Chapter 14

Which of the following linear plots do you expect for a reaction \(A \longrightarrow\) products if the kinetics are (a) zero order, (b) first order, or (c) second order? [Section 14.4]

The accompanying graph shows plots of \(\ln k\) versus \(1 / T\) for two different reactions. The plots have been extrapolated to the \(y\)-intercepts. Which reaction (red or blue) has (a) the larger value for \(E_{a}\) and (b) the larger value for the frequency factor, \(A\) ? [Section 14.5]

(a) What is meant by the term reaction rate? (b) Name three factors that can affect the rate of a chemical reaction. (c) Is the rate of disappearance of reactants always the same as the rate of appearance of products?

For each of the following gas-phase reactions, indicate how the rate of disappearance of each reactant is related to the rate of appearance of each product: (a) \(\mathrm{H}_{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{H}_{2}(g)+\mathrm{O}_{2}(g)\) (b) \(2 \mathrm{~N}_{2} \mathrm{O}(g) \longrightarrow 2 \mathrm{~N}_{2}(g)+\mathrm{O}_{2}(g)\) (c) \(\mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g)\) (d) \(\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{NH}_{2}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{4}(g)+\mathrm{NH}_{3}(g)\)

For each of the following gas-phase reactions, write the rate expression in terms of the appearance of each product and disappearance of each reactant: (a) \(2 \mathrm{H}_{2} \mathrm{O}(g) \longrightarrow 2 \mathrm{H}_{2}(g)+\mathrm{O}_{2}(g)\) (b) \(2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g)\) (c) \(2 \mathrm{NO}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{N}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g)\) (d) \(\mathrm{N}_{2}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{N}_{2} \mathrm{H}_{4}(g)\)

(a) Consider the combustion of ethylene, \(\mathrm{C}_{2} \mathrm{H}_{4}(\mathrm{~g})+\) \(3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g)\). If the concentration of \(\mathrm{C}_{2} \mathrm{H}_{4}\) is decreasing at the rate of \(0.036 \mathrm{M} / \mathrm{s}\), what are the rates of change in the concentrations of \(\mathrm{CO}_{2}\) and \(\mathrm{H}_{2} \mathrm{O}\) ? (b) The rate of decrease in \(\mathrm{N}_{2} \mathrm{H}_{4}\) partial pressure in a closed reaction vessel from the reaction \(\mathrm{N}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g)\) is 74 torr per hour. What are the rates of change of \(\mathrm{NH}_{3}\) partial pressure and total pressure in the vessel?

A reaction \(\mathrm{A}+\mathrm{B} \longrightarrow \mathrm{C}\) obeys the following rate law: Rate \(=k[\mathrm{~B}]^{2}\). (a) If \([\mathrm{A}]\) is doubled, how will the rate change? Will the rate constant change? (b) What are the reaction orders for \(A\) and \(B\) ? What is the overall reaction order? (c) What are the units of the rate constant?

Consider a hypothetical reaction between \(\mathrm{A}, \mathrm{B}\), and \(\mathrm{C}\) that is first order in A, zero order in B, and second order in C. (a) Write the rate law for the reaction. (b) How does the rate change when \([A]\) is doubled and the other reactant concentrations are held constant? (c) How does the rate change when [B] is tripled and the other reactant concentrations are held constant? (d) How does the rate change when \([\mathrm{C}]\) is tripled and the other reactant concentrations are held constant? (e) By what factor does the rate change when the concentrations of all three reactants are tripled? \((f)\) By what factor does the rate change when the concentrations of all three reactants are cut in hal??

The decomposition reaction of \(\mathrm{N}_{2} \mathrm{O}_{5}\) in carbon tetrachloride is \(2 \mathrm{~N}_{2} \mathrm{O}_{5} \longrightarrow 4 \mathrm{NO}_{2}+\mathrm{O}_{2}\). The rate law is first order in \(\mathrm{N}_{2} \mathrm{O}_{5}\). At \(64^{\circ} \mathrm{C}\) the rate constant is \(4.82 \times 10^{-3} \mathrm{~s}^{-1}\). (a) Write the rate law for the reaction. (b) What is the rate of reaction when \(\left[\mathrm{N}_{2} \mathrm{O}_{5}\right]=0.0240 \mathrm{M}\) ? (c) What happens to the rate when the concentration of \(\mathrm{N}_{2} \mathrm{O}_{5}\) is doubled to \(0.0480 \mathrm{M}\) ? (d) What happens to the rate when the concentration of \(\mathrm{N}_{2} \mathrm{O}_{5}\) is halved to \(0.0120 \mathrm{M}\) ?

