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You perform a series of experiments for the reaction \(A \longrightarrow B+C\) and find that the rate law has the form rate \(=k[\mathrm{~A}]^{x}\). Determine the value of \(x\) in each of the following cases: (a) There is no rate change when \([\mathrm{A}]_{0}\) is tripled. (b) The rate increases by a factor of 9 when \([\mathrm{A}]_{0}\) is tripled. (c) When \([\mathrm{A}]_{0}\) is doubled, the rate increases by a factor of 8 .

Short Answer

Expert verified
In the given rate law, the values of x for each case are as follows: (a) \(x = 0\), (b) \(x = 2\), and (c) \(x = 3\).

Step by step solution

01

Case (a) - No rate change when \([\mathrm{A}]_{0}\) is tripled

Initially, the rate law is: rate \(= k[\mathrm{A}]^{x}\) When \([\mathrm{A}]_{0}\) is tripled, the new concentration \([\mathrm{A}]'_{0}\) is: \([\mathrm{A}]'_{0} = 3[\mathrm{A}]_{0}\) Now, let's calculate the new rate using the rate law: rate' \(= k[\mathrm{A}']^{x} = k(3[\mathrm{A}]_{0})^x\) According to the given condition, there is no rate change, which means rate' = rate. Therefore: \(k(\mathrm{3}[\mathrm{A}]_{0})^x = k[\mathrm{A}]_{0}^x\) Divide both sides by \(k[\mathrm{A}]_{0}^x\): \[\frac{\mathrm{(3}[\mathrm{A}]_{0})^^x}{[\mathrm{A}]_{0}^x} = 1\] Simplify the equation: \(3^x = 1\) Since \(3^0 = 1\), we have the value of x: \(x = 0\)
02

Case (b) - Rate increases by a factor of 9 when \([\mathrm{A}]_{0}\) is tripled

As in case (a), let's calculate the new rate when \([\mathrm{A}]_{0}\) is tripled: rate' \(= k(3[\mathrm{A}]_{0})^x\) According to the given condition, the rate increases by a factor of 9, which means rate' = 9 * rate. Therefore: \(k(\mathrm{3}[\mathrm{A}]_{0})^x = 9k[\mathrm{A}]_{0}^x\) Divide both sides by \(k[\mathrm{A}]_{0}^x\): \[\frac{\mathrm{(3}[\mathrm{A}]_{0})^^x}{[\mathrm{A}]_{0}^x} = 9\] Simplify the equation: \(3^x = 9\) Since \(3^2 = 9\), we have the value of x: \(x = 2\)
03

Case (c) - Rate increases by a factor of 8 when \([\mathrm{A}]_{0}\) is doubled

As before, let's calculate the new rate when \([\mathrm{A}]_{0}\) is doubled: rate' \(= k(2[\mathrm{A}]_{0})^x\) According to the given condition, the rate increases by a factor of 8, which means rate' = 8 * rate. Therefore: \(k(\mathrm{2}[\mathrm{A}]_{0})^x = 8k[\mathrm{A}]_{0}^x\) Divide both sides by \(k[\mathrm{A}]_{0}^x\): \[\frac{\mathrm{(2}[\mathrm{A}]_{0})^^x}{[\mathrm{A}]_{0}^x} = 8\] Simplify the equation: \(2^x = 8\) Since \(2^3 = 8\), we have the value of x: \(x = 3\) Thus, in each case we have determined the values of x in the rate law: (a) \(x=0\) (b) \(x=2\) (c) \(x=3\)

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Key Concepts

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

Rate Law
Understanding the rate law is crucial for grasping the nuances of chemical kinetics, a branch of chemistry that studies the rates of chemical reactions. A rate law is a mathematical expression that describes the relationship between the reaction rate and the concentration of reactants. In simpler terms, it shows us how fast a reaction will occur given the amount of starting materials, known as reactants.

The general form of a rate law is: \(\text{rate} = k[\text{A}]^x[\text{B}]^y\cdots\), where \(k\) is the rate constant, \([\text{A}], [\text{B}], \ldots\) are the concentrations of reactants, and \(x, y, \ldots\) are the reaction orders with respect to each reactant. The overall order of the reaction is the sum of these individual orders (\(x+y+\ldots\)).

When analyzing a rate law, as in the exercise where the reaction rate was tested with varying concentrations of reactant \(A\), the goal was to determine the exponent \(x\), which signifies how the rate of the reaction changes with the concentration of \(A\). This involved observing changes in reaction rate when the concentration of \(A\) was altered, and meticulously evaluating the impact of this change.
Reaction Rate
The reaction rate tells us how quickly a chemical reaction occurs. It can be defined as the change in concentration of a reactant or product per unit time. For our exercise, the reaction between \(A\) and \(B\) to produce \(C\), we are interested in how the concentration of \(A\) decreases over time, as \(A\) is transformed into \(B\) and \(C\).

The rate can be affected by various factors like temperature, pressure, the presence of catalysts, and the concentration of reactants. In the exercise examples, we manipulated the concentration to observe changes in reaction rate, illuminating the direct influence concentration has.

