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(a) The gas-phase decomposition of \(\mathrm{SO}_{2} \mathrm{Cl}_{2}, \mathrm{SO}_{2} \mathrm{Cl}_{2}(g)\) \(\longrightarrow \mathrm{SO}_{2}(g)+\mathrm{Cl}_{2}(g),\) is first order in \(\mathrm{SO}_{2} \mathrm{Cl}_{2} .\) At 600 \(\mathrm{K}\) the half-life for this process is \(2.3 \times 10^{5} \mathrm{s}\) . What is the rate constant at this temperature? (b) At 320 "C the rate constant is \(2.2 \times 10^{-5} \mathrm{s}^{-1} .\) What is the half-life at this temperature?

Short Answer

Expert verified
(a) The rate constant at 600K is \(3.01 × 10^{-6} s^{-1}\). (b) The half-life at 320°C is \(3.15 × 10^4 s\).

Step by step solution

01

(a) Calculate the rate constant at 600K using the given half-life

As mentioned earlier, we will use the first-order reaction formula \(t_{1/2} = \frac{\ln{2}}{k}\). Rearranging it to solve for k: \(k = \frac{\ln{2}}{t_{1/2}}\) Given half-life, \(t_{1/2} = 2.3 × 10^5 s\) Calculating k, \(k = \frac{\ln{2}}{2.3 × 10^5 s}\) \(k = 3.01 × 10^{-6} s^{-1}\) So, the rate constant at 600K is \(3.01 × 10^{-6} s^{-1}\).
02

(b) Calculate the half-life at 320°C using the given rate constant

The given rate constant, \(k = 2.2 × 10^{-5} s^{-1}\). Now, we will use the first-order reaction formula \(t_{1/2} = \frac{\ln{2}}{k}\) to calculate half-life. \( t_{1/2} = \frac{\ln{2}}{2.2 × 10^{-5} s^{-1}} \) \( t_{1/2} = 3.15 × 10^4 s \) So, the half-life at 320°C is \(3.15 × 10^4 s\).

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Key Concepts

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

Understanding First-Order Reactions
A first-order reaction is a type of chemical reaction where the rate at which it occurs is directly proportional to the concentration of one of the reactants. In simpler terms, if you were to double the amount of this reactant, the reaction rate would also double.

In mathematical terms, a first-order reaction can be described by the equation: \[ \text{Rate} = k[\text{Reactant}] \]where \( k \) is the rate constant, and \( [\text{Reactant}] \) represents the concentration of the reactant. This kind of reaction has distinctive characteristics, such as a constant half-life regardless of the initial concentration, which makes them especially interesting in fields like pharmacokinetics and radioactive decay.
Rate Constant Calculation
The rate constant, symbolized by \( k \), is a crucial parameter in chemical kinetics as it dictates the speed of the chemical reaction. For first-order reactions, it is related to the half-life of the reaction, which is the time required for the concentration of a reactant to drop to half its initial value.

The formula connecting the half-life (\( t_{1/2} \)) and the rate constant for a first-order reaction is:\[ t_{1/2} = \frac{\ln{2}}{k} \]By rearranging this formula, we can solve for the rate constant if we know the half-life:\[ k = \frac{\ln{2}}{t_{1/2}} \]For instance, given a certain half-life, we can calculate the rate constant, which is essential to predict how fast the reaction proceeds under various conditions. Understanding this relationship is foundational for students studying reaction kinetics.
The Concept of Half-Life in Chemical Kinetics
The half-life of a chemical reaction is a term that describes the duration needed for half of the reactant to undergo the reaction. In the context of a first-order reaction, the half-life is independent of the initial concentration of the reactant, making it a valuable tool for scientists to understand the reaction's behavior over time.

The half-life is inversely proportional to the rate constant, as seen in the equation:\[ t_{1/2} = \frac{\ln{2}}{k} \]This means that a greater rate constant results in a shorter half-life, implying a faster reaction. Conversely, a smaller rate constant indicates a slower reaction with a longer half-life. By measuring the half-life, scientists can deduce the rate constant and vice versa, facilitating the prediction of how long it will take for a reaction to reach a specific stage or to complete.

