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(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 reac- tion is first order with a half-life of \(56.3\) min at this temperature, calculate the rate constant in \(\mathrm{s}^{-1}\).

Short Answer

Expert verified
(a) The half-life at room temperature is calculated using the formula \(t_{1/2} = \frac{0.693}{k}\), resulting in a half-life of 990 seconds. (b) To calculate the rate constant at 415°C, first convert the given half-life of 56.3 minutes to seconds (3378 seconds). Then, use the same half-life formula to solve for the rate constant, resulting in a rate constant of \(2.05 \times 10^{-4} s^{-1}\).

Step by step solution

01

Use the half-life equation for first-order reactions

Use the formula \(t_{1/2} = \frac{0.693}{k}\), where k is the rate constant. In this case, the rate constant k is given as \(7.0 \times 10^{-4} s^{-1}\).
02

Calculate the half-life

Now, plug the value of k into the formula and solve for the half-life as follows: \(t_{1/2} = \frac{0.693}{7.0 \times 10^{-4} s^{-1}} = 990~s\) So, the half-life at this temperature is 990 seconds. (b) Calculate the rate constant at 415°C
03

Convert the half-life to seconds

Given the half-life is 56.3 minutes, we must first convert this to seconds. Recall that there are 60 seconds in a minute: \(56.3~minutes \times \frac{60~s}{1~minute} = 3378~s\)
04

Use the half-life equation for first-order reactions

Use the formula \(t_{1/2} = \frac{0.693}{k}\), where this time, we are solving for the rate constant k, and we have the half-life \(t_{1/2} = 3378~s\).
05

Calculate the rate constant

Now, rearrange the formula and solve for k: \(k = \frac{0.693}{t_{1/2}} = \frac{0.693}{3378~s} = 2.05 \times 10^{-4} s^{-1}\) So, the rate constant at 415°C is \(2.05 \times 10^{-4} s^{-1}\).

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Key Concepts

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

Understanding Half-Life Calculation for First-Order Reactions
In the context of chemical reactions, the half-life is an important measure. It tells us how long it takes for half of the reactant to convert into product. This concept is crucial for first-order reactions, where the rate at which the reaction occurs is directly proportional to the concentration of the reactant.

The formula to calculate the half-life of a first-order reaction is given by the equation:
  • \(t_{1/2} = \frac{0.693}{k}\)
Here, \(t_{1/2}\) represents the half-life, and \(k\) is the rate constant, specific to the reaction conditions.

This equation shows that the half-life of a reaction is inversely proportional to the rate constant. The larger the rate constant, the shorter the half-life. For instance, in the exercise, a rate constant of \(7.0 \times 10^{-4} \mathrm{s}^{-1}\) results in a half-life of 990 seconds. This means, over 990 seconds, half of the reactant decomposes, making it a handy measure to predict the speed of a first-order reaction.
The Importance of the Rate Constant
The rate constant \(k\) is a proportionality factor that plays a significant role in the rate law of a chemical reaction. In first-order reactions, it can be a direct indicator of how fast a reaction will proceed under constant conditions.

The rate constant's units vary with the order of reaction. For first-order reactions, the unit is \(\mathrm{s}^{-1}\), exemplified in the rate constant calculation of the reaction provided in the exercise. Here, given a half-life of 56.3 minutes (or 3378 seconds) for the reaction occurring at 415°C, we calculate \(k\) using the rearranged half-life formula:
  • \(k = \frac{0.693}{t_{1/2}}\)
Substituting the half-life into the formula gives a rate constant of \(2.05 \times 10^{-4} \mathrm{s}^{-1}\).

This indicates that, at the given temperature, the reaction is relatively slower than the first example, as this \(k\) value is lower, showing that rate constants are key to comparing reaction rates at different conditions or for different reactions.
An Overview of Chemical Kinetics
Chemical kinetics is a branch of chemistry that studies the speed or rate at which chemical reactions occur and the factors affecting them. Understanding this helps predict how altering conditions like temperature or concentration influences reaction speed.

Central to chemical kinetics are several concepts:
  • Reaction Rate: How quickly reactants turn into products. For first-order reactions, this depends on the concentration of a single reactant.
  • Rate Law: An equation expressing the relationship between the rate of reaction and the concentrations of reactants. For first-order reactions, it is represented as \(\text{rate} = k[A]\), where \(k\) is the rate constant and \([A]\) is the concentration of the reactant.
  • Half-Life: The time required for the concentration of a reactant to reduce by half, as calculated using the rate constant.
In the given exercise, both parts are excellent examples of how chemical kinetics is applied to calculate the half-life and to determine the rate constant, underlining the predictability of first-order reactions.

