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The initial rate of a reaction doubles as the concentration of one of the reactants is quadrupled. What is the order of this reactant? If a reactant has a \(-1\) order, what happens to the initial rate when the concentration of that reactant increases by a factor of two?

Short Answer

Expert verified
The order of the reactant, when the initial rate doubles as the concentration of the reactant quadruples, is \(1/2\). When the concentration of a reactant with an order of \(-1\) doubles, the initial reaction rate decreases by a factor of \(1/2\), or the reaction rate becomes 50% of the initial rate.

Step by step solution

01

Determine the order of the reactant given the change in the reaction rate and change in concentration

To do this, we can use the formula for the rate law, which is given by: \[R = k[A]^n\] where: - R is the reaction rate - k is the rate constant - [A] is the concentration of the reactant - n is the order of the reactant We are given that the initial rate doubles when the concentration of the reactant quadruples. We can write this as: \[2R_1 = R_2\] and \[4[A_1] = [A_2]\] Plugging these into the rate law equation for the two rates, we have: \[R_1 = k[A_1]^n\] and \[R_2 = k[A_2]^n\] We can now use these equations to determine the order of the reactant (n).
02

Calculate the order of the reactant

To determine the order of the reactant (n), we can divide the second rate law equation by the first rate law equation: \[\frac{R_2}{R_1} = \frac{k[A_2]^n}{k[A_1]^n}\] We know that \(R_2 = 2R_1\) and \([A_2] = 4[A_1]\), so we can substitute these values into the equation: \[\frac{2R_1}{R_1} = \frac{k(4[A_1])^n}{k[A_1]^n}\] Simplify the equation: \[2 = \frac{(4)^n}{1}\] Now, we just need to solve for n: \(2 = 4^n\) Taking the logarithm of both sides: \(\log 2 = \log 4^n\) Using the power rule for logarithms: \(\log 2 = n \log 4\) Finally, solve for n: \(n = \frac{\log 2}{\log 4} = 1/2\) So, the order of the reactant is \(1/2\).
03

Determine the change in reaction rate for a reactant with a -1 order when its concentration doubles

Now, let's consider a reactant with a -1 order. We can use the rate law equation to find the change in the reaction rate when the concentration of the reactant increases by a factor of two: \[R’ = k([A]’)^{-1}\] Since the concentration of the reactant doubles, \([A]’ = 2[A]\). We can substitute this into the rate law equation: \[R’ = k(2[A])^{-1}\] \[R’ = k\frac{1}{2[A]}\] Now, we can divide this equation by the original rate law equation: \[\frac{R’}{R} = \frac{k\frac{1}{2[A]}}{k[A]^{-1}}\] Simplify the equation: \[\frac{R’}{R} = \frac{1}{2}\] This shows that when the concentration of the reactant with a -1 order doubles, the initial reaction rate decreases by a factor of 1/2, or the reaction rate becomes 50% of the initial rate.

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Most popular questions from this chapter

Consider the general reaction $$ \mathrm{aA}+\mathrm{bB} \longrightarrow \mathrm{cC} $$ and the following average rate data over some time period \(\Delta t\) : $$ \begin{aligned} -\frac{\Delta \mathrm{A}}{\Delta t} &=0.0080 \mathrm{~mol} / \mathrm{L} \cdot \mathrm{s} \\ -\frac{\Delta \mathrm{B}}{\Delta t} &=0.0120 \mathrm{~mol} / \mathrm{L} \cdot \mathrm{s} \\ \frac{\Delta \mathrm{C}}{\Delta t} &=0.0160 \mathrm{~mol} / \mathrm{L} \cdot \mathrm{s} \end{aligned} $$ Determine a set of possible coefficients to balance this general reaction.

Consider the reaction $$ 3 \mathrm{~A}+\mathrm{B}+\mathrm{C} \longrightarrow \mathrm{D}+\mathrm{E} $$ where the rate law is defined as $$ -\frac{\Delta[\mathrm{A}]}{\Delta t}=k[\mathrm{~A}]^{2}[\mathrm{~B}][\mathrm{C}] $$ An experiment is carried out where \([\mathrm{B}]_{0}=[\mathrm{C}]_{0}=1.00 \mathrm{M}\) and \([\mathrm{A}]_{0}=1.00 \times 10^{-4} M\) a. If after \(3.00 \mathrm{~min},[\mathrm{~A}]=3.26 \times 10^{-5} M\), calculate the value of \(k\). b. Calculate the half-life for this experiment. c. Calculate the concentration of \(\mathrm{B}\) and the concentration of \(\mathrm{A}\) after \(10.0 \mathrm{~min}\).

The type of rate law for a reaction, either the differential rate law or the integrated rate law, is usually determined by which data is easiest to collect. Explain.

In the Haber process for the production of ammonia, $$ \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g) $$ what is the relationship between the rate of production of ammonia and the rate of consumption of hydrogen?

Which of the following reactions would you expect to proceed at a faster rate at room temperature? Why? (Hint: Think about which reaction would have the lower activation energy.) \(\begin{aligned} 2 \mathrm{Ce}^{4+}(a q)+\mathrm{Hg}_{2}^{2+}(a q) & \longrightarrow 2 \mathrm{Ce}^{3+}(a q)+2 \mathrm{Hg}^{2+}(a q) \\\ \mathrm{H}_{3} \mathrm{O}^{+}(a q)+\mathrm{OH}^{-}(a q) & \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(l) \end{aligned}\)

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