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ELECTROCHEMISTRY

TYPE OF CELL
Galvanic Electrolytic
Chemical to electrical Electrical to chemical
Current due to spontaneous Rex. ∆G= - ve Non- spontaneous Rex. ∆G = + ve
Anode - oxidn (-ve) cathode – Redn (+ve) Anode - oxidn (+ve) cathode – Redn(-ve)

TYPE OF GALVANIC CELL


No matter transfer (Chemical Cell) matter transfer (Conc. Cell)
Chemical cell Conc. Cell
Electrical energy produces due to chemical rex. Electrical energy produces due to transfer of matter
Daniel cell Any conc. cell.

SALT BRIDGE
Need of salt bridge
(1) excess +ve charge on left half + excess -ve charge on right half
(2) Incomplete circuit
(3) To complete circuit and maintain electric neutrality
Salt Bridge
(1) Invert U- shaped tube having inert electrolyte past in agar-agar or gelatin
Inert electrolyte + water +Agar-Agar
(2) Complect internal circuit & maintain electrical neutrality.
(3) Avoid mixing of two electrolyte solutions and minimize the LTP
*Note
(1) Electrolyte which form ppt not used in Salt bridge.
(e.g with Ag, we do not use KCl)
Ag+1 ,Hg+2,Pb+2 with never use KCl, we use NH4NO3 or KNO3 with KCl
(2) Mobility of ions used in salt bridge must be same.
(3) Ions of cathodic and anodic compartment will not be allowed to pass through salt bridge

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VIGYAN VRIKSH |Electrochemistry

Q1. Which of the following statement are correct regarding inert electrolyte used in salt bridge?
(a) The ions of electrolyte should not react with other ions in the solution.
(b) The ions of inert electrolyte should not participate in oxidation and reduction at electrodes.
(c) The mobility of ions of electrolyte should be almost same
(d) All are correct.
Q2. The standard electrode potential of SHE is zero because
(a) Hydrogen is easier to oxidise
(b) Electrode potential is assumed to be zero
(c) H atom has 1 𝑒 −
(d) H is lightest element
Q3. Std. reduction potential of three metals A,B and C are 0.5 V, -3.0V, -1.2V. The reducing power of
metals are
(a) A > B > C (b) C > B > A
(c) A > C > B (d) B > C > A
Q4. A metal can displace H+ from acidic solution resulting into liberation of H2 gas
(a) If it has higher oxidation potential than H2
(b) It has lower oxidation potential than H2
(c) It should have positive reduction potential
(d) It should have negative oxidation potential
0
Q5. The 𝐸𝑚 3+ ⁄𝑀2+ values for Cr, Mn, Fe and Co are – 0.41,+ 1.57, 0.77 and +1.97 respectively, For which

one of these metals, change in O.S. from +2 to + 3 is easiest ?


(a) Fe (b) Mn
(c) Cr (d) Co
Q6. If reduction potential of A is more than B, then
(a) A is better oxidising agent than B
(b) B is better reducing agent than A
(c) A is better reducing agent than B
(d) B is better oxidising agent than A
(a) A and B (b) A and C
(c) B and D (d) C and D
Q7. The standard reduction potentials at 298K for single electrodes are given below:
Electrode Electrode Potential (volt)
Mg2+/Mg -2.34
Zn2+/Zn -0.76
Zn2+/Fe -0.44

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VIGYAN VRIKSH |Electrochemistry

From this we can infer that


(a) Zn can reduce both Mg2+ and Fe2+
(b) Fe can reduce both Mg2+ and Zn2+
(c) Mg can reduce both Zn2+ and Fe2+
(d) Mg can reduce Zn2+ but not Fe2+
Q8. Which of the following properties are extensive ?
(a) ∆G0 (b) Ecell
0 0
(c) 𝐸𝑐𝑒𝑙𝑙 (d) 𝐸𝑐𝑎𝑡ℎ𝑜𝑑𝑒
Q9. Which of the following properties are intensive ?
(a) Ecell (b) ∆G
(c) ∆G0 (d) None of the above
Q10. Given
0 0
ECel2 ⁄cl
− = 1.36 V, E 3+ ⁄
Cr cl = −0.74 V,
0 0
ECe 2− 3+ = 1.33 V, EMnO− ⁄Mn2+ = 1.51V
2 O7 ⁄cl 4