Consider the following reaction: $$ 2 \mathrm{NO}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{N}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g) $$ (a) The rate law for this reaction is first order in \(\mathrm{H}_{2}\) and second order in NO. Write the rate law. (b) If the rate constant for this reaction at \(1000 \mathrm{~K}\) is \(6.0 \times 10^{4} \mathrm{M}^{-2} \mathrm{~s}^{-1}\), what is the reaction rate when \([\mathrm{NO}]=0.035 \mathrm{M}\) and \(\left[\mathrm{H}_{2}\right]=0.015 \mathrm{M}\) ? (c) What is the reaction rate at \(1000 \mathrm{~K}\) when the concentration of \(\mathrm{NO}\) is increased to \(0.10 \mathrm{M}\), while the concentration of \(\mathrm{H}_{2}\) is \(0.010 \mathrm{M}\) ? (d) What is the reaction rate at \(1000 \mathrm{~K}\) if [NO] is decreased to \(0.010 \mathrm{M}\) and \(\left[\mathrm{H}_{2}\right]\) is increased to \(0.030 \mathrm{M}\) ?

The reaction between ethyl bromide \(\left(\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{Br}\right)\) and hydroxide ion in ethyl alcohol at \(330 \mathrm{~K}_{2} \mathrm{C}_{2} \mathrm{H}_{3} \mathrm{Br}(a l c)+\mathrm{OH}^{-}(a l c) \longrightarrow\) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)+\mathrm{Br}^{-}(\)alc \()\), is first order each in ethyl bromide and hydroxide ion. When \(\left[\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Br}\right]\) is \(0.0477 \mathrm{M}\) and \(\left[\mathrm{OH}^{-}\right]\) is \(0.100 M\), the rate of disappearance of ethyl bromide is \(1.7 \times 10^{-7} \mathrm{M} / \mathrm{s}\). (a) What is the value of the rate constant? (b) What are the units of the rate constant? (c) How would the rate of disappearance of ethyl bromide change if the solution were diluted by adding an equal volume of pure ethyl alcohol to the solution?

The iodide ion reacts with hypochlorite ion (the active ingredient in chlorine bleaches) in the following way: \(\mathrm{OCl}^{-}+\mathrm{I}^{-} \longrightarrow \mathrm{OI}^{-}+\mathrm{Cl}^{-}\). This rapid reaction gives the following rate data: (a) Write the rate law for this reaction. (b) Calculate the rate constant with proper units. (c) Calculate the rate when \(\left[\mathrm{OCI}^{-}\right]=2.0 \times 10^{-3} \mathrm{M}\) and \(\left[\mathrm{I}^{-}\right]=5.0 \times 10^{-4} \mathrm{M}\).

(a) Define the following symbols that are encountered in rate equations for the generic reaction \(\mathrm{A} \rightarrow \mathrm{B}:[\mathrm{A}]_{0}, t_{1 / 2}[\mathrm{~A}]_{\mathrm{b}} k\). (b) What quantity, when graphed versus time, will yield a straight line for a first-order reaction? (c) How can you calculate the rate constant for a first- order reaction from the graph you made in part (b)?

(a) For a generic second-order reaction \(\mathrm{A} \longrightarrow \mathrm{B}\), what quantity, when graphed versus time, will yield a straight line? (b) What is the slope of the straight line from part (a)? (c) How do the half-lives of first-order and second-order reactions differ?

