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Sulfuryl chloride, \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\), decomposes by first- order kinetics, and \(k=2.81 \times 10^{-3} \mathrm{~min}^{-1}\) at a certain temperature. (a) Determine the half-life for the reaction. (b) Determine the time needed for the concentration of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) to decrease to \(10 \%\) of its initial concentration. (c) If \(14.0 \mathrm{~g}\) of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) is sealed in a \(2500 .-\mathrm{L}\) reaction vessel and heated to the specified temperature, what mass will remain after \(1.5 \mathrm{~h}\) ?

Short Answer

Expert verified
The half-life is approximately 246.9 minutes. It takes about 544.6 minutes for the concentration to decrease to 10% of its initial concentration. After 1.5 hours, approximately 3.51 g of sulfur dioxide chloride remains.

Step by step solution

01

Determine the half-life for the reaction

The half-life for a first-order reaction can be calculated using the formula: \( t_{1/2} = \frac{\ln(2)}{k} \).
02

Calculate the half-life using the given rate constant

Plug the given rate constant into the half-life equation: \( t_{1/2} = \frac{\ln(2)}{2.81 \times 10^{-3} \text{ min}^{-1}} \). Calculate the value to find the half-life.
03

Determine the time for concentration to reach 10% of the initial concentration

For a first-order reaction, the time required for the concentration to change to a percentage of the initial concentration is given by \( t = \frac{\ln(C_0/C)}{k} \), where \( C_0 \) is the initial concentration, and \( C \) is the final concentration. For 10%, \( \ln(C_0/C) = \ln(10) \).
04

Calculate the time to reach 10% concentration

Use the rate constant \( k \) and the natural logarithm of 10 to find the time: \( t = \frac{\ln(10)}{2.81 \times 10^{-3} \text{ min}^{-1}} \).
05

Calculate the initial moles of \(\mathrm{SO}_{2} \(\mathrm{Cl}_{2}\)\)

Using the molar mass of \(\mathrm{SO}_{2} \(\mathrm{Cl}_{2}\)\), find the initial moles in 14.0 g of the substance.
06

Use the integrated first-order rate law to find remaining moles

Apply the first-order integrated rate law, \( \ln(\frac{[A]_t}{[A]_0}) = -kt \), to calculate the remaining moles after 1.5 hours. Convert hours to minutes to match the minute units in \( k \).
07

Calculate the final mass of \(\mathrm{SO}_{2} \(\mathrm{Cl}_{2}\)\) remaining after 1.5 h

Convert the remaining moles back to grams using the molar mass to find the remaining mass.

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Key Concepts

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

Understanding Chemical Kinetics
Chemical kinetics is the study of the speed or rate at which chemical reactions occur and the factors that affect these rates. It's an essential area of chemistry because it helps us understand reaction mechanisms and predict the behavior of reactions under various conditions.

In kinetics, we often deal with the reaction rate, which is the change in concentration of a reactant or product over a specific period. For a reaction where a substance A transforms into products, the rate can be expressed as the negative change in concentration of A over time, usually denoted by \( -\frac{d[A]}{dt} \).

One crucial aspect of chemical kinetics is the order of the reaction, which relates to how the rate responds to changes in concentration. A first-order reaction implies that the rate is directly proportional to the concentration of the reactant. In simpler terms, if you double the amount of reactant, the reaction rate will also double.
Half-Life Calculation in Chemical Reactions
The half-life of a reaction is the time required for the concentration of a reactant to decrease to half its initial value. In the context of first-order reactions, half-life is a constant, meaning it does not depend on the initial concentration of the reactant.

The formula to calculate half-life for a first-order reaction is \( t_{1/2} = \frac{\ln(2)}{k} \), where \( k \) is the reaction rate constant. This equation is derived from the integrated first-order rate law, and it reflects the exponential nature of the decay in concentration over time.

