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Molecular iodine, \(\mathrm{I}_{2}(g)\), dissociates into iodine atoms at \(625 \mathrm{~K}\) with a first-order rate constant of \(0.271 \mathrm{~s}^{-1}\). (a) What is the half-life for this reaction? (b) If you start with \(0.050 \mathrm{M} \mathrm{I}_{2}\) at this temperature, how much will remain after \(5.12 \mathrm{~s}\) assuming that the iodine atoms do not recombine to form \(\mathrm{I}_{2}\) ?

Short Answer

Expert verified
The half-life for this reaction is approximately \(2.56~\text{s}\). After \(5.12~\text{s}\), the concentration of \(\mathrm{I}_{2}(g)\) remaining is approximately \(0.016~\text{M}\).

Step by step solution

01

Part (a) - Calculate the half-life of the reaction

For first-order reactions, the half-life is given by the equation: \[t_{1/2} = \frac{0.693}{k}\] where \(t_{1/2}\) is the half-life and \(k\) is the rate constant. In this case, the rate constant is given as \(0.271~\text{s}^{-1}\). Plugging the values into the equation, we get: \[t_{1/2} = \frac{0.693}{0.271~\text{s}^{-1}}\] Calculating the half-life, we find: \[t_{1/2} \approx 2.56~\text{s}\] The half-life for this reaction is approximately \(2.56~\text{s}\).
02

Part (b) - Calculate the concentration of \(\text{I}_{2}\) after \(5.12~\text{s}\)

To determine the concentration of \(\text{I}_{2}\) after a certain time, we use the integrated rate law for first-order reactions: \[\ln{\frac{[\text{I}_{2}]_{t}}{[\text{I}_{2}]_{0}}} = -kt\] where \([\text{I}_{2}]_{t}\) is the concentration at time \(t\), \([\text{I}_{2}]_{0}\) is the initial concentration, \(k\) is the rate constant, and \(t\) is the time elapsed. In this case, the initial concentration is \(0.050~\text{M}\), the rate constant is \(0.271~\text{s}^{-1}\), and the time elapsed is \(5.12~\text{s}\). Plugging these values into the equation, we get: \[\ln{\frac{[\text{I}_{2}]_{t}}{0.050~\text{M}}} = -0.271~\text{s}^{-1}(5.12~\text{s})\] Now, we just need to solve for \([\text{I}_{2}]_{t}\): \[\ln{\frac{[\text{I}_{2}]_{t}}{0.050~\text{M}}} \approx -1.387\] \[\frac{[\text{I}_{2}]_{t}}{0.050~\text{M}} = e^{-1.387}\] \[ [\text{I}_{2}]_{t} \approx 0.050~\text{M} \cdot e^{-1.387}\] Calculating the concentration, we find: \[[\text{I}_{2}]_{t} \approx 0.016~\text{M}\] After \(5.12~\text{s}\), the concentration of \(\mathrm{I}_{2}(g)\) remaining is approximately \(0.016~\text{M}\).

