Download JEE MCQs for JEE Chemistry: Electrochemistry
Access targeted multiple-choice questions for Electrochemistry designed to align with the latest JEE academic syllabus for JEE Chemistry. These objective practice sets help students evaluate their conceptual understanding and improve exam readiness.
Chapter-wise Objective Questions: Electrochemistry
Access the complete set of multiple-choice questions for Electrochemistry below. This focused format allows students to isolate specific topics for thorough review and uninterrupted practice alongside official JEE textbooks.
Multiple Choice Questions
(a) 40.3
(b) 18.3
(c) 66
(d) 31.6
Show Answer & Explanation
Answer: (c) 66
Explanation:
1. Chlorine changes from -1 in NaCl to +7 in \( \ce{NaClO4} \): 8 electrons per formula unit.
2. Moles of \( \ce{NaClO4} \) (122.5 g per mol) in 1000 g = 8.16.
3. Faradays = \( 8.16\times8\approx65.3\approx66 \).
Teacher's Note:
1. Faradays = moles x electrons per formula unit.
(a) II only
(b) I only
(c) I and II only
(d) I, II and III
Show Answer & Explanation
Answer: (a) II only
Explanation:
1. The potential depends on pH only if \( \ce{H+} \) (or \( \ce{OH-} \)) appears in the half-reaction.
2. \( \ce{AmO2^{2+} + 4H+ + 2e- -> Am^{4+} + 2H2O} \) contains H+, whereas the other two half-reactions are simple electron transfers without H+.
Teacher's Note:
1. Only half-cell reactions that involve H+ or OH- depend on pH.
(a) 0.03 V
(b) -0.06 V
(c) -0.03 V
(d) 0.06 V
Show Answer & Explanation
Answer: (d) 0.06 V
Explanation:
1. Left: \( [H^+]=K_a\frac{0.1}{1}=10^{-5} \) M. Right: \( [H^+]=K_a\frac11=10^{-4} \) M.
2. \( E=0.0591\log\frac{[H^+]_{right}}{[H^+]_{left}}=0.0591\log10=0.0591\approx0.06 \) V.
Teacher's Note:
1. Each side is a buffer; find [H+] from Henderson's equation.
(a) 0.059 V
(b) -0.0591 V
(c) 0.59 V
(d) 0.0259 V
Show Answer & Explanation
Answer: (b) -0.0591 V
Explanation:
1. For \( \ce{2H+ + 2e- -> H2} \): \( E=0-\frac{0.0591}{2}\log\frac{P_{H_2}}{[H^+]^2} \).
2. \( E=-0.02955\times\log100=-0.0591 \) V.
Teacher's Note:
1. Higher product pressure makes the reduction potential more negative.
(a) 3.04 V, -605.8 kJ per mol, 20000
(b) 3.04 V, -611.8 kJ per mol, 20000
(c) 3.04 V, +611.8 kJ per mol, 20000
(d) 3.13 V, -604 kJ per mol, 20
Show Answer & Explanation
Answer: (b) 3.04 V, -611.8 kJ per mol, 20000
Explanation:
1. \( Q=\frac{[Mg^{2+}]}{[Ag^+]^2}=\frac{0.02}{(0.001)^2}=2\times10^4 \).
2. \( E=3.17-\frac{0.0591}{2}\log(2\times10^4)=3.17-0.127=3.04 \) V.
3. \( \Delta G^\circ=-nFE^\circ=-2\times96500\times3.17=-611.8 \) kJ per mol.
Teacher's Note:
1. dG-standard uses E-standard, not the actual E.
(a) P > S > R > Q
(b) R > S > Q > P
(c) P > Q > R > S
(d) Q > R > S > P
Show Answer & Explanation
Answer: (d) Q > R > S > P
Explanation:
1. \( E=0.34+\frac{0.0591}{2}\log[Cu^{2+}] \).
2. Greater \( [Cu^{2+}] \) gives a higher reduction potential: 0.1 M > 0.01 M > 0.001 M > 0.0001 M.
Teacher's Note:
1. Higher ion concentration favours reduction.
(a) All of these
(b) The cell runs continuously as long as the fuels are supplied
(c) They are more efficient and free from pollution
(d) They are used to provide power and drinking water to astronauts in space programmes
Show Answer & Explanation
Answer: (a) All of these
Explanation:
1. Fuel cells run continuously while reactants are fed in.
2. They convert chemical energy directly with high efficiency and, in the hydrogen-oxygen cell, the only product is water, which is used as drinking water in space missions.
3. So all three statements are correct.
Teacher's Note:
1. H2-O2 fuel cells were used on spacecraft for power and water.
(a) 3, 1 and 2
(b) 3, 1 and 3
(c) 1, 3 and 2
(d) 2, 3 and 2
Show Answer & Explanation
Answer: (c) 1, 3 and 2
Explanation:
1. Equal charge deposits equal numbers of equivalents, so the masses are proportional to the equivalent weights: 2.1 : 2.7 : 7.2 = 7 : 9 : 24.