Rate Measurement

Mathematically, reaction rate can be expressed as: \(\text{rate} = -\frac{\Delta[\text{A}]}{\Delta t}\) for a reactant, where \(\Delta[\text{A}]\) represents the change in concentration and \(\Delta t\) is the change in time. The negative sign indicates that the concentration of reactants diminishes over time. The experiments performed in the exercise aimed to determine how this rate changes under different initial concentrations of reactant \(A\).
Order of Reaction
The order of a reaction provides insight into the dependency of the reaction rate on the concentration of its reactants. It is a key concept in chemical kinetics, as it can be used to predict how changes in concentrations influence the speed of a reaction. In our exercise, the order with respect to reactant \(A\) was determined by observing how the reaction rate changed as the initial concentration of \(A\) was altered.

Orders of reaction are generally determined experimentally, and they can be integers, fractions, or even zero. A zero-order reaction means that the rate is independent of the concentration of the reactant, as was the case in part (a) of the exercise where tripling the concentration of \(A\) did not change the rate, yielding an order of zero (\(x=0\)).

A first-order reaction implies that the rate is directly proportional to one concentration term, while a second-order indicates dependency on either the square of one concentration term or on the product of two different concentrations. Our exercises (b) and (c) revealed that the rate law followed a second and a third-order reaction, respectively, with respect to \(A\), demonstrated by the proportional increase in rate to the increase in \(A\)'s concentration.

Understanding Reaction Orders

Grasping the concept of reaction order is essential for predicting and controlling chemical processes. This knowledge impacts a wide range of applications, from industrial synthesis to pharmaceuticals, where the efficiency and rate of reactions are crucial.

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Most popular questions from this chapter

Enzymes are often described as following the two-step mechanism: $$ \begin{aligned} &\mathrm{E}+\mathrm{S} \rightleftharpoons \mathrm{ES} \quad \text { (fast) } \\\ &\mathrm{ES} \longrightarrow \mathrm{E}+\mathrm{P} \quad \text { (slow) } \end{aligned} $$ where \(\mathrm{E}=\) enzyme, \(\mathrm{S}=\) substrate, \(\mathrm{ES}=\) enzyme-substrate complex, and \(\mathrm{P}=\) product. (a) If an enzyme follows this mechanism, what rate law is expected for the reaction? (b) Molecules that can bind to the active site of an enzyme but are not converted into product are called enzyme inhibitors. Write an additional elementary step to add into the preceding mechanism to account for the reaction of \(E\) with \(I\), an inhibitor.

(a) The reaction \(\mathrm{H}_{2} \mathrm{O}_{2}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\frac{1}{2} \mathrm{O}_{2}(g)\) is first order. Near room temperature, the rate constant equals \(7.0 \times 10^{-4} \mathrm{~s}^{-1}\). Calculate the half-life at this temperature. (b) At \(415^{\circ} \mathrm{C},\left(\mathrm{CH}_{2}\right)_{2} \mathrm{O}\) decomposes in the gas phase, \(\left(\mathrm{CH}_{2}\right)_{2} \mathrm{O}(g) \longrightarrow \mathrm{CH}_{4}(g)+\mathrm{CO}(g)\). If the reaction is first order with a half-life of \(56.3 \mathrm{~min}\) at this temperature, calculate the rate constant in \(\mathrm{s}^{-1}\).

The gas-phase reaction of \(\mathrm{NO}\) with \(\mathrm{F}_{2}\) to form \(\mathrm{NOF}\) and \(\mathrm{F}\) has an activation energy of \(E_{a}=6.3 \mathrm{~kJ} / \mathrm{mol}\). and a frequency factor of \(A=6.0 \times 10^{8} M^{-1} \mathrm{~s}^{-1}\). The reaction is believed to be bimolecular: $$ \mathrm{NO}(g)+\mathrm{F}_{2}(g) \longrightarrow \mathrm{NOF}(g)+\mathrm{F}(g) $$ (a) Calculate the rate constant at \(100{ }^{\circ} \mathrm{C}\). (b) Draw the Lewis structures for the \(\mathrm{NO}\) and the NOF molecules, given that the chemical formula for NOF is misleading because the nitrogen atom is actually the central atom in the molecule. (c) Predict the shape for the NOF molecule. (d) Draw a possible transition state for the formation of NOF, using dashed lines to indicate the weak bonds that are beginning to form. (e) Suggest a reason for the low activation energy for the reaction.

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 \(3.924 \AA\). (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 \(1 \dot{A}=1 \times 10^{-10} \mathrm{~m}\) and \(1 \mathrm{~nm}=1 \times 10^{-9} \mathrm{~m}\). (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 \(2.8 \mathrm{~A}\). (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?

(a) What is meant by the term elementary reaction? (b) What is the difference between a unimolecular and a bimolecular elementary reaction? (c) What is a reaction mechanism? (d) What is meant by the term rate-determining step?

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