(a) The gas-phase decomposition of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}, \mathrm{SO}_{2} \mathrm{Cl}_{2}(g) \longrightarrow\) \(\mathrm{SO}_{2}(g)+\mathrm{Cl}_{2}(g)\), is first order in \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\). At \(600 \mathrm{~K}\) the halflife for this process is \(2.3 \times 10^{5} \mathrm{~s}\). What is the rate constant at this temperature? (b) At \(320^{\circ} \mathrm{C}\) the rate constant is \(2.2 \times 10^{-5} \mathrm{~s}^{-1}\). What is the half-life at this temperature?

Molecular iodine, \(\mathrm{I}_{2}(\mathrm{~g})\), dissociates into iodine atoms at \(625 \mathrm{~K}\) with a first-order rate constant of \(0.271 \mathrm{~s}^{-1}\). (a) What is the half-life for this reaction? (b) If you start with \(0.050 \mathrm{MI}_{2}\) at this temperature, how much will remain after \(5.12 \mathrm{~s}\) assuming that the iodine atoms do not recombine to form \(\mathrm{I}_{2}\) ?

As described in Exercise 14.41, the decomposition of sulfuryl chloride \(\left(\mathrm{SO}_{2} \mathrm{Cl}_{2}\right)\) is a first-order process. The rate constant for the decomposition at \(660 \mathrm{~K}\) is \(4.5 \times 10^{-2} \mathrm{~s}^{-1}\). (a) If we begin with an initial \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) pressure of 450 torr, what is the partial pressure of this substance after \(60 \mathrm{~s}\) ? (b) At what time will the partial pressure of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) decline to one-tenth its initial value?

The first-order rate constant for the decomposition of \(\mathrm{N}_{2} \mathrm{O}_{5}, 2 \mathrm{~N}_{2} \mathrm{O}_{5}(g) \longrightarrow 4 \mathrm{NO}_{2}(g)+\mathrm{O}_{2}(g)\), at \(70^{\circ} \mathrm{C}\) is \(6.82 \times\) \(10^{-3} \mathrm{~s}^{-1}\). Suppose we start with \(0.0250 \mathrm{~mol}\) of \(\mathrm{N}_{2} \mathrm{O}_{5}(\mathrm{~g})\) in a volume of \(2.0 \mathrm{~L}\). (a) How many moles of \(\mathrm{N}_{2} \mathrm{O}_{5}\) will remain after \(5.0 \mathrm{~min}\) ? (b) How many minutes will it take for the quantity of \(\mathrm{N}_{2} \mathrm{O}_{5}\) to drop to \(0.010\) mol? (c) What is the half-life of \(\mathrm{N}_{2} \mathrm{O}_{5}\) at \(70{ }^{\circ} \mathrm{C}\) ?

The reaction $\mathrm{SO}_{2} \mathrm{Cl}_{2}(g) \longrightarrow \mathrm{SO}_{2}(g)+\mathrm{Cl}_{2}(g)\( is first order in \)\mathrm{SO}_{2} \mathrm{Cl}_{2}$. Using the following kinetic data, determine the magnitude and units of the first-order rate constant: $$ \begin{array}{cc} \hline \text { Time (s) } & \text { Pressure } \mathrm{SO}_{2} \mathrm{Cl}_{2}(\mathrm{kPa}) \\ \hline 0 & 101.3 \mathrm{kPa} \\ 2500 & 95.95 \mathrm{kPa} \\ 5000 & 90.69 \mathrm{kPa} \\ 7500 & 85.92 \mathrm{kPa} \\ 10,000 & 81.36 \mathrm{kPa} \\ \hline \end{array} $$

The gas-phase decomposition of $\mathrm{NO}_{2}, 2 \mathrm{NO}_{2}(g) \longrightarrow\( \)2 \mathrm{NO}(g)+\mathrm{O}_{2}(g),$ is studied at \(383^{\circ} \mathrm{C}\), giving the following data: $$ \begin{array}{cc} \hline \text { Time (s) } & {\left[\mathrm{NO}_{2}\right](M)} \\ \hline 0.0 & 0.100 \\ 5.0 & 0.017 \\ 10.0 & 0.0090 \\ 15.0 & 0.0062 \\ 20.0 & 0.0047 \\ \hline \end{array} $$ (a) Is the reaction first order or second order with respect to the concentration of \(\mathrm{NO}_{2} ?(\mathbf{b})\) What is the rate constant? (c) Predict the reaction rates at the beginning of the reaction for initial concentrations of \(0.200 \mathrm{M}, 0.100 \mathrm{M},\) and $0.050 \mathrm{M} \mathrm{NO}_{2}$.

