Electrochemistry Previous Year Questions — JEE Main Chemistry

40 past-year Electrochemistry questions from JEE Main (Chemistry) — page 7.

Q72 (2026)

Consider the following electrochemical cell at 298K $$Pt | HSnO_{2}^{-}(aq) | Sn(OH)_{6}^{2-}(aq) || Bi_{2}O_{3}(s) | Bi(s)$$ If the reaction quotient at a given time is $10^{6}$, then the cell EMF $(E_{\text{cell}})$ is $x \times 10^{-1}\text{ V}$ (Nearest integer). Given the standard half-cell reduction potential as $$E_{Bi_{2}O_{3}/Bi,OH^{-}}^{0} = -0.44\text{ V} \text{ and } E_{Sn(OH)_{6}^{2-}/HSnO_{2}^{-},OH^{-}}^{0} = -0.90\text{ V}$$
### Related Formula $$E_{cell} = E_{cell}^{\circ} - \frac{0.0591}{n} \log Q$$ (Using 0.06 for approximation if needed, as per standard practice unless specified). ### Core Logic First, calculate $E^{\circ}_{cell}$: $$E^{\circ}_{cell} = E^{\circ}_{cathode} - E^{\circ}_{anode}$$ $$E^{\circ}_{cell} = (-0.44\text{ V}) - (-0.90\text{ V}) = +0.46\text{ V}$$ Identify the number of transferred electrons ($n$) for the overall reaction. Anode reaction: $Sn^{2+} \rightarrow Sn^{4+} + 2e^{-}$ (Tin goes from +2 in $HSnO_2^-$ to +4 in $Sn(OH)_6^{2-}$). Cathode reaction: $Bi^{3+} + 3e^{-} \rightarrow Bi$ (Bismuth goes from +3 in $Bi_2O_3$ to 0). To balance the electrons, we multiply anode by 3 and cathode by 2, yielding $n = 6$ total electrons transferred. ### Step 1: Apply Nernst Equation Applying the Nernst equation (approximating 0.0591 to 0.06 for simplicity): $$E_{cell} = E^{\circ}_{cell} - \frac{0.06}{n} \log_{10} Q$$ $$E_{cell} = 0.46 - \frac{0.06}{6} \log_{10}(10^6)$$ $$E_{cell} = 0.46 - 0.01 \times 6$$ $$E_{cell} = 0.46 - 0.06 = 0.40\text{ V}$$ ### Step 2: Format Output The problem asks for the answer in the form $x \times 10^{-1}\text{ V}$. $$0.40 = 4 \times 10^{-1}$$ So, $x = 4$. ### Pattern Recognition Be extremely careful finding 'n'. You must balance the half-reactions. A +2 to +4 change (n=2) and a +3 to 0 change (n=3) resolves to a common multiple of 6. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Electrochemistry

Q67 (2026)

Consider the following reduction processes: $\text{Al}^{3+} + 3e^- \rightarrow \text{Al}(\text{s})$, $E^0 = -1.66\text{ V}$ $\text{Fe}^{3+} + e^- \rightarrow \text{Fe}^{2+}$, $E^0 = +0.77\text{ V}$ $\text{Co}^{3+} + e^- \rightarrow \text{Co}^{2+}$, $E^0 = +1.81\text{ V}$ $\text{Cr}^{3+} + 3e^- \rightarrow \text{Cr}(\text{s})$, $E^0 = -0.74\text{ V}$ The tendency to act as reducing agent decreases in the order:
  1. $\text{Al} > \text{Cr} > \text{Fe}^{2+} > \text{Co}^{2+}$
  2. $\text{Al} > \text{Fe}^{2+} > \text{Cr} > \text{Co}^{2+}$
  3. $\text{Al} > \text{Cr} > \text{Co}^{2+} > \text{Fe}^{2+}$
  4. $\text{Cr} > \text{Fe}^{2+} > \text{Al} > \text{Co}^{2+}$
### Related Formula $$\text{Reducing Power} \propto \frac{1}{\text{Standard Reduction Potential } (E^0_{red})}$$ ### Core Logic Step 1: List standard reduction potential values: - $E^0(\text{Al}^{3+}/\text{Al}) = -1.66\text{ V}$ - $E^0(\text{Cr}^{3+}/\text{Cr}) = -0.74\text{ V}$ - $E^0(\text{Fe}^{3+}/\text{Fe}^{2+}) = +0.77\text{ V}$ - $E^0(\text{Co}^{3+}/\text{Co}^{2+}) = +1.81\text{ V}$ Step 2: Arrange species in increasing order of $E^0_{red}$ (decreasing reducing power): $$\text{Al} > \text{Cr} > \text{Fe}^{2+} > \text{Co}^{2+}$$ ### Pattern Recognition Sees: Reduction potential values for reducing strength ordering. Shortcut: More negative standard reduction potential $\implies$ stronger reducing agent. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Electrochemistry

