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Question #44206

Difficulty: 8/10 | 🟢 Free

The Question

Consider the elementary reversible gas-phase reaction \ceA(g)<=>B(g)\ce{A(g) <=> B(g)} at 300 K300\text{ K}. The standard Gibbs free energy change is ΔG∘=−300R J mol−1\Delta G^\circ = -300 R\text{ J mol}^{-1} and the standard entropy change is ΔS∘=−30R J K−1 mol−1\Delta S^\circ = -30 R\text{ J K}^{-1}\text{ mol}^{-1}. The temperature coefficient (Q10Q_{10}) for the forward reaction between 300 K300\text{ K} and 310 K310\text{ K} is given by ln⁡(Q10,f)=1.5\ln(Q_{10, f}) = 1.5. Assuming ΔH∘\Delta H^\circ and ΔS∘\Delta S^\circ are independent of temperature, what is the value of ln⁡(Q10,b)\ln(Q_{10, b}) for the backward reaction in the same temperature range? (RR is the universal gas constant)

Options

  • A.

    2.52.5

  • B.

    0.50.5

  • C.

    1.51.5

  • D.

    3.53.5

Check Your Answer

Correct Answer

Step-by-Step Solution

Explanation

How the Examiner Thinks

Mechanism_Trap

Don't get tricked by the process! Learn the mechanical traps used in competitive exam questions.

Concepts Behind This Question

State vs Path Functions|Gibbs Energy and Spontaneity|Temperature Coefficient (Q10)

Why This Question Is Tricky

Common Mistakes

This question tests the critical distinction between thermodynamic state functions (ΔG∘\Delta G^\circ, ΔH∘\Delta H^\circ) and path-dependent kinetic parameters (Q10Q_{10}, EaE_a).

The primary trap is the assumption that Gibbs Free Energy (ΔG∘\Delta G^\circ) dictates the temperature dependence of the reaction rate or equilibrium.

Students often erroneously substitute ΔG∘\Delta G^\circ into the Arrhenius or van 't Hoff equations instead of ΔH∘\Delta H^\circ.

A secondary trap involves a sign error in calculating ΔH∘\Delta H^\circ or setting up the ratio ln⁡(Q10,f)−ln⁡(Q10,b)\ln(Q_{10, f}) - \ln(Q_{10, b}), which leads directly to the distractor 0.5.

By forcing the calculation of ΔH∘\Delta H^\circ from ΔG∘\Delta G^\circ and ΔS∘\Delta S^\circ, the problem ensures the student understands that while ΔG∘\Delta G^\circ determines spontaneity at a specific temperature, ΔH∘\Delta H^\circ governs how the equilibrium shifts with temperature.

Quick Facts About This Question

Question Information

SubjectChemistry
ChapterThermodynamics - Class 11 Part 1
ConceptState vs Path Functions
Difficulty8
Cognitive Load7
Target Solve Time160 sec
AccessFree