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Electrochemistry question

2012 · Shift 2 · Q2
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  5. /2012 · Shift 2 · Q2

Electrochemistry question

2012 · Shift 2 · Q2

JEE AdvancedChemistryElectrochemistryMCQ+4 / −1
The electrochemical cell shown below is a concentration cell. M | M2+M^{2+}M2+ (saturated solution of a sparingly soluble salt, MX2MX_2MX2​) || M2+M^{2+}M2+ (0.001 mol dm–3) | M The emf of the cell depends on the difference in concentrations of M2+M^{2+}M2+ ions at the two electrodes. The emf of the cell at 298 K is 0.059 V. The value of ∆G (kJ mol–1) for the given cell is (take 1F = 96500 C mol–1)
  1. A
    –5.7
  2. B
    5.7
  3. C
    11.4
  4. D
    -11.4
View written solutionFree

Correct answer: D

  1. Use the relation between Gibbs free energy and emf

For an electrochemical cell,

ΔG=−nFEcell\Delta G = -n F E_{\text{cell}}ΔG=−nFEcell​

where:

  • nnn = number of electrons transferred
  • F=96500 C mol−1F = 96500\ \text{C mol}^{-1}F=96500 C mol−1
  • Ecell=0.059 VE_{\text{cell}} = 0.059\ \text{V}Ecell​=0.059 V
  1. Find nnn

The electrode process is:

M2++2e−⇌MM^{2+} + 2e^- \rightleftharpoons MM2++2e−⇌M

So, the number of electrons transferred is

n=2n=2n=2
  1. Calculate ΔG\Delta GΔG
ΔG=−(2)(96500)(0.059)\Delta G = -(2)(96500)(0.059)ΔG=−(2)(96500)(0.059)

First compute:

96500×0.059=5693.596500 \times 0.059 = 5693.596500×0.059=5693.5

Then,

ΔG=−2×5693.5=−11387 J mol−1\Delta G = -2 \times 5693.5 = -11387\ \text{J mol}^{-1}ΔG=−2×5693.5=−11387 J mol−1
  1. Convert to kJ mol−1^{-1}−1
ΔG=−11.387 kJ mol−1\Delta G = -11.387\ \text{kJ mol}^{-1}ΔG=−11.387 kJ mol−1

Rounding,

ΔG≈−11.4 kJ mol−1\Delta G \approx -11.4\ \text{kJ mol}^{-1}ΔG≈−11.4 kJ mol−1
  1. Match with the options

The correct option is:

D: −11.4\boxed{\text{D: } -11.4}D: −11.4​
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