Understanding half-life is extremely useful as it provides a clear and measurable understanding of how quickly a reaction proceeds. It's a common concept not just in chemistry, but also in physics, biology, and even pharmacology.
Determining the Reaction Rate Constant
The reaction rate constant, denoted as \( k \) in equations, is a proportionality factor that relates the reaction rate to the reactant concentrations. In a first-order reaction, the rate constant can tell us how quickly the reaction occurs. A higher value of \( k \) indicates a faster reaction.

We obtain \( k \) experimentally by measuring the concentration of reactants or products over time and fitting this data to a kinetic model. The units of \( k \) vary depending on the order of the reaction, and for first-order reactions, it has units of reciprocal time (e.g., \( s^{-1} \) or \( min^{-1} \)).

Knowing the rate constant is fundamental for calculating other kinetics parameters, such as half-life, and for predicting how long it will take for a reaction to reach a certain conversion level, as in the case of the textbook exercise provided.
The Integrated Rate Law for First-Order Reactions
The integrated rate law is an expression that describes the concentration of a reactant in a reaction over time. For first-order reactions, this law takes the form \( \ln(\frac{[A]_t}{[A]_0}) = -kt \), where \( [A]_0 \) is the initial concentration of the reactant A, \( [A]_t \) is the concentration of A at time \( t \) and \( k \) is the reaction rate constant. This mathematical relationship is derived from the differential rate law by integrating it over the time the reaction has been proceeding.

By using this equation, we can calculate the concentration of a reactant at any point in time during a first-order reaction. It's a powerful tool for chemists because it connects the measurable quantities of concentration and time to the underlying kinetics of a reaction. In practical terms, this lets us determine, among other things, how much reactant remains after a certain period, just as we might calculate in the given textbook exercise.

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Most popular questions from this chapter

The Michaelis constant \(\left(K_{M}\right)\) is an index of the stability of an enzyme-substrate complex. Does a high Michaelis constant indicate a stable or an unstable enzyme-substrate complex? Explain your reasoning.

Because partial pressures are proportional to concentrations, rate laws for gas-phase reactions can also be expressed in terms of partial pressures, for instance, as Rate \(=\) \(k P_{\mathrm{X}}\) for a first-order reaction of a gas \(\mathrm{X}\). What are the units for the rate constants when partial pressures are expressed in torr and time is expressed in seconds for (a) zero-order reactions; (b) first-order reactions; (c) second-order reactions?

The mechanism proposed for the oxidation of iodide ion by the hypochlorite ion in aqueous solution is as follows: Step \(1 \mathrm{ClO}^{-}+\mathrm{H}_{2} \mathrm{O} \longrightarrow \mathrm{HClO}+\mathrm{OH}^{-}\)and its reverse (both fast, equilibrium) Step \(2 \mathrm{I}^{-}+\mathrm{HClO} \longrightarrow \mathrm{HIO}+\mathrm{Cl}^{-}\)(slow) Step \(3 \mathrm{HIO}+\mathrm{OH}^{-} \longrightarrow \mathrm{IO}^{-}+\mathrm{H}_{2} \mathrm{O}\) (fast) Write the rate law for the formation of HIO implied by this mechanism.

Determine which of the following statements about catalysts are true. If the statement is false, explain why. (a) A heterogeneous catalyst works by binding one or more of the molecules undergoing reaction to the surface of the catalyst. (b) Enzymes are naturally occurring proteins that serve as catalysts in biological systems. (c) The equilibrium constant for a reaction is greater in the presence of a catalyst. (d) A catalyst changes the pathway of a reaction in such a way that the reaction becomes more exothermic.

The decomposition of A has the rate law Rate \(=k[\mathrm{~A}]^{a}\). Show that for this reaction the ratio \(t_{1 / 2} / t_{3 / 4}\), where \(t_{1 / 2}\) is the halflife and \(t_{3 / 4}\) is the time for the concentration of A to decrease to \(\frac{3}{4}\) of its initial concentration, can be written as a function of \(a\) alone and can therefore be used to make a quick assessment of the order of the reaction in A.

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