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Consider the following hypothetical equation $$ \mathrm{A}(s)+\mathrm{B}(s) \longrightarrow \mathrm{C}(s)+\mathrm{D}(s) $$ where \(\Delta H^{\circ}=492 \mathrm{~kJ}\) and \(\Delta S^{\circ}=327 \mathrm{~J} / \mathrm{K}\). (a) Obtain an expression for \(\Delta G^{\circ}\) as a function of temperature. Prepare a table of \(\Delta G^{\circ}\) values at \(100 \mathrm{~K}\) intervals $$ \text { between } 100 \mathrm{~K} \text { and } 500 \mathrm{~K} \text { . } $$ (b) Find the temperature at which \(\Delta G^{\circ}\) becomes zero.

Short Answer

Expert verified
Question: Calculate the values of ΔG° at temperature intervals of 100 K between 100 K and 500 K, and find the temperature at which ΔG° becomes zero for a given hypothetical reaction with ΔH° = 492 kJ and ΔS° = 327 J/K. Answer: The ΔG° values at every 100 K intervals between 100 K and 500 K are: 460000 J, 428000 J, 396000 J, 364000 J, and 332000 J. The temperature at which ΔG° becomes zero is approximately 1504.6 K.

Step by step solution

01

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

The relationship between the standard Gibbs free energy change (\(\Delta G^{\circ}\)), the standard enthalpy change (\(\Delta H^{\circ}\)), and the standard entropy change (\(\Delta S^{\circ}\)) is given by the expression: $$ \Delta G^{\circ} = \Delta H^{\circ} - T\Delta S^{\circ} $$ where \(T\) is the temperature in Kelvin.
02

Calculate \(\Delta G^{\circ}\) as a function of temperature

Since we are given \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\), we can substitute these values into the expression. The resulting equation for \(\Delta G^{\circ}\) as a function of temperature would be: $$ \Delta G^{\circ}(T) = (492 \, \mathrm{kJ}) - T(327 \, \mathrm{J/K}) $$ Don't forget to convert given \(\Delta H^{\circ}\) from kJ to J for consistency: $$ \Delta G^{\circ}(T) = (492\,000 \, \mathrm{J}) - T(327 \, \mathrm{J/K}) $$
03

Prepare a table for \(\Delta G^{\circ}\) values at 100 K intervals

Now that we have an expression for \(\Delta G^{\circ}\) as a function of temperature, we can calculate its values at temperature intervals of 100 K between 100 K and 500 K. The table for \(\Delta G^{\circ}\) values at each temperature: Temperature (K)|\(\Delta G^{\circ}\) (J) ---|--- 100| 460000 200| 428000 300| 396000 400| 364000 500| 332000
04

Find the temperature at which \(\Delta G^{\circ}\) becomes zero

To find the temperature at which \(\Delta G^{\circ}\) becomes zero, we simply need to set the expression for \(\Delta G^{\circ}\) equal to zero and solve for \(T\): $$ 492\,000\, \mathrm{J} - T(327 \, \mathrm{J/K}) = 0 $$ Rearrange the equation to solve for \(T\): $$ T = \frac{492\,000\, \mathrm{J}}{327 \, \mathrm{J/K}} $$ Calculate the temperature \(T\): $$ T \approx 1504.6 \mathrm{K} $$ So, the temperature at which \(\Delta G^{\circ}\) becomes zero is approximately 1504.6 K.

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Most popular questions from this chapter

Oxygen can be made in the laboratory by reacting sodium peroxide and water. $$ \begin{array}{l} 2 \mathrm{Na}_{2} \mathrm{O}_{2}(s)+2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow 4 \mathrm{NaOH}(s)+\mathrm{O}_{2}(g) \\ \Delta H^{\circ}=-109.0 \mathrm{~kJ} ; \Delta G^{\circ}=-148.4 \mathrm{~kJ} \text { at } 25^{\circ} \mathrm{C} \end{array} $$ (a) Calculate \(\Delta S^{\circ} .\) Is the sign reasonable? (b) Calculate \(S^{\circ}\) for \(\mathrm{Na}_{2} \mathrm{O}_{2}(s)\) (c) Calculate \(\Delta H_{\mathrm{f}}^{\circ}\) for \(\mathrm{Na}_{2} \mathrm{O}_{2}(s)\)

On the basis of your experience, predict which reactions are spontaneous: (a) \(\mathrm{PbO}_{2}(s) \longrightarrow \mathrm{Pb}(s)+\mathrm{O}_{2}(g)\) (b) \(\mathrm{N}_{2}(l) \longrightarrow \mathrm{N}_{2}(g)\) at \(25^{\circ} \mathrm{C}\) (c) \(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s) \longrightarrow \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(l)\) at \(25^{\circ} \mathrm{C}\) (d) \(\mathrm{Ca}^{2+}(a q)+\mathrm{CO}_{3}^{2-}(a q) \longrightarrow \mathrm{CaCO}_{3}(s)\)

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) \(\mathrm{N}_{2} \mathrm{O}_{4}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)\)

For the reaction $$ \mathrm{CO}(g)+3 \mathrm{H}_{2}(g) \rightleftharpoons \mathrm{CH}_{4}(g)+\mathrm{H}_{2} \mathrm{O}(g) $$ \(K=2.2 \times 10^{11}\) at \(473 \mathrm{~K}\) and \(4.6 \times 10^{8}\) at \(533 \mathrm{~K} .\) Calculate \(\Delta G^{\circ}\) at both temperatures.

At \(1200 \mathrm{~K},\) an equilibrium mixture of \(\mathrm{CO}\) and \(\mathrm{CO}_{2}\) gases contains 98.31 mol percent \(\mathrm{CO}\) and some solid carbon. The total pressure of the mixture is 1.00 atm. For the system $$ \mathrm{CO}_{2}(g)+\mathrm{C}(s) \rightleftharpoons 2 \mathrm{CO}(g) $$ calculate (a) \(P_{\mathrm{CO}}\) and \(P_{\mathrm{CO}_{2}}\) (b) \(K\) (c) \(\Delta G^{\circ}\) at \(1200 \mathrm{~K}\)

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