Among the following , the strongest reducing agent is


(a) Cr 3+ (b) Cl−
(c) Cr (d) Mn2+
Q11. Find ∆G0 for the given reaction
Zn+2Ag+→ 2Ag + Zn2+
0 0
EAg ∗ ⁄Ag = 0.80V, E
Zn2+ ⁄Zn = −0.76V,

(a) 301 KJ mol-1 (b) -301KJ mol-1


(c) -301J mol-1 (d) -150KJ mol-1
Q12. Cd2++2e-→Cd(s)E0=-0.40V
Ag++e-→Ag(s)E0=-0.80V
Find ∆G0for 2Ag++Cd(s)→2Ag(s)+Cd2+(∆G)
(a) 115.8 KJ mol-1 (b) -115.8 KJ mol-1
(c) -231.6 KJ mol-1 (d) +231.6 KJ mol-1
0 0 0
Q13. Given the 𝐸𝐹𝑒 2+ ⁄𝐹𝑒 = -0.44V and 𝐸𝐹𝑒 3+ ⁄𝐹𝑒 2+ = 0.77V, the 𝐸𝐹𝑒 3+ ⁄𝐹𝑒 is :

(a) 1.21V (b) 0.33V


(c) -0.036V (d) 0.036V
Q14. The statement that is correct for both electrochemical (galvanic) cells and electrolytic cell is :
(a) ∆G= -nFE
(b) Free energy decreases in both cells

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VIGYAN VRIKSH |Electrochemistry

(c) The cell potential are temperature independent


(d) Chemical energy is converted into electrical energy in both cells
Q15. Given the standard potential for the following half-cell reaction at 298K
Cu+ (aq) + e− → Cu (s) E0 = 0.52V
Cu2+ (aq) + e− → Cu+ (aq) E0 = 0.16V
Calculate the ∆G0 (KJ) for the reaction,2Cu+ (aq)→ Cu(s)+ Cu2+
(a) -34.740 (b) -65.720
(c) -69.480 (d) -131.40
Q16. Given that 𝐸0 (Fe3+,Fe) = - 0.04 V and E0 (𝐹𝑒 2+ , 𝐹𝑒) =- 0.44 V, the value of E0(𝐹𝑒 3+ , 𝐹𝑒 2+ ) is :
(a) 0.76 V (b) -0.40V
(c) -0.76V (d) 0.40V
Q17. Ag++ 𝑒 − → Ag 𝐸 0 = 0.80
Ni2++ 2𝑒 − → Ni 𝐸 0 = −0.25
0
Find 𝐸𝑐𝑒𝑙𝑙 of the cell formed by combining these two electrodes
(a) +1.05V (b) -1.05V
(c) 0.55V (d) +1.35V
Q18. Consider following E0 values
0 0
𝐸𝐹𝑒 3+ ⁄𝐹𝑒 2+ = +0.77 𝑉, 𝐸𝑆𝑛2+ ⁄𝑆𝑛 = −0.14 𝑉

Under standard conditions, potential for the reaction


Sn(s) + 2Fe3+(aq) → 2Fe2+ (aq)+Sn2+(aq)
(a) 0.63V (b) 1.40V
(c) 1.68V (d) 0.91V
0 0
Q19. 𝐸𝐶𝑙 − ⁄𝐴𝑔𝐶𝑙 ⁄𝐴𝑔 = 0.22 V 𝐸
𝐴𝑔+ ⁄𝐴𝑔 = 0.80 V

Find E0 for the given reaction


Ag+ (aq) + 𝐶𝑙 − (aq) → AgCl(s)
(a) 1.02V (b) 0.58V
(c) -0.58V (d) -1.02V
0 0
Q20. 𝐸𝐹𝑒 3+ ⁄𝐹𝑒 = -0.036 V, 𝐸𝐹𝑒 +2 ⁄𝐹𝑒 = -0.439 V,

Value of standard electrode fotential for the change


𝐹𝑒 3+ +𝑒 − → 𝐹𝑒 2+ will be
(a) 0.772V (b) -0.27V
(c) -0.072V (d)0.385V

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VIGYAN VRIKSH |Electrochemistry

Q21. Given electrode potential :