2. Equivalent weight = atomic weight / valency: A = 7/1, B = 27/3 = 9, C = 48/2 = 24.
3. Valencies are 1, 3 and 2.
Teacher's Note:
1. Faraday's second law: mass is proportional to equivalent weight.
(a) Different acids are used in the two compartments
(b) The EMF of a cell depends on the molarities of the acids used
(c) The pH of 0.1 M HCl and 0.1 M acetic acid is not the same
(d) The temperature is constant
Show Answer & Explanation
Answer: (c) The pH of 0.1 M HCl and 0.1 M acetic acid is not the same
Explanation:
1. Both electrodes are hydrogen electrodes at 1 atm, so the EMF depends only on the difference in \( [H^+] \).
2. HCl is strong (\( [H^+]=0.1 \) M) while acetic acid is weak (\( [H^+]\approx1.3\times10^{-3} \) M), so a potential develops.
Teacher's Note:
1. A concentration cell has zero EMF only if the two sides have equal [H+].
(a) \( \ce{Sn^{2+}} \) is a more powerful reducing agent than \( \ce{Hg2^{2+}} \)
(b) \( \ce{Pb^{2+}} \) is a more powerful reducing agent than \( \ce{Sn^{2+}} \)
(c) \( \ce{Sn^{4+}} \) is a more powerful oxidising agent than \( \ce{Pb^{4+}} \)
(d) \( \ce{Hg^{2+}} \) is a more powerful oxidising agent than \( \ce{Pb^{4+}} \)
Show Answer & Explanation
Answer: (a) \( \ce{Sn^{2+}} \) is a more powerful reducing agent than \( \ce{Hg2^{2+}} \)
Explanation:
1. The lower the reduction potential of a couple, the stronger the reducing agent of its reduced form.
2. \( \ce{Sn^{2+}} \) (0.15 V) is a stronger reductant than \( \ce{Hg2^{2+}} \) (0.92 V), and \( \ce{Pb^{2+}} \) (1.45 V) is a weaker reductant than Sn2+.
3. Pb(IV) (1.45 V) is a stronger oxidant than both Hg(II) (0.92 V) and Sn(IV) (0.15 V).
Teacher's Note:
1. High E means strong oxidant (oxidised form) and weak reductant (reduced form).
(a) 2 : 1
(b) 1 : 1
(c) 4 : 1
(d) 1 : 2
Show Answer & Explanation
Answer: (d) 1 : 2
Explanation:
1. CuCl contains \( \ce{Cu+} \): 1 F deposits 63.5 g.
2. \( \ce{CuSO4} \) contains \( \ce{Cu^{2+}} \): 1 F deposits 31.75 g.
3. Ratio \( \ce{CuSO4} \) : CuCl = 1 : 2.
Teacher's Note:
1. Mass deposited is inversely proportional to the charge on the ion for the same charge passed.
(a) 0.25
(b) 0.125
(c) 0.0125
(d) 1.25
Show Answer & Explanation
Answer: (b) 0.125
Explanation:
1. \( \Lambda_M=\frac{1000k}{C}=\frac{1000\times4.95\times10^{-5}}{0.00099}=50 \) S cm\(^2\) mol\(^{-1}\).
2. \( \alpha=\frac{\Lambda_M}{\Lambda_M^\infty}=\frac{50}{400}=0.125 \).
Teacher's Note:
1. Degree of dissociation = molar conductance / limiting molar conductance.
(a) 260
(b) 270
(c) 250
(d) 255
Show Answer & Explanation
Answer: (b) 270
Explanation:
1. Kohlrausch's law for strong electrolytes: \( \Lambda_m=\Lambda_m^\infty-A\sqrt C \).
2. \( 260=\Lambda^\infty-0.5A \) and \( 250=\Lambda^\infty-A \): subtracting gives \( A=20 \).
3. \( \Lambda^\infty=260+10=270 \).
Teacher's Note:
1. Plot or solve two equations in the square root of concentration.
(a) \( \ce{Ce^{4+}} > \ce{Cr2O7^{2-}} > \ce{Sn^{4+}} > \ce{MnO4-} \)
(b) \( \ce{Cr2O7^{2-}} > \ce{Sn^{4+}} > \ce{Ce^{4+}} > \ce{MnO4-} \)
(c) \( \ce{MnO4-} > \ce{Ce^{4+}} > \ce{Sn^{4+}} > \ce{Cr2O7^{2-}} \)
(d) \( \ce{Ce^{4+}} > \ce{MnO4-} > \ce{Cr2O7^{2-}} > \ce{Sn^{4+}} \)
Show Answer & Explanation
Answer: (d) \( \ce{Ce^{4+}} > \ce{MnO4-} > \ce{Cr2O7^{2-}} > \ce{Sn^{4+}} \)
Explanation:
1. A higher reduction potential means a stronger oxidising agent.
2. Order of E: 1.61 (Ce4+) > 1.51 (MnO4-) > 1.33 (Cr2O7 2-) > 0.15 (Sn4+).
Teacher's Note:
1. Rank by standard reduction potential.
(a) 2
(b) 1
(c) 3
(d) 4
Show Answer & Explanation
Answer: (a) 2
Explanation:
1. \( \ce{2H2 + O2 -> 2H2O} \) involves 4 electrons for 2 mol of water.