Q71 (2026)

Consider the following electrochemical cell: $$\text{Pt} \mid \text{O}_2(\text{g}) (1\text{ bar}) \mid \text{HCl}(\text{aq}) \mid\mid \text{M}^{2+}(\text{aq}, 1.0\text{ M}) \mid \text{M}(\text{s})$$ The pH above which, oxygen gas would start to evolve at anode is ____ (nearest integer). Given: $E^0_{\text{M}^{2+}/\text{M}} = 0.994\text{ V}$, $E^0_{\text{O}_2/\text{H}_2\text{O}} = 1.23\text{ V}$ standard reduction potential and $\frac{RT}{F}(2.303) = 0.059\text{ V}$ at the given condition
### Related Formula $$E_{\text{cell}} = E_{\text{Red}}(\text{cathode}) + E_{\text{Oxi}}(\text{anode}) > 0$$ $$E_{\text{Oxi}}(\text{anode}) = -E^0_{\text{O}_2/\text{H}_2\text{O}} - \frac{0.059}{2} \log \left([\text{H}^+]^2 P_{\text{O}_2}^{1/2}\right)$$ ### Core Logic Step 1: Set spontaneous cell reaction threshold ($E_{\text{cell}} = 0$): $$E_{\text{Oxi}}(\text{anode}) = -E_{\text{Red}}(\text{cathode}) = -0.994\text{ V}$$ Step 2: Anodic reaction: $$\text{H}_2\text{O} \rightarrow 2\text{H}^+ + \frac{1}{2}\text{O}_2 + 2e^-$$ $$E_{\text{Oxi}} = -1.23 - \frac{0.059}{2} \log \left([\text{H}^+]^2 \times 1^{1/2}\right) = -1.23 + 0.059 \times \text{pH}$$ Step 3: Equate oxidation potential: $$-0.994 = -1.23 + 0.059 \times \text{pH}$$ $$0.059 \times \text{pH} = 0.236$$ $$\text{pH} = \frac{0.236}{0.059} = 4$$ ### Pattern Recognition Sees: Minimum pH for gas evolution at anode. Shortcut: Apply $E_{\text{cell}} = 0$ threshold equation $-0.994 = -1.23 + 0.059 \text{pH} \implies \text{pH} = 4$. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Electrochemistry

Q55 (2026)

