 9.65 3600
4 =
109 96500
M = 9.81 g
18. Ans. 3
E0cell = E0Zn/Zn+2 + E0M+ /M
19. Ans. 1
G° = –RT ln K
–2 × 96000 × 2 = –8 × 300 ln K
ln K = 160
K = e160
20. Ans. 2
0.059
E0Cell = logK
n
0.059
E0cell = log(1016 )
2
= 0.472 0.4736 V
21. Ans. 1
dE0 S0
= = −5 10−4
dT nF
S0
= −5 10−4
2 96000
S0 = –96 J/Kmol
G = H − TS
−2 96000 2 96
= H + 300
1000 1000
–384 – 28.8 = H°
H° = –412.8 KJ/mol
22. Ans. 2
0HA = 100.5 + 425.9 − 126.4
0HA = 400
5 10−5 1000
0.001
HA = = 50 Scm2 mol–1
10−3
0.001 50
HA = HA0 = = 0.125
HA 400
23. Ans. 2
Reducing power depends on oxidation potential.
So, Ni < Zn < Mg < Ca
24. Ans. 1
½ H2(g) ⎯→ H+(aq)+ e
e + AgCl(s) ⎯→ Ag(s) + Cl(aq)
1
H2(g ) + AgCl(s) → Ag(s) + Cl(aq) + H(aq.)
2
0.06 [H+ ][Cl − ]
E = E − log
n (PH2 )1/2
( )(
10−6 10−6 )
0.92 = EH( 0
+
2 /H
+ ECl /AgCl/Ag
0
) −
0.06
1
log
1
0.92 = 0 + E0Cl /AgCl/Ag + 0.72
25. Ans. 3
Eq. (PbSO4) = no. of faraday
mPbSO4
2 = 0.05
303
mPbSO4 = 7.575 gm
7.6 gm
26. Ans. 1
2e + Cu+2 (aq) ⎯→ Cu (s) E10 = 0.34
Cu (s) ⎯→ Cu+(aq) + e– E02 = −0.522
e + Cu+2 (aq) ⎯→ Cu+ (aq)
E0 × 1 = 0.34 × 2 – 0.522 x 1
E0 = 0.158 V
27. Ans. 1
(1) 0m (NaBr) = 0m (NaI) + 0m (KBr) − 0m (NaBr)
0m (NaBr) = 0m (I ) + 0m (K + )
Incorrect
(2) 0H2O = 0m (HCl) + 0m (NaOH) − 0m (NaCl)
0H2O = 0m (H+ ) + 0m (OH )
Correct
(3) 0m (KCl) = 0m(NaCl) + 0KBr − 0NaBr
0m (KCl) = 0m (Cl ) + 0(K + )
Correct
(4) 0m (NaBr) = 0m (NaCl) + 0m (KBr) − 0m (KCl)
0m (NaBr) = 0m (Na + ) + 0m (Br )
Correct
At equilibrium
[Sn+2 ]
0 = ( +0.14 − 0.13) − 0.03log
[Pb+2 ]
[Sn +2 ]
0.01 = 0.03log
[Pb+2 ]
1 [Sn +2 ]
10 3 =
[Pb+2 ]
[Sn+2 ]
= 2.15
[Pb+2 ]