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Question #44068

Difficulty: 8/10 | 🟢 Free

The Question

The standard Gibbs free energy change for the dissolution and dissociation of a gaseous weak acid \ceHA(g)\ce{HA(g)} in water at 320 K320\text{ K} is ΔG∘=12.25 kJ mol−1\Delta G^\circ = 12.25\text{ kJ mol}^{-1}. \ceHA(g)<=>H+(aq)+A−(aq)\ce{HA(g) <=> H+(aq) + A-(aq)} The standard states are defined as P∘=1 barP^\circ = 1\text{ bar} for the gas and m∘=1 mol kg−1m^\circ = 1\text{ mol kg}^{-1} for the aqueous species. At 320 K320\text{ K}, the density of pure water is 0.95 kg L−10.95\text{ kg L}^{-1}.

If the equilibrium pressure of \ceHA(g)\ce{HA(g)} is maintained at 1 atm1\text{ atm} (1 atm=1.013 bar1\text{ atm} = 1.013\text{ bar}), what is the equilibrium concentration of \ceH+(aq)\ce{H+(aq)} in molarity (mol L−1\text{mol L}^{-1})?

Assume ideal behavior for the gas and the solution, and that the solution is sufficiently dilute such that its density equals that of pure water. (Given: R=8.314 J K−1 mol−1R = 8.314\text{ J K}^{-1}\text{ mol}^{-1}, e−4.604=0.01e^{-4.604} = 0.01)

Options

  • A.

    0.0956 mol L−10.0956\text{ mol L}^{-1}

  • B.

    0.1006 mol L−10.1006\text{ mol L}^{-1}

  • C.

    0.0950 mol L−10.0950\text{ mol L}^{-1}

  • D.

    0.1000 mol L−10.1000\text{ mol L}^{-1}

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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

Relationship between Kp and Kc|Concentration Units Dependency|Spontaneity Criteria

Why This Question Is Tricky

Common Mistakes

This question tests the rigorous thermodynamic definition of the equilibrium constant K∘K^\circ using activities.

Students often fall into two traps: (1) Ignoring the standard state pressure (1 bar1\text{ bar}) and directly using 1 atm1\text{ atm}, which leads to an incorrect activity for the gas. (2) Assuming that K∘K^\circ directly yields molarity (mol L−1\text{mol L}^{-1}).

In rigorous thermodynamics, the standard state for solutes is molality (1 mol kg−11\text{ mol kg}^{-1}).

To find molarity, one must account for the solvent's density at the given temperature.

Failing the pressure conversion yields 0.0950 M0.0950\text{ M}, failing the density conversion yields 0.1006 M0.1006\text{ M}, and failing both yields 0.1000 M0.1000\text{ M}.

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Question Information

SubjectChemistry
ChapterEquilibrium - Class 11 Part 1
ConceptRelationship between Kp and Kc
Difficulty8
Cognitive Load7
Target Solve Time160 sec
AccessFree