Fe3+ + e− →Fe2+ E0 = 0.771 Volts
𝐼2 + 2e− → 2I- E0 = 0.536 Volts
0
𝐸𝑐𝑒𝑙𝑙 for the cell reaction
2Fe3+ + 2I− → 2Fe2+ + I2 is
(a) (2 × 0.771-0.563) = 1.006 V
(b) (0.771-0.5× 0.536) = 0.5.3 V
(c) 0.771 -0.530 = 0.235 V
(d) 0.536-0.771 = - 0.235 V
Q22. Calculate E0 for 2Cu+ → Cu + Cu2+
0 0
Given 𝐸𝐶𝑢 + ⁄𝐶𝑢 = 0.52V , 𝐸𝐶𝑢2+ ⁄𝐶𝑢+ = 0.16 V

(a) 0.36V (b) 0.68V


(c) 0.84V (d)1.20V
Q23. Given the E0 values for the following reaction sequence,

Mn 6+ ⎯⎯⎯→ Mn5+ ⎯⎯⎯


→ Mn 4+ ⎯⎯⎯
→ Mn3+ ⎯⎯⎯
→ Mn 2+
1.28V 2.9V 0.96 1.5V

the computed value of E0 for Mn6+ → Mn2+ (in volts) is ____.


Q24. The Latimer diagram of oxygen is given below. The value of x is _______V. (Upto two decimal
places)

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VIGYAN VRIKSH |Electrochemistry

TYPE OF ELECTRODES
(A) Metal Metal ion
(B) Metal -Metal insoluble salt anion -electrodes
(i) Ag| AgCl |Cl-||Cl-|AgCl |Ag

(ii) Fe +3OH-→Fe(OH)3 Fe +(OH)3+3e- →Fe+3OH-

(C) Gas- ion Half cell


(D) Oxidn- redn half cell or redox half cell electrodes
(E) Metal -amalgam electrodes
Ques. Write Down the Net Cell Reaction of following
(i). Pt|CO2| H2C2O4, H+ ||Mn𝑜4− , Mn+2 , H+|Pt
(ii) Ag | Ag Cl | KCl || Hg2 Cl2 |Hg

Ques.
(iii) Pt |H2 |H+ || OH- |O2 |pt
(iv) Pt | PbCl2 |PbCl2 | AgCl |Ag
Ques. Write down cell representation from following cell Reaction

(i)Zn(s) + H2SO4 (aq)→ZnSO4 + H2 (g)


(ii)AgCl(s) + e-→Ag(s)+Cl-(aq)
1
(iii)Ag(s) +2 Br2(l)→AgBr(s)

(iv)H2O(s)+H2(g) → Hg + H2O
Q25. Al(s)|Al3+(0.01M)||Fe2+(0.1M)|Fe(s)
0 0
Find 𝐸𝑐𝑒𝑙𝑙 . Given 𝐸𝐴𝑙 3+ /𝐴𝑙 = - 1.66V and 𝐸𝐹𝑒 2+ /𝐹𝑒 = - 0.44V

(a) 0.23V (b) 1.23V


(c) 1.48V (d) 0.48V
Q26. Determine the standard equilibrium constant of the following reaction at 298 K
2Fe3+ + Sn2+ → 2Fe2+ + Sn4+
(a) 1015 (b) 1021
(c) 1048 (d) 1032
Q27. The emf of the cell
Zn|Zn2+(0.01M)||Fe2+ (0.001M)|Fe
at 298 K is 0.2905 volt. Then the value of equilibrium constant for the cell reaction is

