Part - I: Subjective Questions: Section (A) : Galvanic Cell, Its Representation & Salt Bridge

Electrochemistry
 Marked Questions may have for Revision Questions.
PART - I : SUBJECTIVE QUESTIONS

Section (A) : Galvanic cell, its Representation & salt bridge
Commit to memory :
Notation for Galvanic cell :
 LOAN  left oxidation- Anode-negative

A-1. In the galvanic cell Cu | Cu2+ || Ag+ | Ag, the electrons flow from Cu-electrode to Ag-electrode. Answer
the following questions regarding this cell :
(a) Which is the anode ?
(b) Which is the cathode ?
(c) What happens at anode-reduction or oxidation ?
(d) What happens at cathode-oxidation or reduction ?
(e) Which electrode loses mass ?
(f) Which electrode gains mass ?
(g) Write the electrode reactions.
(h) Write the cell reaction
(i) Which metal has greater tendency to loss electron-Cu or Ag ?
(j) Which is the more reactive metal-Cu or Ag ?
(k) What is the function of salt bridge represented by the symbol || ?
A-2. Write cell reaction of the following cells :
(a) Cu | Cu2+(aq) | | Ag+(aq) | Ag (b) Pt | Fe2+, Fe3+ | | MnO4–, Mn2+, H+ | Pt
(c) Pt, Cl2 | Cl–(aq) | | Ag+(aq) | Ag (d) Cd | Cd2+(aq) | | H+(aq) | H2 | Pt
A-3. Write cell notation of each cell with following cell reactions :
(a) Zn(s) + 2H+(aq)  Zn2+(aq) + H2(g)
(b) 2Fe3+(aq) + Sn2+(aq)  2Fe2+(aq) + Sn4+(aq)
(c) Pb(s) + Br2(I)  Pb2+(aq) + 2Br–(aq)
Section (B) : Electrochemical series & its Applications
Commit to memory :
1 1
SRP  Oxidising power   Non-metallic character 
reducing power Metallic character
B-1. The reduction potential values are given below

Al3+/Al = –1.67 volt, Mg2+/Mg = –2.34 volt, Cu2+/Cu = +0.34 volt, 2/– = +0.53 volt.
Which one is the best reducing agent ?
B-2. The standard reduction potential value of the three metallic cations X, Y and Z are 0.52, –3.03 and
–1.18 V respectively. Write the decreasing order of reducing power of the corresponding metals :
B-3. (i) Which of the following oxides is reduced by hydrogen ?
MgO, CuO and Na2O
(ii) Which of the following oxides will decompose most easily on heating ?
ZnO, CuO, MgO and Ag2O
(iii) The value of EºOX for electrode reactions,
Fe Fe2+ + 2e–, Cu Cu2+ + 2e– and Zn  Zn2+ + 2e–
are 0.444, –0.337 and 0.763 volt respectively. State which of these metals can replace the
other two from the solution of their salts ?
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Electrochemistry
B-4. For the cell reaction 2Ce4+ + Co  2Ce3+ + Co2+, EºCell is 1.89 V. If ECo2 |Co is – 0.28 V, what is the
value of ECe4  |Ce3  ?
B-5. Determine the standard reduction potential for the half reaction :
Cl2 + 2e–  2Cl–
Given Pt2+ + 2Cl–  Pt + Cl2, EºCell = – 0.15 V
Pt2+ + 2e–  Pt E° = 1.20 V
B-6. What is EºCell if :
2Cr + 3H2O + 3OCl–  2Cr3+ + 3Cl– + 6 OH–
Cr3+ + 3e–  Cr, E° = – 0.74 V
OCl– + H2O + 2e–  Cl– + 2OH– E° = 0.94 V
Section (C) : Concept of G

Commit to memory :
Eºcell is an intensive property, so on multiplying or dividing electrode reaction, Eºcell remains same.
Calcualte Eºcell for 3rd reaction with the help of 1st and 2nd reaction using Gº = –nF Eºcell.
n1E1  n2E 2
Eºtarget = where n1 = electrons participating in 1st reaction.
ntarget
n2 = electrons participating in 2nd reaction.
ntarget = electrons participating in target reaction.
  
C-1. If EFe2
|Fe
=–0.44 V, EFe3
|Fe2 
= 0.77 V. Calculate EFe3
|Fe
C-2. Consider the standard reduction potentials (in volts) as shown in Fig. Find Eº.
0.936 0.576 1
SO24   SO32   S2O32
2
E  ? __________
|____________________ 
1.5 V 1.0 V
C-3. The standard oxidation potentials for Mn3+ ion acid solution are Mn2+   Mn3+   MnO2.
Is the reaction 2 Mn + 2 H2O  Mn + MnO2 + 4H spontaneous under conditions of unit activity ?
3+ 2+ +
What is the change in free energy ?
C-4. Using the Gº for the reactions

C + O2  CO2 Gº = 395 kJ / mole,
2Al() + 3/2O2  Al2O3(s) Gº = 1269 kJ/mole
Al2O3(s)  Al2O3 (melt) Gº = 16 kJ/mole
Calculate the EMF for the cell reaction 2Al2O3 (melt) + 3C  4Al() + 3CO2(g). The number of electrons
involved in the reaction is 12.
Section (D) : Nernst equation & its Applications (including concentration cells)
Commit to memory :
RT
Nernst equation : Ecell = Eºcell – ln Q
nf
0.0591
At 25ºC, Ecell = Eºcell– log Q
n
where, n = number of transferred electron, Q = reaction quotient.
For concentration cell Eºcell = 0
D-1. Calculate the oxidation potential of a hydrogen electrode at pH = 1 (T = 298 K).
D-2. Calculate the equilibrium constant for the reaction :
Fe2+ + Ce4+  Fe3+ + Ce3+, [Given E0Ce4  / Ce3  : = 1.61 V; EFe
0
3
/ Fe2 
= 0.77V]
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Electrochemistry
D-3. The standard reduction potential of Cu2+ / Cu couple is 0.34 V at 25°C. Calculate the reduction potential
at pH = 14 for this couple.
(Given : Ksp, Cu (OH)2 = 1.0 × 10–19).
D-4. The EMF of the cell M |Mn+ (0.02 M) || H+ (1M) | H2 (g) (1 atm), Pt at 25°C is 0.81V. Calculate the
valency of the metal if the standard oxidation potential of the metal is 0.76V.
D-5. Consider the following electrochemical cell :
(a) Write a balanced net ionic equation for the spontaneous reaction that take place in the cell.
(b) Calculte the standard cell potential Eº for the cell reaction.
(c) If the cell emf is 1.6 V, what is the concentration of Zn2+ ?
(d) How will the cell potential be affected if KI is added to Ag+ half-cell ?
D-6. NO3  NO2 (acid medium), Eº = 0.790 V

NO3  NH3OH+ (acid medium), Eº = 0.731 V.
At what pH, the above two will have same E value? Assume the concentration of all other species
NH3OH+ except [H+] to be unity.
D-7. The standard oxidation potential of Zn referred to SHE is 0.76V and that of Cu is –0.34V at 25ºC. When
excess of Zn is added to CuSO4, Zn displaces Cu2+ till equilibrium is reached. What is the approx value
[Zn2 ]
of log at equilibrium?
[Cu2 ]
Section (E) : Electrolysis

Commit to memory :
Higher SOP means higher tendency of oxidation.
Higher SRP means higher tendency of reduction.
SOP order : SO42– < NO3– < Cl– < H2O < Br– < Ag < I– < OH– < Cu.....< Li
SRP order : Follow ECS
E-1. ELECTROLYTE ANODE Product CATHODE Product
1 NaCl (Molten) with Pt electrode
2 NaCl (aq) with Pt electrode
3 Na2SO4 (aq) with Pt electrode
4 NaNO3 (aq) with Pt electrode
5 AgNO3 (aq) with Pt electrode
6 CuSO4 (aq) with Inert electrode
7 CuSO4 (aq) with Copper electrode
Section (F) : Faraday laws & its Applictions

Commit to memory :
Faraday's law of electrolysis :
EQ
Ist law W = ZQ =
96500
Q = it
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Electrochemistry
W1 Z E
2nd law = 1 = 1 (Q = same)
W2 Z2 E2
actual amount of product
Current efficiency () = × 100
theortical amount of product
 EQ  
W actual = 
 96500  100
F-1. Find the number of electrons involved in the electrodeposition of 63.5 g of copper from a solution of
copper sulphate is :
F-2. A current 0.5 ampere when passed through AgNO3 solution for 193 sec. deposited 0.108 g of Ag . Find
the equivalent weight of Ag :
F-3. A certain metal salt solution is electrolysed in series with a silver coulometer. The weights of silver and
the metal deposited are 0.5094 g and 0.2653g. Calculate the valency of the metal if its atomic weight is
nearly that of silver.
F-4. 3A current was passed through an aqueous solution of an unknown salt of Pd for 1Hr. 2.977g of Pd +n
was deposited at cathode. Find n. (Given Atomic mass of Pd = 106.4)
F-5. How long a current of 2A has to be passed through a solution of AgNO 3 to coat a metal surface of
80cm2 with 5m thick layer? Density of silver = 10.8g/cm 3.
F-6. A certain electricity deposited 0.54g of Ag from AgNO 3 Solution. What volume of hydrogen will the
same quantity of electricity liberate at STP (Vm = 22.4 L/mol).
F-7. A current of 3.7A is passed for 6hrs. between Ni electrodes in 0.5L of 2M solution of Ni(NO 3)2. What will
be the molarity of solution at the end of electrolysis?
F-8. Cd amalgam is prepared by electrolysis of a solution of CdCl 2 using a mercury cathode. How long
should a current of 5A be passed in order to prepare 12% Cd-Hg amalgam when 2 g Hg is used as
cathode (atomic weight of Cd = 112.4)
F-9. Electrolysis of a solution of HSO4– ions produces S2O82–. Assuming 75% current efficiency, what current
should be employed to achieve a production rate of 1 mole of S2O82– per hour ?
Section (G) : Commercial Cells & Corrosion
Commit to memory :
At STP, Vm (molar volume of the gas) = 22.4 L/mol
Volume of gas required at STP = moles of gas × 22.4
G-1. A fuel cell uses CH4(g) and forms CO32– at the anode. It is used to power a car with 80 Amp. for 0.96 hr.
How many litres of CH4(g) (STP) would be required ? (Vm = 22.4 L/mol) (F = 96500). Assume 100%
efficiency.
G-2. Find Eº of cell formed for rusting of iron ?
0
EFe / Fe2 
= +0.44 V
0
EH O|O |H
= –1.23 V
2 2
Section (H) : Electrical Conductance

