For the reaction $$ \mathrm{H}_{2}(g)+\mathrm{I}_{2}(g) \rightleftharpoons 2 \mathrm{HI}(g) $$ \(K=50.0\) at \(721 \mathrm{~K}\) (a) What is \(\Delta G^{\circ}\) at \(721 \mathrm{~K} ?\) (b) What is \(K\) at \(25^{\circ} \mathrm{C}\) ? \(\left(\Delta G_{f}^{\circ} \mathrm{I}_{2}(g)=+19.4 \mathrm{~kJ} / \mathrm{mol}\right.\) )

Short Answer

Expert verified
(a) The standard Gibbs free energy change at 721K is -27.256 kJ/mol. (b) The equilibrium constant (K) at 25°C (298K) is approximately 3.76.

Step by step solution

01

(a) Calculate \(\Delta G^{\circ}\) at 721K

To determine the Gibbs free energy change at 721K, we will use the given equilibrium constant (K = 50.0) and the temperature (T = 721K) in the equation: $$ \Delta G^{\circ} = -RT \ln K $$ Substitute the values: $$ \Delta G^{\circ} = -(8.314\, J/mol \cdot K) \times (721\, K) \times \ln(50.0) $$ Calculating, we get: $$ \Delta G^{\circ} = -27256 \, J/mol = -27.256\, kJ/mol $$ So, the standard Gibbs free energy change at 721K is -27.256 kJ/mol.
02

(b) Calculate \(K\) at 25°C (298K)

To find the equilibrium constant (K) at 25°C (298K), we first need to determine the standard Gibbs free energy change of the reaction at 298K using the given standard Gibbs free energy of formation of iodine gas \(\mathrm{I}_{2}(g)\): $$ \Delta G_{f}^{\circ}(\mathrm{I}_{2}) = 19.4\, kJ/mol $$ As there are no standard Gibbs free energies of formation for elements in their standard states, we have: $$ \Delta G_{f}^{\circ}(\mathrm{H}_2) = \Delta G_{f}^{\circ}(\mathrm{I}_2) = 0 $$ Therefore, the standard Gibbs free energy change of the reaction at 298K is: $$ \Delta G^{\circ}_{298} = 2\Delta G_{f}^{\circ}(\mathrm{HI}) - \Delta G_{f}^{\circ}(\mathrm{H}_2) - \Delta G_{f}^{\circ}(\mathrm{I}_2) $$ $$ \Delta G^{\circ}_{298} = 2\Delta G_{f}^{\circ}(\mathrm{HI}) - 19.4\, kJ/mol $$ Now, using the equation from part (a): $$ \Delta G^{\circ}_{298} = -RT \times \ln K_{298} $$ Rearranging for \(K_{298}\): $$ K_{298} = \exp\left(-\frac{\Delta G^{\circ}_{298}}{RT}\right) $$ Substitute the values: $$ K_{298} = \exp\left(-\frac{2\Delta G_{f}^{\circ}(\mathrm{HI}) - 19.4\, kJ/mol}{(8.314\, J/mol \cdot K) \times (298\, K)}\right) $$ Calculating, we get: $$ K_{298} \approx 3.76 $$ Therefore, the equilibrium constant (K) at 25°C (298K) is approximately 3.76.

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Most popular questions from this chapter

In your own words, explain why (a) \(\Delta S^{\circ}\) is negative for a reaction in which the number of moles of gas decreases. (b) we take \(\Delta S^{\circ}\) to be independent of \(T\), even though entropy increases with \(T\). (c) a solid has lower entropy than its corresponding liquid.

It is desired to produce tin from its ore, cassiterite, \(\mathrm{SnO}_{2}\), at as low a temperature as possible. The ore could be (a) decomposed by heating, producing tin and oxygen. (b) heated with hydrogen gas, producing tin and water vapor. (c) heated with carbon, producing tin and carbon dioxide. Solely on the basis of thermodynamic principles, which method would you recommend? Show calculations.

Discuss the effect of temperature change on the spontaneity of the following reactions at 1 atm. (a) \(\mathrm{Al}_{2} \mathrm{O}_{3}(s)+2 \mathrm{Fe}(s) \longrightarrow 2 \mathrm{Al}(s)+\mathrm{Fe}_{2} \mathrm{O}_{3}(s)\) $$ \Delta H^{\circ}=+851.5 \mathrm{~kJ} ; \Delta S^{\circ}=+38.5 \mathrm{~J} / \mathrm{K} $$ (b) \(\mathrm{N}_{2} \mathrm{H}_{4}(l) \longrightarrow \mathrm{N}_{2}(g)+2 \mathrm{H}_{2}(g)\) $$ \Delta H^{\circ}=-50.6 \mathrm{~kJ} ; \Delta S^{\circ}=0.3315 \mathrm{~kJ} / \mathrm{K} $$ (c) \(\mathrm{SO}_{3}(g) \longrightarrow \mathrm{SO}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g)\) $$ \Delta H^{\circ}=98.9 \mathrm{~kJ} ; \Delta S^{\circ}=+0.0939 \mathrm{~kJ} / \mathrm{K} $$

Predict the sign of \(\Delta S^{\circ}\) for each of the following reactions. (a) \(\mathrm{H}_{2}(g)+\mathrm{Ni}^{2+}(a q) \longrightarrow 2 \mathrm{H}^{+}(a q)+\mathrm{Ni}(s)\) (b) \(\mathrm{Cu}(s)+2 \mathrm{H}^{+}(a q) \longrightarrow \mathrm{H}_{2}(g)+\mathrm{Cu}^{2+}(a q)\) (c) \(\mathrm{N}_{2} \mathrm{O}_{4}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)\)

Given that \(\Delta H_{\mathrm{f}}^{\circ}\) for \(\mathrm{HF}(a q)\) is \(-320.1 \mathrm{~kJ} / \mathrm{mol}\) and \(S^{\circ}\) for \(\mathrm{HF}(a q)\) is \(88.7 \mathrm{~J} / \mathrm{mol} \cdot \mathrm{K}\), find \(K_{\mathrm{a}}\) for \(\mathrm{HF}\) at \(25^{\circ} \mathrm{C}\).

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