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The relationship between \(\Delta G^{\circ}\) and \(T\) is linear. Draw the graph of a reaction with the properties described below. You need only label the point at which \(\Delta G^{\circ}=0\). The reaction is exothermic. \(\Delta n_{\mathrm{g}}<0\left(\Delta n_{\mathrm{g}}=\right.\) moles of gas products \(-\) moles of gas reactants). At \(300 \mathrm{~K},\) the system is at equilibrium and \(K=1\).

Short Answer

Expert verified
The temperature at which ΔG°=0 for the given exothermic reaction with Δng<0 is 300 K. This is because, at equilibrium with K=1, ΔG° becomes 0 according to the equation ΔG° = -RT ln K.

Step by step solution

01

Recall the mathematical relationship between \(\Delta G^{\circ}\), \(\Delta H^{\circ}\), \(\Delta S^{\circ}\), and \(T\)

The relationship between Gibbs free energy change, enthalpy change, entropy change, and temperature is given by the following equation: \[\Delta G^{\circ} = \Delta H^{\circ} - T\Delta S^{\circ}\] We know that the reaction is exothermic, which means \(\Delta H^{\circ} < 0\). As \(\Delta n_{\mathrm{g}}<0\), the entropy change must be negative, which means \(\Delta S^{\circ} < 0\).
02

Determine \(\Delta G^{\circ}\) when \(K=1\)

At equilibrium, we can use the relationship between Gibbs free energy change and the equilibrium constant K: \[\Delta G^{\circ} = -RT \ln K\] Since at \(300\mathrm{~K}\), the system is at equilibrium and \(K=1\), we can substitute these values into the equation: \[\Delta G^{\circ}_{300} = - (8.314)(300) \ln1\] As \(\ln1 = 0\), we get \(\Delta G^{\circ}_{300} = 0\).
03

Draw the graph

Plot the Temperature \(T\) on the x-axis and Gibbs free energy change \(\Delta G^{\circ}\) on the y-axis. The graph of the reaction will be linear. Since we know that \(\Delta G^{\circ}_{300}=0\), we can label this point on the graph as \((300,0)\). Now, considering that the reaction is exothermic and \(\Delta n_{\mathrm{g}}<0\), the line should have a positive slope. In summary, the graph is a straight line with positive slope, having a point \((300,0)\) where \(\Delta G^{\circ}=0\).

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Most popular questions from this chapter

Consider the reaction $$ 2 \mathrm{HI}(g) \rightleftharpoons \mathrm{H}_{2}(g)+\mathrm{I}_{2}(g) $$ At \(500^{\circ} \mathrm{C}\), a flask initially has all three gases, each at a partial pressure of \(0.200 \mathrm{~atm}\). When equilibrium is established, the partial pressure of HI is determined to be 0.48 atm. What is \(\Delta G^{\circ}\) for the reaction at \(500^{\circ} \mathrm{C} ?\)

Predict the sign of \(\Delta S^{\circ}\) for each of the following reactions. (a) \(2 \mathrm{Na}(s)+\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{NaCl}(s)\) (b) \(2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)\) (c) \(\mathrm{C}_{2} \mathrm{H}_{4}(g)+3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)+3 \mathrm{H}_{2} \mathrm{O}(l)\) (d) \(\mathrm{NH}_{4} \mathrm{NO}_{3}(s)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow 2 \mathrm{NH}_{3}(g)+\mathrm{O}_{2}(g)\)

Consider the reaction $$ 2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g) $$ (a) Calculate \(\Delta G^{\circ}\) at \(25^{\circ} \mathrm{C}\). (b) If the partial pressures of \(\mathrm{SO}_{2}\) and \(\mathrm{SO}_{3}\) are kept at 0.400 atm, what partial pressure should \(\mathrm{O}_{2}\) have so that the reaction just becomes nonspontaneous (i.e., \(\Delta G=\) \(+1.0 \mathrm{~kJ}) ?\)

Discuss the effect of temperature on the spontaneity of reactions with the following values for \(\Delta H^{\circ}\) and \(\Delta S^{\circ} .\) $$ \begin{array}{l} \text { (a) } \Delta H^{\circ}=128 \mathrm{~kJ} ; \Delta S^{\circ}=89.5 \mathrm{~J} / \mathrm{K} \\ \text { (b) } \Delta H^{\circ}=-20.4 \mathrm{~kJ} ; \Delta S^{\circ}=-156.3 \mathrm{~J} / \mathrm{K} \end{array} $$ (c) \(\Delta H^{\circ}=-127 \mathrm{~kJ} ; \Delta S^{\circ}=43.2 \mathrm{~J} / \mathrm{K}\)

Consider the reaction $$ \mathrm{AgCl}(s) \longrightarrow \mathrm{Ag}^{+}(a q)+\mathrm{Cl}^{-}(a q) $$ (a) Calculate \(\Delta G^{\circ}\) at \(25^{\circ} \mathrm{C}\). (b) What should the concentration of \(\mathrm{Ag}^{+}\) and \(\mathrm{Cl}^{-}\) be so that \(\Delta G=-1.0 \mathrm{~kJ}\) (just spontaneous)? Take \(\left[\mathrm{Ag}^{+}\right]=\) \(\left[\mathrm{Cl}^{-}\right]\) (c) The \(K_{\mathrm{sp}}\) for \(\mathrm{AgCl}\) is \(1.8 \times 10^{-10} .\) Is the answer to \((\mathrm{b})\) reasonable?

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