Given the following data: $$\begin{array}{lr}2 \mathrm{C}_{6} \mathrm{H}_{6}(l)+15 \mathrm{O}_{2}(g) \longrightarrow 12 \mathrm{CO}_{2}(g)+6 \mathrm{H}_{2} \mathrm{O}(l) \\ \Delta G^{\circ}=-6399 \mathrm{~kJ} \\\\\mathrm{C}(s)+\mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g) & \Delta G^{\circ}=-394 \mathrm{~kJ} \\ \mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l) & \Delta G^{\circ}=-237 \mathrm{~kJ} \end{array}$$ calculate \(\Delta G^{\circ}\) for the reaction $$6 \mathrm{C}(s)+3 \mathrm{H}_{2}(g) \longrightarrow \mathrm{C}_{6} \mathrm{H}_{6}(l)$$

Short Answer

Expert verified
The standard Gibbs free energy change for the formation of benzene, \(C_6H_6(l)\), from its elements, carbon and hydrogen, is \(\Delta G^{\circ}_{target} = 124.5 \ \text{kJ}\).

Step by step solution

01

Analyze the reactions and manipulate them to cancel out unwanted terms

Start by looking at the three given reactions. The target reaction is: $$6 C(s) + 3 H_2(g) \longrightarrow C_6H_6(l)$$ We need to manipulate the given reactions so that we can add them together to get the target reaction. This may involve reversing and/or scaling the reactions.
02

Reverse the first reaction, and scale it by 1/2

Reverse the first reaction in order to obtain \(\Delta G^{\circ}\) for: $$12 CO_2(g) + 6 H_2O(l) \longrightarrow 2 C_6H_6(l) + 15 O_2(g)$$ The new free energy change associated with this reaction is: \(\Delta G^{\circ}_{1\_reversed} = 6399 \ \text{kJ}\) Now, divide both sides of the reversed reaction by 2: $$6 CO_2(g) + 3 H_2O(l) \longrightarrow C_6H_6(l) + 7.5 O_2(g)$$ The new free energy change associated with this reaction is: \(\Delta G^{\circ}_{1\_scaled} = \frac{1}{2} * 6399 \ \text{kJ} = 3199.5 \ \text{kJ}\)
03

Scale the second reaction by 6

Multiply the second reaction by 6 to have the same number of carbon atoms as in the target reaction: $$6 C(s) + 6 O_2(g) \longrightarrow 6 CO_2(g)$$ The new free energy change associated with this reaction is: \(\Delta G^{\circ}_{2\_scaled} = 6 * (-394) \ \text{kJ} = -2364 \ \text{kJ}\)
04

Scale the third reaction by 3

Multiply the third reaction by 3 to have the same number of hydrogen atoms as in the target reaction: $$3 H_2(g) + 1.5 O_2(g) \longrightarrow 3 H_2O(l)$$ The new free energy change associated with this reaction is: \(\Delta G^{\circ}_{3\_scaled} = 3 * (-237) \ \text{kJ} = -711 \ \text{kJ}\)
05

Add the manipulated reactions to obtain the target reaction

Now, add the reactions from Steps 2, 3, and 4. This will cancel out unwanted terms and result in the target reaction. \( (6 CO_2(g) + 3 H_2O(l) \longrightarrow C_6H_6(l) + 7.5 O_2(g)) \newline(+ 6 C(s) + 6 O_2(g) \longrightarrow 6 CO_2(g)) \newline(+ 3 H_2(g) + 1.5 O_2(g) \longrightarrow 3 H_2O(l))\) The sum of these reactions gives us the target reaction: $$6 C(s) + 3 H_2(g) \longrightarrow C_6H_6(l)$$ Now, sum up the associated free energy changes for each reaction: \(\Delta G^{\circ}_{target} = \Delta G^{\circ}_{1\_scaled} + \Delta G^{\circ}_{2\_scaled} + \Delta G^{\circ}_{3\_scaled} = 3199.5 + (-2364) + (-711) = 124.5 \ \text{kJ}\) Thus, the standard Gibbs free energy change for the formation of benzene, \(C_6H_6(l)\), from its elements is \(\Delta G^{\circ}_{target} = 124.5 \ \text{kJ}\).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Consider the system $$\mathrm{A}(g) \longrightarrow \mathrm{B}(g)$$ at \(25^{\circ} \mathrm{C}\). a. Assuming that \(G_{\mathrm{A}}^{\circ}=8996 \mathrm{~J} / \mathrm{mol}\) and \(G_{\mathrm{B}}^{\circ}=11,718 \mathrm{~J} / \mathrm{mol}\), cal- culate the value of the equilibrium constant for this reaction. b. Calculate the equilibrium pressures that result if \(1.00 \mathrm{~mol} \mathrm{~A}(\mathrm{~g})\) at \(1.00\) atm and \(1.00 \mathrm{~mol} \mathrm{~B}(g)\) at \(1.00 \mathrm{~atm}\) are mixed at \(25^{\circ} \mathrm{C}\). c. Show by calculations that \(\Delta G=0\) at equilibrium.