In the given electrochemical cell, $Ag(s)|AgCl(s)|Cl^{-}(aq) || FeCl_{2}(aq), FeCl_{3}(aq)|Pt(s)$ at 298 K, the cell potential ($E_{\text{cell}}$) will increase when : (A) Concentration of $Fe^{2+}$ is increased. (B) Concentration of $Fe^{3+}$ is decreased. (C) Concentration of $Fe^{2+}$ is decreased. (D) Concentration of $Fe^{3+}$ is increased. (E) Concentration of $Cl^{-}$ is increased. Choose the correct answer from the options given below :
  1. $\text{A and B only}$
  2. $\text{A and E only}$
  3. $\text{B only}$
  4. $\text{C, D and E only}$
### Related Formula $$E_{\text{cell}} = E^{\circ}_{\text{cell}} - \frac{0.059}{n} \log Q$$ ### Core Logic First, write the complete balanced cell reaction. At Anode (Oxidation): $Ag_{(s)} + Cl^-_{(aq)} \rightarrow AgCl_{(s)} + e^-$ At Cathode (Reduction): $Fe^{3+}_{(aq)} + e^- \rightarrow Fe^{2+}_{(aq)}$ Overall cell reaction: $$Ag_{(s)} + Cl^-_{(aq)} + Fe^{3+}_{(aq)} \rightarrow AgCl_{(s)} + Fe^{2+}_{(aq)}$$ ### Step 1: Applying the Nernst Equation Applying the Nernst equation at $298 \text{ K}$ with $n = 1$: $$E_{\text{cell}} = E^{\circ}_{\text{cell}} - \frac{0.059}{1} \log \frac{[Fe^{2+}]}{[Cl^-][Fe^{3+}]}$$ ### Step 2: Analysis of Variables To increase $E_{\text{cell}}$, the value of the logarithmic term $\log \frac{[Fe^{2+}]}{[Cl^-][Fe^{3+}]}$ must decrease. This happens if the numerator decreases or the denominator increases. - Decreasing $[Fe^{2+}]$ (Statement C) - Increasing $[Fe^{3+}]$ (Statement D) - Increasing $[Cl^-]$ (Statement E) Thus, statements C, D, and E will increase the cell potential. ### Pattern Recognition Nernst equation trick: $E_{\text{cell}}$ increases when product concentrations decrease or reactant concentrations increase (Le Chatelier's perspective of pushing the forward reaction). ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Electrochemistry

Q53 (2026)

{{IMG1}} Consider the above electrochemical cell where a metal electrode (M) is undergoing redox reaction by forming $M^{+}$ ($M \rightarrow M^{+} + e^{-}$). The cation $M^{+}$ is present in two different concentrations $c_{1}$ and $c_{2}$ as shown above. Which of the following statement is correct for generating a positive cell potential?
  1. $\text{If } c_1 \text{ is present at anode, then } c_1 = c_2$
  2. $\text{If } c_1 \text{ is present at cathode, then } c_1 < c_2$
  3. $\text{If } c_1 \text{ is present at cathode, then } c_1 > c_2$
  4. $\text{If } c_1 \text{ is present at anode, then } c_1 > c_2$
### Related Formula $$E_{\text{cell}} = E^{\circ}_{\text{cell}} - \frac{0.0591}{n} \log Q$$ For a concentration cell, $E^{\circ}_{\text{cell}} = 0$, so: $$E_{\text{cell}} = - \frac{0.0591}{n} \log \left( \frac{[\text{Anode}]}{[\text{Cathode}]} \right)$$ ### Core Logic For a concentration cell to have a positive cell potential ($E_{\text{cell}} > 0$), the ratio $\frac{[\text{Anode}]}{[\text{Cathode}]}$ must be less than $1$. This implies that $[\text{Anode}] < [\text{Cathode}]$. Let's evaluate the given conditions: **Case 1: If $c_1$ is at the anode.** Then $c_2$ is at the cathode. Cell reaction: $M(s) + M^{+}(c_2) \rightarrow M(s) + M^{+}(c_1)$ $$E_{\text{cell}} = -0.059 \log \frac{c_1}{c_2}$$ For $E_{\text{cell}} > 0$, we need $c_1 < c_2$. Option 1 says $c_1 = c_2$ (Incorrect). Option 4 says $c_1 > c_2$ (Incorrect). ### Step 1: Check Cathode Conditions **Case 2: If $c_1$ is at the cathode.** Then $c_2$ is at the anode. Cell reaction: $M(s) + M^{+}(c_1) \rightarrow M(s) + M^{+}(c_2)$ $$E_{\text{cell}} = -0.059 \log \frac{c_2}{c_1}$$ For $E_{\text{cell}} > 0$, we need $\frac{c_2}{c_1} < 1 \implies c_2 < c_1 \implies c_1 > c_2$. Option 2 says $c_1 < c_2$ (Incorrect). Option 3 says $c_1 > c_2$ (Correct). ### Pattern Recognition In any spontaneous concentration cell, ions flow from the higher concentration compartment to the lower concentration compartment. Thus, for a positive voltage, the cathode must always have the higher concentration. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Electrochemistry
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JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%) | JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%)

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