Download JEE MCQs for JEE Chemistry: Electrochemistry
Review structured MCQ sets for JEE Chemistry Electrochemistry. Built according to official JEE guidelines, these downloadable questions support daily revision and core concept reinforcement.
Chapter-wise Objective Questions: Electrochemistry
Navigate directly to the 50 objective questions for Electrochemistry using the digital viewer below. Each practice set includes verified answer keys, allowing students to instantly cross-check their work and identify areas requiring further revision.
Multiple Choice Questions
(a) 347 S cm² mol⁻¹
(b) 271.6 S cm² mol⁻¹
(c) 42.7 S cm² mol⁻¹
(d) 195.3 S cm² mol⁻¹
Show Answer & Explanation
Answer: (b) 271.6 S cm² mol⁻¹
Explanation:
1. CaCl₂ gives one Ca²⁺ and two Cl⁻.
2. Λ°m = 119 + 2 × 76.3 = 271.6 S cm² mol⁻¹.
Teacher's Note:
1. Multiply each ionic value by the number of ions in the formula.
2. Kohlrausch's law for molar conductivity.
(a) BrO₃⁻
(b) BrO₄⁻
(c) Br₂
(d) HBrO
Show Answer & Explanation
Answer: (d) HBrO
Explanation:
1. A species disproportionates if its reduction potential to the lower state is greater than the potential for the oxidation to the upper state.
2. For HBrO, E° for HBrO → Br₂ is 1.595 V, which is greater than 1.5 V for BrO₃⁻ → HBrO, so HBrO disproportionates.
Teacher's Note:
1. The right-hand potential must exceed the left-hand potential.
2. Check each intermediate species in the same way.
(a) 100
(b) 1000
(c) 500
(d) 50
Show Answer & Explanation
Answer: (b) 1000
Explanation:
1. κ = (1/R)(ℓ/A) = (1/1000) × 100 = 0.1 S cm⁻¹.
2. Λm = κ × 1000 / M = 0.1 × 1000 / 0.1 = 1000 S cm² mol⁻¹.
Teacher's Note:
1. Cell constant is ℓ/A = 100 cm⁻¹.
2. Resistance 1 kΩ is 1000 Ω.
(a) 2.67
(b) 2.13
(c) 3.27
(d) 3.041
Show Answer & Explanation
Answer: (d) 3.041
Explanation:
1. E = 3.17 − (0.0591/2) log(0.02/(10⁻³)²) = 3.17 − 0.02955 × log(2 × 10⁴).
2. log(2 × 10⁴) = 4.301, so E = 3.17 − 0.127 = 3.043 V ≈ 3.04 V.
Teacher's Note:
1. Substitute the ion concentrations into the reaction quotient.
2. The Ag⁺ concentration is squared.
(a) 630 ohm⁻¹ cm² mol⁻¹
(b) 315 ohm⁻¹ cm² mol⁻¹
(c) 100 ohm⁻¹ cm² mol⁻¹
(d) 6.300 ohm⁻¹ cm² mol⁻¹
Show Answer & Explanation
Answer: (a) 630 ohm⁻¹ cm² mol⁻¹
Explanation:
1. Λm = κ × 1000 / M = 6.3 × 10⁻² × 1000 / 0.1.
2. = 630 ohm⁻¹ cm² mol⁻¹.
Teacher's Note:
1. Multiply κ by 1000 and divide by the molarity.
2. Check that κ is in ohm⁻¹ cm⁻¹.
(a) 0.1 M fluoroacetic acid
(b) 0.1 M difluoroacetic acid
(c) 0.1 M acetic acid
(d) 0.1 M chloroacetic acid
Show Answer & Explanation
Answer: (b) 0.1 M difluoroacetic acid
Explanation:
1. Fluorine is strongly electron withdrawing, and two fluorine atoms make difluoroacetic acid the strongest acid of the four.