For each of the following pairs of substances, which substance has the greater value of \(S^{\circ} ?\) a. \(C_{\text {graphite }}(s)\) or \(C_{\text {diamond }}(s)\) b. \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)\) or \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(\mathrm{g})\) c. \(\mathrm{CO}_{2}(s)\) or \(\mathrm{CO}_{2}(g)\)

Consider the following reaction: \(\mathrm{H}_{2} \mathrm{O}(g)+\mathrm{Cl}_{2} \mathrm{O}(g) \rightleftharpoons 2 \mathrm{HOCl}(g) \quad K_{298}=0.090\) For \(\mathrm{Cl}_{2} \mathrm{O}(g)\), \(\Delta G_{\mathrm{f}}^{\circ}=97.9 \mathrm{~kJ} / \mathrm{mol}\) \(\Delta H_{\mathrm{f}}^{\circ}=80.3 \mathrm{~kJ} / \mathrm{mol}\) \(S^{\circ}=266.1 \mathrm{~J} / \mathrm{K} \cdot \mathrm{mol}\) a. Calculate \(\Delta G^{\circ}\) for the reaction using the equation \(\Delta G^{\circ}=\) \(-R T \ln (K)\) b. Use bond energy values (Table 8.4) to estimate \(\Delta H^{\circ}\) for the reaction. c. Use the results from parts a and \(b\) to estimate \(\Delta S^{\circ}\) for the reaction. d. Estimate \(\Delta H_{\mathrm{f}}^{\circ}\) and \(S^{\circ}\) for \(\mathrm{HOCl}(g)\). e. Estimate the value of \(K\) at \(500 . \mathrm{K}\). f. Calculate \(\Delta G\) at \(25^{\circ} \mathrm{C}\) when \(P_{\mathrm{H}_{2} \mathrm{O}}=18\) torr, \(P_{\mathrm{Cl}_{2} \mathrm{O}}=2.0\) torr, and \(P_{\mathrm{HOCl}}=0.10\) torr.

If wet silver carbonate is dried in a stream of hot air, the air must have a certain concentration level of carbon dioxide to prevent silver carbonate from decomposing by the reaction $$\mathrm{Ag}_{2} \mathrm{CO}_{3}(s) \rightleftharpoons \mathrm{Ag}_{2} \mathrm{O}(s)+\mathrm{CO}_{2}(g)$$ \(\Delta H^{\circ}\) for this reaction is \(79.14 \mathrm{~kJ} / \mathrm{mol}\) in the temperature range of 25 to \(125^{\circ} \mathrm{C}\). Given that the partial pressure of carbon dioxide in equilibrium with pure solid silver carbonate is \(6.23 \times 10^{-3}\) torr at \(25^{\circ} \mathrm{C}\), calculate the partial pressure of \(\mathrm{CO}_{2}\) necessary to prevent decomposition of \(\mathrm{Ag}_{2} \mathrm{CO}_{3}\) at \(110 .{ }^{\circ} \mathrm{C}\). (Hint: Manipulate the equation in Exercise 71 .)

Ethanethiol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{SH} ;\right.\) also called ethyl mercaptan) is commonly added to natural gas to provide the "rotten egg" smell of a gas leak. The boiling point of ethanethiol is \(35^{\circ} \mathrm{C}\) and its heat of vaporization is \(27.5 \mathrm{~kJ} / \mathrm{mol}\). What is the entropy of vaporization for this substance?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free