Commit to memory :
1
Conductivity () = C × = ×
A R A
where, = cell constant, C = conductance, R = resistance.
A
A = surface area of electrodes, = distance between electrodes.
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Electrochemistry
  1000
Molar conductance (m) = S cm2 mol–1
M
  1000
Equivalent conductance (eq) = S cm2 eq–1
N
where, M = molarity, N = normality and N = M × valence factor
H-1. The resistance of a M/10 KCl solution in 245 ohms. Calculate the specific conductance and the molar
conductance of the solution if the electrodes in the cell are 4 cm apart and each having an area of 7.0
sq. cm.
H-2. The equivalent conductance of 0.10 N solution of MgCl 2 is 97.1 mho cm2 eq.–1 at 25°C. A cell with
electrodes that are 1.50 cm 2 in surface area and 0.50 cm apart is filled with 0.1N MgCl 2 solution. How
much current will flow when the potential difference between the electrodes is 5 volts ?
H-3. The specific conductance of a N/10 KCl solution at 18°C is 1.12 × 10–2 mho cm–1. The resistance of the
solution contained in the cell is found to be 65 ohms. Calculate the cell constant.
Section (I) : Kohlrausch law and its applications
Commit to memory :
Kohlrausch law : At infinite dilution, ºm, electrolyte =   ºm +   ºm
where,  + = number of cations in one formula unit of electrolyte.
– = number of anions in one formula unit of electrolyte.
At infinite dilution equivalent conductance : ºeq, electrolyte = ºeq+ + ºeq–
m  eq
Degree of dissociation (D.O.D.) =  = = 0
 ºm  eq
C 2
For weak electrolyte, dissociation constant (Ka) = , where, C = concentration of electrolyte.
1 
  1000
Solubility (s) = and Ksp = S2 for AB type salt.
 ºm
I-1. The molar conductance of an infinitely dilute solution of NH4Cl is 150 and the ionic conductances of
OH– and Cl– ions are 198 and 76 respectively. What will be the molar conductance of the solution of
NH4OH at infinite dilution. If the molar conductance of a 0.01 M solution NH4OH is 9.6, what will be its
degree of dissociation?
I-2. Given the molar conductance of sodium butyrate, sodium chloride and hydrogen chloride as 83, 127
and 426 mho cm2 mol–1 at 25°C respectively. Calculate the molar conductance of butyric acid at infinite
dilution.
I-3. Calculate Ka of acetic acid if its 0.05 N solution has equivalent conductance of 7.36 mho cm 2 at 25°C.

(  CH3 COOH
 390.7) .
I-4. The specific conductance of a saturated solution of AgCl at 25°C after subtracting the specific
conductance of conductivity of water is 2.28 × 10–6 mho cm–1. Find the solubility product of AgCl at
25°C. (  AgCl  138.3 mho cm2 )
Section (J) : Conductometric Titration

Commit to memory :
H+ and OH– ions are highly conducting.
J-1. Draw approximate titration curve for following –
(1) HCl(aq) is titrated with NaOH
(2) CH3COOH(aq) is titrated with NaOH
(3) Equimolar mixture of HCl and HCN titrated withNaOH
(4) NH4Cl(aq) is titrated withNaOH
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Electrochemistry
PART - II : ONLY ONE OPTION CORRECT TYPE
* Marked Questions are having more than one correct option.
Section (A) : Galvanic cell, its Representation & salt bridge
A-1. In a galvanic cell
(A) Chemical reaction produces electrical energy (B) electrical energy produces chemical reaction
(C) reduction occurs at anode (D) oxidation occurs at cathode
A-2. Which of the following is/are function(s) of salt-bridge ?
(A) It completes the electrical circuit with electrons flowing from one electrode to the other through
external wires and a flow of ions between the two compartments through salt - bridge
(B) it minimises the liquid - liquid junction potential
(C) both correct
(D) none of these
A-3. Salt bridge contains :
(A) calomel (B) sugar (C) H2O (D) agar-agar paste
A-4. The emf of the cell, Ni | Ni2+ (1.0 M) || Ag+ (1.0M) | Ag [E° for Ni2+ / Ni = –0.25 volt, E° for Ag+/Ag = 0.80
volt] is given by -
(A) –0.25 + 0.80 = 0.55 volt (B) –0.25 – (+0.80) = –1.05 volt
(C) 0 + 0.80 – (–0.25) = + 1.05 volt (D) –0.80 – (–0.25) = – 0.55 volt
Section (B) : Electrochemical series & its Applications

1
B-1. Eº for F2 + 2e  2F– is 2.8 V, Eº for F2 + e  F– is
2
(A) 2.8 V (B) 1.4 V (C) – 2.8 V (D) – 1.4 V
º º
B-2. Consider the cell potentials = EMg2
| Mg
– 2.37 V and EFe3
| Fe
= – 0.04 V. The best reducing agent would
be
(A) Mg2+ (B) Fe3+ (C) Mg (D) Fe
B-3. If a spoon of copper metal is placed in a solution of ferrous sulphate -
(A) Cu will precipitate out (B) iron will precipitate
(C) Cu and Fe will precipitate (D) no reaction will take place
B-4. The position of some metals in the electrochemical series in decreasing electropositive character is
given as Mg > Al > Zn > Cu > Ag. What will happen if a copper spoon is used to stir a solution of
aluminium nitrate ?
(A) The spoon will get coated with aluminium (B) An alloy of aluminium and copper is formed
(C) The solution becomes blue (D) There is no reaction
B-5. For Zn2+ / Zn, E° = –0.76 V, for Ag+/Ag E° = 0.799 V. The correct statement is -
(A) the reaction Zn getting reduced Ag getting oxidized is spontaneous
(B) Zn undergoes reduction and Ag is oxidized
(C) Zn undergoes oxidation Ag+ gets reduced
(D) No suitable answer
B-6. Electrode potential data are given below.
Fe3+ (aq) + e– Fe2+ (aq); Eº = + 0.77
Al3+ (aq) + 3e–  Al (s); Eº = – 1.66 V
Br2 (aq) + 2e–  2Br– (aq) ; Eº = + 1.08 V
Based one the data given above, reducing power of Fe2+, Al and Br– will increase in the order :
(A) Br– < Fe2+ < Al (B) Fe2+ < Al < Br– (C) Al < Br– < Fe2+ (D) Al < Fe2+ < Br–
B-7. KCl can be used in salt bridge as electrolyte in which of the following cells?
(A) Zn | ZnCl2 || AgNO3 | Ag (B) Pb | Pb(NO3)2 || Cu(NO3)2 | Cu
(C) Cu | CuSO4 || AuCl3 | Au (D) Fe | FeSO4 || Pb(NO3)2 | Pb
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Electrochemistry
B-8. Consider the following Eº values :
0
EFe 3
/ Fe2 
= + 0.77 V ; E0Sn2  / Sn = – 0.14 V
Under standard conditions the potential for the reaction is
Sn (s) + 2 Fe3+ (aq)  2Fe2+ (aq) + Sn2+ (aq)
(A) 1.68V (B) 1.40 V (C) 0.91 V (D) 0.63 V
Section (C) : Concept of G

C-1. Given standard electrode potentials :
Fe3+ + 3e–  Fe ; E° = –0.036 volt
Fe + 2e  Fe;
2+ –
E° = –0.440 volt
The standard electrode potential E° for Fe3+ + e–  Fe2+
(A) –0.476 volt (B) –0.404 volt (C) 0.440 volt (D) 0.772 volt
C-2. Cu+ + e–  Cu, E° = x1 volt; Cu2+ + 2e–  Cu, E° = x 2 volt, then for Cu2+ + e–  Cu+, E° (volt)
will be -
(A) x1 – 2x2 (B) x1 + 2x2 (C) x1 – x2 (D) 2x2 – x1
C-3. Which of the following statements about the spontaneous reaction occurring in a galvanic cell is always
true?
(A) Eºcell > 0, Gº < 0, and Q < K (B) Eºcell > 0, Gº < 0, and Q > K
(C) Eºcell > 0, Gº > 0, and Q > K (D) Ecell > 0, G < 0, and Q < K
Section (D) : Nernst equation & its Applications (including concentration cells)
D-1. The standard emf for the cell reaction Zn + Cu2+  Zn2+ + Cu is 1.10 volt at 25°C. The emf for the cell
reaction when 0.1 M Cu2+ and 0.1 M Zn2+ solutions are used at 25°C is
(A) 1.10 volt (B) 0.110 volt (C) –1.10 volt (D) –0.110 volt
H2 (Pt) H3 O (aq) Ag

D-2. Consider the cell Ag. The measured EMF of the cell is 1.0 V. What is the
1 atm pH  5.03 x M
value of x ? E0Ag ,Ag = + 0.8 V. [T = 25°C] ; E0Ag ,Ag = + 0.8 V. [T = 25°C]

(A) 2 × 10–2 M (B) 2 × 10–3 M (C) 1.5 × 10–3 M (D) 1.5 × 10–2 M
D-3. Zn | Zn2+ (C1)|| Zn2+ (C2)|Zn. for this cell G is negative if -
(A) C1 = C2 (B) C1 > C2 (C) C2 > C1 (D) None
H2 H H H2
D-4. Pt Pt (where p1 and p2 are pressures) cell reaction will be
(p1 ) (1 M) (1 M) (p 2)
spontaneous if :
(A) p1 = p2 (B) p1 > p2 (C) p2 > p1 (D) p1 = 1 atm
D-5. Pt | (H2) | pH = 1 || pH = 2 | (H2)Pt
1 atm 1 atm
The cell reaction for the given cell is :
(A) spontaneous (B) non - spontaneous (C) equilibrium (D) none of these
M
D-6. The EMF of a concentration cell consisting of two zinc electrodes, one dipping into sol. of zinc
4
M
sulphate & the other into sol. of the same salt at 25C is
16
(A) 0.0125 V (B) 0.0250 V (C) 0.0178 V (D) 0.0356 V
Section (E) : Electrolysis

E-1. In an electrolytic cell of Ag/AgNO3/Ag, when current is passed, the concentration of AgNO3
(A) Increases (B) Decreases (C) Remains same (D) None of these
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Electrochemistry
E-2. If 0.224 L of H2 gas is formed at the cathode, the volume of O2 gas formed at the anode under identical
conditions, is
(A) 0.224 L (B) 0.448 L (C) 0.112 L (D) 1.12 L
E-3. The two aqueous solutions, A (AgNO3) and B (LiCl) were electrolysed using Pt. electrodes. The pH of
the resulting solutions will
(A) increase in A and decrease in B (B) decrease in both
(C) increase in both (D) decrease in A and increase in B.
E-4. In the electrolysis of aqueous CuBr2 using Pt electrodes :

(A) Br2 gas is not evolved at the anode
(B) Cu (s) is deposited at the cathode
(C) Br2 gas is evolved at anode and H2 gas at cathode
(D) H2 gas is evolved at anode.
E-5. During electrolysis of CuSO4 using Pt-electrodes, the pH of solution

(A) increases (B) decreases (C) remains unchanged (D) cannot be predicted
Section (F) : Faraday laws & its Applictions

