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Question #44210

Difficulty: 8/10 | 🟢 Free

The Question

Consider the following gas-phase equilibria at 298 K298\text{ K}:

(1) \ceX(g)+2Y(g)⇌2Z(g)Kp1=2×108\ce{X(g) + 2Y(g) \rightleftharpoons 2Z(g)} \quad K_{p1} = 2 \times 10^8 (2) \ceZ(g)⇌W(g)+Y(g)Kp2=5×10−4\ce{Z(g) \rightleftharpoons W(g) + Y(g)} \quad K_{p2} = 5 \times 10^{-4}

A rigid reaction vessel at 298 K298\text{ K} contains the gases with the following instantaneous partial pressures: PX=0.5 barP_X = 0.5\text{ bar}, PY=2.0 barP_Y = 2.0\text{ bar}, PZ=1.0 barP_Z = 1.0\text{ bar}, and PW=5.0 barP_W = 5.0\text{ bar}.

For the overall transformation \ceX(g)⇌2W(g)\ce{X(g) \rightleftharpoons 2W(g)}, determine the standard Gibbs free energy change (ΔG∘\Delta G^\circ) and the actual Gibbs free energy change (ΔG\Delta G) at this instant.

Options

  • A.

    ΔG∘=−RTln⁡(50)\Delta G^\circ = -RT \ln(50), ΔG=0\Delta G = 0

  • B.

    ΔG∘=−RTln⁡(2×105)\Delta G^\circ = -RT \ln(2 \times 10^5), ΔG=−RTln⁡(4×103)\Delta G = -RT \ln(4 \times 10^3)

  • C.

    ΔG∘=−RTln⁡(105)\Delta G^\circ = -RT \ln(10^5), ΔG=−RTln⁡(2×103)\Delta G = -RT \ln(2 \times 10^3)

  • D.

    ΔG∘=−RTln⁡(50)\Delta G^\circ = -RT \ln(50), ΔG=RTln⁡(50)\Delta G = RT \ln(50)

Check Your Answer

Correct Answer

Step-by-Step Solution

Explanation

How the Examiner Thinks

Numerical_Precision

Improve calculation stamina and avoid rounding errors in high-stakes competitive examinations.

Concepts Behind This Question

State vs Path Functions|Stoichiometric Coefficient Division|Reaction Quotient vs. Equilibrium Constant

Why This Question Is Tricky

Common Mistakes

This problem tests the distinction between extensive state functions (ΔG∘\Delta G^\circ) and equilibrium constants (KK).

A common trap is treating KK linearly when multiplying stoichiometric coefficients (e.g., calculating Koverall=Kp1×2Kp2K_{overall} = K_{p1} \times 2K_{p2}), which leads to Option B.

Furthermore, it highlights a profound thermodynamic concept: an overall coupled reaction can have ΔG=0\Delta G = 0 (no driving force) even if its constituent elementary steps are far from equilibrium, emphasizing that QQ must be calculated strictly for the target stoichiometry.

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