Sucrose \(\left(\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\right),\) commonly known as table sugar, reacts in dilute acid solutions to form two simpler sugars, glucose and fructose, both of which have the formula \(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}\). At \(23^{\circ} \mathrm{C}\) and in \(0.5 \mathrm{M} \mathrm{HCl}\), the following data were obtained for the disappearance of sucrose: $$ \begin{array}{cc} \hline \text { Time (min) } & {\left[\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\right](\mathrm{M})} \\ \hline 0 & 0.316 \\ 39 & 0.274 \\ 80 & 0.238 \\ 140 & 0.190 \\ 210 & 0.146 \\ \hline \end{array} $$

(a) What factors determine whether a collision between two molecules will lead to a chemical reaction? (b) According to the collision model, why does temperature affect the value of the rate constant? (c) Does the rate constant for a reaction generally increase or decrease with an increase in reaction temperature?

(a) In which of the following reactions would you expect the orientation factor to be least important in leading to reaction: \(\mathrm{NO}+\mathrm{O} \longrightarrow \mathrm{NO}_{2}\) or \(\mathrm{H}+\mathrm{Cl} \longrightarrow \mathrm{HCl}\) ? (b) How does the kinetic-molecular theory help us understand the temperature dependence of chemical reactions?

(a) The activation energy for the isomerization of methyl isonitrile (Figure 14.7) is \(160 \mathrm{~kJ} / \mathrm{mol}\). Calculate the fraction of methyl isonitrile molecules that has an energy of \(160.0 \mathrm{~kJ}\) or greater at \(500 \mathrm{~K}\). (b) Calculate this fraction for a temperature of \(520 \mathrm{~K}\). What is the ratio of the fraction at \(520 \mathrm{~K}\) to that at \(500 \mathrm{~K} ?\)

For the elementary process \(\mathrm{N}_{2} \mathrm{O}_{5}(g) \longrightarrow \mathrm{NO}_{2}(g)+\mathrm{NO}_{3}(g)\) the activation energy \(\left(E_{a}\right)\) and overall \(\Delta E\) are \(154 \mathrm{~kJ} / \mathrm{mol}\) and \(136 \mathrm{~kJ} / \mathrm{mol}\), respectively. (a) Sketch the energy profile for this reaction, and label \(E_{a}\) and \(\Delta E\). (b) What is the activation energy for the reverse reaction?

Indicate whether each statement is true or false. (a) If you compare two reactions with similar collision factors, the one with the larger activation energy will be faster. (b) A reaction that has a small rate constant must have a small frequency factor. (c) Increasing the reaction temperature increases the fraction of successful collisions between reactants.

Indicate whether each statement is true or false. (a) If you measure the rate constant for a reaction at different temperatures, you can calculate the overall enthalpy change for the reaction. (b) Exothermic reactions are faster than endothermic reactions. (c) If you double the temperature for a reaction, you cut the activation energy in half.

Based on their activation energies and energy changes and assuming that all collision factors are the same, which of the following reactions would be fastest and which would be slowest? (a) \(E_{a}=45 \mathrm{~kJ} / \mathrm{mol} ; \Delta E=-25 \mathrm{~kJ} / \mathrm{mol}\) (b) \(E_{a}=35 \mathrm{~kJ} / \mathrm{mol} ; \Delta E=-10 \mathrm{~kJ} / \mathrm{mol}\) (c) \(E_{a}=55 \mathrm{~kJ} / \mathrm{mol} ; \Delta E=10 \mathrm{~kJ} / \mathrm{mol}\)

(a) A certain first-order reaction has a rate constant of \(2.75 \times 10^{-2} \mathrm{~s}^{-1}\) at \(20^{\circ} \mathrm{C}\). What is the value of \(k\) at \(60^{\circ} \mathrm{C}\) if \(E_{a}=75.5 \mathrm{~kJ} / \mathrm{mol}\) ? (b) Another first-order reaction also has a rate constant of \(2.75 \times 10^{-2} \mathrm{~s}^{-1}\) at \(20^{\circ} \mathrm{C}\) What is the value of \(k\) at \(60^{\circ} \mathrm{C}\) if \(E_{a}=125 \mathrm{~kJ} / \mathrm{mol}\) ? (c) What assumptions do you need to make in order to calculate answers for parts (a) and (b)?