F-1. How many faradays are required to reduce one mol of MnO4¯ to Mn2+ -
(A) 1 (B) 2 (C) 3 (D) 5
F-2. Three faradays of electricity was passed through an aqueous solution of iron (II) bromide. The mass of
iron metal (at. mass 56) deposited at the cathode is -
(A) 56 g (B) 84 g (C) 112 g (D) 168 g
F-3. A current of 2 A was passed for 1 h through a solution of CuSO4 0.237 g of Cu2+ ions were discharged
at cathode. The current efficiency is
(A) 42.2% (B) 26.1% (C) 10% (D) 40.01%
F-4. A current of 9.65 ampere is passed through the aqueous solution NaCl using suitable electrodes for
1000 s. The amount of NaOH formed during electrolysis is
(A) 2.0 g (B) 4.0 g (C) 6.0 g (D) 8.0 g
F-5. Salts of A (atomic mass 15), B (atomic mass 27) and C (atomic mass 48) were electrolysed using same
amount of charge. It was found that when 4.5 g of A was deposited, the mass of B and C deposited
were 2.7g and 9.6 g. The valencies of A, B and C respectively.
(A) 1, 3 and 2 (B) 3, 1 and 3 (C) 2, 6 and 3 (D) 3, 1 and 2
Section (G) : Commercial Cells & Corrosion

G-1. During discharge of a lead storage cell the density of sulphuric acid in the cell :
(A) Increasing (B) decreasing
(C) remians unchanged (D) initially increases but decrease subsequently
G-2. In H2O2 fuel cell the reaction occuring at cathode is :

(A) 2 H2O + O2 + 4 e  4 OH (B) 2H2 + O2  2H2O (l)
1
(C) H+ + OH  H2O (D) H+ + e  H2 .
2
G-3. Which is not correct method for prevention of iron from Rusting -
(A) Galvanisation (B) Connecting to sacrificial electrode of Mg
(C) Making medium alkaline (D) Making medium acidic
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Electrochemistry
Section (H) : Electrical Conductance
H-1. Which of the following curve represents the variation of M with C for AgNO3 ?
(A) (B) (C) (D)
C C C C
H-2. Which has maxmium conductivity :

(A) [Cr(NH3)3 Cl3] (B) [Cr(NH3)4 Cl2]Cl (C) [Cr(NH3)5Cl]Cl2 (D) [Cr(NH3)6]Cl3
H-3. Resistance of decimolar solution is 50 ohm. If electrodes of surface area 0.0004 m 2 each are placed at
a distance of 0.02 m then conductivity of solution is :
(A) 1 s cm– (B) 0.01 s cm– (C) 0.001 s cm– (D) 10 s cm–
Section (I) : Kohlrausch law and its applications

I-1. The ionization constant of a weak electrolyte (HA) is 25 × 10–6 while the equivalent conductance of its
0.01 M solution is 19.6 S cm 2 eq–1. The equivalent conductance of the electrolyte at infinite dilution
(in S cm2 eq–1 ) will be
(A) 250 (B) 196 (C) 392 (D) 384
I-2. The conductivity of a saturated solution of BaSO4 is 3.06 × 10–6 ohm–1 cm–1 and its equivalent
conductance is 1.53 ohm–1 cm2 equiv–1. The Ksp for BaSO4 will be
(A) 4 × 10–12 (B) 2.5 × 10–13 (C) 25 × 10–9 (D) 10–6
I-3. Molar conductance of 0.1 M acetic acid is 7 ohm 1 cm2 mol 1. If the molar cond. of acetic acid at infinite
dilution is 380.8 ohm 1 cm2 mol 1, the value of dissociation constant will be :
(A) 226  10 5 mol dm 3 (B) 1.66  10 3 mol dm 1
(C) 1.66  10 mol dm
2 3
(D) 3.442  10 5 mol dm 3
I-4. The conductivity of a solution of AgCl at 298 K is found to be 1.382 × 10–6 –1 cm–1. The ionic
conductance of Ag+ and Cl– at infinite dilution are 61.9 –1 cm2 mol–1 and 76.3 –1 cm2 mol–1,
respecitvley. The solubility of AgCl is
(A) 1.4 × 10–5 mol L–1 (B) 1 × 10–2 mol L–1 (C) 1 × 10–5 mol L–1 (D) 1.9 × 10–5 mol L–1
I-5. Molar conductances of BaCl2, H2SO4 and HCl at infinite dilutions are x 1, x2 and x3, respectively.
Equivalent conductance of BaSO4 at infinite dilution will be :
[x  x 2  x3 ] [x  x 2  x3 ] [x  x2  2x3 ]
(A) 1 (B) 1 (C) 2 (x1 + x2 – 2x3) (D) 1
2 2 2
Section (J) : Conductometric Titration

J-1. 20 ml KOH solution was titrated with 0.2 mol/l H2SO4 solution in
Conductivity
conductivity cell. Concentration of KOH solution was –

(A) 0.3 M
(B) 0.15 15 30
(C) 0.12 0 Volume of H2 SO 4 (ml)
(D) None of these
ADVECH - 37
Electrochemistry
J-2. Following curve for conductometric titration is obtained when –
Conduction
x = Equivalence point
x
Volume of Solutions 
(A) NaOH solution is added in to HCl solution

(B) NaOH solution is added in to CH3COOH solution
(C) NH4OH solution is added in to HCl solution
(D) NH4OH solution is added in to CH3COOH solution
PART - III : MATCH THE COLUMN
1. Match the column
Column I Column II
Zn | Zn+2 | | Mg2+ | Mg
(A) (p) Ecell = 0
c1 c2 (c1 = c2)
(B) Zn | Zn+2 | | Ag+ | Ag at. equilibrium (q) E0cell 0
Ag | Ag+ | | Ag+ | Ag
(C) (r) E0cell = +ve
c1 c2 (c1 = c2)
Fe | Fe+2 | | Ag | Ag+
(D) (s) E0cell = –ve
c1 c2 (c1 = c2)
2.^ Match Matrix ( E0Ag / Ag = 0.8).
Column I Column II
+ +
(A) Pt | H2 (0.1 bar) | H (0.1 M) || H (1 M) | H2 (0.01 bar) | Pt (p) Concentration cell
(B) Ag | Ag+ (10–9 M) || Ag+ (10–2 M) | Ag (q) Ecell > 0
(C) Cu | Cu2+ (0.1 M) || Cu2+ (0.01 M) | Cu (r) Eºcell = 0
but cell is working.
(D) Pt | Cl2 (1bar) | HCl (0.1 M) || NaCl (0.1M) | Cl2 | Pt (1 bar) (s) non working condition

 Marked Questions may have for Revision Questions.
PART - I : ONLY ONE OPTION CORRECT TYPE

1. Given : Eº(Cu2+ | Cu) = 0.337 V and Eº (Sn2+ | Sn) = – 0.136 V. Which of the following statements is
correct?
(A) Cu2+ ions can be reduced by H2(g) (B) Cu can be oxidized by H+
(C) Sn2+ ions can be reduced by H2(g) (D) Cu can reduce Sn2+
ADVECH - 38
Electrochemistry
2. Using the standard potential values given below, decide which of the statements I, II, III, IV are correct.
Choose the right answer from (a), (b), (c) and (d)
Fe2+ + 2e– = Fe, Eº = – 0.44 V
Cu2+ + 2e– = Cu, Eº = + 0.34 V
Ag+ + e– = Ag, Eº = + 0.80 V
I. Copper can displace iron from FeSO4 solution
II. Iron can displace copper from CuSO4 solution
III. Silver can displace Cu from CuSO4 solution
IV. Iron can displace silver from AgNO3 solution
(A) I and II (B) II and III (C) II and IV (D) I and IV
3. Red hot carbon will remove oxygen from the oxide AO and BO but not from MO, while B will remove
oxygen from AO. The activity of metals A, B and M in decreasing order is
(A) A > B > M (B) B > A > M (C) M > B > A (D) M > A > B
4. Which statement is correct.
(A) In SHE, the pressure of dihydrogen gas should be low and pH of solution should be zero.
(B) In the reaction H2O2 + O3  2H2O + 2O2, H2O2 is oxidised to H2O.
(C) The absolute value of electrode potential cannot be determined.
(D) According to IUPAC conventions, the standard electrode potential pertains to oxidation reactions
only.
5. The electrode oxidation potential of electrode M(s)  Mn+(aq) (2M) + ne– at 298 K is E1. When
temperature (in ºC) is doubled and concentration is made half, then the electrode potential becomes E2.
Which of the following represents the correct relationship between E1 and E2 ?
(A) E1 > E2 (B) E1 < E2 (C) E1 = E2 (D) Cann’t be predicted
6. A galvanic cell is composed of two hydrogen electrodes, one of which is a standard one. In which of the
following solutions should the other electrode be immersed to get maximum emf ?
Ka(CH3COOH) = 2 × 10–5, Ka(H3PO4) = 10–3.
(A) 0.1 M HCl (B) 0.1 M CH3COOH (C) 0.1 M H3PO4 (D) 0.1 M H2SO4
7. Two weak acid solutions HA1 and HA2 each with the same concentration and
having pKa values 3 and 5 are placed in contact with hydrogen electrode (1
atm, 25ºC) and are interconnected through a salt bridge. The emf of the cell
is :
(A) 0.21 V (B) 0.059 V
(C) 0.018 V (D) 0.021 V
8. A hydrogen electrode placed in a buffer solution of CH3COONa and CH3COOH in the ratios of x : y and
y : x has electrode potential values E1 volts and E2 volts, respectively at 25ºC. The pKa values of acetic
acid is (E1 and E2 are oxidation potentials)
E  E2 E  E1 E  E2 E  E2
(A) 1 (B) 2 (C) – 1 (D) 1
0.118 0.118 0.118 0.118
AgBr (s), Br¯ Fe3  , Fe2

9. What is the emf at 25° C for the cell, Ag, Pt
a  0.34 a  0.1 a  0.02
The standard reduction potentials for the half-reactions AgBr + e–  Ag + Br– and Fe3+ + e–  Fe2+
are + 0.0713 V and + 0.770 V respectively.
(A) 0.474 volt (B) 0.529 volt (C) 0.356 volt (D) 0.713 volt
10. When the sample of copper with zinc impurity is to be purified by electolysis, the appropriate electrode
are
(A) pure zinc as cathode and pure copper as anode
(B) impure sample as cathode and pure copper as anode
(C) impure zinc as cathode and impure sample as anode
(D) pure copper as cathode and impure sample as anode
ADVECH - 39
Electrochemistry
11. Four moles of electrons were transferred from anode to cathode in an experiment on electrolysis of
water. The total volume of the two gases (dry and at STP) produced will be approximately (in litres)
(A) 22.4 (B) 44.8 (C) 67.2 (D) 89.4
12. Electrolysis of a solution of MnSO4 in aqueous sulphuric acid is a method for the preparation of MnO 2.
Passing a current of 27A for 24 hours gives 1kg of MnO2. The current efficiency in this process is :
(A) 100% (B) 95.185% (C) 80% (D) 82.951%
13. During the preparation of H2S2O8 (per disulphuric acid) O2 gas also releases at anode as byproduct,
When 9.72 L of H2 releases at cathode and 2.35 L O2 at anode at STP, the weight of H2S2O8 produced
in gram is
(A) 87.12 (B) 43.56 (C) 83.42 (D) 51.74
14. When the electric current is passed through a cell having an electrolyte, the positive ions move towards
cathode and negative ions towards the anode. If the cathode is pulled out of the solution
(A) the positive and negative ions will move towards anode
(B) the positive ions will start moving towards the anode while negative ions will stop moving
(C) the negative ions will continue to move towards anode while positive ions will stop moving
(D) the positive and negative ions will start moving randomly
15. When iron is rusted, it is :
(A) reduced (B) oxidised (C) evaporated (D) decomposed
PART - II : NUMERICAL VALUE QUESTIONS

