The addition of 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?

Short Answer

Expert verified
(a) The overall chemical equation for the reaction is: \(\mathrm{N}_{2} \mathrm{O}(g) \longrightarrow \mathrm{N}_{2}(g) + \mathrm{O}_{2}(g)\) (b) NO is serving as a catalyst in this reaction. (c) The absence of measurable NO₂ accumulation does not rule out the proposed mechanism, as it might suggest that the second step of the mechanism is much faster than the first step.

Step by step solution

01

Find the overall reaction equation

To determine the overall chemical equation, we will add the two steps of the reaction mechanism: \[ \begin{aligned} \mathrm{NO}(g)+\mathrm{N}_{2} \mathrm{O}(g) & \longrightarrow \mathrm{N}_{2}(g)+\mathrm{NO}_{2}(g) \\ 2 \mathrm{NO}_{2}(g) & \longrightarrow 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \end{aligned} \] Add both equations together and cancel any species that appear on both sides of the equation (in this case, NO and NO₂): \[ \begin{aligned} \cancel{\mathrm{NO}(g)}+\cancel{\mathrm{N}_{2} \mathrm{O}(g)} + 2 \cancel{\mathrm{NO}_{2}(g)} & \longleftrightarrow \mathrm{N}_{2}(g)+\cancel{\mathrm{NO}_{2}(g)} + 2 \cancel{\mathrm{NO}(g)}+\mathrm{O}_{2}(g) \end{aligned} \] This simplifies to: \[ \mathrm{N}_{2} \mathrm{O}(g) \longrightarrow \mathrm{N}_{2}(g) + \mathrm{O}_{2}(g) \]
02

Determine the role of NO

To understand whether NO is serving as a catalyst or an intermediate, we should analyze how it behaves in the reaction mechanism. A catalyst speeds up the reaction by participating in the reaction steps but is not consumed in the overall reaction. An intermediate is formed and consumed during the reaction steps. In the mechanism, NO is consumed in the first step and then regenerated in the second step. Since it is not consumed in the overall reaction, NO is acting as a catalyst.
03

Discuss the effect of non-accumulating NO₂ on the proposed mechanism

The fact that experiments do not show measurable accumulation of NO₂ during the decomposition of N₂O does not necessarily rule out the proposed mechanism. It might indicate that the second step of the reaction mechanism (the decomposition of NO₂) is much faster than the first step (the reaction between NO and N₂O). In this case, the intermediate NO₂ would be rapidly consumed as soon as it is produced, making it difficult to detect its accumulation experimentally. In conclusion: (a) The overall chemical equation for the reaction is: \(\mathrm{N}_{2} \mathrm{O}(g) \longrightarrow \mathrm{N}_{2}(g) + \mathrm{O}_{2}(g)\) (b) NO is serving as a catalyst in this reaction. (c) The absence of measurable NO₂ accumulation does not rule out the proposed mechanism, as it might suggest that the second step of the mechanism is much faster than the first step.

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Most popular questions from this chapter

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. \((\mathbf{b})\) 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 \(21^{\circ} \mathrm{C} ?(\mathbf{d})\) On the basis of parts (c) and (d), what can you conclude about the difference in activation energies for the catalyzed and uncatalyzed reactions?

(a) For the generic reaction \(\mathrm{A} \rightarrow \mathrm{B}\) what quantity, when graphed versus time, will yield a straight line for a first- order reaction? (b) How can you calculate the rate constant for a first-order reaction from the graph you made in part (a)?

For a first order reaction \(\mathrm{A} \longrightarrow \mathrm{B}+\mathrm{C},\) if the half-life of \(\mathrm{A}\) at \(25^{\circ} \mathrm{C}\) is $3.05 \times 10^{4} \mathrm{~s},\( what is the rate constant \)k$ at this temperature? What percentage of A will not have reacted after one day?

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) \(25^{\circ} \mathrm{C},(\mathbf{b}) 125^{\circ} \mathrm{C} ?\)

Consider the following hypothetical aqueous reaction: $\mathrm{A}(a q) \rightarrow \mathrm{B}(a q)\(. A flask is charged with \)0.065 \mathrm{~mol}$ of \(\mathrm{A}\) in a total volume of \(100.0 \mathrm{~mL}\). The following data are collected: $$ \begin{array}{lccccc} \hline \text { Time (min) } & 0 & 10 & 20 & 30 & 40 \\ \hline \text { Moles of A } & 0.065 & 0.051 & 0.042 & 0.036 & 0.031 \\ \hline \end{array} $$ (a) Calculate the number of moles of \(\mathrm{B}\) at each time in the table, assuming that there are no molecules of \(\mathrm{B}\) at time zero and that A cleanly converts to B with no intermediates. (b) Calculate the average rate of disappearance of A for each 10 -min interval in units of \(M /\) s. (c) Between \(t=0 \mathrm{~min}\) and \(t=30 \mathrm{~min},\) what is the average rate of appearance of \(\mathrm{B}\) in units of \(\mathrm{M} / \mathrm{s}\) ? Assume that the volume of the solution is constant.

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