Understanding the high-temperature behavior of nitrogen oxides is essential for controlling pollution generated in automobile engines. The decomposition of nitric oxide \((\mathrm{NO})\) to \(\mathrm{N}_{2}\) and \(\mathrm{O}_{2}\) is second order with a rate constant of \(0.0796 \mathrm{M}^{-1} \mathrm{~s}^{-1}\) at \(737^{\circ} \mathrm{C}\) and \(0.0815 \mathrm{M}^{-1} \mathrm{~s}^{-1}\) at \(947{ }^{\circ} \mathrm{C}\). Calculate the activation energy for the reaction.

The temperature dependence of the rate constant for a reaction is tabulated as follows: $$ \begin{array}{ll} \hline \text { Temperature (K) } & k\left(M^{-1} \mathrm{~s}^{-1}\right) \\ \hline 600 & 0.028 \\ 650 & 0.22 \\ 700 & 1.3 \\ 750 & 6.0 \\ 800 & 23 \\ \hline \end{array} $$ Calculate \(E_{a}\) and \(A\).

(a) What is meant by the term elementary reaction? (b) What is the difference between a unimolecular and a bimolecular elementary reaction? (c) What is a reaction mechanism? (d) What is meant by the term rate-determining step?

(a) What is meant by the term molecularity? (b) Why are termolecular elementary reactions so rare? (c) What is an intermediate in a mechanism? (d) What are the differences between an intermediate and a transition state?

What is the molecularity of each of the following elementary reactions? Write the rate law for each. (a) \(\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{Cl}(g)\) (b) \(\mathrm{OCl}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{HOCl}(a q)+\mathrm{OH}^{-}(a q)\) (c) \(\mathrm{NO}(g)+\mathrm{Cl}_{2}(g) \longrightarrow \mathrm{NOCl}_{2}(g)\)

What is the molecularity of each of the following elementary reactions? Write the rate law for each. (a) \(2 \mathrm{NO}(g) \longrightarrow \mathrm{N}_{2} \mathrm{O}_{2}(g)\) (b) \(\mathrm{H}_{2} \mathrm{C}-\mathrm{CH}_{2}(g) \longrightarrow \mathrm{CH}_{2}=\mathrm{CH}-\mathrm{CH}_{3}(g)\) (c) \(\mathrm{SO}_{3}(g) \longrightarrow \mathrm{SO}_{2}(g)+\mathrm{O}(g)\)

The following mechanism has been proposed for the gasphase reaction of \(\mathrm{H}_{2}\) with \(\mathrm{ICl}\) : $$ \begin{aligned} &\mathrm{H}_{2}(g)+\mathrm{ICl}(g) \longrightarrow \mathrm{HI}(g)+\mathrm{HCl}(g) \\ &\mathrm{HI}(g)+\mathrm{ICl}(g) \longrightarrow \mathrm{I}_{2}(g)+\mathrm{HCl}(g) \end{aligned} $$ (a) Write the balanced equation for the overall reaction. (b) Identify any intermediates in the mechanism. (c) If the first step is slow and the second one is fast, which rate law do you expect to be observed for the overall reaction?

The decomposition of hydrogen peroxide is catalyzed by iodide ion. The catalyzed reaction is thought to proceed by a two-step mechanism: $$ \begin{aligned} \mathrm{H}_{2} \mathrm{O}_{2}(a q)+\mathrm{I}^{-}(a q) & \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{IO}^{-}(a q) \quad \text { (slow) } \\ \mathrm{IO}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}_{2}(a q) & \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{O}_{2}(g)+\mathrm{I}^{-}(a q) \text { (fast) } \end{aligned} $$ (a) Write the chemical equation for the overall process. (b) Identify the intermediate, if any, in the mechanism. (c) Assuming that the first step of the mechanism is rate determining, predict the rate law for the overall process.