1. H4XeO6 + 2H+ + 2e–  XeO3 + 3H2O Eº = 3 V
F2 + 2e–  2F– Eº = 2.87 V
O3 + 2H+ + 2e–  O2 + H2O Eº = 2.07 V
Ce4+ + e–  Ce3+ Eº = 1.67 V
2HClO + 2H+ + 2e–  Cl2 + 2H2O Eº = 1.63 V
ClO4– + 2H+ + 2e–  ClO3– + H2O Eº = 1.23 V
ClO– + H2O + 2e–  Cl¯ + 2OH– Eº = 0.89 V
BrO– + H2O + 2e–  Br¯ + 2OH– Eº = 0.76 V
ClO4– + H2O + 2e–  ClO3– + 2OH– Eº = 0.36 V
[Fe(CN)6]3– + e–  [Fe(CN)6]4– Eº = 0.36 V
Based on the above data, how many of the following statements are correct ?
(A) F2 is better oxidizing agent than H4X6O6.
(B) Ozone can oxidize Cl2
(C) ClO4– is better oxidizing agent in basic medium than in acidic medium
(D) Ferrocyanide ion can be easily oxidized by ClO–, Ce4+, Li+, BrO–
(E) ClO– can oxidize Br– and ClO3– in basic medium
(F) Ce4+ can oxidize Cl2 in acidic medium under standard conditions.
2. A hydrogen gas electrode is made by dipping platinum wire in a solution of NaOH of pH = 10 and by
passing hydrogen gas around the platinum wire at one atm pressure. The oxidation potential of
2.303 RT
electrode is 10x milivolt. Find x ? (Take = 0.059)
F
3. Estimate the cell potential of a Daniel cell having 1.0M Zn2+ and originally having 1.0M Cu2+ after
sufficient NH3 has been added to the cathode compartment to make NH3 concentration 2.0M at
equilibrium. Given Kf for [Cu(NH3)4]2+ = 1 × 1012, E° for the reaction, Zn + Cu2+  Zn2+ + Cu 1.1V.
2.303 RT
(Take = 0.06, log 6.25 = 0.8) Respond as 10  your answer.
F
ADVECH - 40
Electrochemistry
4. Molar conductivity of 0.04 MgCl2 solution at 298 k is 200 Scm2mole–1. A conductivity cell which is filled
with MgCl2 have area of cross-section of electrode 4cm 2 & distance between electrode is 8 cm. If
potential difference between electrode is 10V then find current flow in miliampere.
The conductivity of a solution which is 0.1 M in Ba(NO 3)2 and 0.2 M in AgNO3 is 5.3 Sm–1. If (Ag ) =
o
5.
6 × 10–3 Sm2 mol–1 & (Ba2 ) = 13 × 10–3 Sm2 mol–1, determine (NO3– ) in same unit. Report your answer
o o
after multiplying by 1000.


6. m (weak mono basic HA acid) = 390.7 S cm 2 mol–1
m of HA at 0.01 M is 3.907 S cm 2 mol–1
Find pH of 0.01 M HA ?
7. For a saturated solution of AgCl at 25°C,  = 3.4 × 10–6 ohm–1 cm–1 and that of H2O() used is
2.02 × 10–6 ohm–1 cm–1. m for AgCl is 138 ohm–1 cm2 mol–1 then the solubility of AgCl in mili moles per
m3 will be :
8. At 298 K, the conductivity of pure water is 5.5 × 10–6 S m–1. Calculate the ionic product of water using
the following data :
ºm values (in S m2 mol–1) : Ba(OH)2 = 5.3 × 10–2, HCl = 4.25 × 10–2, BaCl2 = 2.8 × 10–2 .
Does your answer match with experimental value. Write 20 for yes & 40 for No.

9. How many of the following comparisons are correct with respect to their  m ?
(A) K+ > Na+ (B) K+ > H3O+ (C) Ca2+ > Na+ (D) Mg2+ > NH4+
(E) H3O+ > Mg2+ (F) K+ > Mg2+
PART - III : ONE OR MORE THAN ONE OPTIONS CORRECT TYPE

   
1. Given EAg /Ag = 0.80V, E Mg2 / Mg = –2.37V, E Cu2 / Cu = 0.34V, EHg2 / Hg = 0.79 V.
Which of the following statements is/are correct
(A) AgNO3 can be stored in copper vessel (B) Mg(NO3)2 can be stored in copper vessel
(C) CuCl2 can be stored in silver vessel (D) HgCl2 can be stored in copper vessel
2. Any redox reaction would occur spontaneously, if :
(A) the free energy change ( G) is negative (B) the Gº is positive
(C) the cell e.m.f. (Eº) is negative (D) the cell e.m.f. is positive
3. Consider an electrolytic cell E being powered by a galvenic cell G, as shown in the figure. Then :
(A) Anode of E is connected to cathode of G (B) Anode of E is connected to anode of G

(C) Cathode of E is connected to anode of G (D) Cathode of E is connected to cathode of G
4. On electrolysis, in which of the following, O2 would be liberated at the anode ?
(A) dilute H2SO4 with Pt electrodes (B) aqueous AgNO3 solution with Pt electrodes
(C) dilute H2SO4 with Cu electrodes (D) aqueous NaOH with a Fe cathode & a Pt anode
ADVECH - 41
Electrochemistry
5. A current of 2.68 A is passed for one hour through an aqueous solution of CuSO 4 using copper
electrodes. Select the correct statement(s) from the following :
(A) increase in mass of cathode = 3.174 g
(B) decrease in mass of anode = 3.174 g
(C) no change in masses of electrodes
(D) the ratio between the change of masses of cathode and anode is 1 : 2.
6. Three moles of electrons are passed through three solutions in succession containing AgNO 3, CuSO4
and AuCl3, respectively. The molar ratio of amounts of cations reduced at cathode will be
1 1 1
(A) 1 : 2 : 3 (B) : : (C) 3 : 2 : 1 (D) 6 : 3 : 2
1 2 3
7. If same quantity of electricity is passed through three electrolytic cells containing FeSO4, Fe2(SO4)3 and
Fe(NO3)3, then
(A) the amount of iron deposited in FeSO4 and Fe2(SO4)3 are equal
(B) the amount of iron deposited in FeSO4 is 1.5 times of the amount of iron deposited in Fe(NO3)3.
(C) the amount of iron deposited in Fe2(SO4)3 and Fe(NO3)3 are equal
(D) the same amount of gas is evolved in all three cases at the anode.
8. When a lead storage battery is discharged then :

(A) SO2 is evolved (B) lead sulphate is produced at both electrodes
(C) sulphuric acid is consumed (D) water is formed
9. Mark out the correct statement(s) regarding electrolytic molar conductivity.
(A) It increase as temperature increases.
(B) It experiences resistance due to vibration of ion at the mean position.
(C) Increase in concentration decreases the electrolytic molar conductivity of both the strong as well as
the weak electrolyte.
(D) Greater the polarity of solvent, greater is the electrolytic molar conduction.
10. On increasing dilution following will increase :

(A) Equivalent conductivity (B) Conductivity
(C) Molar conductivity (D) All of these
11. The resistances of following solutions of KCl were measured using conductivity cells of different cell
constants, at same temperature. (Consider that at concentration less than 0.1 M, the specific
conductivity of solution is directly proportional to the concentration of solution.)
Concentration of Solution Cell Constant
1. 0.1 M 1 cm–1
2. 0.01 M 10 cm–1
3. 0.005 M 5 cm–1
4. 0.0025 M 25 cm–1
Which of the following comparisons between their conductances (G) is/are correct ?
(A) G1 is maximum (B) G4 is minimum (C) G3 >> G2 (D) G4 is maximum
12. Identify correct statements :
(A) Kohlraush law is applicable only on weak electrolyte.
(B) On increasing dilution conductance, molar conductivity, equivalent conductivity increases but
conductivity decreases.
K
(C) m = following formula has units m – dm2/mol, K  – dm—1, C  mol/.
C
(D) Equation m = m  b C is applicable on weak as well as strong electrolyte.
ADVECH - 42
Electrochemistry
13. Select the correct option(s):
ºeq Al3  ºeq SO 2– 
(A)
3
º
 
= m Al & 3
2
4
= m SO24– 
º
º
m Al  ºm SO 2 
(B)  eq Al3  = &  eq SO 24  =
º 3 º 4
3 2
ºm Al3  ºm SO 2 
(C)  eq (Al2(SO4) 3) =
º 4
+
3 2
(D) ºm (Al2(SO4) 3) = 6 ×  eq (Al2(SO4) 3)
º
14. Which of the following order is correct related to their mobility in solution:
     2  
(A) Csaq > Rbaq > K aq > Naaq > Liaq (B) Beaq > Liaq > Csaq
  2  2    2
(C) Haq > Liaq > Beaq > Naaq > Mg aq (D) Haq  > Naaq  > Liaq  > Beaq 
15. For strong electrolyte M increases slow with dilution and can be represented by the equation
 M = M
o
– AC½
Select correct statement
(A) Plot of M against C½ is obtain a straight line with intercept M
o
& and slope ‘–A’
(B) Value of A depends upon temperature solvent and nature of electrolyte.
(C) NaCl and KCl have different value of constant ‘A’
(D) NaCl and MgSO4 have different value of constant ‘A’
PART - IV : COMPREHENSION
Read the following passage carefully and answer the questions.
Comprehension # 1
If an element can exist in several oxidation states, it is convenient to display the reduction potentials
corresponding to the various half reactions in diagrammatic form, known as Latimer diagram. The
Latimer diagram for chlorine in acid solution is
1.20 V 1.18 V 1.60 V 1.67 V 1.36 V
ClO4–   ClO3–  HClO2  HClO   Cl2   Cl–
in basic solution.
0.37 V 0.30 V 0.68 V 0.42 V 1.36 V
ClO4–   ClO3–   ClO2–   ClO–   Cl2   Cl–
The standard potentials for two nonadjacent species can also be calculated by using the concept that
G° as an additive property but potential is not an additive property and G° = – nFx0. If a given
oxidation state is a stronger oxidising agent than in the next higher oxidation state, disproportionation
can occur. The reverse of disproportionation is called comproportionation. The relative stabilities of the
oxidation state can also be understood by drawing a graph of G°/F against oxidation state, known as
Frost diagram, choosing the stability of zero oxidation state arbitrarily as zero. The most stable
oxidation state of a species lies lowest in the diagram. Disproportionation is spontaneous if the species
lies above a straight line joining its two product species.
1. Which of the following couple have same value of potential at pH = 0 and pH = 14?
ClO4 ClO2 ClO Cl
(A) 
(B) (C) (D) 2
ClO3 Cl2 Cl2 Cl
ClO 
2. What is the potential of couple at pH = 14 ?
Cl
(A) 1.78 V (B) – 0.94 V (C) 0.89 V (D) – 0.89 V
3. Which of the following statement is correct ?
(A) Cl2 undergoes disproportionation into Cl– and ClO– both at pH = 0 and pH = 14.
(B) Cl2 undergoes disproportionation into Cl– and ClO– at pH = 14 but not at pH = 0.
(C) Cl2 undergoes disproportionation into Cl– and ClO– at pH = 0 but not at pH = 14.
(D) None of these
ADVECH - 43
Electrochemistry
4. For a hypothetical element, the Frost diagram is shown in figure?
Which of the following oxidation state is least stable?