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VIGYAN VRIKSH |Electrochemistry
0.32 0.32
(a) 𝑒 0.0295 (b) 100.0295
0.26 0.32
(c) 100.0295 (d) 100.0591
Q28. In a cell that utilizes the reaction
Zn(s) +2H+(aq)→Zn2+(aq)+H2(g)
Addition of H2SO4 to the cathode compartment will
(a) Lower the E and shift equilibrium to the left
(b) Lower the E and shift equilibrium to the right
(c) Increases the E and shift equilibrium to the right
(d) Increases the E and shift equilibrium to the left
Q29. Evaluate standard equilibrium constant for formation of triiodide ion
I2(aq) + I-→I3−
Given I2(aq) + 2e-→2I− , E0 = 0.6197V
I3− + 2e-→3I − , E0 = 0.535V
(a) 608 (b) 400
(c) 735 (d) 7080
Q30. For a cell constructed with Cu(s)Cu2+ (aq) anode and Ag+ (aq)|Ag(s)cathode at 250C . Calculate cell
potential at 250C under non standard conditions.
[Cu2+]=0.3 M and [Ag+] = 0.05M
(a) 0.398V (b) -0.398V
(c) 0.46V (d) 1.46V
Given Ag + e- → Ag E0 = 0.80V
Cu → Cu2+ +2e- E0 = 0.34V
Q31. A hydrogen electrode is dipped in a solution of pH = 3 at 250C. The potential of the cell will be
(a) 0.177V (b) 0.087
(c) -0.177 (d) 0.059V
Q32. A cell contains two hydrogen electordes. The negative electrode is in contact with a solution of 10-6 M
H+ ions. The emf of cell is 0.118 at 250C. Calculate the concentration of hydrogen at the positive
electrode.
(a) 10-1 (b) 10-7
(c) 10-4 (d) 10-6

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VIGYAN VRIKSH |Electrochemistry

1
Q33. H++ 𝑒 − → 2 𝐻2

R.P of this reaction


(a) ↑ with ↑ in Ph of solution
(b) ↓ with ↑ in Ph of solution
(c) ↑ with ↑ in in conc. of H+
(d) ↓ with ↑ in conc. of H+
Q34. From the standard potentials,
Tl+ + 𝑒 − ⇌ Tl(s) 𝐸 0 = −0.336𝑉
TlCl(s)+ 𝑒 − ⇌ Tl(s)+Cl- 𝐸 0 = −0.557𝑉
The solubility product of TICl at 250C is 10x .The value of x is _________(Round off to two decimal
places)
2.303𝑅𝑇
[Given: = 0.0591 at 250C]
𝐹

Q35. The solubility product of AgBr is _______ ×10-13 in water if250C from the cell Ag,AgBr [standard
0 0
solution]/AgBr(s).Ag, The standard potentials are 𝐸𝐴𝑔𝐵𝑟/𝐴𝑔 = 0.071V and 𝐸𝐴𝑔 + /𝐴𝑔 = 0.799V (upto

one place of decimal)


Q36. The solubility product of AgCl in Cl-|AgCl| Ag electrode is 1.8×-5 at 250C The standard electrode
0
potential of the half-cell Cl-|AgCl| Ag is ______V(𝐸𝐴𝑔 + ⁄𝐴𝑔 =0.80V)

[Round off to two decimal places ]


Q37. Consider the following Latimer diagram,

BrO−4 ⎯⎯⎯→ BrO3− ⎯⎯⎯


→ HBrO ⎯⎯⎯→ Br2 ⎯⎯⎯→ Br −
1.82V 1.5V 1.59V 1.06V

The species that will undergo disproportionation is


(a) Br𝑂3− (b) HBrO
(c) Br2 (d) Br𝑂4−
0 0 0
Q38. The value of 𝐸𝐶𝐼𝑂 −
3 ⁄𝐶𝑙2
is [Given : 𝐸𝐶𝑙𝑂 −
3 ⁄𝐶𝑙
− = 0.627V and 𝐸𝐶𝑙 − ⁄𝐶𝑙 − = 1.36V ]
2

(a) 0.4804V (b) 0.2804V


(c) 0.1804V (d) 0.1038V
Q39. For a cell reaction E (at 250C) =1.26V,n =2 and S = - 96.5 JK-1 mol-1.Ecell at 850C by assuming S to
be independent of temperature is _____(V). [Given F = 96500 Cmol-1][Round off to two decimal
places].
Q40. For a cell Ag(s)|AgBr(s)|KBr(aq)|Hg2Br2(s)|Hg(ℓ), the emfs at several temperatures are
T/K 293 298 303
emf/V 0.0663 0.06839 0.07048
The change in entropy at 298K is _____JK-1.(Round off to two decimal places)(1F =96500C)

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VIGYAN VRIKSH |Electrochemistry

Q41. Determine the value of E0 for the given cell reaction is _____
+2
𝐶𝑟(𝑎𝑞) + 2𝑒 − →Cr(s)
From the one -electron ‘s reduction potential for Cr3+ and the three-electrons reduction potential for
𝐶𝑟 3+ ?
0 0
(𝐸𝐶𝑟 3+ ⁄𝐶𝑟 = −0.744V and 𝐸𝐶𝑟 3+ ⁄𝐶𝑟 3+ = 0.407V ) (Round off to two decimal places.)