2. It ionises most, giving the highest ion concentration and the highest conductivity.
Teacher's Note:
1. Conductivity of a weak electrolyte depends on its degree of ionisation.
2. More electron-withdrawing groups give a stronger acid.
(a) 124 × 10⁻⁴ S m² mol⁻¹
(b) 1240 × 10⁻⁴ S m² mol⁻¹
(c) 1.24 × 10⁻⁴ S m² mol⁻¹
(d) 12.4 × 10⁻⁴ S m² mol⁻¹
Show Answer & Explanation
Answer: (a) 124 × 10⁻⁴ S m² mol⁻¹
Explanation:
1. Cell constant = κR = 1.29 × 100 = 129 m⁻¹.
2. For 0.02 M, κ = 129/520 = 0.2481 S m⁻¹, and Λm = κ / C = 0.2481 / 20 mol m⁻³ = 1.24 × 10⁻² S m² mol⁻¹ = 124 × 10⁻⁴ S m² mol⁻¹.
Teacher's Note:
1. In SI units the concentration must be in mol m⁻³ (0.02 M = 20 mol m⁻³).
2. Find the cell constant from the first solution.
(a) λC = λ∞ − B√C
(b) λC = λ∞ + B√C
(c) λC = λ∞ + B C
(d) λC = λ∞ − B C
Show Answer & Explanation
Answer: (a) λC = λ∞ − B√C
Explanation:
1. The Debye-Hückel-Onsager equation for strong electrolytes is Λ = Λ° − b√C.
2. So λC = λ∞ − B√C.
Teacher's Note:
1. A graph of Λ against √C is a straight line with negative slope for strong electrolytes.
2. The intercept gives the limiting value.
(a) Electrons flow from the copper electrode to the zinc electrode
(b) Current flows from the zinc electrode to the copper electrode
(c) Cations move towards the copper electrode
(d) Cations move towards the zinc electrode
Show Answer & Explanation
Answer: (c) Cations move towards the copper electrode
Explanation:
1. Zn is the anode and Cu is the cathode.
2. Electrons flow from Zn to Cu and the current flows from Cu to Zn in the external wire, and cations move towards the cathode (Cu), so (c) is true.
Teacher's Note:
1. Cations go to the cathode and anions go to the anode in any cell.
2. Check electrons and current directions separately.
(a) −3.26 V
(b) +1.66 V
(c) −1.66 V
(d) +3.26 V
Show Answer & Explanation
Answer: (c) −1.66 V
Explanation:
1. Al is the anode and Ag is the cathode.
2. E°cell = 0.80 − E°(Al) = 2.46, so E°(Al³⁺/Al) = −1.66 V.
Teacher's Note:
1. Al displaces hydrogen, so its reduction potential is negative.
2. Solve for the unknown anode potential.
(a) 1.07 V
(b) 0.82 V
(c) 2.14 V
(d) 1.80 V
Show Answer & Explanation
Answer: (a) 1.07 V
Explanation:
1. E = E° − (0.0591/2) log([Zn²⁺]/[Cu²⁺]) = 1.10 − 0.02955 × log(1/0.1).
2. = 1.10 − 0.02955 = 1.07 V.
Teacher's Note:
1. Product concentration greater than reactant concentration lowers E.
2. n = 2 for this cell.
(a) increase the Ecell and shift the equilibrium to the right
(b) lower the Ecell and shift the equilibrium to the right
(c) lower the Ecell and shift the equilibrium to the left
(d) increase the Ecell and shift the equilibrium to the left
Show Answer & Explanation
Answer: (a) increase the Ecell and shift the equilibrium to the right
Explanation:
1. H⁺ is a reactant, and adding acid increases [H⁺] and so lowers Q.
2. E = E° − (0.0591/2) log Q rises, and the equilibrium shifts to the right.
Teacher's Note:
1. Raising a reactant concentration favours the forward reaction.
2. The emf rises as Q falls.
(a) p(H₂) = 2 atm and [H⁺] = 1.0 M
(b) p(H₂) = 2 atm and [H⁺] = 2.0 M
(c) p(H₂) = 1 atm and [H⁺] = 2.0 M
(d) p(H₂) = 1 atm and [H⁺] = 1.0 M
Show Answer & Explanation
Answer: (a) p(H₂) = 2 atm and [H⁺] = 1.0 M
Explanation:
