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NEET-UG and JEE Main Chemistry · Class 11

Cell potential, Gibbs energy and the equilibrium constant — NEET & JEE Questions

Cell potential, Gibbs energy and the equilibrium constant is a topic in Redox Reactions and Electrochemistry, a Class 11 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 12 published NEET-UG and JEE Main questions on Cell potential, Gibbs energy and the equilibrium constant, each with the marking scheme of the real paper.

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Cell potential, Gibbs energy and the equilibrium constant MCQs with solutions

10 of the 12 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.

  1. Question 1 · difficulty L1 · recall

    For an electrochemical cell reaction transferring nn electrons, the standard Gibbs energy change is related to standard cell potential by

    • A. ΔG∘=−nFE∘\Delta G^\circ=-nFE^\circ
    • B. ΔG∘=nFE∘\Delta G^\circ=nFE^\circ
    • C. ΔG∘=−FE∘/n\Delta G^\circ=-FE^\circ/n
    • D. ΔG∘=RT/E∘\Delta G^\circ=RT/E^\circ
  2. Question 2 · difficulty L2 · understanding

    A spontaneous galvanic cell reaction under standard conditions has

    • A. Ecell∘>0E^\circ_{cell}>0 and ΔG∘<0\Delta G^\circ<0
    • B. Ecell∘<0E^\circ_{cell}<0 and ΔG∘<0\Delta G^\circ<0
    • C. Ecell∘=0E^\circ_{cell}=0 always
    • D. Ecell∘>0E^\circ_{cell}>0 and ΔG∘>0\Delta G^\circ>0
  3. Question 3 · difficulty L2 · understanding

    At equilibrium for the overall cell reaction, the cell potential is

    • A. zero
    • B. always 1 V
    • C. infinite
    • D. equal to E∘E^\circ for every system
  4. Question 4 · difficulty L2 · understanding

    The relation between standard Gibbs energy and equilibrium constant is

    • A. ΔG∘=−RTln⁡K\Delta G^\circ=-RT\ln K
    • B. ΔG∘=RTln⁡K\Delta G^\circ=RT\ln K
    • C. ΔG∘=−KRT\Delta G^\circ=-KRT
    • D. K=−RT/ΔG∘K=-RT/\Delta G^\circ
  5. Question 5 · difficulty L3 · application

    A cell has E∘=1.10 VE^\circ=1.10\,\text{V} and transfers 2 electrons. What is ΔG∘\Delta G^\circ approximately? Take F=96500 C mol−1F=96500\,\text{C mol}^{-1}.

    • A. −212 kJ mol−1-212\,\text{kJ mol}^{-1}
    • B. −106 kJ mol−1-106\,\text{kJ mol}^{-1}
    • C. +212 kJ mol−1+212\,\text{kJ mol}^{-1}
    • D. +106 kJ mol−1+106\,\text{kJ mol}^{-1}
  6. Question 6 · difficulty L3 · application

    If Ecell∘E^\circ_{cell} is negative for a reaction as written, what can be concluded under standard conditions?

    • A. The reaction as written is non-spontaneous and the reverse is favoured
    • B. The reaction is necessarily at equilibrium
    • C. The reaction is spontaneous because voltage has a magnitude
    • D. No thermodynamic conclusion can be drawn
  7. Question 7 · difficulty L3 · application

    At 298 K, a cell transfers 2 electrons and has E∘=0.0591 VE^\circ=0.0591\,\text{V}. Approximately what is log⁡10K\log_{10}K?

    • A. 1
    • B. 2
    • C. 4
    • D. 10
  8. Question 8 · difficulty L3 · application

    If K=1K=1 for a cell reaction under standard-state definition at a given temperature, then

    • A. ΔG∘=0\Delta G^\circ=0 and E∘=0E^\circ=0
    • B. ΔG∘<0\Delta G^\circ<0 and E∘>0E^\circ>0
    • C. ΔG∘>0\Delta G^\circ>0 and E∘<0E^\circ<0
    • D. E∘E^\circ must be 1 V
  9. Question 9 · difficulty L4 · application

    A cell reaction has n=1n=1 and E∘=0.1182 VE^\circ=0.1182\,\text{V} at 298 K. What is KK approximately?

    • A. 1010
    • B. 10210^2
    • C. 10410^4
    • D. 10−210^{-2}
  10. Question 10 · difficulty L4 · application

    A reaction has ΔG∘=−57.9 kJ mol−1\Delta G^\circ=-57.9\,\text{kJ mol}^{-1} and transfers 2 electrons. Take F=96500F=96500. What is E∘E^\circ approximately?

    • A. 0.15 V
    • B. 0.30 V
    • C. 0.60 V
    • D. 1.20 V

Common mistakes in Cell potential, Gibbs energy and the equilibrium constant

Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.

  • Uses $0.0591\log K$ without dividing by the electron number.
  • Treats the equilibrium constant as independent of the electrochemical driving force.

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