Chapter 19

(a) Using data in Appendix \(C\), estimate the temperature at which the free- energy change for the transformation from \(\mathrm{I}_{2}(s)\) to \(\mathrm{I}_{2}(g)\) is zero. (b) Use a reference source, such as Web Elements (www.webelements.com), to find the experimental melting and boiling points of \(I_{2}\). (c) Which of the values in part (b) is closer to the value you obtained in part (a)?

Acetylene gas, \(\mathrm{C}_{2} \mathrm{H}_{2}(g)\), is used in welding. (a) Write a balanced equation for the combustion of acetylene gas to \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(l) .(\mathbf{b})\) How much heat is produced in burning \(1 \mathrm{~mol}\) of \(\mathrm{C}_{2} \mathrm{H}_{2}\) under standard conditions if both reactants and products are brought to \(298 \mathrm{~K} ?\) (c) What is the maximum amount of useful work that can be accomplished under standard conditions by this reaction?

Indicate whether \(\Delta G\) increases, decreases, or stays the same for each of the following reactions as the partial pressure of \(\mathrm{O}_{2}\) is increased: (a) \(\mathrm{HgO}(s) \longrightarrow \mathrm{Hg}(l)+\mathrm{O}_{2}(g)\) (b) \(2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g)\) (c)

Indicate whether \(\Delta G\) increases, decreases, or does not change when the partial pressure of \(\mathrm{H}_{2}\) is increased in each of the following reactions: (a) \(\mathrm{H}_{2}(g)+\mathrm{NiO}(s) \longrightarrow \mathrm{Ni}(s)+\mathrm{H}_{2} \mathrm{O}(g)\) (b) \(\mathrm{H}_{2}(g)+\mathrm{S}(s) \longrightarrow \mathrm{H}_{2} \mathrm{~S}(g)\) (c) \(\mathrm{C}(s)+\mathrm{H}_{2} \mathrm{O}(g) \longrightarrow \mathrm{CO}(g)+\mathrm{H}_{2}(g)\)

Consider the reaction \(2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)\) (a) Using data from Appendix \(\mathrm{C},\) calculate \(\Delta G^{\circ}\) at \(298 \mathrm{~K}\). (b) Calculate \(\Delta G\) at \(298 \mathrm{~K}\) if the partial pressures of all gases are \(33.4 \mathrm{kPa}\).

Consider the reaction \(\mathrm{CH}_{4}(\mathrm{~g})+4 \mathrm{Cl}_{2}(g) \longrightarrow \mathrm{CCl}_{4}(g)+\) \(4 \mathrm{HCl}(g) .\). (a) Using data from Appendix C, calculate \(\Delta G^{\circ}\) at \(298 \mathrm{~K} .(\mathbf{b})\) Calculate \(\Delta G\) at \(298 \mathrm{~K}\) if the reaction mixture consists of \(50.7 \mathrm{kPa}\) of \(\mathrm{CH}_{4}(g), 25.3 \mathrm{kPa}\) of \(\mathrm{Cl}_{2}(g), 10.13 \mathrm{kPa}\) of \(\mathrm{CCl}_{4}(\mathrm{~g})\) and \(15.2 \mathrm{kPa}\) of \(\mathrm{HCl}(\mathrm{g})\)

Use data from Appendix \(C\) to calculate the equilibrium constant, \(K,\) and \(\Delta G^{\circ}\) at \(298 \mathrm{~K}\) for each of the following reactions: (a) \(\mathrm{H}_{2}(g)+\mathrm{I}_{2}(g) \rightleftharpoons 2 \mathrm{HI}(g)\) (b) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(g) \rightleftharpoons \mathrm{C}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2} \mathrm{O}(g)\) (c) \(3 \mathrm{C}_{2} \mathrm{H}_{2}(g) \rightleftharpoons \mathrm{C}_{6} \mathrm{H}_{6}(g)\)