(A) – 1 (B) 0 (C) + 2 (D) + 3
5. Which of the following statement is correct ? According to Q.4

(A) A+1 undergoes disproportionation into A and A2+.
(B) A2+ undergoes disporportionation in A and A3+.
(C) A undergoes comporportionation in A+1 and A–1.
(D) All of the above.
Comprehension # 2
The molar conductance of NaCl varies with the concentration as shown in the following table and all
values follows the equation

m
C
= m –b C Where  m
C
= molar specific conductance

m = molar specific conductance at infinite dilution
C = molar concentration
Molar Concentration of NaCl Molar Conductance in ohm–1 cm2 mole–1

4 × 10–4 107
9 × 10–4 97
16 × 10–4 87
When a certain conductivity cell (C) was filled with 25 x 10–4 (M) NaCl solution. The resistance of the
cell was found to be 1000 ohm. At Infinite dilution, conductance of Cl – and SO4–2 are 80 ohm–1 cm2
mole–1 and 160 ohm–1 cm2 mole–1 respectively.
6. What is the molar conductance of NaCl at infinite dilution ?

(A) 147 ohm–1 cm2 mole–1 (B) 107 ohm–1 cm2s mole–1
–1 –1
2
(C) 127 ohm cm mole (D) 157 ohm–1 cm2 mole–1
7. What is the cell constant of the conductivity cell (C)

(A) 0.385 cm–1 (B) 3.85 cm–1 (C) 38.5 cm–1 (D) 0.1925 cm–1
8. If the cell (C) is filled with 5 x 10–3 (N) Na2SO4 the observed resistance was 400 ohm. What is the molar
conductance of Na2SO4.
(A) 19.25 ohm–1 cm2 mole–1 (B) 96.25 ohm–1 cm2 mole–1
–1 –1
(C) 385 ohm cm mole 2
(D) 192.5 ohm–1 cm2s mole–1
9. If a 100 mL solution of 0.1M HBr is titrated using a very concentrated solution of NaOH, then the
conductivity (specific conductance) of this solution at the equivalence point will be (assume volume
change is negligible due to addition of NaOH) . Report your answer after multipling it with 10 in Sm –1.
[Given  º(Na ) = 8 × 10–3 Sm2 mol–1 ,  º(Br  ) = 4 × 10–3 S m2 mol–1]
(A) 6 (B) 12 (C) 15 (D) 24
ADVECH - 44
Electrochemistry
Comprehension # 3
Answer 10, Q.11 and Q.12 by appropriately matching the information given in the three columns of the
following table.
The curves in Column 1 shows the variation of conductivity during different titrations. The analyte and titrants
has been listed in Column 2 & Column 3 respectively.
Column-1 Column-2 (Titrate) Column-3 (Titrant)
Conductivity decreases
(I) (i) (C2H5)2NH (P) HCl
initially then increases slowly
then increases rapidly
(II) (ii) CH3COOH (Q) NaOH
initially then increases
(III) initially then remains (iii) HBr (R) CH3COOH
approximately same
Conductivity increases initially

(IV) then remains approximately (iv) NaOH (S) NH4OH
same
10. Which of the following is an incorrect combination of curves in Column 1.
(A) (II) (iii) (Q) (B) (I) (i) (P) (C) (I) (iii) (S) (D) (I) (ii) (Q)
11. The correct combination for a titration in which conductance at equivalent point is lower than initial
(A) (I) (ii) (Q) (B) (I) (iii) (S) (C) (III) (iv) (R) (D) (IV) (ii) (S)
12. Select the correct combination
(A) (I) (iii) (Q) (B) (IV) (ii) (S) (C) (I) (iii) (S) (D) (I) (iv) (R)
PART - I : JEE (ADVANCED) / IIT-JEE PROBLEMS (PREVIOUS YEARS)

* Marked Questions are having one or more than one correct options.
1. Standard electrode potential data are useful for understanding the suitability of an oxidant in a redox
titration. Some half cell reactions and their standard potentials are given below : [JEE 2002, 3/84]
MnO4–(aq.) + 8H+(aq.) + 5e–  Mn2+(aq.) + 4H2O() Eº = 1.51 V
Cr2O72–(aq.) + 14H+(aq.) + 6e–  2Cr3+(aq.) + 7H2O() Eº = 1.38 V
Fe3+(aq.) + e–  Fe2+(aq.) Eº = 0.77 V
Cl2(g) + 2e–  2Cl–(aq.) Eº = 1.40 V
Identify the only INCORRECT statement regarding the quantitative estimation of aqueous Fe(NO3)2 :
(A) MnO4– can be used in aqueous HCl. (B) Cr2O72– can be used in aqueous HCl.
(C) MnO4– can be used in aqueous H2SO4. (D) Cr2O72– can be used in aqueous H2SO4.
2. Two students use the same stock solution of ZnSO4 and different solutions of CuSO4 to make Daniel
cell. The emf of one cell is 0.03 V higher than the other. The concentration of CuSO 4 solution in the cell
with higher emf value is 0.5 M. Find out the concentration of CuSO 4 solution in the other cell.
 2.303 RT 
 Given :  0.06 . [JEE 2003, 2/60]
F 
3. The emf of the cell, Zn | Zn2+(0.01 M) || Fe2+(0.001 M) | Fe at 298 K is 0.2905 V. Then the value of
equilibrium constant for the cell reaction is : [JEE 2004, 3/84]
0.32 0.32 0.26 0.32
0.0295 0.0295 0.0295 0.059
(A) e (B) 10 (C) 10 (D) 10
ADVECH - 45
Electrochemistry
4. Find the equilibrium constant at 298 K for the reaction : [JEE 2004, 4/60]
Cu2+(aq) + In2+(aq) Cu+(aq) + In3+(aq)
Given that EºCu2+ / Cu+ = 0.15 V, EºIn3+ / In+ = – 0.42 V, EºIn2+ / In+ = – 0.40 V.
5. The half cell reactions for rusting of iron are :
1
2H+ + O2 + 2e– H2O; Eº = +1.23 V & Fe2+ + 2e– Fe ; Eº = – 0.44 V
2
Gº (in kJ/mol) for the overall reaction is : [JEE 2005, 3/84]
(A) – 76 (B) – 322 (C) – 122 (D) – 176
Comprehension # 1
Tollen’s reagent is used for the detection of aldehyde. When a solution of AgNO 3 is added to glucose
with NH4OH, then gluconic acid is formed.
Ag+ + e– Ag ; Eºred = 0.8 V
C6H12O6 + H2O  C6H12O7 (Gluconic acid) + 2H+ + 2e– ; Eºoxd = – 0.05 V
Ag(NH3)2+ + e– Ag(s) + 2NH3 ; Eº = – 0.337 V
RT F
[Use 2.303 × = 0.0592 and = 38.92 at 298 K]
F RT
Now answer the following three questions :
6. 2Ag+ + C6H12O6 + H2O  2Ag(s) + C6H12O7 + 2H+
Find ln K of this reaction : [JEE 2006, 5/184]
2Ag+ + C6H12O6 + H2O  2Ag(s) + C6H12O7 + 2H+
(A) 66.13 (B) 58.38 (C) 28.30 (D) 46.29
7. When ammonia is added to the solution, pH is raised to 11. Which half-cell reaction is affected by pH
and by how much : [JEE 2006, 5/184]
(A) Eoxd will increase by a factor of 0.65 for Eºoxd (B) Eoxd will decrease by a factor of 0.65 for Eºoxd
(C) Ered will increase by a factor of 0.65 for Eºred (D) Ered will decrease by a factor of 0.65 for Eºred
8. Ammonia is always is added in this reaction. Which of the following must be INCORRECT :
(A) NH3 combines with Ag+ to form a complex. [JEE 2006, 5/184]
(B) Ag(NH3)2+ is a weaker oxidising reagent than Ag+.
(C) In absence of NH3, silver salt of gluconic acid is formed.
(D) NH3 has affected the standard reduction potential of glucose/gluconic acid electrode.
9. We have taken a saturated solution of AgBr. Ksp of AgBr is 12 × 10–14. If 10–7 mole of AgNO3 are added
to 1 litre of this solution, find conductivity (specific conductance) of this solution in terms of 10–7 Sm–1.
Given : º(Ag+) = 6 × 10–3 Sm2mol–1, º(Br–) = 8 × 10–3 Sm2mol–1, º(NO3–) = 7 × 10–3 Sm2mol–1.
[JEE 2006, 6/184]
Comprehension # 2
Chemical reactions involve interaction of atoms and molecules. A large number of atoms/molecules
(approximately 6.023 × 1023) are present in a few grams of any chemical compound varying with its
atomic/molecular masses. To handle such large number conveniently, the mole concept was
introduced. This concept has implications in diverse areas such as analytical chemistry, biochemistry,
electrochemistry and radiochemistry. The following example illustrates a typical case, involving
chemical/electrochemical reaction, which requires a clear understanding of the mole concept.
A 4.0 molar aqueous solution of NaCl is prepared and 500 mL of this solution is electrolysed. This leads
to the evolution of chlorine gas at one of the electrodes.
(Given : Atomic masses : Na = 23, Hg = 200 ; 1 Faraday = 96500 coulombs)
Now answer the following three questions :
10. The total number of moles of chlorine gas evolved is : [JEE 2007, 4/162]
(A) 0.5 (B) 1.0 (C) 2.0 (D) 3.0
11. If the cathode is Hg electrode, the maximum weight (in g) of amalgam formed from this solution is :
[JEE 2007, 4/162]
(A) 200 (B) 225 (C) 400 (D) 446
12. The total charge (in coulombs) required for complete electrolysis is : [JEE 2007, 4/162]
(A) 24125 (B) 48250 (C) 96500 (D) 193000
ADVECH - 46
Electrochemistry
Comprehension # 3
Redox reactions play a pivoted role in chemistry and biology. The values of standard redox potential
(Eº) of two half-cell reactions decide which way the reaction is expected to proceed. A simple example
is a Daniel cell in which zinc goes into solution and copper gets deposited. Given below is a set of half-
cell reactions (acidic medium) along with their Eº values with respect to normal hydrogen electrode.
Using this data, obtain the correct explanations to questions 13 - 14.
I2 + 2e– 2I– Eº = 0.54 V
Cl2 + 2e– 2Cl– Eº = 1.36 V
Mn 3+
+ e Mn
– 2+
Eº = 1.50 V
Fe + e Fe
3+ – 2+
Eº = 0.77 V
O2 + 4H+ + 4e– 2H2O Eº = 1.23 V
13. Among the following, identify the correct statement : [JEE 2007, 4/162]
(A) Chloride ion is oxidised by O2 (B) Fe2+ is oxidised by iodine
(C) Iodine ion is oxidised by chlorine (D) Mn2+ is oxidised by chlorine
14. While Fe3+ is stable, Mn3+ is not stable in acid solution, because : [JEE 2007, 4/162]
(A) O2 oxidises Mn2+ to Mn3+ (B) O2 oxidises both Mn2+ to Mn3+ and Fe2+ to Fe3+
(C) Fe3+ oxidises H2O to O2 (D) Mn3+ oxidises H2O to O2
15. Electrolysis of dilute aqueous NaCl solution was carried out by passing 10 milliampere current. The
time required to liberate 0.01 mole of H2 gas at the cathode is : (1 Faraday = 96500 C)
[JEE 2008, 3/163]
4 4 4
(A) 9.65 × 10 sec (B) 19.3 × 10 sec (C) 28.95 × 10 sec (D) 38.6 × 104 sec
16.* For the reduction of NO3– ion in an aqueous solution, Eº is +0.96 V. Values of Eº for some metal ions
are given below :
V2+(aq) + 2e– V Eº = –1.19 V
Fe3+(aq) + 3e–  Fe Eº = –0.04 V
Au3+(aq) + 3e–  Au Eº = +1.40 V
Hg2+(aq) + 2e– Hg Eº = +0.86 V
The pair(s) of metals that is(are) oxidized by NO3– in aqueous solution is(are) : [JEE 2009, 4/160]
(A) V and Hg (B) Hg and Fe (C) Fe and Au (D) Fe and V
Comprehension # 4
The concentration of potassium ions inside a biological cell is at least twenty times higher than the
outside. The resulting potential difference across the cell is important in several processes such as
transmission of nerve impulses and maintaining the ion balance. A simple model for such a
concentration cell involving a metal M is :
M(s) | M+(aq ; 0.05 molar) || M+(aq ; 1 molar) | M(s)
For the above electrolytic cell, the magnitude of the cell potential is | Ecell | = 70 mV.
Now answer the following two questions :
17. For the above cell : [JEE 2010, 3/163]