The reaction \(2 \mathrm{NO}(g)+\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{NOCl}(g)\) was performed and the following data obtained under conditions of constant \(\left[\mathrm{Cl}_{2}\right]\) : (a) Is the following mechanism consistent with the data? $$ \begin{aligned} \mathrm{NO}(g)+\mathrm{Cl}_{2}(g) & \longrightarrow \mathrm{NOCl}_{2}(g) \text { (fast) } \\ \mathrm{NOCl}_{2}(g)+\mathrm{NO}(g) & \longrightarrow 2 \mathrm{NOCl}(g) \text { (slow) } \end{aligned} $$ (b) Does the linear plot guarantee that the overall rate law is second order?

You have studied the gas-phase oxidation of \(\mathrm{HBr}\) by \(\mathrm{O}_{2}\) : $$ 4 \mathrm{HBr}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(g)+2 \mathrm{Br}_{2}(g) $$ You find the reaction to be first order with respect to \(\mathrm{HBr}\) and first order with respect to \(\mathrm{O}_{2}\). You propose the following mechanism: $$ \begin{aligned} \mathrm{HBr}(g)+\mathrm{O}_{2}(g) & \longrightarrow \operatorname{HOOBr}(g) \\\ \mathrm{HOOBr}(g)+\operatorname{HBr}(g) & \longrightarrow 2 \operatorname{HOBr}(g) \\ \mathrm{HOBr}(g)+\operatorname{HBr}(g) & \longrightarrow \mathrm{H}_{2} \mathrm{O}(g)+\mathrm{Br}_{2}(g) \end{aligned} $$ (a) Confirm that the elementary reactions add to give the overall reaction. (b) Based on the experimentally determined rate law, which step is rate determining? (c) What are the intermediates in this mechanism? (d) If you are unable to detect HOBr or HOOBr among the products, does this disprove your mechanism?

(a) What is a catalyst? (b) What is the difference between a homogeneous and a heterogeneous catalyst? (c) Do catalysts affect the overall enthalpy change for a reaction, the activation energy, or both?

(a) Most commercial heterogeneous catalysts are extremely finely divided solid materials. Why is particle size important? (b) What role does adsorption play in the action of a heterogeneous catalyst?

In solution, chemical species as simple as \(\mathrm{H}^{+}\)and \(\mathrm{OH}^{-}\)can serve as catalysts for reactions. Imagine you could measure the \(\left[\mathrm{H}^{+}\right.\)] of a solution containing an acid- catalyzed reaction as it occurs. Assume the reactants and products themselves are neither acids nor bases. Sketch the \(\left[\mathrm{H}^{+}\right]\)concentration profile you would measure as a function of time for the reaction, assuming \(t=0\) is when you add a drop of acid to the reaction.

The oxidation of \(\mathrm{SO}_{2}\) to \(\mathrm{SO}_{3}\) is accelerated by \(\mathrm{NO}_{2}\). The reaction proceeds according to: $$ \begin{aligned} &\mathrm{NO}_{2}(g)+\mathrm{SO}_{2}(g) \longrightarrow \mathrm{NO}(g)+\mathrm{SO}_{3}(g) \\ &2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g) \end{aligned} $$ (a) Show that, with appropriate coefficients, the two reactions can be summed to give the overall oxidation of \(\mathrm{SO}_{2}\) by \(\mathrm{O}_{2}\) to give \(\mathrm{SO}_{3}\). (b) \(\mathrm{Do}\) we consider \(\mathrm{NO}_{2}\) a catalyst or an intermediate in this reaction? (c) Is this an example of homogeneous catalysis or heterogeneous catalysis?