Using data from Appendix \(\mathrm{C}\), write the equilibrium-constant expression and calculate the value of the equilibrium constant and the free- energy change for these reactions at \(298 \mathrm{~K}:\) (a) \(\mathrm{NaHCO}_{3}(s) \rightleftharpoons \mathrm{NaOH}(s)+\mathrm{CO}_{2}(g)\) (b) \(2 \mathrm{HBr}(g)+\mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{HCl}(g)+\mathrm{Br}_{2}(g)\) (c) \(2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{SO}_{3}(g)\)

Consider the reaction $$ \mathrm{PbCO}_{3}(s) \rightleftharpoons \mathrm{PbO}(s)+\mathrm{CO}_{2}(g) $$ Using data in Appendix \(\mathrm{C}\), calculate the equilibrium pressure of \(\mathrm{CO}_{2}\) in the system at $$ \text { (a) } 400^{\circ} \mathrm{C} \text { and } $$ $$ \text { (b) } 180^{\circ} \mathrm{C} \text { . } $$

The value of \(K_{a}\) for nitrous acid \(\left(\mathrm{HNO}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix D. (a) Write the chemical equation for the equilibrium that corresponds to \(K_{a}\). (b) By using the value of \(K_{a}\) calculate \(\Delta G^{\circ}\) for the dissociation of nitrous acid in aqueous solution. (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=5.0 \times 10^{-2} \mathrm{M}\), \(\left[\mathrm{NO}_{2}^{-}\right]=6.0 \times 10^{-4} \mathrm{M},\) and \(\left[\mathrm{HNO}_{2}\right]=0.20 \mathrm{M} ?\)

The \(K_{b}\) for methylamine \(\left(\mathrm{CH}_{3} \mathrm{NH}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix \(D\). (a) Write the chemical equation for the equilibrium that corresponds to \(K_{b}\). (b) By using the value of \(K_{b}\), calculate \(\Delta G^{\circ}\) for the equilibrium in part (a). (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=6.7 \times 10^{-9} \mathrm{M},\left[\mathrm{CH}_{3} \mathrm{NH}_{3}^{+}\right]=2.4 \times 10^{-3} \mathrm{M}\) and \(\left[\mathrm{CH}_{3} \mathrm{NH}_{2}\right]=0.098 \mathrm{M} ?\)

(a) Which of the thermodynamic quantities \(p, H, q, w,\) and \(G\) are state functions? (b) Consider a system going from state 1 to state 2 in a reversible and an irreversible way. Compare \(q_{\text {rev }}\) and \(q_{\text {irtev }}\) (c) Consider a system going from state 1 to state 2 in a reversible and an irreversible way. Compare \(w_{\text {rev }}\) and \(w_{\text {trev }}\). (d) For a reversible isothermal process, write an expression for \(\Delta H\) and an expression for \(\Delta G\) in terms of \(q, w\) and \(T, p\) and \(\Delta V\).

The crystalline hydrate \(\mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2} \cdot 4 \mathrm{H}_{2} \mathrm{O}(s)\) loses water when placed in a large, closed, dry vessel at room temperature: $$ \mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2} \cdot 4 \mathrm{H}_{2} \mathrm{O}(s) \longrightarrow \mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2}(s)+4 \mathrm{H}_{2} \mathrm{O}(g) $$ This process is spontaneous and \(\Delta H^{\circ}\) is positive at room temperature. (a) What is the sign of \(\Delta S^{\circ}\) at room temperature? (b) If the hydrated compound is placed in a large, closed vessel that already contains a large amount of water vapor, does \(\Delta S^{\circ}\) change for this reaction at room temperature?

Indicate whether each of the following statements is trueor false. If it is false, correct it. (a) The feasibility of manufacturing \(\mathrm{NH}_{3}\) from \(\mathrm{N}_{2}\) and \(\mathrm{H}_{2}\) depends entirely on the value of \(\Delta H\) for the process \(\mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g) .\) (b) The reaction of \(\mathrm{Na}(s)\) with \(\mathrm{Cl}_{2}(g)\) to form \(\mathrm{NaCl}(s)\) is a spontaneous process. (c) A spontaneous process can in principle be conducted reversibly. (d) Spontaneous processes in general require that work be done to force them to proceed. (e) Spontaneous processes are those that are exothermic and that lead to a higher degree of order in the system.