(A) Ecell < 0 ; G > 0 (B) Ecell > 0 ; G < 0 (C) Ecell < 0 ; Gº > 0 (D) Ecell > 0 ; Gº < 0
18. If the 0.05 molar solution of M+ is replaced by a 0.0025 molar M+ solution, then the magnitude of the cell
potential would be : [JEE 2010, 3/163]
(A) 35 mV (B) 70 mV (C) 140 mV (D) 700 mV
ADVECH - 47
Electrochemistry
19. AgNO3(aq.) was added to an aqueous KCl solution gradually and the conductivity of the solution was
measured. The plot of conductance () versus the volume of AgNO3 is : [JEE 2011, 3/180]
(A) (P) (B) Q (C) (R) (D) (S)
20. Consider the following cell reaction : [JEE 2011, 3/180]

2Fe (s) + O2 (g) + 4H (aq)  2Fe
+ 2+
(aq) + 2H2O (l) Eº = 1.67 V
2+ –3
At [Fe ] = 10 M, P(O2) = 0.1 atm and pH = 3, the cell potential at 25ºC is :
2.303 R (298)
(Take = 0.06)
F
(A) 1.47 V (B) 1.77 V (C) 1.87 V (D) 1.57 V
Comprehension # 5
The electrochemical cell shown below is a concentration cell.
M|M2+ (saturated solution of a sparingly soluble salt,MX2)|| M2+ (0.001 mol dm–3) |M
The emf of the cell depends on the difference in concetration of M2+ ions at the two electrodes. The emf
of the cell at 298 is 0.059 V.
21. The solubility product (Ksp ; in mol3 dm–9) of MX2 at 298 K based on the information available in the
given concentration cell is : (Take 2.303× R × 298/F = 0.059 V) [IIT-JEE 2012, 3/66]
(A) 1 × 10–15 (B) 4 × 10–15 (C) 1 × 10– 12 (D) 4 × 10–12
22. The value of G (in kJ mol–1) for the given cell is : (Take 1F = 96500 C mol–1 ) [IIT-JEE 2012, 3/136]
(A) – 5.7 (B) 5.7 (C) 11.4 (D) –11.4
23. An aqueous solution of X is added slowly to an aqueous solution of Y as shown in list I. The variation in
conductivity of these reactions is given in List II. Match List I with List II and select the correct answer
using the code given below the lists : [JEE(Advanced) 2013, 3/120]
List I List II
P. (C2H5)3N + CH3COOH 1. Conductivity decreases and then increases
X Y
Q. KI (0.1M) + AgNO3(0.01M) 2. Conductivity decreases and then does not change
X Y much
R. CH3COOH + KOH 3. Conductivity increases and then does not change much
X Y
S. NaOH + HI 4. Conductivity does not change much and then increases
X Y
Codes :
P Q R S P Q R S
(A) 3 4 2 1 (B) 4 3 2 1
(C) 2 3 4 1 (D) 1 4 3 2
ADVECH - 48
Electrochemistry
24. The standard reduction potential data at 25ºC is given below. [JEE(Advanced) 2013, 3/120]
Eº (Fe3+.Fe2+) = + 0.77 V; Eº (Fe2+.Fe) = – 0.44 V;
Eº (Cu2+.Cu) = + 0.34 V; Eº (Cu+.Cu) = + 0.52 V;
Eº (O2(g) + 4H + 4e 2H2O) = + 1.23 V ;
+ –
Eº (O2(g) + 2H2O + 4e– 4OH) = + 0.40 V
Eº (Cr .Cr) = – 0.74 V;
3+
Eº (Cr2+.Cr) = – 0.91 V
Match Eº of the rebox pair in List I with the values given in List II and select the correct answer using
the code given below the lists :
List I List II
P. Eº (Fe3+, Fe) 1. – 0.36 V
Q. Eº (4H2O 4H+ + 4OH–) 2. –0.4 V
R. Eº (Cu2+ + Cu  2Cu+) 3. –0.04 V
S. Eº(Cr3+, Cr+2) 4. –0.83 V
Codes :
P Q R S P Q R S
(A) 4 1 2 3 (B) 2 3 4 1
(C) 1 2 3 4 (D) 3 4 1 2
25. In a galvanic cell, the salt bridge [JEE(Advanced) 2014, 3/120]
(A) does not participate chemically in the cell reaction.
(B) stops the diffusion of ions from one electrode to another.
(C) is necessary for the occurrence of the cell reaction.
(D) ensures mixing of the two electrolytic solutions.
26. All the energy released from the reaction X  Y, rGº = –193 kJ mol–1 is used for oxidizing M+ as M+ 
M3+ + 2e– , Eº = – 0.25 V. Under standard conditions, the number of moles of M+ oxidized when one
mole of X is converted to Y is : [F = 96500 C mol –1] [JEE(Advanced) 2015, 4/168]
27. The molar conductivity of a solution of a weak acid HX (0.01 M) is 10 times smaller than the molar
conductivity of a solution of a weak acid HY (0.10 M). If 0 –  0 – , the difference in their pKa values,
X Y
pKa (HX) – pKa (HY), is (consider degree of ionization of both acids to be <<1)
[JEE(Advanced) 2015, 4/168]
28. For the following electrochemical cell at 298 K,
M2  (aq) 
 
Pt(s) | H2(g, 1 bar) | H+(aq, 1 M) || M4+(aq) | M2+(aq) | Pt(s), Ecell= 0.092 V when = 10x.
M4  (aq)
 
Given : EM0 4 / M2 = 0.151 V; 2.303 RT = 0.059 V
F
The value of x is : [JEE(Advanced) 2016, 3/124]
(A) –2 (B) –1 (C) 1 (D) 2
29. The conductance of a 0.0015 M aqueous solution of a weak monobasic acid was determined by using a
conductivity cell consisting of platinized Pt electrodes. The distance between the electrodes is 120 cm
with an area of cross section of 1 cm 2. The conductance of this solution was found to be 5 × 10–7 S. The
pH of the solution is 4. The value of limiting molar conductivity (ºm) of this weak monobasic acid in
aqueous solution is Z × 102 S cm–1 mol–1. The value of Z is [JEE(Advanced) 2017, 3/122]
30. For the following cell, Zn(s) | ZnSO4(aq) || CuSO4 (aq) | Cu(s) when the concentration of Zn2+ is 10
times the concentration of Cu2+, the expression for G (in J mol–1) is : [JEE(Advanced) 2017, 3/122]
[F is Faraday constant; R is gas constant; T is temperature; Eº(cell) = 1.1 V]
(A) 2.303 RT + 1.1 F (B) 1.1 F (C) 2.303 RT – 2.2 F (D) –2.2 F
31. For the electrochemical cell, Mg(s) | Mg2+ (aq,1 M) || Cu2+ (aq,1M) | Cu(s)
the standard emf of the cell is 2.70 V at 300 K. When the concentration of Mg2+ is changed to x M, the
F
cell potential changes to 2.67 V at 300 K. The value of x is ____. (Given, = 11500 K V−1, where F is
R
the Faraday constant and R is the gas constant, ln(10) = 2.30). [JEE(Advanced) 2018, 3/120]
32. Consider an electrochemical cell : A(s) | An+(aq, 2 M) || B2n+(aq, 1 M) | B(s). The value of H° for the cell
reaction is twice that of G° at 300 K. If the emf of the cell is zero, the S°(in J K–1mol–1) of the cell
reaction per mole of B formed at 300 K is____.
(Given : ln (2) = 0.7, R(universal gas constant) = 8.3 J K–1 mol–1. H, S and G are enthalpy, entropy and
Gibbs energy, respectively.) [JEE(Advanced) 2018, 3/120]
ADVECH - 49
Electrochemistry
PART - II : JEE (MAIN) ONLINE PROBLEMS (PREVIOUS YEARS)
1. The standard electrode potentials EMº  / M  of four metals A, B, C and D are –1.2 V, 0.6 V, 0.85 V and –
0.76 V, respectively. The sequence of deposition of metals on applying potential is :
[JEE(Main) 2014 Online (09-04-14), 4/120]
(1) A, C, B, D (2) B, D, C, A (3) C, B, D, A (4) D, A, B, C
2. A current of 10.0 A flows for 2.00 h through an electrolytic cell containing a molten salt of metal X. This
results in the decomposition of 0.250 mol of metal X at the cathode. The oxidation state of X in the
molten salt is : (F = 96,500 C) [JEE(Main) 2014 Online (09-04-14), 4/120]
(1) 1 + (2) 2 + (3) 3 + (4) 4 +
3. Given : Fe3+ (aq) + e–  Fe2+ (aq) ; Eº = + 0.77 V
Al3+ (aq) + 3e–  Al(s); Eº = –1.66 V
Br2 (aq) + 2e–  2Br– ; Eº = +1.09 V
Considering the electrode potentials, which of the following represents the correct order of reducing
power?
[JEE(Main) 2014 Online (11-04-14), 4/120]
(1) Fe2+ < Al < Br– (2) Br– < Fe2+ < Al (3) Al < Br– < Fe2+ (4) Al < Fe2+ < Br–
4. How many electrons would be required to deposit 6.35 g of copper at the cathode during the
electrolysis of an aqueous solution of copper sulphate ? (Atomic mass of copper = 63.5 u, N A =
Avogadro's constant). [JEE(Main) 2014 Online (12-04-14), 4/120]
N N N N
(1) A (2) A (3) A (4) A
20 10 5 2
5. A variable, opposite external potential (Eext) is applied to the cell Zn|Zn2+ (1 M) || Cu2+ (1M) | Cu, of
potential 1.1 V. When Eext < 1.1 V and Eext > 1.1 V respectively electrons flow from :
[JEE(Main) 2015 Online (10-04-15), 4/120]
(1) Cathode to anode in both cases (2) cathode to anode and anode to cathode
(3) anode to cathode and cathode to anode (4) anode to cathode in both cases
6. 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
 RT 
Br2|Br, and 0.54 V for 2|–. At pH = 3, permanganate is expected to oxidize :   0.059 V 
 F 
[JEE(Main) 2015 Online (11-04-15), 4/120]
(1) Cl–, Br– and – (2) Br– and – (3) Cl– and Br– (4) – only
7. What will occur if a block of copper metal is dropped into a beaker containing a solution of 1M ZnSO 4?
[JEE(Main) 2016 Online (09-04-16), 4/120]
(1) The copper metal will dissolve and zinc metal will be deposited.
(2) The copper metal will dissolve with evolution of oxygen gas.
(3) The copper metal will dissolve with evolution of hydrogen gas.
(4) No reaction will occur.
8. Identify the correct statement: [JEE(Main) 2016 Online (10-04-16), 4/120]
(1) Corrosion of iron can be minimized by forming an impermeable barrier at its surface.
(2) Iron corrodes in oxygen-free water.
(3) Iron corrodes more rapidly in salt water because its electrochemical potential is higher.
(4) Corrosion of iron can be minimized by forming a contact with another metal with a higher reduction
potential.
9. What is the standard reduction potential (Eº) for Fe3+  Fe ?
Given that : [JEE(Main) 2017 Online (08-04-17), 4/120]
Fe + 2e  Fe; EFe2  /Fe = – 0.47 V
2+ – º
Fe3+ + e–  Fe2+ ; EFe

