Chapter 12: Problem 15
Define what is meant by unimolecular and bimolecular steps. Why are termolecular steps infrequently seen in chemical reactions?
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Chapter 12: Problem 15
Define what is meant by unimolecular and bimolecular steps. Why are termolecular steps infrequently seen in chemical reactions?
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The activation energy for a reaction is changed from 184 \(\mathrm{kJ} /\) \(\mathrm{mol}\) to 59.0 \(\mathrm{kJ} / \mathrm{mol}\) at \(600 . \mathrm{K}\) by the introduction of a catalyst. If the uncatalyzed reaction takes about 2400 years to occur, about how long will the catalyzed reaction take? Assume the frequency factor \(A\) is constant, and assume the initial concentrations are the same.
Draw a rough sketch of the energy profile for each of the following cases: a. \(\Delta E=+10 \mathrm{kJ} / \mathrm{mol}, E_{\mathrm{a}}=25 \mathrm{kJ} / \mathrm{mol}\) b. \(\Delta E=-10 \mathrm{kJ} / \mathrm{mol}, E_{\mathrm{a}}=50 \mathrm{kJ} / \mathrm{mol}\) c. \(\Delta E=-50 \mathrm{kJ} / \mathrm{mol}, E_{\mathrm{a}}=50 \mathrm{kJ} / \mathrm{mol}\)
Each of the statements given below is false. Explain why. a. The activation energy of a reaction depends on the overall energy change \((\Delta E)\) for the reaction. b. The rate law for a reaction can be deduced from examination of the overall balanced equation for the reaction. c. Most reactions occur by one-step mechanisms.
Sulfuryl chloride undergoes first-order decomposition at \(320 .^{\circ} \mathrm{C}\) with a half-life of 8.75 \(\mathrm{h}\) . $$ \mathrm{SO}_{2} \mathrm{Cl}_{2}(g) \longrightarrow \mathrm{SO}_{2}(g)+\mathrm{Cl}_{2}(g) $$ What is the value of the rate constant, \(k,\) in \(\mathrm{s}^{-1}\) ? If the initial pressure of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) is 791 torr and the decomposition occurs in a \(1.25-\mathrm{L}\) container, how many molecules of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) remain after 12.5 \(\mathrm{h}\) ?
For enzyme-catalyzed reactions that follow the mechanism $$ \begin{aligned} \mathrm{E}+\mathrm{S} & \rightleftharpoons \mathrm{E} \cdot \mathrm{S} \\ \mathrm{E} \cdot \mathrm{S} & \rightleftharpoons \mathrm{E}+\mathrm{P} \end{aligned} $$ a graph of the rate as a function of [S], the concentration of the substrate, has the following appearance: Note that at higher substrate concentrations the rate no longer changes with [S]. Suggest a reason for this.
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