For each of the following processes, indicate whether the signs of \(\Delta S\) and \(\Delta H\) are expected to be positive, negative, or about zero. (a) A solid sublimes. (b) The temperature of a sample of \(\mathrm{Co}(s)\) is lowered from \(60^{\circ} \mathrm{C}\) to \(25^{\circ} \mathrm{C} .\) (c) Ethyl alcohol evaporates from a beaker. (d) A diatomic molecule dissociates into atoms. (e) A piece of charcoal is combusted to form \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(g)\).

The reaction \(2 \mathrm{Mg}(s)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{MgO}(s)\) is highly spontaneous. A classmate calculates the entropy change for this reaction and obtains a large negative value for \(\Delta S^{\circ}\). Did your classmate make a mistake in the calculation? Explain.

Consider a system that consists of two standard playing dice, with the state of the system defined by the sum of the values shown on the top faces. (a) The two arrangements of top faces shown here can be viewed as two possible microstates of the system. Explain. (b) To which state does each microstate correspond? (c) How many possible states are there for the system? (d) Which state or states have the highest entropy? Explain. (e) Which state or states have the lowest entropy? Explain. (f) Calculate the absolute entropy of the two-dice system.

Ammonium nitrate dissolves spontaneously and endothermally in water at room temperature. What can you deduce about the sign of \(\Delta S\) for this solution process?

A standard air conditioner involves a \(r\) frigerant that is typically now a fluorinated hydrocarbon, such as \(\mathrm{CH}_{2} \mathrm{~F}_{2}\). An air- conditioner refrigerant has the property that it readily vaporizes at atmospheric pressure and is easily compressed to its liquid phase under increased pressure. The operation of an air conditioner can be thought of as a closed system made up of the refrigerant going through the two stages shown here (the air circulation is not shown in this diagram). During expansion, the liquid refrigerant is released into an expansion chamber at low pressure, where it vaporizes. The vapor then undergoes compression at high pressure back to its liquid phase in a compression chamber. (a) What is the sign of \(q\) for the expansion? (b) What is the sign of \(q\) for the compression? (c) In a central air-conditioning system, one chamber is inside the home and the other is outside. Which chamber is where, and why? (d) Imagine that a sample of liquid refrigerant undergoes expansion followed by compression, so that it is back to its original state. Would you expect that to be a reversible process? (e) Suppose that a house and its exterior are both initially at \(31^{\circ} \mathrm{C}\). Some time after the air conditioner is turned on, the house is cooled to \(24^{\circ} \mathrm{C}\). Is this process spontaneous of nonspontaneous?

Trouton's rule states that for many liquids at their normal boiling points, the standard molar entropy of vaporization is about \(88 \mathrm{~J} / \mathrm{mol}-\mathrm{K} .(\) a) Estimate the normal boiling point of bromine, \(\mathrm{Br}_{2}\), by determining \(\Delta H_{\text {vap }}^{\circ}\) for \(\mathrm{Br}_{2}\) using data from Appendix \(C\). Assume that \(\Delta H_{\text {vap }}^{\circ}\) remains constant with temperature and that Trouton's rule holds. (b) Look up the normal boiling point of \(\mathrm{Br}_{2}\) in a chemistry handbook or at the WebElements website (www.webelements.com) and compare it to your calculation. What are the possible sources of error, or incorrect assumptions, in the calculation?

(a) Write the chemical equations that correspond to \(\Delta G_{i}^{9}\) for \(\mathrm{CH}_{4}(g)\) and for \(\mathrm{NaCl}(s) .\) (b) For these formation reactions, compare \(\Delta G_{f}^{\circ}\) and \(\Delta H_{f}\). (c) In general, under which condition is \(\Delta G\), more negative (less positive) than \(\Delta H_{f}\) ? (i) When the temperature is high, (ii) when \(\Delta S_{f}^{\circ}\) is positive, (iii) when the reaction is reversible.

