Problem 41
Question
The first-order rate constant for the decomposition of a certain hormone in water at \(25^{\circ} \mathrm{C}\) is \(3.42 \times 10^{-4}\) day \(^{-1}\). (a) A \(0.0200-\mathrm{M}\) solution of the hormone is stored at \(25^{\circ} \mathrm{C}\) for two months. Calculate its concentration at the end of that period. (b) Calculate how long it takes for the concentration of the solution to drop from \(0.0200 \mathrm{M}\) to \(0.00350 \mathrm{M}\). (c) Determine the half-life of the hormone.
Step-by-Step Solution
Verified Answer
(a) Concentration is approximately 0.0160 M; (b) it takes roughly 195 days; (c) the half-life is approximately 2027 days.
1Step 1: Understanding the First-Order Reaction
First-order reactions have a rate law of the form \( r = k[A] \), where \( k \) is the rate constant and \([A]\) is the concentration of the reactant. The relationship between the concentration and time for a first-order reaction is given by the equation \( [A] = [A]_0 e^{-kt} \).
2Step 2: Calculate Concentration After Two Months
To find the concentration of the hormone after two months (approximately 60 days), use the equation for first-order kinetics.Given: Initial concentration \([A]_0 = 0.0200 \, \text{M}\), \( k = 3.42 \times 10^{-4} \, \text{day}^{-1} \), and \( t = 60 \, \text{days} \).Substitute these into the equation: \([A] = 0.0200 \, \text{M} \times e^{-3.42 \times 10^{-4} \, \text{day}^{-1} \times 60 \, \text{days}} \)After calculation, \([A] \approx 0.0160 \, \text{M}\).
3Step 3: Calculate Time for Concentration to Drop to 0.00350 M
Use the integrated rate law equation again:\([A] = [A]_0 e^{-kt} \)Rearranging the formula to solve for \( t \):\(t = \frac{-\ln \left( \frac{[A]}{[A]_0} \right)}{k} \)Given \([A]_0 = 0.0200 \, \text{M}\), \([A] = 0.00350 \, \text{M}\), and \( k = 3.42 \times 10^{-4} \, \text{day}^{-1}\):\(t = \frac{-\ln \left( \frac{0.00350}{0.0200} \right)}{3.42 \times 10^{-4}} \)After calculation, \( t \approx 195 \, \text{days} \).
4Step 4: Determine the Half-Life of the Hormone
For a first-order reaction, the half-life \( t_{1/2} \) is independent of the initial concentration and is given by:\(t_{1/2} = \frac{0.693}{k} \)Plugging in the value for \( k \):\(t_{1/2} = \frac{0.693}{3.42 \times 10^{-4} \, \text{day}^{-1}} \)After calculation, \( t_{1/2} \approx 2027 \, \text{days}\).
Key Concepts
Rate ConstantIntegrated Rate LawHalf-Life Calculation
Rate Constant
A rate constant is a pivotal concept in chemical kinetics, especially when dealing with first-order reactions. This constant, denoted as \( k \), signifies the speed at which a reaction proceeds. In simplest terms, it's like the throttle of a reaction, dictating how fast the reactants convert to products. For first-order reactions, the rate of reaction is directly proportional to the concentration of one reactant. The equation \( r = k[A] \) captures this idea, where \( r \) is the reaction rate and \([A]\) is the concentration. For our exercise, the rate constant \( k \) is given as \(3.42 \times 10^{-4} \text{ day}^{-1}\), a value indicating how quickly the hormone decomposes in water at \(25^{\circ} \mathrm{C}\). Understanding this value helps predict how the reactant concentrations will change over time.
Moreover, knowing the rate constant allows us to calculate critical aspects like how much of a reactant will remain after a certain period or how long it takes for the reactant concentration to drop to a specified level. As such, the value of \( k \) serves as the cornerstone for analysis and prediction in chemical kinetics.
Moreover, knowing the rate constant allows us to calculate critical aspects like how much of a reactant will remain after a certain period or how long it takes for the reactant concentration to drop to a specified level. As such, the value of \( k \) serves as the cornerstone for analysis and prediction in chemical kinetics.
Integrated Rate Law
The integrated rate law for a first-order reaction is a powerful tool that provides a relationship between the concentration of a reactant and the elapsed time. It translates chemical kinetics into an equation form, making it easier to calculate time-dependent concentration changes. The integrated rate law equation is: \[ [A] = [A]_0 e^{-kt} \]where \([A]_0\) is the initial concentration, \([A]\) is the concentration at time \( t \), and \( k \) is the rate constant.
By substituting known values into the integrated rate law, you can explore the behavior of the reaction through step-by-step calculations.
- The equation expresses how the concentration declines exponentially over time.
- It allows us to calculate the concentration of a reactant remaining after any given time.
- It can also be rearranged to determine the time needed for the concentration to reach a certain level.
By substituting known values into the integrated rate law, you can explore the behavior of the reaction through step-by-step calculations.
Half-Life Calculation
The concept of half-life is particularly intuitive in first-order reactions as it describes the time required for a reactant's concentration to decrease by half. This concept applies broadly, from radioactive decay to biological processes. For first-order reactions, the half-life formula is: \[ t_{1/2} = \frac{0.693}{k} \]This formula strikingly shows why half-life is unique in first-order reactions:
This fact reveals a slowly degrading substance, highlighting the stabilizing nature and the long periods involved in the evolution of certain chemical and biological contexts. Recognizing the half-life allows comprehension of the persistence and time-resolved dynamics of a reaction.
- It remains constant regardless of the starting concentration.
- It's solely dependent on the rate constant \( k \).
- This constancy makes it extremely useful for comparing different reactions or understanding how quickly a substance reduces to half its quantity.
This fact reveals a slowly degrading substance, highlighting the stabilizing nature and the long periods involved in the evolution of certain chemical and biological contexts. Recognizing the half-life allows comprehension of the persistence and time-resolved dynamics of a reaction.
Other exercises in this chapter
Problem 38
The compound \(\mathrm{Xe}\left(\mathrm{CF}_{3}\right)_{2}\) decomposes in a first-order reaction to elemental Xe with a half-life of \(30 . \mathrm{min}\). If
View solution Problem 40
The compound \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) decomposes in a first-order reaction $$ \mathrm{SO}_{2} \mathrm{Cl}_{2}(\mathrm{~g}) \longrightarrow \mathrm{SO
View solution Problem 44
Assume that each gas-phase reaction occurs via a single bimolecular step. For which reaction would you expect the steric factor to be more important? Why? \(\ma
View solution Problem 45
Assume that each gas-phase reaction occurs via a single bimolecular step. For which reaction would you expect the steric factor to be more important? Why? $$ \b
View solution