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Most popular questions from this chapter

The enzyme urease catalyzes the reaction of urea, \(\left(\mathrm{NH}_{2} \mathrm{CONH}_{2}\right),\) with water to produce carbon dioxide and ammonia. In water, without the enzyme, the reaction proceeds with a first-order rate constant of \(4.15 \times 10^{-5} \mathrm{s}^{-1}\) at \(100^{\circ} \mathrm{C} .\) In the presence of the enzyme in water, the reaction proceeds with a rate constant of \(3.4 \times 10^{4} \mathrm{s}^{-1}\) at \(21^{\circ} \mathrm{C}\) . (a) Write out the balanced equation for the reaction catalyzed by urease. (b) If the rate of the catalyzed reaction were the same at \(100^{\circ} \mathrm{C}\) as it is at \(21^{\circ} \mathrm{C},\) what would be the difference in the activation energy between the catalyzed and uncatalyzed reactions? (c) In actuality, what would you expect for the rate of the catalyzed reaction at \(100^{\circ} \mathrm{Cas} \mathrm{com}-\) pared to that at \(21^{\circ} \mathrm{C} ?(\mathbf{d})\) On the basis of parts \((\mathrm{c})\) and \((\mathrm{d}),\) what can you conclude about the difference in activation energies for the catalyzed and uncatalyzed reactions?

The gas-phase reaction of NO with \(\mathrm{F}_{2}\) to form \(\mathrm{NOF}\) and \(\mathrm{F}\) has an activation energy of \(E_{a}=6.3 \mathrm{kJ} / \mathrm{mol} .\) and a frequency factor of \(A=6.0 \times 10^{8} M^{-1} \mathrm{s}^{-1} .\) The reaction is believed to be bimolecular: $$ \mathrm{NO}(g)+\mathrm{F}_{2}(g) \longrightarrow \mathrm{NOF}(g)+\mathrm{F}(g)$$ (a) Calculate the rate constant at \(100^{\circ} \mathrm{C}\) . (b) Draw the Lewis structures for the NO and the NOF molecules, given that the chemical formula for NOF is misleading because the nitrogen atom is actually the central atom in the molecule, (c) Predict the shape for the NOF molecule.Draw a possible transition state for the formation of NOF, using dashed lines to indicate the weak bonds that are beginning to form. (e) Suggest a reason for the low activation energy for the reaction.

One of the many remarkable enzymes in the human body is carbonic anhydrase, which catalyzes the interconversion of carbon dioxide and water with bicarbonate ion and protons. If it were not for this enzyme, the body could not rid itself rapidly enough of the \(\mathrm{CO}_{2}\) accumulated by cell metabolism. The enzyme catalyzes the dehydration (release to air) of up to \(10^{7} \mathrm{CO}_{2}\) molecules per second. Which components of this description correspond to the terms enzyme, substrate, and turnover number?

The reaction between ethyl iodide and hydroxide ion in ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) solution, \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{I}(a l c)+\mathrm{OH}^{-}(a l c) \longrightarrow\) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)+\mathrm{I}^{-}(a l c),\) has an activation energy of 86.8 \(\mathrm{kJ} / \mathrm{mol}\) and a frequency factor of \(2.10 \times 10^{11} \mathrm{M}^{-1} \mathrm{s}^{-1}\) (a) Predict the rate constant for the reaction at \(35^{\circ} \mathrm{C} .\) (b) A g \(\mathrm{KOH}\) in ethanol to form 250.0 \(\mathrm{mL}\) of solution. Similarly, 1.453 \(\mathrm{g}\) of \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{I}\) is dissolved in ethanol to form 250.0 \(\mathrm{mL}\) of solution. Equal volumes of the two solutions are mixed. Assuming the reaction is first order in each reac-solution of \(\mathrm{KOH}\) in ethanol is made up by dissolving 0.335 g KOH in ethanol to form 250.0 \(\mathrm{mL}\) of solution. Similarly, 1.453 \(\mathrm{g}\) of \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{I}\) is dissolved in ethanol to form 250.0 \(\mathrm{mL}\) of solution. Equal volumes of the two solutions are mixed. Assuming the reaction is first order in each reactant, what is the initial rate at \(35^{\circ} \mathrm{C} ?(\mathbf{c})\) Which reagent in the reaction is limiting, assuming the reaction proceeds to completion? Assuming the frequency factor and activation energy do not change as a function of temperature, calculate the rate constant for the reaction at \(50^{\circ} \mathrm{C}\) .

Consider the reaction \(\mathrm{A}+\mathrm{B} \longrightarrow \mathrm{C}+\mathrm{D} .\) Is each of the following statements true or false? (a) The rate law for the reaction must be Rate \(=k[\mathrm{A}][\mathrm{B}] .\) (b) If the reaction is an elementary reaction, the rate law is second order. (c) If the reaction is an elementary reaction, the rate law of the reverse reaction is first order. (d) The activation energy for the reverse reaction must be greater than that for the forward reaction.

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