Using the data in Appendix \(C\) and given the pressures listed, calculate \(K_{\mathrm{p}}\) and \(\Delta G\) for each of the following reactions: $$ \begin{array}{l} \text { (a) } \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g) \\ \quad R_{\mathrm{N}_{2}}=263.4 \mathrm{kPa}, P_{\mathrm{H}_{2}}=597.8 \mathrm{kPa}, P_{\mathrm{NH}_{3}}=101.3 \mathrm{kPa} \\ \text { (b) } 2 \mathrm{~N}_{2} \mathrm{H}_{4}(g)+2 \mathrm{NO}_{2}(g) \longrightarrow 3 \mathrm{~N}_{2}(g)+4 \mathrm{H}_{2} \mathrm{O}(g) \end{array} $$ \(P_{\mathrm{N}_{2} \mathrm{H}_{4}}=P_{\mathrm{NO}_{2}}=5.07 \mathrm{kPa}\) $$ \begin{array}{l} \quad R_{\mathrm{N}_{2}}=50.7 \mathrm{kPa}, P_{\mathrm{H}_{2} \mathrm{O}}=30.4 \mathrm{kPa} \\ \text { (c) } \mathrm{N}_{2} \mathrm{H}_{4}(g) \longrightarrow \mathrm{N}_{2}(g)+2 \mathrm{H}_{2}(g) \\ P_{\mathrm{N}_{2} \mathrm{H}_{4}}=101.3 \mathrm{kPa}, P_{\mathrm{N}_{2}}=152.0 \mathrm{kPa}, P_{\mathrm{H}_{2}}=253.3 \mathrm{kPa} \end{array} $$

(a) For each of the following reactions, predict the sign of \(\Delta H^{*}\) and \(\Delta S^{\circ}\) without doing any calculations. (b) Based on your general chemical knowledge, predict which of these reactions will have \(K>1\) at \(25^{\circ} \mathrm{C} .(\mathbf{c})\) In each case, indicate whether \(K\) should increase or decrease with increasing temperature. (i) \(2 \mathrm{Fe}(s)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{FeO}(s)\) (ii) \(\mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{Cl}(g)\) (iii) \(\mathrm{NH}_{4} \mathrm{Cl}(s) \rightleftharpoons \mathrm{NH}_{3}(g)+\mathrm{HCl}(g)\) (iv) \(\mathrm{CO}_{2}(\mathrm{~g})+\mathrm{CaO}(s) \rightleftharpoons \mathrm{CaCO}_{3}(s)\)

The oxidation of glucose \(\left(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}\right)\) in body tissue produces \(\mathrm{CO}_{2}\) and \(\mathrm{H}_{2} \mathrm{O} .\) In contrast, anaerobic decomposition, which occurs during fermentation, produces ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) and \(\mathrm{CO}_{2}\). (a) Using data given in Appendix \(\mathrm{C}\), compare the equilibrium constants for the following reactions: $$ \begin{array}{r} \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s)+6 \mathrm{O}_{2}(g) \rightleftharpoons 6 \mathrm{CO}_{2}(g)+6 \mathrm{H}_{2} \mathrm{O}(l) \\ \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s) \rightleftharpoons 2 \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(I)+2 \mathrm{CO}_{2}(g) \end{array} $$ (b) Compare the maximum work that can be obtained from these processes under standard conditions.

