JEE Challenger
More from Electrochemistry

Gibbs Free Energy Change for Given Concentration Cell

Comprehension Passage

Paragraph for Questions 31 and 32

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\text{M} \mid \text{M}^{2+} (\text{saturated solution of a sparingly soluble salt, MX}_2) \parallel \text{M}^{2+} (0.001 \text{ mol dm}^{-3}) \mid \text{M}

The emf of the cell depends on the difference in concentrations of M2+\text{M}^{2+} ions at the two electrodes. The emf of the cell at 298 K298 \text{ K} is 0.059 V0.059 \text{ V}.

The value of ΔG\Delta G (kJ mol−1\text{kJ mol}^{-1}) for the given cell is (take 1F=96500 C mol−11\text{F} = 96500 \text{ C mol}^{-1})

Options

A

−5.7-5.7

B

5.75.7

C

11.411.4

D

−11.4-11.4

Correct

Step-by-Step Solution

To calculate the change in Gibbs free energy (ΔG\Delta G) for the given concentration cell, we use the fundamental thermodynamic relation:

ΔG=−nFEcell\Delta G = -nFE_{\text{cell}}

Step 1: Identify the cell reactions and number of transferred electrons (nn)

The given cell representation is: M(s)∣Manode2+∥Mcathode2+∣M(s)\text{M(s)} \mid \text{M}^{2+}_{\text{anode}} \parallel \text{M}^{2+}_{\text{cathode}} \mid \text{M(s)}

The half-cell reactions are:

  • At Anode (Oxidation): M(s)→Manode2++2e−\text{M(s)} \rightarrow \text{M}^{2+}_{\text{anode}} + 2e^-
  • At Cathode (Reduction): Mcathode2++2e−→M(s)\text{M}^{2+}_{\text{cathode}} + 2e^- \rightarrow \text{M(s)}

Net Cell Reaction: Mcathode2+→Manode2+\text{M}^{2+}_{\text{cathode}} \rightarrow \text{M}^{2+}_{\text{anode}}

From the half-cell reactions, the number of moles of electrons transferred per mole of reaction is n=2n = 2.


Step 2: Calculate ΔG\Delta G

Given data:

  • n=2n = 2
  • F=96500 C mol−1F = 96500 \text{ C mol}^{-1}
  • Ecell=0.059 VE_{\text{cell}} = 0.059 \text{ V}

Substituting these values into the formula: ΔG=−2×96500 C mol−1×0.059 V\Delta G = -2 \times 96500 \text{ C mol}^{-1} \times 0.059 \text{ V}

ΔG=−11387 J mol−1\Delta G = -11387 \text{ J mol}^{-1}

Converting Joules to kilojoules (kJ\text{kJ}): ΔG=−113871000 kJ mol−1=−11.387 kJ mol−1≈−11.4 kJ mol−1\Delta G = -\frac{11387}{1000} \text{ kJ mol}^{-1} = -11.387 \text{ kJ mol}^{-1} \approx -11.4 \text{ kJ mol}^{-1}

Thus, the value of ΔG\Delta G is −11.4 kJ mol−1-11.4 \text{ kJ mol}^{-1}.

Correct Option: D