The decomposition of hydrogen peroxide is catalyzed by iodide ion. The catalyzed reaction is thought to proceed by a two-step mechanism: $$ \begin{aligned} \mathrm{H}_{2} \mathrm{O}_{2}(a q)+\mathrm{I}^{-}(a q) & \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{IO}^{-}(a q)(\text { slow }) \\ \mathrm{IO}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}_{2}(a q) & \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{O}_{2}(g)+\mathrm{I}^{-}(a q) \quad(\text { fast }) \end{aligned} $$ (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.

Short Answer

Expert verified
(a) The overall chemical equation for the decomposition of hydrogen peroxide catalyzed by iodide ions is: \(\mathrm{2H}_{2} \mathrm{O}_{2}(a q) + \mathrm{I}^{-}(a q) \longrightarrow \mathrm{2H}_{2} \mathrm{O}(l) + \mathrm{O}_{2}(g) + \mathrm{I}^{-}(a q)\) (b) The intermediate in the mechanism is \(\mathrm{IO}^{-}(a q)\). (c) The rate law for the overall process, assuming the first step is rate determining, is: Rate \(= k[\mathrm{H}_{2} \mathrm{O}_{2}][\mathrm{I}^{-}]\).

Step by step solution

01

1. Writing the chemical equation for the overall process

To find the overall chemical equation, we can add the two given equations and then cancel out any species that appear on both sides of the equation. First, let's write down the two equations provided: (i) \(\mathrm{H}_{2} \mathrm{O}_{2}(a q)+\mathrm{I}^{-}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{IO}^{-}(a q)\) (ii) \(\mathrm{IO}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}_{2}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{O}_{2}(g)+\mathrm{I}^{-}(a q)\)
02

2. Identifying the intermediate

An intermediate is a species that is produced in one step of a mechanism and consumed in another step. In this case, \(\mathrm{IO}^{-}(a q)\) is produced in step (i) and consumed in step (ii), so it is the intermediate.
03

3. Predicting the rate law for the overall process

Since the first step of the mechanism is rate determining (slow), the rate law for the overall process will be determined by the rate law of the first step. In the first step, we have: \(\mathrm{H}_{2} \mathrm{O}_{2}(a q)+\mathrm{I}^{-}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{IO}^{-}(a q)\) The rate law for this elementary reaction is given by: Rate \(= k[\mathrm{H}_{2} \mathrm{O}_{2}][\mathrm{I}^{-}]\) where k is the rate constant, and the concentration of each reactant is raised to the power of its stoichiometric coefficient (which is 1 for both reactants in this case). So, the rate law for the overall process is given by: Rate \(= k[\mathrm{H}_{2} \mathrm{O}_{2}][\mathrm{I}^{-}]\).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

In a hydrocarbon solution, the gold compound $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{AuPH}_{3}\( decomposes into ethane \)\left(\mathrm{C}_{2} \mathrm{H}_{6}\right)$ and a different gold compound, \(\left(\mathrm{CH}_{3}\right) \mathrm{AuPH}_{3} .\) The following mechanism has been proposed for the decomposition of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{AuPH}_{3}:$ Step 1: $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{AuPH}_{3} \underset{k-1}{\stackrel{k_{1}}{\rightleftharpoons}}\left(\mathrm{CH}_{3}\right)_{3} \mathrm{Au}+\mathrm{PH}_{3} \quad$ (fast) Step 2: $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{Au} \stackrel{\mathrm{k}_{2}}{\longrightarrow} \mathrm{C}_{2} \mathrm{H}_{6}+\left(\mathrm{CH}_{3}\right) \mathrm{Au} \quad$ (slow) Step 3: $\left(\mathrm{CH}_{3}\right) \mathrm{Au}+\mathrm{PH}_{3} \stackrel{k_{3}}{\longrightarrow}\left(\mathrm{CH}_{3}\right) \mathrm{AuPH}_{3} \quad$ (fast) (a) What is the overall reaction? (b) What are the intermediates in the mechanism? (c) What is the molecularity of each of the elementary steps? (d) What is the rate-determining step? (e) What is the rate law predicted by this mechanism? (f) What would be the effect on the reaction rate of adding \(\mathrm{PH}_{3}\) to the solution of $\left(\mathrm{CH}_{3}\right)_{3} \mathrm{AuPH}_{3} ?$

The isomerization of methyl isonitrile $\left(\mathrm{CH}_{3} \mathrm{NC}\right)\( to acetonitrile \)\left(\mathrm{CH}_{3} \mathrm{CN}\right)$ was studied in the gas phase at \(215^{\circ} \mathrm{C}\), and the following data were obtained: $$ \begin{array}{rc} \hline \text { Time (s) } & {\left[\mathrm{CH}_{3} \mathrm{NC}\right](M)} \\ \hline 0 & 0.0165 \\ 2000 & 0.0110 \\ 5000 & 0.00591 \\ 8000 & 0.00314 \\ 12,000 & 0.00137 \\ 15,000 & 0.00074 \\ \hline \end{array} $$ (a) Calculate the average rate of reaction, in \(M / s\), for the time interval between each measurement. (b) Calculate the average rate of reaction over the entire time of the data from \(t=0\) to \(t=15,000 \mathrm{~s} .(\mathbf{c})\) Which is greater, the average rate between \(t=2000\) and $t=12,000 \mathrm{~s}\(, or between \)t=8000\( and \)t=15,000 \mathrm{~s} ?(\mathbf{d})$ Graph \(\left[\mathrm{CH}_{3} \mathrm{NC}\right]\) versus time and determine the instantaneous rates in \(M / \mathrm{s}\) at \(t=5000 \mathrm{~s}\) and $t=8000 \mathrm{~s}$.

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), \quad\( at \)\quad 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}(g)\( in a volume of \)2.0 \mathrm{~L} .(\mathbf{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 \mathrm{~mol}\( ? (c) What is the half-life of \)\mathrm{N}_{2} \mathrm{O}_{5}$ at \(70{ }^{\circ} \mathrm{C}\) ?

Platinum nanoparticles of diameter \(\sim 2 \mathrm{nm}\) are important catalysts in carbon monoxide oxidation to carbon dioxide. Platinum crystallizes in a face-centered cubic arrangement with an edge length of \(392.4 \mathrm{pm} .(\mathbf{a})\) Estimate how many platinum atoms would fit into a \(2.0-\mathrm{nm}\) sphere; the volume of a sphere is $(4 / 3) \pi r^{3} .\( Recall that \)1 \mathrm{pm}=1 \times 10^{-12} \mathrm{~m}\( and \)1 \mathrm{nm}=1 \times 10^{-9} \mathrm{~m} .(\mathbf{b})$ Estimate how many platinum atoms are on the surface of a 2.0-nm Pt sphere, using the surface area of a sphere \(\left(4 \pi r^{2}\right)\) and assuming that the "footprint" of one Pt atom can be estimated from its atomic diameter of \(280 \mathrm{pm}\) (c) Using your results from (a) and (b), calculate the percentage of \(\mathrm{Pt}\) atoms that are on the surface of a \(2.0-\mathrm{nm}\) nanoparticle. (d) Repeat these calculations for a 5.0-nm platinum nanoparticle. (e) Which size of nanoparticle would you expect to be more catalytically active and why?

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?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free