Q42. Given for the reaction, 2M+6H+ ⇆ 2M+3+3H2 for which ∆H0 =-3.0 kcal. The molar entropies are
6.5cal/K for M,-22.2cal/K for M+3, 31.2 cal/K for H2 and -10.0 cal/K for H+
The value of E0 for the half cell , M+3 + 3𝑒 − ⇆M is __________[Round off to two decimal places].
0
Q43. If the 𝐸𝑐𝑒𝑙𝑙 for a reaction has a negative value , which of the following give the correct relationships
for the values of G0 and Keq.
(a) G0 > 0 ; 𝐾𝑒𝑞 < 1
(b) G0 > 0 ; 𝐾𝑒𝑞 > 1
(c) G0 < 0 ; 𝐾𝑒𝑞 > 1
(d) G0 < 0 ; 𝐾𝑒𝑞 < 1
Q44. EMF of the cell at 298K when pH = 5.0 is
Pt|Q,QH2,H+|| KCl (1M)|Hg2Cl2(s) |Hg |Pt
0 0
Given;𝐸𝑆𝐶𝐸 = 0.28𝑉 and 𝐸𝑄,𝑄𝐻 +
2 ,𝐻 |𝑃𝑡
= 0.70V
(a) -0.23V (b) 0.23V
(c) 0.13V (d) -0.13V
Q45. The EMF of the cell was found to be 0.264V at 250C. The pH of the solution at this temperature when
0
𝐸𝑐𝑎𝑙𝑜𝑚𝑒𝑙 = 0.2422V and 𝐸(𝐻 + ,,𝐻 ) = 0.6996 is __________(Round off to two decimal places),
2

Q46. A conc. Cell with two hydrogen electrode at two different pressure as –
Pt|H2(g)|HCl (aq)| H2(g)| Pt
The potential of cell

RT P RT P
(a) ln P2 (b) ln P2
f 1 2f 1

RT P RT P
(c) ln P1 (d) ln P1
f 2 2f 2

Q47. When conc. of K+ across a cell membrane drops from 0.01M to 0.001M. The potential

Difference across the membranes is :


(a) 0.01V (b)0.059V
(c) 0.0059V (d)0.59V

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VIGYAN VRIKSH |Electrochemistry

Q48. The emf of the cell corresponding to the cell reaction, Zn (s) +2AgCl(s)→ZnCl2(aq).+Ag(s) is 1.08 V
at 300K.if the temperature coefficient of the cell is -4.2×10-4 VK-1, then the for the given cell reaction
at 300 K is
(a) 232 KJ/mol (b) -232 KJ/mol
(c) 172 KJ/mol (d) -172 KJ/mol
Q49. Consider the following concentration cell
Pt|H2(1bar)|HCl(a1):HCl(a2)|H2(1bar)|Pt
The overall reaction for the passage of 1 Faraday of charge is (t denotes the transport number)
(a) t + HCl(a1 ) →t + HCl(a2 )
(b) t + HCl(a2 ) →t + HCl(a1 )
(c) t − HCl(a1 ) →t − HCl(a2 )
(d) t − HCl(a2 ) →t − HCl(a1 )

Q50. The equilibrium constant of the cell reaction , 2Ag+ + Zn 2Ag + Zn 2+ occurring in the zinc-silver
cell at 250C when concentration of both Zn2+ and Ag+ is 0.10M.(emf of the cell is 1.60V)
(a) 1054.2 (b) 1055.2
(c) 1058.2 (d) 1059.2
Q51. The potential of the Ag+|Ag electrode (E0 = 0.799V) in a saturated solution of AgI (Ksp=10-16) is
[Given : 2.303 RT/F =0.06]
(a) 1.297V (b) 0.319V
(c) -1.279V (d) -0.319V
Q52. The chemical potential of the 2 molal Na2SO4 solution is expressed in term of mean
ionic activity coefficient () is :-