1. E = −(0.0591/2) log (p(H₂)/[H⁺]²).
2. E is negative when p(H₂)/[H⁺]² > 1, which is true for p = 2 atm and [H⁺] = 1 M (ratio 2).
Teacher's Note:
1. Compare p(H₂) with [H⁺]².
2. Options (b) and (c) give a ratio below 1, option (d) gives E = 0.
(a) 10
(b) 1 × 10¹⁰
(c) 1 × 10⁻¹⁰
(d) 29.5 × 10⁻²
Show Answer & Explanation
Answer: (b) 1 × 10¹⁰
Explanation:
1. log K = nE° / 0.0591 = 2 × 0.295 / 0.0591 = 9.98.
2. K ≈ 10¹⁰.
Teacher's Note:
1. Use n = 2.
2. Round the logarithm to the nearest whole number.
(a) −ve, < 1, −ve
(b) −ve, > 1, −ve
(c) −ve, > 1, +ve
(d) +ve, > 1, −ve
Show Answer & Explanation
Answer: (c) −ve, > 1, +ve
Explanation:
1. A spontaneous reaction has ΔG < 0.
2. Then E°cell = −ΔG°/nF > 0 and K > 1.
Teacher's Note:
1. ΔG = −nFE and ΔG° = −RT ln K.
2. All three quantities point the same way.
(a) 2.14 V
(b) 4.28 V
(c) 6.42 V
(d) 8.56 V
Show Answer & Explanation
Answer: (a) 2.14 V
Explanation:
1. Four electrons are transferred per mole of O₂ in the reaction.
2. E = −ΔG / nF = 827000 / (4 × 96500) = 2.14 V.
Teacher's Note:
1. The minimum emf for electrolysis equals the emf of the reverse galvanic reaction.
2. n = 4 for one O₂.
(a) −0.33 V ; the reaction will not occur
(b) −0.33 V ; the reaction will occur
(c) −2.69 V ; the reaction will not occur
(d) −2.69 V ; the reaction will occur
Show Answer & Explanation
Answer: (c) −2.69 V ; the reaction will not occur
Explanation:
1. Mn²⁺ is both reduced to Mn (E° = −1.18 V) and oxidised to Mn³⁺ (reverse of +1.51 V).
2. E°cell = −1.18 − 1.51 = −2.69 V, which is negative, so the disproportionation will not occur.
Teacher's Note:
1. Add the reduction potential of the reduced step and the oxidation potential of the oxidised step.
2. A negative E° means the reaction is non-spontaneous.
(a) −8.12
(b) +8.612
(c) −37.83
(d) −16.13
Show Answer & Explanation
Answer: (d) −16.13
Explanation:
1. AgI(s) ⇌ Ag⁺ + I⁻ is obtained by adding Ag → Ag⁺ + e⁻ (−0.800 V) and AgI + e⁻ → Ag + I⁻ (−0.152 V).
2. E° = −0.952 V, so log Ksp = nE°/0.059 = −0.952 / 0.059 = −16.13.
Teacher's Note:
1. Reverse the first given reaction to get the reduction of AgI.
2. The solubility product is very small, so log Ksp is a large negative number.
(a) Cu
(b) Cr
(c) Ag
(d) Ca
Show Answer & Explanation
Answer: (d) Ca
Explanation:
1. In an aqueous solution, water is reduced in preference to Ca²⁺ because Ca has a much lower reduction potential (−2.87 V).
2. So calcium cannot be obtained by electrolysis of aqueous solutions.
Teacher's Note:
1. Highly electropositive metals such as Na, K and Ca are obtained from molten salts.
2. Cu, Cr and Ag can be electroplated.
(a) 5.49 × 10⁴ C of electric charge
(b) 5.49 × 10¹ C of electric charge
(c) 5.49 × 10⁷ C of electric charge
(d) 1.83 × 10⁷ C of electric charge
Show Answer & Explanation
Answer: (c) 5.49 × 10⁷ C of electric charge
Explanation:
1. 5.12 kg = 5120 g = 189.6 mol of Al, needing 3 F per mole, which is 568.9 F.