The addition of \(\mathrm{NO}\) accelerates the decomposition of \(\mathrm{N}_{2} \mathrm{O}\), possibly by the following mechanism: $$ \begin{aligned} \mathrm{NO}(g)+& \mathrm{N}_{2} \mathrm{O}(g) \longrightarrow \mathrm{N}_{2}(g)+\mathrm{NO}_{2}(g) \\ 2 \mathrm{NO}_{2}(g) & \longrightarrow 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \end{aligned} $$ (a) What is the chemical equation for the overall reaction? Show how the two steps can be added to give the overall equation. (b) Is NO serving as a catalyst or an intermediate in this reaction? (c) If experiments show that during the decomposition of \(\mathrm{N}_{2} \mathrm{O}, \mathrm{NO}_{2}\) does not accumulate in measurable quantities, does this rule out the proposed mechanism?

Many metallic catalysts, particularly the precious-metal ones, are often deposited as very thin films on a substance of high surface area per unit mass, such as alumina \(\left(\mathrm{Al}_{2} \mathrm{O}_{3}\right)\) or silica \(\left(\mathrm{SiO}_{2}\right)\). (a) Why is this an effective way of utilizing the catalyst material compared to having powdered metals? (b) How does the surface area affect the rate of reaction?

(a) If you were going to build a system to check the effectiveness of automobile catalytic converters on cars, what substances would you want to look for in the car exhaust? (b) Automobile catalytic converters have to work at high temperatures, as hot exhaust gases stream through them. In what ways could this be an advantage? In what ways a disadvantage? (c) Why is the rate of flow of exhaust gases over a catalytic converter important?

Heterogeneous catalysts that perform hydrogenation reactions, as illustrated in Figure 14.24, are subject to "poisoning," which shuts down their catalytic ability. Compounds of sulfur are often poisons. Suggest a mechanism by which such compounds might act as poisons.

The enzyme carbonic anhydrase catalyzes the reaction \(\mathrm{CO}_{2}(g)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{HCO}_{3}{\underline{\phantom{xx}}}^{-}(a q)+\mathrm{H}^{+}(a q)\). In water, without the enzyme, the reaction proceeds with a rate constant of \(0.039 \mathrm{~s}^{-1}\) at \(25^{\circ} \mathrm{C}\). In the presence of the enzyme in water, the reaction proceeds with a rate constant of \(1.0 \times 10^{6} \mathrm{~s}^{-1}\) at \(25^{\circ} \mathrm{C}\). Assuming the collision factor is the same for both situations, calculate the difference in activation energies for the uncatalyzed versus enzyme-catalyzed reaction.

The enzyme urease catalyzes the reaction of urea, \(\left(\mathrm{NH}_{2} \mathrm{CONH}_{2}\right)\), with water to produce carbon dioxide and ammonia. In water, without the enzyme, the reaction proceeds with a first-order rate constant of \(4.15 \times 10^{-5} \mathrm{~s}^{-1}\) at \(100^{\circ} \mathrm{C}\). In the presence of the enzyme in water, the reaction proceeds with a rate constant of \(3.4 \times 10^{4} \mathrm{~s}^{-1}\) at \(21^{\circ} \mathrm{C}\). (a) Write out the balanced equation for the reaction catalyzed by urease. (b) If the rate of the catalyzed reaction were the same at \(100^{\circ} \mathrm{C}\) as it is at \(21^{\circ} \mathrm{C}\), what would be the difference in the activation energy between the catalyzed and uncatalyzed reactions? (c) In actuality, what would you expect for the rate of the catalyzed reaction at \(100^{\circ} \mathrm{C}\) as compared to that at \(21^{\circ} \mathrm{C}\) ? (d) On the basis of parts (c) and (d), what can you conclude about the difference in activation energies for the catalyzed and uncatalyzed reactions?

The activation energy of an uncatalyzed reaction is \(95 \mathrm{~kJ} / \mathrm{mol}\). The addition of a catalyst lowers the activation energy to \(55 \mathrm{~kJ} / \mathrm{mol}\). Assuming that the collision factor remains the same, by what factor will the catalyst increase the rate of the reaction at (a) \(25^{\circ} \mathrm{C}\), (b) \(125^{\circ} \mathrm{C}\) ?