(a) μ0 + 5RT 𝑙n 2 +3RT ln 


(b) μ0 + 3RT 𝑙n 
(c) μ0 + 3RT 𝑙n 2 + 3RT In 
(d) μ0 + 4RT 𝑙n 
Q53. For the cell : Cd(Hg)|CdSO4(8/3)H2O(S)|CdSO4(aq, satd.)|Hg2SO4(s)|Hg
The temperature dependence of emf in Volts is given by
B =1.0185 — 4.05× 10-5 (T-293)-9.5×10-7 (T-293)2
The change in entropy at 250C for the cell reaction is
(a) -253K-1mol-1
(b) -9.65JK-1mol-1
(c) -8.3× 10-4JK-1mol-1
(d) Zero

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VIGYAN VRIKSH |Electrochemistry

Q54. For the reaction,Hg2Cl2(s)+H2(g)→2Hg(ℓ)+2HCl(aq).the correct representation of the cell and the
thermodynamic properties ∆G, ∆H and ∆S at 298 K respectively, are (given:𝐸298 = 0.2684𝑉 and
temperature coefficient = -3 ×10-4VK-1)
(a) Pt|H2(g,1atm)|HCl(aq)|Hg2Cl2(s)|Hg(ℓ)
∆G = -51.8kJmol-1,∆H= -69kJmol-1,∆S= -58JK-1mol-1
(b) Pt|H2(g,1atm)|HCl(aq)|Hg2Cl2(s)|Hg(ℓ)
∆G = -25.9kJmol-1,∆H= -34.5kJmol-1,∆S= -29JK-1mol-1
(c) Hg(ℓ)Hg2Cl2(s)|HCl(aq)|H2(g,1 atm)|Pt
∆G = -51.8kJmol-1,∆H= -69kJmol-1,∆S= -58JK-1mol-1
(d) Hg(ℓ)Hg2Cl2(s)|HCl(aq)|H2(g,1 atm)|Pt
∆G = -51.8kJmol-1,∆H= -69kJmol-1,∆S= -58JK-1mol-1
Q55. From the data of two half-cell reactions :
AgCl(s) + e− → Ag(s)+Cl− (aq) E 0 = +0.22V
Ag+(aq) + e− → Ag(s) E 0 = +0.80𝑉
the solubility product of AgCl at 298K, is calculated to be
(a) 1.5 × 10-10 (b) 2.1 × 10-7
(c) 3.0 × 10-3 (d) 1.2 × 10-5
Q56. Given the standard potential for the following half-cell reaction at 298K
Cu+ (aq) + e− → Cu (s) E0 = 0.52V
Cu2+ (aq) + e− → Cu+ (aq) E0 = 0.16V
Calculate the ∆G0 (KJ) for the reaction,2Cu+ (aq)→ Cu(s)+ Cu2+
(a) -34.740 (b) -65.720
(c) -69.480 (d) -131.40
Q57. For the concentration cell
M|𝑀+ (aq,0.01moldm-3) || M+ (aq,0.1mol dm-3)
the EMF (E) of the cell at temperate (T)equals
RT RT
(a) 2.303 F (b) -2.303 F
0 RT 0 RT
(c) Em + ⁄M + 2.303 (d) Em + ⁄M − 2.303
F F

Q58. Consider the cell :


Zn|Zn2+(a=0.01)||𝐹𝑒 2+ (𝑎 = 0.001),𝐹𝑒 3+ (a =0.01)|Pt
𝐸𝑐𝑒𝑙𝑙 = 1.71𝑉 at 250C for the above cell . The equilibrium constant for the reaction:
Zn + 2𝐹𝑒 3+ ⇄ 𝑍𝑛2+ + 2𝐹𝑒 2+ at 250 𝐶 would be close to
(a) 1027 (b) 1054
(c) 1081 (d) 1040

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VIGYAN VRIKSH |Electrochemistry