2. Charge = 568.9 × 96500 = 5.49 × 10⁷ C.
Teacher's Note:
1. Convert kilograms to grams before finding moles.
2. Each Al³⁺ needs 3 electrons.
(a) 0.4012 g and 0.8024 g
(b) 0.4012 g and 0.2006 g
(c) 0.2006 g and 0.4012 g
(d) 0.1003 g and 0.2006 g
Show Answer & Explanation
Answer: (c) 0.2006 g and 0.4012 g
Explanation:
1. 0.216 g Ag is 0.002 mol, so 0.002 F passed.
2. Hg²⁺ (cell Q) needs 2 F per mole, giving 0.001 mol = 0.2006 g, and Hg⁺ (cell R) needs 1 F per mole, giving 0.002 mol = 0.4012 g.
Teacher's Note:
1. Mercuric ion is Hg²⁺ and mercurous nitrate contains Hg⁺ (as Hg₂²⁺ in the dimer, the charge per Hg is 1).
2. The same charge passes through all cells in series.
(a) 1.1 hr
(b) 46 hr
(c) 53.6 hr
(d) 24.00 hr
Show Answer & Explanation
Answer: (c) 53.6 hr
Explanation:
1. Zn = 100/65 = 1.54 mol but Cu²⁺ = 1.0 mol only, so Cu²⁺ is the limiting reagent.
2. Charge available = 1.0 × 2 F = 193000 C, and t = 193000 / 1.0 A = 193000 s = 53.6 hours.
Teacher's Note:
1. Find the limiting reactant first.
2. The cell stops when either the zinc or Cu²⁺ is used up.
(a) 1.1180 g
(b) 0.11180 g
(c) 5.590 g
(d) 0.5590 g
Show Answer & Explanation
Answer: (b) 0.11180 g
Explanation:
1. Charge = 0.5 × 200 = 100 C.
2. Mass = Z × Q = 0.0011180 × 100 = 0.1118 g.
Teacher's Note:
1. Electrochemical equivalent is the mass deposited per coulomb.
2. W = Z I t.
(a) 2.0 g
(b) 8.0 g
(c) 4.0 g
(d) 1.0 g
Show Answer & Explanation
Answer: (c) 4.0 g
Explanation:
1. Charge = 9.65 × 1000 = 9650 C = 0.1 F, and one mole of OH⁻ (hence NaOH) is formed per faraday.
2. Mass of NaOH = 0.1 × 40 = 4.0 g.
Teacher's Note:
1. At the cathode, 2H₂O + 2e⁻ → H₂ + 2OH⁻.
2. One F gives one mole of OH⁻.
(a) 56 cm³
(b) 550 cm³
(c) 5.6 cm³
(d) 11.2 cm³
Show Answer & Explanation
Answer: (c) 5.6 cm³
Explanation:
1. 0.108 g Ag = 0.001 mol, so the charge is 0.001 F.
2. O₂ evolved = 0.001/4 = 0.00025 mol = 0.00025 × 22400 cm³ = 5.6 cm³.
Teacher's Note:
1. Four faradays liberate one mole of O₂.
2. Equal charge passes through both voltameters.
(a) ΔH / ΔG
(b) nFE / ΔG
(c) −nFE / ΔH
(d) zero
Show Answer & Explanation
Answer: (c) −nFE / ΔH
Explanation:
1. Efficiency = (useful electrical work) / (enthalpy change) = ΔG / ΔH.
2. Since ΔG = −nFE, this equals −nFE / ΔH.
Teacher's Note:
1. Maximum work is −ΔG = nFE.
2. The enthalpy change is the total energy available.
(a) M/2
(b) M/4
(c) M
(d) zero
Show Answer & Explanation
Answer: (d) zero
Explanation:
1. Cu²⁺ + 2e⁻ → Cu, so 2 F deposits 1 mol of Cu²⁺.
2. The solution contained only 1 mol, so all Cu²⁺ is used up and the molarity becomes zero.
Teacher's Note:
1. Compare the charge passed with the charge required for complete deposition.
2. Here both are equal.
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Practice MCQs for JEE Chemistry Electrochemistry
About Electrochemistry MCQs for JEE Chemistry
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