Overall, mastering chemical kinetics provides valuable insights into reaction mechanisms and the optimization of industrial chemical processes, making it an invaluable area of study for chemists.

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Most popular questions from this chapter

The iodide ion reacts with hypochlorite ion (the active ingredient in chlorine bleaches) in the following way: \(\mathrm{OCl}^{-}+\mathrm{I}^{-} \longrightarrow \mathrm{OI}^{-}+\mathrm{Cl}^{-} .\) This rapid reaction gives the following rate data: \begin{tabular}{lll} \hline \(\left.\mathrm{OCl}^{-}\right](\mathrm{M})\) & {\(\left[\mathrm{I}^{-}\right](M)\)} & Rate \((M / \mathrm{s})\) \\ \hline \(1.5 \times 10^{-3}\) & \(1.5 \times 10^{-3}\) & \(1.36 \times 10^{-4}\) \\ \(3.0 \times 10^{-3}\) & \(1.5 \times 10^{-3}\) & \(2.72 \times 10^{-4}\) \\ \(1.5 \times 10^{-3}\) & \(3.0 \times 10^{-3}\) & \(2.72 \times 10^{-4}\) \\ \hline \end{tabular} (a) Write the rate law for this reaction. (b) Calculate the rate constant. (c) Calculate the rate when \(\left[\mathrm{OCl}^{-}\right]=\) \(2.0 \times 10^{-3} M\) and \(\left[1^{-}\right]=5.0 \times 10^{-4} M\)

Dinitrogen pentoxide \(\left(\mathrm{N}_{2} \mathrm{O}_{5}\right)\) decomposes in chloroform as a solvent to yield \(\mathrm{NO}_{2}\) and \(\mathrm{O}_{2}\). The decomposition is first order with a rate constant at \(45^{\circ} \mathrm{C}\) of \(1.0 \times 10^{-5} \mathrm{~s}^{-1}\). Calculate the partial pressure of \(\mathrm{O}_{2}\) produced from \(1.00\) L of \(0.600 \mathrm{M} \mathrm{N}_{2} \mathrm{O}_{5}\) solution at \(45^{\circ} \mathrm{C}\) over a period of \(20.0 \mathrm{~h}\) if the gas is collected in a \(10.0-\mathrm{L}\) container. (Assume that the products do not dissolve in chloroform.)

You perform a series of experiments for the reaction \(\mathrm{A} \longrightarrow \mathrm{B}+\mathrm{C}\) and \(\mathrm{find}\) 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 [A] is tripled. (b) The rate increases by a factor of 9 when \([\mathrm{A}]\) is tripled. (c) When [A] is doubled, the rate increases by a factor of 8 . [Section \(14.3]\)

You have studied the gas-phase oxidation of \(\mathrm{HBr}\) by \(\mathrm{O}_{2}\) : $$ 4 \mathrm{HBr}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(g)+2 \mathrm{Br}_{2}(g) $$ You find the reaction to be first order with respect to \(\mathrm{HBr}\) and first order with respect to \(\mathrm{O}_{2}\). You propose the following mechanism: $$ \begin{aligned} \mathrm{HBr}(g)+\mathrm{O}_{2}(g) & \cdots & \mathrm{HOOBr}(g) \\ \mathrm{HOOBr}(g)+\mathrm{HBr}(g) & \longrightarrow 2 \mathrm{HOBr}(g) \\ \mathrm{HOBr}(g)+\mathrm{HBr}(g) & \longrightarrow \mathrm{H}_{2} \mathrm{O}(g)+\mathrm{Br}_{2}(g) \end{aligned} $$ (a) Indicate how the elementary reactions add to give the overall reaction. (Hint: You will need to multiply the coefficients of one of the equations by 2.) (b) Based on the rate law, which step is rate determining? (c) What are the intermediates in this mechanism? (d) If you are unable to detect HOBr or HOOBr among the products, does this disprove your mechanism?

The gas-phase reaction \(\mathrm{Cl}(g)+\mathrm{HBr}(g) \longrightarrow \mathrm{HCl}(g)+\) \(\mathrm{Br}(g)\) has an overall enthalpy change of \(-66 \mathrm{~kJ}\). The activation energy for the reaction is \(7 \mathrm{~kJ}\). (a) Sketch the energy profile for the reaction, and label \(E_{a}\) and \(\Delta E\). (b) What is the activation energy for the reverse reaction?

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