Consider the decomposition of liquid benzene, \(\mathrm{C}_{6} \mathrm{H}_{6}(l),\) to gaseous acetylene, \(\mathrm{C}_{2} \mathrm{H}_{2}(g):\) $$ \mathrm{C}_{6} \mathrm{H}_{6}(l) \longrightarrow 3 \mathrm{C}_{2} \mathrm{H}_{2}(g) \quad \Delta H=+630 \mathrm{~kJ} $$ (a) What is the enthalpy change for the reverse reaction? (b) What is \(\Delta H\) for the formation of 1 mol of acetylene? (c) Which is more likely to be thermodynamically favored, the forward reaction or the reverse reaction? (d) If \(\mathrm{C}_{6} \mathrm{H}_{6}(g)\) were consumed instead of \(\mathrm{C}_{6} \mathrm{H}_{6}(l),\) would you expect the magnitude of \(\Delta H\) to increase, decrease, or stay the same? Explain.

Short Answer

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(a) The enthalpy change for the reverse reaction is -630 kJ. (b) The enthalpy change for the formation of 1 mol of acetylene is +210 kJ. (c) The reverse reaction is more likely to be thermodynamically favored since it has a negative enthalpy change. (d) If gaseous benzene is consumed instead of liquid benzene, the magnitude of ΔH would increase due to the additional energy needed for the phase change.

Step by step solution

01

(a) Calculate the enthalpy change for the reverse reaction

To find the enthalpy change for the reverse reaction, we simply change the sign of the given enthalpy change for the forward reaction. In this case, the enthalpy change for the reverse reaction is: \[-\Delta H = -(+630 \,\text{kJ}) = -630 \,\text{kJ}\]
02

(b) Calculate the enthalpy change for the formation of 1 mol of acetylene

We are given that the formation of 3 moles of acetylene has an enthalpy change of \(+630\) kJ. To find the enthalpy change for 1 mole of acetylene, we simply divide this value by 3: \[\Delta H_{1 \,\text{mol of } C_2H_2} = \frac{+630 \,\text{kJ}}{3} = +210 \,\text{kJ}\]
03

(c) Determine which reaction is thermodynamically favored

In general, a reaction with a negative enthalpy change (\(\Delta H<0\)) is exothermic and tends to be thermodynamically favored since it releases energy. A reaction with a positive enthalpy change (\(\Delta H>0\)) is endothermic and tends to be less thermodynamically favored since it absorbs energy. In this case, the forward reaction has a positive enthalpy change while the reverse reaction has a negative enthalpy change. Therefore, the reverse reaction is more likely to be thermodynamically favored.
04

(d) Expected change in enthalpy if gaseous benzene is consumed

Changing the phase of benzene from liquid to gas requires energy (known as the heat of vaporization). Therefore, if gaseous benzene were to be consumed instead of liquid benzene in the reaction, additional energy would be needed to turn liquid benzene into gaseous benzene before the reaction can occur. This would result in an increased magnitude of the enthalpy change (\(\Delta H\)) for the reaction.

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Most popular questions from this chapter

For each of the following compounds, write a balanced thermochemical equation depicting the formation of one mole of the compound from its elements in their standard states and use Appendix \(\mathrm{C}\) to obtain the value of \(\Delta H_{f}^{\circ}\) : (a) \(\mathrm{NO}_{2}(g)\) (b) \(\mathrm{SO}_{3}(g),(\mathrm{c}) \mathrm{NaBr}(s)\) (d) \(\mathrm{Pb}\left(\mathrm{NO}_{3}\right)_{2}(s)\)

Consider the combustion of liquid methanol, \(\mathrm{CH}_{3} \mathrm{OH}(l):\) $$ \begin{aligned} \mathrm{CH}_{3} \mathrm{OH}(l)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l) & \\ \Delta H=&-726.5 \mathrm{~kJ} \end{aligned} $$ (a) What is the enthalpy change for the reverse reaction? (b) Balance the forward reaction with whole-number coefficients. What is \(\Delta H\) for the reaction represented by this equation? (c) Which is more likely to be thermodynamically favored, the forward reaction or the reverse reaction? (d) If the reaction were written to produce \(\mathrm{H}_{2} \mathrm{O}(g)\) instead of \(\mathrm{H}_{2} \mathrm{O}(l)\) would you expect the magnitude of \(\Delta H\) to increase, decrease, or stay the same? Explain.

Three common hydrocarbons that contain four carbons are listed here, along with their standard enthalpies of formation: (a) For each of these substances, calculate the molar enthalpy of combustion to \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(l) .\) (b) Calculate the fuel value in \(\mathrm{kJ} / \mathrm{g}\) for each of these compounds. \((\mathrm{c})\) For each hydrocarbon, determine the percentage of hydrogen by mass. (d) By comparing your answers for parts (b) and (c), propose a relationship between hydrogen content and fuel value in hydrocarbons.

Suppose an Olympic diver who weighs \(52.0 \mathrm{~kg}\) executes a straight dive from a \(10-\mathrm{m}\) platform. At the apex of the dive, the diver is \(10.8 \mathrm{~m}\) above the surface of the water. (a) What is the potential energy of the diver at the apex of the dive, relative to the surface of the water? (b) Assuming that all the potential energy of the diver is converted into kinetic energy at the surface of the water, at what speed in \(\mathrm{m} / \mathrm{s}\) will the diver enter the water? (c) Does the diver do work on entering the water? Explain.

In what two ways can an object possess energy? How do these two ways differ from one another?

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