The conversion of natural gas, which is mostly methane, into products that contain two or more carbon atoms, such as ethane \(\left(\mathrm{C}_{2} \mathrm{H}_{6}\right)\), is a very important industrial chemical process. In principle, methane can be converted into ethane and hydrogen: $$ 2 \mathrm{CH}_{4}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{6}(g)+\mathrm{H}_{2}(g) $$ In practice, this reaction is carried out in the presence of oxygen: $$ 2 \mathrm{CH}_{4}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{6}(g)+\mathrm{H}_{2} \mathrm{O}(g) $$ (a) Using the data in Appendix \(C\), calculate \(K\) for these reactions at \(25^{\circ} \mathrm{C}\) and \(500^{\circ} \mathrm{C}\). (b) Is the difference in \(\Delta G^{\circ}\) for the two reactions due primarily to the enthalpy term \((\Delta H)\) or the entropy term \((-T \Delta S)\) ? (c) Explain how the preceding reactions are an example of driving a nonspontaneous reaction, as discussed in the "Chemistry and Life" box in Section 19.7. (d) The reaction of \(\mathrm{CH}_{4}\) and \(\mathrm{O}_{2}\) to form \(\mathrm{C}_{2} \mathrm{H}_{6}\) and \(\mathrm{H}_{2} \mathrm{O}\) must be carried out carefully to avoid a competing reaction. What is the most likely competing reaction?

The potassium-ion concentration in blood plasma is about \(5.0 \times 10^{-3} \mathrm{M}\), whereas the concentration in muscle-cell fluid is much greater \((0.15 \mathrm{M})\). The plasma and intracellular fluid are separated by the cell membrane, which we assume is permeable only to \(\mathrm{K}^{+}\). (a) What is \(\Delta G\) for the transfer of \(1 \mathrm{~mol}\) of \(\mathrm{K}^{+}\) from blood plasma to the cellular fluid at body temperature \(37^{\circ} \mathrm{C} ?\) (b) What is the minimum amount of work that must be used to transfer this \(\mathrm{K}^{+} ?\)

Most liquids follow Trouton's rule (see Exercise 19.93 ), which states that the molar entropy of vaporization is approximately \(88 \pm 5 \mathrm{~J} / \mathrm{mol}-\mathrm{K}\). The normal boiling points and enthalpies of vaporization of several organic liquids are as follows: \begin{tabular}{lcc} \hline & Normal Boiling & \\ Substance & Point \(\left({ }^{\circ} \mathrm{C}\right)\) & \(\Delta H_{\text {vap }}(\mathrm{k} / / \mathrm{mol})\) \\ \hline Acetone, \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CO}\) & 56.1 & 29.1 \\\ Dimethyl ether, \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{O}\) & -24.8 & 21.5 \\\ Ethanol, \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\) & 78.4 & 38.6 \\ Octane, \(\mathrm{C}_{\mathrm{s}} \mathrm{H}_{18}\) & 125.6 & 34.4 \\ Pyridine, \(\mathrm{C}_{5} \mathrm{H}_{\mathrm{S}} \mathrm{N}\) & 115.3 & 35.1 \\\ \hline \end{tabular} (a) Calculate \(\Delta S_{\text {vap }}\) for each of the liquids. Do all the liquids obey Trouton's rule? (b) With reference to intermolecular forces (Section 11.2), can you explain any exceptions to the rule? (c) Would you expect water to obey Trouton's rule? By using data in Appendix \(\mathrm{B}\), check the accuracy of your conclusion. (d) Chlorobenzene \(\left(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{Cl}\right)\) boils at \(131.8^{\circ} \mathrm{C}\). Use Trouton's rule to estimate \(\Delta H_{\text {vap }}\) for this substance.

In chemical kinetics, the entropy of activation is the entropy change for the process in which the reactants reach the activated complex. Predict whether the entropy of activation for a bimolecular process is usually positive or negative.

The following processes were all discussed in Chapter 18 , "Chemistry of the Environment." Estimate whether the entropy of the system increases or decreases during each process: (a) photodissociation of \(\mathrm{O}_{2}(g),(\mathbf{b})\) formation of ozone from oxygen molecules and oxygen atoms, (c) diffusion of CFCs into the stratosphere, (d) desalination of water by reverse osmosis.