º
2
/Fe
º
EFe 2
/Fe 2 
= + 0.77 V
(1) + 0.30 V (2) – 0.057 V (3) + 0.057 V (4) – 0.30 V
ADVECH - 50
Electrochemistry
10. Consider the following standard electrode potentials (Eº in volts) in aqueous solution :
Element M3+ / M M+ / M [JEE(Main) 2017 Online (08-04-17), 4/120]
Al –1.66 + 0.55
Tl +1.26 – 0.34
Based on these data, which of the following statements is correct ?
(1) Al+ is more stable than Al3+ (2) Tl3+ is more stable than Al3+
+ 3+
(3) Tl is more stable than Al (4) Tl+ is more stable than Al+
11. Which of the following ions does not liberate hydrogen gas on reaction with dilute acids ?
[JEE(Main) 2017 Online (09-04-17), 4/120]
(1) Mn2+ (2) Ti2+ (3) V2+ (4) Cr2+
12. 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+ + 3e– M at 298 K will be : [JEE(Main) 2017 Online (09-04-17), 4/120]
(Given EAg / Ag at 298 K = 0.80 volt)
(1) 0.32 Volt (2) 0.66 Volt (3) 0.38 Volt (4) 1.28 Volt
13. 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 :
[JEE(Main) 2018 Online (15-04-2018), 4/120]
(1) 2.0 (2) 0.1 (3) 0.5 (4) 1.0
14.^ When 9.65 ampere current was passed for 1.0 hour into nitrobenzene in acidic medium, the amount of
p-aminophenol produced is : [JEE(Main) 2018 Online (16-04-2018), 4/120]
Note : Nitrobenzene actually convert into aniline in reduction in acidic medium.
(1) 109.0 g (2) 98.1 g (3) 9.81 g (4) 10.9 g
15. 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 PbSO 4 = 303 g mol–1)
[JEE(Main) 2019 Online (09-01-2019), 4/120]
(1) 15.2 (2) 22.8 (3) 7.6 (4) 11.6
16. 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–1mol, F = 96000 C mol–1)
[JEE(Main) 2019 Online (09-01-2019), 4/120]
(1) e320 (2) e –80 (3) e160 (4) e–160
17. Consider the following reduction processes :
Zn2+ + 2e–  Zn(s) ; E0 = –0.76 V
Ca + 2e  Ca(s) ;
2+ –
E0 = –2.86 V
Mg + 2e  Mg(s) ; E0 = –2.36 V
2+ –
Ni2+ + 2e–  Ni(s); E0 = –0.25 V

The reducing power of the metals increases in the order: [JEE(Main) 2019 Online (10-01-2019), 4/120]
(1) Ca < Mg < Zn < Ni (2) Ni < Zn < Mg < Ca (3) Ca < Zn < Mg < Ni (4) Zn < Mg < Ni < Ca
18. In the cell, Pt(s) | H2(g,1bar) | HCl(aq) | AgCl (s) | Ag(s)| Pt(s)
The cell potential is 0.92 V when a 10–6 molal HCl solution is used. The standard electrode potential of
 2.303RT 
(AgCl / Ag, Cl–) electrode is : Given,  0.06Vat298k 
 F 
[JEE(Main) 2019 Online (10-01-2019), 4/120]
(1) 0.76 V (2) 0.20 V (3) 0.94 V (4) 0.40 V
19. The electrolytes usually used in the electroplating of gold and silver, respectively, are:
[JEE(Main) 2019 Online (10-01-2019), 4/120]
(1) [Au(CN)2]– and [AgCl2]– (2) [Au(NH3)2]+ and [Ag(CN)2]–
(3) [Au(CN)2]– and [Ag(CN)2]– (4) [Au(OH)4]– and [Ag(OH)2]–
ADVECH - 51
Electrochemistry
20. 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)
EMx  / M/( V ) 1.40 0.80 0.77 –0.44
If EZn2 / Zn = –0.76 V, which cathode will give a maximum value of Ecell per electron transferred ?
[JEE(Main) 2019 Online (11-01-2019), 4/120]
(1) Au3+ / Au (2) Fe3+ / Fe2+ (3) Fe2+ / Fe (4) Ag+ / Ag
21. Given the equilibrium constant : KC of the reaction Cu(s) + 2Ag+(aq)  Cu2+ (aq) + 2Ag(s) is 10 × 1015,
 RT 
caluclate the E 0cell of this reaction at 298 K : 2.303 at298K  0.059 V 
 F 
[JEE(Main) 2019 Online (11-01-2019), 4/120]
(1) 0.4736 mV (2) 0.04736 V (3) 0.4736 V (4) 0.04736 mV
 dE 
22. The standard electrode potential E and its temperature coefficient   for a cell are 2 V 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 (rH) at 300 K in kJ mol–1 is :
(Use R = 8JK–1 mol–1 and F = 96,000 Cmol–1) [JEE(Main) 2019 Online (12-01-2019), 4/120]
(1) 206.4 (2) –384.0 (3) 192.0 (4) –412.8
23. ºm for NaCl, HCl and NaA are 126.4, 425.9 and 100.5 S cm 2mol–1, respectively. If the conductivity of
0.001 M HA is 5 × 10–5 S cm–1, degree of dissociation of HA is:
[JEE(Main) 2019 Online (12-01-2019), 4/120]
(1) 0.125 (2) 0.50 (3) 0.75 (4) 0.25

24. Given that] EO  1.23V
2 / H2O
ES O2– / SO2  2.05V

2 8 4

EBr –  1.09V;
2 / Br
E Au 3  / Au  1.4 V
The strongest oxidizing agent is : [JEE(Main) 2019 Online (08-04-19)S1, 4/120]
(1) O2 (2) Br2 (3) Au3+ (4) S 2O 82 –
25. Calculate the standard cell potential (in V) of the cell in which following reaction takes place :
Fe2+ (aq) + Ag+ (aq)  Fe3+ (aq) + Ag(s)
Given that
E0Ag  / Ag  xV
0
EFe 2
/ Fe
 yV
0
EFe 3
/ Fe
 zV [JEE(Main) 2019 Online (08-04-19)S2, 4/120]
(1) x – z (2) x – y (3) x + y – z (4) x + 2y – .3z
26. The standard Gibbs energy for the given cell reaction in kJ mol–1 at 298 K is :
Zn(s) + Cu2+(aq)  Zn2+(aq) + Cu(s).
Eº = 2 V at 298 K
(Faraday's constant, F = 96000 C mol–1) [JEE(Main) 2019 Online (09-04-19)S1, 4/120]
27. A solution of Ni(NO3)2 is electrolyzed between platinum electrodes using 0.1 Faraday electricity. How
many mole of Ni will be deposited at the cathode?
[JEE(Main) 2019 Online (09-04-19)S2, 4/120]
(1) 0.20 (2) 0.15 (3) 0.10 (4) 0.05
ADVECH - 52
Electrochemistry
28. Consider the statements Statement-1 and Statement-2 :
Statement-1 : Conductivity always increases with decrease in the concentration of electrolyte.
Statement-2 : Molar conductivity always increase with decrease in the concentration of electrolyte.
The correct option among the following is :
[JEE(Main) 2019 Online (10-04-19)S1, 4/120]
(1) Both Statement-1 and Statement-2 are correct
(2) Both Statement-1 and Statement-2 are wrong
(3) Statement-1 is wrong and Statement-2 is correct
(4) Statement-1 is correct and Statement-2 is wrong
29. Which one of the following graphs between molar conductivity (Am) versus C is correct?
[JEE(Main) 2019 Online (10-04-19)S2, 4/120]
KCl
Am Am Am Am
(1) NaCl (2) NaCl (3) KCl (4) KCl
KCl NaCl NaCl
C C C C
30. Given
Co3+ + e–  Co2+ ; Eº = +1.81V ; Pb4+ + 2e– Pb2 ; E0 = + 1.67 V
Ce + e  Ce ; Eº = + 1.61 V ;
4+ – 3+
Bi3+ + 3e–  Bi ; Eº = +0.20 V
Oxidizing power of the species will increase in the order :[JEE(Main) 2019 Online (12-04-19)S1, 4/120]
(1) Ce4+ < Pb4+ < Bi3+ < Co3+ (2) Bi3+ < Ce4+ < Pb4+ < Co3+
(3) Co3+ < Pb4+ < Ce4+ < Bi3+ (4) Co3+ < Ce4+ < Bi3+ < Pb4+
31. The decreasing order of electrical conductivity of the following aqueous solution is :
[JEE(Main) 2019 Online (12-04-19)S2, 4/120]
0.1 M Formic acid (A) ; 0.1 M Acetic acid (B) ; 0.1 M Benzoic acid (C)
(1) A > B > C (2) A > C > B (3) C > A > B (4) C > B > A
32. 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: [JEE(Main) 2020 Online (07-01-20)S1, 4/120]
(1) +0.158 V (2) –0.182 V (3) 0.182 V (4) –0.158 V
33. The equation that is incorrect is: [JEE(Main) 2020 Online (07-01-20)S2, 4/120]
 
