Given the following data: $$\begin{aligned}2 \mathrm{H}_{2}(g)+\mathrm{C}(s) \longrightarrow \mathrm{CH}_{4}(g) & & \Delta G^{\circ}=-51 \mathrm{~kJ} \\ 2 \mathrm{H}_{2}(\mathrm{~g})+\mathrm{O}_{2}(g) & \Delta \mathrm{H}_{2} \mathrm{O}(l) & & \Delta G^{\circ}=-474 \mathrm{~kJ} \\ \mathrm{C}(s)+\mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g) & \Delta G^{\circ} &=-394 \mathrm{~kJ}\end{aligned}$$ Calculate \(\Delta G^{\circ}\) for \(\mathrm{CH}_{4}(\mathrm{~g})+2 \mathrm{O}_{2}(\mathrm{~g}) \rightarrow \mathrm{CO}_{2}(\mathrm{~g})+2 \mathrm{H}_{2} \mathrm{O}(l) .\)

Short Answer

Expert verified
The standard Gibbs free energy change for the target reaction, \( \mathrm{CH}_{4}(g)+2\ \mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g)+2\ \mathrm{H}_{2}O(l) \), is \(\Delta G^{\circ} = -131\ \mathrm{kJ}\).

Step by step solution

01

Identify the target reaction

The target reaction for which we have to find the standard Gibbs free energy change is: \( \mathrm{CH}_{4}(g)+2\ \mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g)+2\ \mathrm{H}_{2}O(l) \)
02

Combine given reactions to match the target reaction

We need to find a way to combine the given reactions in a way that will result in the target reaction. After examination, we can see that adding the 1st and 2nd reactions, and then the 3rd reaction in reverse, will resemble our target reaction: (1) \( 2 \mathrm{H}_{2}(g)+\mathrm{C}(s) \longrightarrow \mathrm{CH}_{4}(g) \) (2) \( 2 \mathrm{H}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{H}_{2}O(l) \) (3, reverse) \( \mathrm{CO}_{2}(g) \longrightarrow \mathrm{C}(s)+\mathrm{O}_{2}(g) \) >equals> \( \mathrm{CH}_{4}(g) + 2\ \mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g) + 2\ \mathrm{H}_{2}O(l) \)
03

Calculate \(\Delta G^{\circ}\) for the target reaction

To find the standard Gibbs free energy change for the target reaction, we will sum the respective \(\Delta G^{\circ}\) values of the reactions we used in Step 2, considering the appropriate signs: \(\Delta G^{\circ}_{\text{target}} = \Delta G^{\circ}_{1} + \Delta G^{\circ}_{2} - \Delta G^{\circ}_{3}\) (Note that we subtracted \(\Delta G^{\circ}_{3}\) since we used the reverse form of reaction 3) Now, plug in the given values: \(\Delta G^{\circ}_{\text{target}} = (-51\ \mathrm{kJ}) + (-474\ \mathrm{kJ}) - (-394\ \mathrm{kJ})\) \(\Delta G^{\circ}_{\text{target}} = -51\ \mathrm{kJ} - 474\ \mathrm{kJ} + 394\ \mathrm{kJ}\) \(\Delta G^{\circ}_{\text{target}} = -131\ \mathrm{kJ}\) Thus, the standard Gibbs free energy change for the target reaction is \(\Delta G^{\circ} = -131\ \mathrm{kJ}\).

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Most popular questions from this chapter

As \(\mathrm{O}_{2}(I)\) is cooled at \(1 \mathrm{~atm}\), it freezes at \(54.5 \mathrm{~K}\) to form solid \(\mathrm{I}\). At a lower temperature, solid I rearranges to solid II, which has a different crystal structure. Thermal measurements show that \(\Delta H\) for the \(\mathrm{I} \rightarrow\) II phase transition is \(-743.1 \mathrm{~J} / \mathrm{mol}\), and \(\Delta S\) for the same transition is \(-17.0 \mathrm{~J} / \mathrm{K} \cdot \mathrm{mol}\). At what temperature are solids I and II in equilibrium?

. What information can be determined from \(\Delta G\) for a reaction? Does one get the same information from \(\Delta G^{\circ}\), the standard free energy change? \(\Delta G^{\circ}\) allows determination of the equilibrium constant \(K\) for a reaction. How? How can one estimate the value of \(K\) at temperatures other than \(25^{\circ} \mathrm{C}\) for a reaction? How can one estimate the temperature where \(K=1\) for a reaction? Do all reactions have a specific temperature where \(K=1 ?\)

At 1 atm, liquid water is heated above \(100^{\circ} \mathrm{C}\). For this process, which of the following choices (i-iv) is correct for \(\Delta S_{\text {sur }}\) ? \(\Delta S\) ? \(\Delta S_{\text {univ }} ?\) Explain each answer. i. greater than zero ii. less than zero iii. equal to zero iv. cannot be determined

Calculate \(\Delta G^{\circ}\) for \(\mathrm{H}_{2} \mathrm{O}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \rightleftharpoons \mathrm{H}_{2} \mathrm{O}_{2}(g)\) at \(600 . \mathrm{K}\) using the following data: \(\mathrm{H}_{2}(\mathrm{~g})+\mathrm{O}_{2}(g) \rightleftharpoons \mathrm{H}_{2} \mathrm{O}_{2}(g) \quad K=2.3 \times 10^{6}\) at \(600 . \mathrm{K}\) \(2 \mathrm{H}_{2}(\mathrm{~g})+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{H}_{2} \mathrm{O}(g) \quad K=1.8 \times 10^{37}\) at 600. \(\mathrm{K}\)

Predict the sign of \(\Delta S^{\circ}\) for each of the following changes. a. \(\mathrm{Na}(s)+\frac{1}{2} \mathrm{Cl}_{2}(g) \longrightarrow \mathrm{NaCl}(s)\) b. \(\mathrm{N}_{2}(\mathrm{~g})+3 \mathrm{H}_{2}(\mathrm{~g}) \longrightarrow 2 \mathrm{NH}_{3}(\mathrm{~g})\) c. \(\mathrm{NaCl}(s) \longrightarrow \mathrm{Na}^{+}(a q)+\mathrm{Cl}^{-}(a q)\) d. \(\mathrm{NaCl}(s) \longrightarrow \mathrm{NaCl}(l)\)

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