An ice cube with a mass of \(25 \mathrm{~g}\) at \(-18{ }^{\circ} \mathrm{C}\) (typical freezer temperature) is dropped into a cup that holds \(250 \mathrm{~mL}\) of hot water, initially at \(85^{\circ} \mathrm{C}\). What is the final temperature in the cup? The density of liquid water is \(1.00 \mathrm{~g} / \mathrm{mL}\); the specific heat capacity of ice is \(2.03 \mathrm{~J} / \mathrm{g}{\underline{\phantom{xx}}}^{\circ} \mathrm{C} ;\) the specific heat capacity of liquid water is \(4.184 \mathrm{~J} / \mathrm{g}-\mathrm{K} ;\) the enthalpy of fusion of water is \(6.01 \mathrm{~kJ} / \mathrm{mol}\).

Carbon disulfide \(\left(C S_{2}\right)\) is a toxic, highly flammable substance. The following thermodynamic data are available for \(\mathrm{CS}_{2}(I)\) and \(\mathrm{CS}_{2}(g)\) at \(298 \mathrm{~K}\) \begin{tabular}{lcc} \hline & \(\Delta H_{i}(\mathrm{k} / \mathrm{mol})\) & \(\Delta G_{i}^{\prime}(\mathrm{kJ} / \mathrm{mol})\) \\ \hline\(C S_{2}(l)\) & 89.7 & 65.3 \\ \(C S_{2}(g)\) & 117.4 & 67.2 \\ \hline \end{tabular} (a) Draw the Lewis structure of the molecule. What do you predict for the bond order of the \(\mathrm{C}-\mathrm{S}\) bonds? \((\mathbf{b})\) Use the VSEPR method to predict the structure of the \(\mathrm{CS}_{2}\) molecule. (c) Liquid \(\mathrm{CS}_{2}\) burns in \(\mathrm{O}_{2}\) with a blue flame, forming \(\mathrm{CO}_{2}(g)\) and \(\mathrm{SO}_{2}(g)\). Write a balanced equation for this reaction. (d) Using the data in the preceding table and in Appendix \(C,\) calculate \(\Delta H^{\circ}\) and \(\Delta G^{\circ}\) for the reaction in part \((c) .\) Is the reaction exothermic? Is it spontaneous at \(298 \mathrm{~K} ?\) (e) Use the data in the table to calculate \(\Delta S^{\circ}\) at \(298 \mathrm{~K}\) for the vaporization of \(\mathrm{CS}_{2}(I) .\) Is the sign of \(\Delta S^{\circ}\) as you would expect for a vaporization? (f) Using data in the table and your answer to part (e), estimate the boiling point of \(\mathrm{CS}_{2}(l)\). Do you predict that the substance will be a liquid or a gas at \(298 \mathrm{~K}\) and \(101.3 \mathrm{kPa}\) ?

The reaction $$ \mathrm{SO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{~S}(g) \rightleftharpoons 3 \mathrm{~S}(s)+2 \mathrm{H}_{2} \mathrm{O}(g) $$ is the basis of a suggested method for removal of \(\mathrm{SO}_{2}\) from power-plant stack gases. The standard free energy of each substance is given in Appendix C. (a) What is the equilibrium constant for the reaction at \(298 \mathrm{~K} ?(\mathbf{b})\) In principle, is this reaction a feasible method of removing \(\mathrm{SO}_{2}\) ? (c) If \(P_{5 \mathrm{O}_{2}}=P_{\mathrm{H}_{2}}\) s and the vapor pressure of water is \(3.33 \mathrm{kPa}\), calculate the equilibrium \(\mathrm{SO}_{2}\) pressure in the system at \(298 \mathrm{~K}\). (d) Would you expect the process to be more or less effective at higher temperatures?

When most elastomeric polymers (e.g., a rubber band) are stretched, the molecules become more ordered, as illustrated here: Suppose you stretch a rubber band. (a) Do you expect the entropy of the system to increase or decrease? (b) If the rubber band were stretched isothermally, would heat need to be absorbed or emitted to maintain constant temperature? (c) Try this experiment: Stretch a rubber band and wait a moment. Then place the stretched rubber band on your upper lip, and let it return suddenly to its unstretched state (remember to keep holding on!). What do you observe? Are your observations consistent with your answer to part (b)?