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Give the individual reaction orders for all substances and the overall reaction order from the following rate law: $$ \text { Rate }=k\left[\mathrm{BrO}_{3}^{-}\right]\left[\mathrm{Br}^{-}\right]\left[\mathrm{H}^{+}\right]^{2} $$

Short Answer

Expert verified
The orders are: \[\text{BrO}_3^-: 1, \text{Br}^-: 1, \text{H}^+: 2\]. The overall order is 4.

Step by step solution

01

Identify the Rate Law

The rate law given is \[\text{Rate} = k[\text{BrO}_3^-][\text{Br}^-][\text{H}^+]^2\]
02

Determine the Order of Each Substance

Look at the exponents of each reactant in the rate law: \[\text{BrO}_3^-\text{: Order = 1}\] \[\text{Br}^-\text{: Order = 1}\] \[\text{H}^+\text{: Order = 2}\]
03

Calculate the Overall Reaction Order

Sum the orders of all reactants: \[1 + 1 + 2 = 4\] So, the overall reaction order is 4.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

rate law
In chemistry, a rate law is a mathematical equation that describes how the concentration of reactants affects the rate of a chemical reaction. The general form of a rate law is: \(\text{Rate} = k[A]^m[B]^n...\) where: \(\text{Rate}\) is the reaction rate, \(k\) is the rate constant, \[A\] and \[B\] are the concentrations of reactants, \(m\) and \(n\) are the reaction orders with respect to each reactant. The rate constant \(k\) is a proportionality constant unique to a particular reaction at a given temperature. Its value changes with temperature but does not depend on the concentration of reactants. Reaction orders (\(m\) and \(n\)) indicate how the rate is affected by the concentration of each reactant. These orders are determined experimentally and do not necessarily correspond to the stoichiometric coefficients in the balanced chemical equation, though they often do. In the given rate law: \(\text{Rate} = k[\text{BrO}_3^-][\text{Br}^-][\text{H}^+]^2\), the exponents indicate the reaction order with respect to each reactant.
overall reaction order
The overall reaction order is the sum of the individual reaction orders of all reactants in the rate law. It gives a general idea of how the reaction rate will change if the concentrations of all reactants are varied simultaneously. To find the overall reaction order, you add up the exponents of all the reactants in the rate law. For example, in the given rate law: \[ \text{Rate} = k[\text{BrO}_3^-][\text{Br}^-][\text{H}^+]^2 \], the exponents are: 1 for \(\text{BrO}_3^-\text{ORDER}\), 1 for \(\text{Br}^-\text{ORDER}\), and 2 for \(\text{H}^+\text{ORDER}\). So, the overall reaction order is \[ 1 + 1 + 2 = 4 \]. This means the reaction is fourth-order overall, implying that the rate of reaction is very sensitive to changes in the concentration of reactants.
individual reaction orders
Individual reaction orders specify how the rate of reaction depends on the concentration of a single reactant. These orders are represented by the exponents in the rate law formula. They must be determined experimentally and are not necessarily related to the stoichiometry of the reaction. For each reactant in the given rate law: \[ \text{Rate} = k[\text{BrO}_3^-][\text{Br}^-][\text{H}^+]^2 \], we find the following individual reaction orders: \(\text{BrO}_3^-\text{: Order = 1}\) \(\text{Br}^-\text{: Order = 1}\) \(\text{H}^+\text{: Order = 2}\). This means: - The rate of the reaction increases linearly with the concentration of \[ \text{BrO}_3^- \]. - The rate of the reaction also increases linearly with the concentration of \[ \text{Br}^- \]. - The rate of the reaction increases quadratically with the concentration of \[ \text{H}^+ \]. Understanding these orders helps in predicting how changes in reactant concentrations will affect the reaction rate.

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Most popular questions from this chapter

Define reaction rate. Assuming constant temperature and a closed reaction vessel, why does the rate change with time?

Consider the following mechanism: (1) \(\mathrm{ClO}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}(l) \rightleftharpoons \mathrm{HClO}(a q)+\mathrm{OH}^{-}(a q) \quad\) [fast (2) \(\mathrm{I}^{-}(a q)+\mathrm{HClO}(a q) \longrightarrow \mathrm{HIO}(a q)+\mathrm{Cl}^{-}(a q)\) [slow] (3) \(\mathrm{OH}^{-}(a q)+\mathrm{HIO}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{IO}^{-}(a q)\) [fast (a) What is the overall equation? (b) Identify the intermediate(s), if any. (c) What are the molecularity and the rate law for each step? (d) Is the mechanism consistent with the actual rate law: Rate = \(k\left[\mathrm{ClO}^{-}\right]\left[\mathrm{I}^{-}\right] ?\)

The compound \(\mathrm{AX}_{2}\) decomposes according to the equation \(2 \mathrm{AX}_{2}(g) \rightarrow 2 \mathrm{AX}(g)+\mathrm{X}_{2}(g) .\) In one experiment, \(\left[\mathrm{AX}_{2}\right]\) was measured at various times and these data were obtained: $$ \begin{array}{cc} \text { Time (s) } & {\left[A X_{2}\right](\mathrm{mol} / \mathrm{L})} \\ \hline 0.0 & 0.0500 \\ 2.0 & 0.0448 \\ 6.0 & 0.0300 \\ 8.0 & 0.0249 \\ 10.0 & 0.0209 \\ 20.0 & 0.0088 \end{array} $$ (a) Find the average rate over the entire experiment. (b) Is the initial rate higher or lower than the rate in part (a)? Use graphical methods to estimate the initial rate.

Define the half-life of a reaction. Explain on the molecular level why the half-life of a first-order reaction is constant.

16.103 Even when a mechanism is consistent with the rate law, later work may show it to be incorrect. For example, the reaction between hydrogen and iodine has this rate law: rate \(=k\left[\mathrm{H}_{2}\right]\left[\mathrm{I}_{2}\right]\). The long-accepted mechanism had a single bimolecular step; that is, the overall reaction was thought to be elementary: \(\mathrm{H}_{2}(g)+\mathrm{I}_{2}(g) \longrightarrow 2 \mathrm{HI}(g)\) In the 1960 s, however, spectroscopic evidence showed the presence of free I atoms during the reaction. Kineticists have since proposed a three-step mechanism: (1) \(\mathrm{I}_{2}(g) \rightleftharpoons 2 \mathrm{I}(g)\) [fast] (2) \(\mathrm{H}_{2}(g)+\mathrm{I}(g) \rightleftharpoons \mathrm{H}_{2} \mathrm{I}(g)\) [fast] (3) \(\mathrm{H}_{2} \mathrm{I}(g)+\mathrm{I}(g) \longrightarrow 2 \mathrm{HI}(g) \quad[\) slow \(]\) Show that this mechanism is consistent with the rate law.

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