2. So 1 mol of water needs 2 mol of electrons, that is 2 faraday.
Teacher's Note:
1. Water has oxygen going from 0 to -2: two electrons per mole of water.
(a) 22.4
(b) 44.8
(c) 67.2
(d) 89.4
Show Answer & Explanation
Answer: (c) 67.2
Explanation:
1. \( \ce{2H2O -> 2H2 + O2} \) requires 4 mol of electrons for 2 mol \( \ce{H2} \) and 1 mol \( \ce{O2} \).
2. Total gas = 3 mol = \( 3\times22.4=67.2 \) L.
Teacher's Note:
1. 4 mol of e- gives 2 mol H2 at the cathode and 1 mol O2 at the anode.
(a) 250
(b) 196
(c) 392
(d) 384
Show Answer & Explanation
Answer: (c) 392
Explanation:
1. For a weak electrolyte, \( \alpha=\sqrt{K/C}=\sqrt{\frac{25\times10^{-6}}{0.01}}=0.05 \).
2. \( \Lambda^\infty=\frac{\Lambda}{\alpha}=\frac{19.6}{0.05}=392 \).
Teacher's Note:
1. Use alpha = root of K over C for a weak electrolyte.
(a) 6 : 3 : 2
(b) 1 : 2 : 3
(c) 2 : 1 : 3
(d) 3 : 2 : 1
Show Answer & Explanation
Answer: (a) 6 : 3 : 2
Explanation:
1. Ag+ needs 1 e-: 3 mol Ag. Cu2+ needs 2 e-: 1.5 mol Cu. Au3+ needs 3 e-: 1 mol Au.
2. Ratio = 3 : 1.5 : 1 = 6 : 3 : 2.
Teacher's Note:
1. Moles deposited = moles of electrons / charge on the ion.
(a) \( \frac{10^3y}{2(x_1+x_2-2x_3)} \)
(b) \( \frac{10^6y^2}{(x_1+x_2-2x_3)^2} \)
(c) \( \frac{x_1+x_2-2x_3}{10^6y} \)
(d) \( \frac{10^6y^2}{4(x_1+x_2-x_3)^2} \)
Show Answer & Explanation
Answer: (d) \( \frac{10^6y^2}{4(x_1+x_2-x_3)^2} \)
Explanation:
1. \( \Lambda^\infty_{eq}(\ce{BaSO4})=x_1+x_2-x_3 \) (Kohlrausch's law with equivalent conductances).
2. Normality of the saturated solution \( N=\frac{1000y}{x_1+x_2-x_3} \); molar solubility \( S=\frac N2 \) because 1 mol gives 2 equivalents.
3. \( K_{sp}=S^2=\frac{10^6y^2}{4(x_1+x_2-x_3)^2} \).
Teacher's Note:
1. For a sparingly soluble salt, Lambda at the saturation concentration is about Lambda-infinity.
(a) Only: Fe\(^{2+}\) solution is not stable in air
(b) All of these: Fe\(^{2+}\) solution is not stable in air, Fe nails can prevent oxidation of Fe\(^{2+}\) to Fe\(^{3+}\) by air, and corrosion of iron takes place by air
(c) Only: Fe nails can prevent oxidation of Fe\(^{2+}\) to Fe\(^{3+}\) by air
(d) Only: corrosion of iron takes place by air
Show Answer & Explanation
Answer: (b) All of these: Fe\(^{2+}\) solution is not stable in air, Fe nails can prevent oxidation of Fe\(^{2+}\) to Fe\(^{3+}\) by air, and corrosion of iron takes place by air
Explanation:
1. \( \ce{O2} \) oxidising \( \ce{Fe^{2+}} \): \( E=1.23-0.77=+0.46 \) V, spontaneous, so Fe2+ is not stable in air.
2. Fe reducing \( \ce{Fe^{3+}} \): \( E=0.77+0.44=+1.21 \) V, spontaneous, so iron nails keep iron in the +2 state.
3. Fe oxidised by \( \ce{O2} \): \( E=1.23+0.44=+1.67 \) V, so iron corrodes in air. All three are correct.
Teacher's Note:
1. Check the sign of the cell EMF for each pairing.
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