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The compound \(\mathrm{Xe}\left(\mathrm{CF}_{3}\right)_{2}\) decomposes in a first-order reaction to elemental Xe with a half-life of \(30 .\) minutes. If you place \(7.50 \mathrm{mg}\) of \(\mathrm{Xe}\left(\mathrm{CF}_{3}\right)_{2}\) in a flask, how long must you wait until only 0.25 mg of \(\mathrm{Xe}\left(\mathrm{CF}_{3}\right)_{2}\) remains?

Short Answer

Expert verified
Wait approximately 147 minutes.

Step by step solution

01

Understand the First-Order Reaction

In a first-order reaction, the rate of decomposition depends only on the concentration of the compound. The formula for the remaining amount of a substance in a first-order reaction is \( A(t) = A_0 \times e^{-kt} \), where \( A(t) \) is the amount at time \( t \), \( A_0 \) is the initial amount, and \( k \) is the first-order rate constant.
02

Determine the Rate Constant

The half-life (\( T_{1/2} \)) for a first-order reaction is related to the rate constant \( k \) by the formula \( T_{1/2} = \frac{0.693}{k} \). Here, \( T_{1/2} = 30 \) minutes. Solving for \( k \), we find \( k = \frac{0.693}{30} \approx 0.0231 \text{ min}^{-1} \).
03

Set Up the Equation for Remaining Amount

We want to find how long it takes for the compound to decrease from 7.50 mg to 0.25 mg. Using the equation for first-order reactions, set \( A(t) = 0.25 \) mg and \( A_0 = 7.50 \) mg. The equation becomes \( 0.25 = 7.50 \times e^{-0.0231t} \).
04

Solve for Time (t)

Rearrange the equation to isolate \( e^{-0.0231t} \): \( \frac{0.25}{7.50} = e^{-0.0231t} \). Simplify to find \( 0.0333 = e^{-0.0231t} \). Apply the natural logarithm to both sides: \( \ln(0.0333) = -0.0231t \).
05

Calculate Time

Solving \( \ln(0.0333) \approx -3.4012 \), we substitute back into the equation: \( -3.4012 = -0.0231t \). Solve for \( t \) by dividing: \( t = \frac{3.4012}{0.0231} \approx 147.3 \) minutes.

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Key Concepts

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

Rate Constant
The rate constant (\( k \)) is a crucial component in the study of first-order reactions. It is a measure of the speed at which a chemical reaction occurs. For a first-order reaction, the concentra...lf-life is independent of the initial concentration, which is a unique feature of first-order reactions. Chemists use the half-life to predict when a certain amount of a reactant will have decomposed, making it a valuable tool in chemical analysis.
Natural Logarithm
The natural logarithm (\( \ln \)) is a mathematical function that is essential in calculating rates and times in first-order reactions. It is the inverse function of exponential growth and decay, describing the relationships between time a...ay intuitive. The natural logarithmic function helps us to linearize these equations, making it easier to calculate the unknowns such as time (\( t \)). Mastering the use of logarithms is essential for anyone studying thermodynamics and kinetics.
Chemical Decomposition
Chemical decomposition is a type of chemical reaction where one compound breaks down into two or more simpler substances. In a first-order decomposition reaction, such as the breakdown of \( \text{Xe(CF}_3\text{)}_2 \), the reaction rate ...nel of Xe gas and fluorine compounds. This process is important in a variety of chemical manufacturing and waste treatment processes. Monitoring decomposition rates is critical for predicting the stability and shelf-life of chemical products.

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Most popular questions from this chapter

When heated to a high temperature, cyclobutane, \(\mathrm{C}_{4} \mathrm{H}_{8}\) decomposes to ethylene: $$\mathrm{C}_{4} \mathrm{H}_{8}(\mathrm{g}) \rightarrow 2 \mathrm{C}_{2} \mathrm{H}_{4}(\mathrm{g})$$ The activation energy, \(E_{a},\) for this reaction is \(260 \mathrm{kJ} / \mathrm{mol} .\) At \(800 \mathrm{K},\) the rate constant \(k=0.0315 \mathrm{s}^{-1} .\) Determine the value of \(k\) at \(850 \mathrm{K}.\)

What is the rate law for each of the following elementary reactions? (a) \(\mathrm{Cl}(\mathrm{g})+\mathrm{ICl}(\mathrm{g}) \rightarrow \mathrm{I}(\mathrm{g})+\mathrm{Cl}_{2}(\mathrm{g})\) (b) \(\mathrm{O}(\mathrm{g})+\mathrm{O}_{3}(\mathrm{g}) \rightarrow 2 \mathrm{O}_{2}(\mathrm{g})\) (c) \(2 \mathrm{NO}_{2}(\mathrm{g}) \rightarrow \mathrm{N}_{2} \mathrm{O}_{4}(\mathrm{g})\)

If the rate constant for a reaction triples when the temperature rises from \(3.00 \times 10^{2} \mathrm{K}\) to \(3.10 \times 10^{2} \mathrm{K},\) what is the activation energy of the reaction?

The decomposition of HOF occurs at \(25^{\circ} \mathrm{C}\) $$\mathrm{HOF}(\mathrm{g}) \rightarrow \mathrm{HF}(\mathrm{g})+1 / 2 \mathrm{O}_{2}(\mathrm{g})$$ Using the data in the table below, determine the rate law, and then calculate the rate constant. $$\begin{array}{cc}{[\mathrm{HOF}](\mathrm{mol} / \mathrm{L})} & \mathrm{Time}(\mathrm{min}) \\ \hline 0.850 & 0 \\\0.810 & 2.00 \\\0.754 & 5.00 \\\0.526 & 20.0 \\\0.243 & 50.0 \\\\\hline\end{array}$$

To determine the concentration dependence of the rate of the reaction $$\mathrm{H}_{2} \mathrm{PO}_{3}^{-}(\mathrm{aq})+\mathrm{OH}^{-}(\mathrm{aq}) \rightarrow \mathrm{HPO}_{3}^{2-}(\mathrm{aq})+\mathrm{H}_{2} \mathrm{O}(\ell)$$ you might measure \(\left[\mathrm{OH}^{-}\right]\) as a function of time using a pH meter. (To do so, you would set up conditions under which \(\left[\mathrm{H}_{2} \mathrm{PO}_{3}^{-}\right]\) remains constant by using a large excess of this reactant.) How would you prove a second-order rate dependence for \(\left[\mathrm{OH}^{-}\right] ?\)

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