Q59. At 298K,the EMF of the cell


Pt|H2(1bar)|H+(solution)||𝐶𝑙 − |Hg2Cl2|Hg
is 0.7530V. The standard potential of the calomel electrode is 0.2802V. If the liquid junction potential
is zero, the pH of the solution is :
(a) 4.7 (b) 7.4
(c) 8.0 (d) 12.7
Q60. The solubility product of AgBr (s)is 5 × 10-13 at 298K. If the standard reduction potential of the half-
0 0
cell, 𝐸𝐴𝑔|𝐴𝑔𝐵𝑟(𝑠)𝐵𝑟 − is 0.07V, the standard reduction potential 𝐸 +
𝐴𝑔 |𝐴𝑔 (in volts)is ______.
𝜕𝐸
Q61. The temperature derivative of electrochemical potential E at constant pressure, (𝜕𝑇 ) is given by
𝑃
∆𝑆 ∆𝑆
(a) − 𝑛𝐹 (b) 𝑛𝐹
∆𝑆 ∆𝑆
(c) 𝑛𝐹𝑇 (d) − 𝑛𝐹𝑇

Q62. Given that 𝐸 0 (𝐶𝑙2⁄𝐶𝑙 − ) = 1.35𝑉 and 𝐾𝑠𝑝 (AgCl) = 10−10 at 250C, 𝐸 0 corresponding to the electrode
reaction
1 2.303𝑅𝑇
𝐶𝑙2 (𝑔) + 𝐴𝑔+ (so In.)+𝑒 − →AgCl(s) is [ = 0.06𝑉]
2 𝐹

(a) 0.75V (b) 1.05V


(c) 1.65V (d) 1.95V
Q63. The predicted electromotive force (emf) of the electrochemical cell
Fe (S)/𝐹𝑒 2+ (aq)(0.01M)||𝐶𝑑 2+ (aq)(0.01M)/Cd(s) is
0 0
(𝐸(𝐹𝑒 2+ ⁄𝐹𝑒 ) = −0.447𝑉 𝑎𝑛𝑑 𝐸(𝐶𝑑2+ ⁄𝐶𝑑) = −0.403𝑉)

(a) -0.850 V (b) -0.044 V


(c) +0.850 V (d) -0.044 V
0 0 0
Q64. The value of 𝐸𝐶𝑙𝑂 −
3 ⁄𝐶𝑙2
is [Given : 𝐸𝐶𝑙𝑂 −
3 ⁄𝐶𝑙
− = 0.627V and 𝐸𝐶𝑙 ⁄𝐶𝑙 − =1.36V]
2

(a) 0.4804V (b) 0.2804V


(c) 0.1804V (d) 0.1038V
Q65. For a cell Ag(s)|AgBr(s)|KBr(aq)|Hg2Br2(s)|Hg(ℓ), the emfs at several temperatures are
T/K 293 298 303
emf/V 0.0663 0.06839 0.07048
The change in entropy at 298K is _____JK-1.(Round off to two decimal places)(1F =96500C)
𝜕𝐸 0
Q66. For a half cell reaction of Mn𝑂4− → Mn𝑂2 in alkaline medium, ( 𝜕𝑇 ) = 7.6 ×10−5 𝑉𝐾 −1. The
𝑃

entropy change for the reaction in JK-1 is


(a) 82 (b) 54
(c) 36 (d) 22

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VIGYAN VRIKSH |Electrochemistry

Q67. The standard electrode potential of Cu/Cu+2 is -0.34 volt. At what concentration of ions will this
electrode potential be zero.
(a) 3.12 × 10-12 M (b) 4.12 × 10-14 M
(c) 5.60 × 10-16 M (d) 4.12 × 10-16 M
Q68. The chemical potential () of the 3 molal Na3PO4 in terms of mean ionic activity coefficient () at
temperature T is expressed as :-
(a) 0 + RT 𝑙n 3 +3RT ln 
(b) 0 + 7RT 𝑙n 3+ 4RT In 

(c) 0 + 3RT 𝑙n 3 + 2RT In 


(d) 0 + 4RT 𝑙n 
Q69. What will be the equilibrium constant of the following reaction at 298K
2𝐹𝑒 3+ + 𝑆𝑛2+ → 2𝐹𝑒 2+ + 𝑆𝑛4+
0 0
𝐸𝐹𝑒 3+ ⁄𝐹𝑒 2+ = 0.771V 𝐸𝑆𝑛 2+ ⁄𝑆𝑛+4 = -0.150V

(a) 1021 (b) 1031


(c) 1041 (d) None of these
Q70. The potential of the Ag+|Ag electrode (E0 = 0.799V) in a saturated solution of AgI (Ksp=10-16) is
[Given : 2.303 RT/F =0.06]
(a) 1.297V (b) 0.319V
(c) -1.279V (d) -0.319V

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