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Key Concepts

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

First-Order Reaction
In chemical kinetics, first-order reactions are a fundamental type that describes how the rate of a reaction is directly proportional to the concentration of a single reactant. This means that as the concentration of the reactant decreases, so does the rate of the reaction. These reactions are commonly represented by the following general form:
  • A single substance decomposes into products: A → Products
  • The rate law of the reaction: rate = k[A]
In this setup, - **A** stands for the reactant, - **k** is the rate constant, - **[A]** is the concentration of the reactant. The simplicity of first-order reactions makes them particularly useful for understanding the principles of reaction kinetics.
Half-Life Calculation
The concept of half-life is an essential aspect of first-order reactions and kinetics. It refers to the time required for half of the reactant to be converted into products. This property is unique because, for first-order reactions, the half-life remains constant irrespective of the initial concentration of the reactant.The formula for calculating the half-life, given a first-order reaction, is:\[t_{1/2} = \frac{0.693}{k}\]where:- **\(t_{1/2}\)** is the half-life,- **\(k\)** is the rate constant.For instance, when dealing with a reaction involving molecular iodine dissociating, the use of this formula allows for quick determination of how long it takes for half of the iodine to convert, providing insights into the reaction's behavior over time.
Rate Constant
In the context of reaction kinetics, the rate constant, denoted as **k**, plays a crucial role in understanding the speed of a chemical reaction. In a first-order reaction, this constant makes the connection between the rate of the reaction and the concentration of the reactant through the rate law:\[ ext{rate} = k[A]\]The value of **k** is influenced by:- **Temperature**: Higher temperatures usually increase the rate constant.- **Nature of reactants**: Different chemical species react at different rates.In the exercise example of iodine dissociation at a temperature of \(625 \mathrm{~K}\), the rate constant \(k\) was given as \(0.271 \mathrm{~s}^{-1}\). Understanding this helps chemists and students predict how fast reactions will proceed under various conditions.
Integrated Rate Law
The integrated rate law provides a mathematical description of how the concentration of reactants changes over time in a chemical reaction. For a first-order reaction, the integrated rate law is:\[\ln{\left(\frac{[A]_t}{[A]_0}\right)} = -kt\]Here,- **\([A]_t\)** is the concentration of the reactant at time **t**,- **\([A]_0\)** is the initial concentration,- **k** is the rate constant,- **t** is the elapsed time.This formula is very useful for calculating the concentration of a reactant left after a certain period, which helps in understanding the progress of the reaction. For example, using the iodine dissociation problem, it can predict the remaining concentration after a given time, showing the decay of the iodine molecules efficiently over time with precise calculations.

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Most popular questions from this chapter

From the following data for the first-order gas-phase isomerization of \(\mathrm{CH}_{3} \mathrm{NC}\) at \(215^{\circ} \mathrm{C}\), calculate the firstorder rate constant and half-life for the reaction: $$ \begin{array}{rl} \hline \text { Time (s) } & \text { Pressure CH }_{3} \text { NC (torr) } \\ \hline 0 & 502 \\ 2,000 & 335 \\ 5,000 & 180 \\ 8,000 & 95.5 \\ 12,000 & 41.7 \\ 15,000 & 22.4 \end{array} $$

The reaction \(2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)\) is second order in \(\mathrm{NO}\) and first order in \(\mathrm{O}_{2}\). When \([\mathrm{NO}]=0.040 \mathrm{M}\) and \(\left[\mathrm{O}_{2}\right]=0.035 \mathrm{M}\), the observed rate of disappearance of \(\mathrm{NO}\) is \(9.3 \times 10^{-5} \mathrm{M} / \mathrm{s}\). (a) What is the rate of disappearance of \(\mathrm{O}_{2}\) at this moment? (b) What is the value of the rate constant? (c) What are the units of the rate constant? (d) What would happen to the rate if the concentration of NO were increased by a factor of \(1.8\) ?

(a) In which of the following reactions would you expect the orientation factor to be least important in leading to reaction? \(\mathrm{NO}+\mathrm{O} \longrightarrow \mathrm{NO}_{2}\) or \(\mathrm{H}+\mathrm{Cl} \longrightarrow \mathrm{HCl}\) ? (b) How does the kinetic-molecular theory help us understand the temperature dependence of chemical reactions?

(a) For a second-order reaction, what quantity, when graphed versus time, will yield a straight line? (b) How do the half-lives of first-order and second- order reactions differ?

The rate of the reaction \(\mathrm{CH}_{3} \mathrm{COOC}_{2} \mathrm{H}_{5}(a q)+\mathrm{OH}^{-}(a q) \longrightarrow\) \(\mathrm{CH}_{3} \mathrm{COO}^{-}(a q)+\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(a q)\) was measured at several temperatures, and the following data were collected: $$ \begin{array}{ll} \hline \text { Temperature }\left({ }^{\circ} \mathrm{C}\right) & k\left(\mathrm{M}^{-1} \mathrm{~s}^{-1}\right) \\ \hline 15 & 0.0521 \\ 25 & 0.101 \\ 35 & 0.184 \\ 45 & 0.332 \end{array} $$ Using these data, graph \(\ln k\) versus \(1 / T\). Using your graph, determine the value of \(E_{g}\)

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