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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 \(\Delta G^{\circ}_{target} = 124.5 \ \text{kJ}\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Chemical Reactions
Chemical reactions are processes where substances interact to form new products. In our exercise, the reaction involves the formation of benzene (labeled as \( C_6H_6(l) \)) from carbon \( C(s) \) and hydrogen \( H_2(g) \). Understanding these reactions requires knowledge of breaking and forming chemical bonds, as energy is transformed. Within this context:
  • The conversion of carbon and hydrogen into benzene requires very specific conditions.
  • This particular reaction involves manipulating initial reactions to achieve a desired one.
Each compound reacts differently, so calculations must account for different energetic properties. This is where we apply concepts like Gibbs Free Energy, which helps determine if the reaction occurs spontaneously.
Thermodynamics
Thermodynamics deals with the principles governing energy transformations, especially as heat and work. In chemical reactions, it allows us to predict if and how a reaction will occur.
For the reaction of forming benzene, thermodynamic principles guide:
  • Energy balance: Ensuring energy entering the system equals energy leaving the system.
  • Entropy and enthalpy: These concepts come into play to predict reaction spontaneity.
The Gibbs Free Energy is a key component. By calculating the changes, we determine if the process energetically favors the formation of benzene. Negative \( \Delta G \) means spontaneous reactions under set conditions.
Enthalpy
Enthalpy is the measure of total heat content in a thermodynamic system, crucial in determining reaction feasibility. It represents the bond energy required or released when substances change.
For benzene formation:
  • Reactions release heat when forming \( CO_2 \) and \( H_2O \).
  • These processes require calculating changes in enthalpy to predict how energy is absorbed or released.
By evaluating enthalpy and combining it with entropy, the overall Gibbs Free Energy is found. This provides insight into the energy landscape of chemical reactions and helps predict the direction and feasibility of reactions.

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Most popular questions from this chapter

Some nonelectrolyte solute (molar mass \(=142 \mathrm{~g} / \mathrm{mol}\) ) was dissolved in \(150 . \mathrm{mL}\) of a solvent (density \(=0.879 \mathrm{~g} / \mathrm{cm}^{3}\) ). The elevated boiling point of the solution was \(355.4 \mathrm{~K}\). What mass of solute was dissolved in the solvent? For the solvent, the enthalpy of vaporization is \(33.90 \mathrm{~kJ} / \mathrm{mol}\), the entropy of vaporization is \(95.95\) \(\mathrm{J} / \mathrm{K} \cdot \mathrm{mol}\), and the boiling-point elevation constant is \(2.5 \mathrm{~K} \cdot \mathrm{kg} / \mathrm{mol}\).

For mercury, the enthalpy of vaporization is \(58.51 \mathrm{~kJ} / \mathrm{mol}\) and the entropy of vaporization is \(92.92 \mathrm{~J} / \mathrm{K} \cdot \mathrm{mol}\). What is the normal boiling point of mercury?

a. Using the free energy profile for a simple one-step reaction, show that at equilibrium \(K=k_{\mathrm{f}} / k_{\mathrm{r}}\), where \(k_{\mathrm{f}}\) and \(k_{\mathrm{r}}\) are the rate constants for the forward and reverse reactions. Hint: Use the relationship \(\Delta G^{\circ}=-R T \ln (K)\) and represent \(k_{\mathrm{f}}\) and \(k_{\mathrm{r}}\) using the Arrhenius equation \(\left(k=A e^{-E_{2} / R T}\right)\). b. Why is the following statement false? "A catalyst can increase the rate of a forward reaction but not the rate of the reverse reaction."

Carbon monoxide is toxic because it bonds much more strongly to the iron in hemoglobin (Hgb) than does \(\mathrm{O}_{2}\). Consider the following reactions and approximate standard free energy changes: $$\begin{array}{clr}\mathrm{Hgb}+\mathrm{O}_{2} \longrightarrow \mathrm{HgbO}_{2} & \Delta G^{\circ}=-70 \mathrm{~kJ} \\ \mathrm{Hgb}+\mathrm{CO} \longrightarrow \mathrm{HgbCO} & \Delta G^{\circ}=-80 \mathrm{~kJ} \end{array}$$ Using these data, estimate the equilibrium constant value at \(25^{\circ} \mathrm{C}\) for the following reaction: $$\mathrm{HgbO}_{2}+\mathrm{CO} \rightleftharpoons \mathrm{HgbCO}+\mathrm{O}_{2}$$

Consider the following energy levels, each capable of holding two objects: \(E=2 \mathrm{~kJ}\) ______ \(E=1 \mathrm{~kJ}\) ______ \(E=0 \quad \mathrm{XX}\) Draw all the possible arrangements of the two identical particles (represented by X) in the three energy levels. What total energy is most likely, that is, occurs the greatest number of times? Assume that the particles are indistinguishable from each other.

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