(1)  0
m NaBr  
– 0
m NaI  
 0
m KBr  
–  0
m NaBr (2)   0
m HO
2
 
 m0
HCl
 
 m0
NaOH
 
– m0
NaCl
(3)    0
m KCl –  
0
m NaCl   
0
m KBr –  0
m NaBr (4)   0
m NaBr –   0
m NaCl   
0
m KBr –   0
m KCl
34. 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 ; Temp = 298 K ; oxygen under std.
pressure of 1 bar) [JEE(Main) 2020 Online (08-01-20)S1, 4/120]
35. For an electrochemical cell [JEE(Main) 2020 Online (08-01-20)S2, 4/120]
2
[Sn ]
Sn(s) | Sn2+(aq, 1M)||Pb2+ (aq, 1M)|Pb(s) the ratio when this cell attains equilibrium is _____
[Pb2 ]
   2.303RT 
 Given :ESn2 |Sn  –0.14V, EPb2 |Pb  –0.13V,  0.06 
 F 
36. 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(Main) 2020 Online (09-01-20)S1, 4/120]
37. Amongst the following, the form of water with the lowest ionic conductance at 298 K is:
[JEE(Main) 2020 Online (09-01-20)S2, 4/120]
(1) distilled water (2) sea water
(3) water from a well (4) saline water used for intravenous injection
ADVECH - 53
Electrochemistry
EXERCISE - 1
PART - I
A-1. (a) Cu (b) Ag (c) oxidation (d) reduction
(e) Cu (f) Ag (g) anode-Cu Cu2+ + 2e–; cathode-Ag+ + e–  Ag
(h) Cu + 2Ag+ Cu2+ + 2Ag (i) Cu (j) Cu
(k) to complete circuit and maintain electrical neutrality in solution
A-2. (a) 2Ag+ + Cu  2Ag + Cu2+ (b) 8H+ + MnO4– 5Fe3+ + Mn2+ + 4H2O
(c) 2Ag+ + 2Cl–  2Ag + Cl2 (d) Cd + 2H+  Cd2+ + H2
A-3. (a) Zn | Zn2+ | | H+ | H2 | Pt (b) Pt | Sn2+, Sn4+ | | Fe3+, Fe2+ | Pt (c) Pb | Pb2+ | | Br– | | Br2 | Pt
B-1. Mg B-2. Y>Z>X
B-3. (i) CuO : Cu is below hydrogen in series, so it can reduce from CuO to Cu.
(ii) Ag2O: Lower in series stability of oxide become lesser.
(iii) Lower S.R.P. metal can displace higher S.R.P. metals ions from solution.
B-4. 1.61 V B-5. 1.35 V B-6. 1.68 V C-1. – 0.036 V
C-2. 0.756 V C-3. Spontaneous,  48250 J C-4. 1.14 volt

D-1. 0.059 volt D-2. 1014 D-3. – 0.2214 V D-4. n=2
D-5. (a) The spontaneous cell reaction: Zn + 2Ag+ (aq) Zn2+ (aq) + 2Ag (s)
(b) 1.56 V (c) [Zn2+] = 4 × 10–4 M
(d) As we add KI to cathode chamber, some Ag+ will precipitate out as:
Ag+ + I– AgI
The above reaction reducing [Ag+] from cathode chamber. This will reduce Ecell according to Nernst’s
equation.
D-6. pH = 1.5. D-7. log [Zn2+] / [Cu2+] = 37.22
E-1.
ELECTROLYTE ANODE Product CATHODE Product
1 NaCl (Molten) with Pt electrode Cl2(g) Na
2 NaCl (aq) with Pt electrode Cl2(g) H2(g)
3 Na2SO4 (aq) with Pt electrode O2(g) H2(g)
4 NaNO3 (aq) with Pt electrode O2(g) H2(g)
5 AgNO3 (aq) with Pt electrode O2(g) Ag
6 CuSO4 (aq) with Inert electrode O2(g) Cu
7 CuSO4 (aq) with Copper electrode Cu dissolve Cu
ADVECH - 54
Electrochemistry
F-1. 12.04 x 1023 F-2. 108. F-3. 2 F-4. n=4 F-5. t = 193 sec.
F-6. V(H2 ) = 56.0 mL. F-7. Ni2+ = 2M F-8. t = 93.65 sec. F-9.  71.5 amp
G-1. 8 G-2. 1.67 V H-1. 2.332 × 10–3 mho cm–1, 23.32 mho cm2 mol–1.
H-2. 0.1456 amp H-3. 0.728 cm–1. I-1. 272, 0.0353 I-2. 382 mho cm2 mol–1.
I-3. 1.76 × 10–5 mole/litre. I-4. 2.70 × 10–10 (mole/litre)2.

Conductance
Conductance
Conductance
J-1. (1) (2) (3) (4)
Volume of NaOH Volume of NaOH Volume of NaOH
PART - II
A-1. (A) A-2. (C) A-3. (D) A-4. (C) B-1. (A)
B-2. (C) B-3. (D) B-4. (D) B-5. (C) B-6. (A)
B-7. (C) B-8. (C) C-1. (D) C-2. (D) C-3. (D)
D-1. (A) D-2. (A) D-3. (C) D-4. (B) D-5. (B)
D-6. (C) E-1. (C) E-2. (C) E-3. (D) E-4. (B)
E-5. (B) F-1. (D) F-2. (B) F-3. (C) F-4. (B)
F-5. (C) G-1. (B) G-2. (A) G-3. (D) H-1. (A)
H-2. (D) H-3. (B) I-1. (C) I-2. (D) I-3. (D)
I-4. (C) I-5. (D) J-1. (A) J-2. (C)
PART – III
1. (A - s) ; (B - p,r) ; (C - p,q) ; (D - r) 2. (A - p, q, r) ; (B - p, q, r) ; (C - p, s) ; (D - p, s)
EXERCISE - 2
PART - I
1. (A) 2. (C) 3. (C) 4. (C) 5. (B)
6. (B) 7. (B) 8. (A) 9. (D) 10. (D)
11. (C) 12. (B) 13. (B) 14. (D) 15. (B)
ADVECH - 55
Electrochemistry
PART - II
1. 3 (B, E & F) 2. 59 3. E° = 7 V. 4. 40
5. (NO
o
– 2
) = 7 Sm mol
–1
6. 4 7. 10 8. 20 9. 4
3
PART - III
1. (BC) 2. (AD) 3. (AC) 4. (ABD) 5. (AB)
6. (BD) 7. (BCD) 8. (BCD) 9. (ACD) 10. (AC)
11. (AB) 12. (BC) 13. (BCD) 14. (A) 15. (ABD)
PART – IV
1. (D) 2. (C) 3. (B) 4. (D) 5. (A)
6. (C) 7. (D) 8. (D) 9. (B) 10. (C)
11. (C) 12. (B)
EXERCISE – 3
PART - I
1. (A) 2. 0.05 M 3. (B) 4. KC = 1010 5. (B)
6. (B) 7. (A) 8. (D) 9. 55 S m–1 10. (B)
11. (D) 12. (D) 13. (C) 14. (D) 15. (B)
16. (ABD) 17. (B) 18. (C) 19. (D) 20. (D)
21. (B) 22. (D) 23. (A) 24. (D) 25. (A)
26. 4 27. 3 28. (D) 29. 6 30. (C)
–1 –1
31. 10 32. –11.62 JK mol
PART – II
1. (3) 2. (3) 3. (2) 4. (3) 5. (4)

6. (2) 7. (4) 8. (1) 9. (2) 10. (4)
11. (1) 12. (1) 13. (4) 14. (3) 15. (3)
16. (3) 17. (2) 18. (2) 19. (3) 20. (1)
21. (3) 22. (4) 23. (1) 24. (4) 25. (4)
26. (2) 27. (4) 28. (3) 29. (3) 30. (2)
31. (2) 32. (1) 33. (1) 34. –0.93 to –0.94
35. 2.13 to 2.17 36. 5.66 to 5.68 37. (1)
ADVECH - 56

Part - I: Subjective Questions: Section (A) : Galvanic Cell, Its Representation & Salt Bridge

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Electrochemistry

 Marked Questions may have for Revision Questions.

PART - I : SUBJECTIVE QUESTIONS

 LOAN  left oxidation- Anode-negative

B-1. The reduction potential values are given below

Section (C) : Concept of G

What is the change in free energy ?

C-4. Using the Gº for the reactions

D-6. NO3  NO2 (acid medium), Eº = 0.790 V

Section (E) : Electrolysis

Section (F) : Faraday laws & its Applictions

Section (H) : Electrical Conductance

Section (J) : Conductometric Titration

Section (B) : Electrochemical series & its Applications

Section (C) : Concept of G

H2 (Pt) H3 O (aq) Ag

value of x ? E0Ag ,Ag = + 0.8 V. [T = 25°C] ; E0Ag ,Ag = + 0.8 V. [T = 25°C]

Section (E) : Electrolysis

E-4. In the electrolysis of aqueous CuBr2 using Pt electrodes :

E-5. During electrolysis of CuSO4 using Pt-electrodes, the pH of solution

Section (F) : Faraday laws & its Applictions

Section (G) : Commercial Cells & Corrosion

G-2. In H2O2 fuel cell the reaction occuring at cathode is :

(A) (B) (C) (D)

H-2. Which has maxmium conductivity :

Section (I) : Kohlrausch law and its applications

Section (J) : Conductometric Titration

conductivity cell. Concentration of KOH solution was –

(D) None of these

(A) NaOH solution is added in to HCl solution

PART - III : MATCH THE COLUMN

1. Match the column

2.^ Match Matrix ( E0Ag / Ag = 0.8).

PART - I : ONLY ONE OPTION CORRECT TYPE

AgBr (s), Br¯ Fe3  , Fe2

PART - II : NUMERICAL VALUE QUESTIONS

after multiplying by 1000.

PART - III : ONE OR MORE THAN ONE OPTIONS CORRECT TYPE

(A) Anode of E is connected to cathode of G (B) Anode of E is connected to anode of G

8. When a lead storage battery is discharged then :

10. On increasing dilution following will increase :

Which of the following oxidation state is least stable?

5. Which of the following statement is correct ? According to Q.4

Molar Concentration of NaCl Molar Conductance in ohm–1 cm2 mole–1

6. What is the molar conductance of NaCl at infinite dilution ?

7. What is the cell constant of the conductivity cell (C)

Conductivity increases initially

PART - I : JEE (ADVANCED) / IIT-JEE PROBLEMS (PREVIOUS YEARS)

17. For the above cell : [JEE 2010, 3/163]

(A) (P) (B) Q (C) (R) (D) (S)

20. Consider the following cell reaction : [JEE 2011, 3/180]

Fe3+ + e–  Fe2+ ; EFe

Ni2+ + 2e–  Ni(s); E0 = –0.25 V

ES O2– / SO2  2.05V

B-4. 1.61 V B-5. 1.35 V B-6. 1.68 V C-1. – 0.036 V

C-2. 0.756 V C-3. Spontaneous,  48250 J C-4. 1.14 volt

I-3. 1.76 × 10–5 mole/litre. I-4. 2.70 × 10–10 (mole/litre)2.

Volume of NaOH Volume of NaOH Volume of NaOH