Urea \(\left(\mathrm{NH}_{2} \mathrm{CONH}_{2}\right)\) is the end product in protein metabolism in animals. The decomposition of urea in $0.1 \mathrm{M} \mathrm{HCl}$ occurs according to the reaction $$ \mathrm{NH}_{2} \mathrm{CONH}_{2}(a q)+\mathrm{H}^{+}(a q)+2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow 2 \mathrm{NH}_{4}^{+}(a q)+\mathrm{HCO}_{3}^{-}(a q) $$ The reaction is first order in urea and first order overall. When \(\left[\mathrm{NH}_{2} \mathrm{CONH}_{2}\right]=0.200 \mathrm{M},\) the rate at \(61.05^{\circ} \mathrm{C}\) $$ \text { is } 8.56 \times 10^{-5} \mathrm{M} / \mathrm{s} $$ (a) What is the rate constant, \(k\) ? (b) What is the concentration of urea in this solution after $4.00 \times 10^{3} \mathrm{~s}\( if the starting concentration is \)0.500 \mathrm{M}$ ? (c) What is the half-life for this reaction at \(61.05^{\circ} \mathrm{C}\) ?

Short Answer

Expert verified
(a) The rate constant, \(k\) is \(4.28 \times 10^{-4}\, s^{-1}\). (b) The concentration of urea after \(4.00 \times 10^3\, s\) is \(0.213\, M\). (c) The half-life for this reaction at \(61.05^{\circ}C\) is \(1.62 \times 10^3\, s\).

Step by step solution

01

Write the rate law for the reaction

The decomposition of urea follows first-order kinetics. Since the reaction is first order in urea and first order overall, the rate law for this reaction is: $$ \text{rate} = k[\mathrm{NH}_{2}\mathrm{CONH}_{2}] $$
02

Calculate the rate constant k using the given rate and initial concentration

We are given that the reaction rate at an initial concentration of \(0.200 M\) is \(8.56 \times 10^{-5} M/s\). We can use this information to find the rate constant k. $$ \text{rate} = k[\mathrm{NH}_{2}\mathrm{CONH}_{2}] $$ Plug in the given values: $$ 8.56 \times 10^{-5} M/s = k (0.200 M) $$ Solve for k: $$ k = \frac{8.56 \times 10^{-5} M/s}{0.200 M} = 4.28 \times 10^{-4} s^{-1} $$
03

Calculate the concentration of urea after a certain time

To find the concentration of urea after \(4.00 \times 10^3 s\), we can use the first-order kinetics equation: $$ \ln\frac{[\mathrm{NH}_{2}\mathrm{CONH}_{2}]_t}{[\mathrm{NH}_{2}\mathrm{CONH}_{2}]_0} = -kt $$ We know \([\mathrm{NH}_{2}\mathrm{CONH}_{2}]_0 = 0.500 M\), \(k = 4.28 \times 10^{-4} s^{-1}\), and \(t = 4.00 \times 10^3 s\). Now, plug in these values and solve for \([\mathrm{NH}_{2}\mathrm{CONH}_{2}]_t\): $$ \ln\frac{[\mathrm{NH}_{2}\mathrm{CONH}_{2}]_t}{0.500 M} = -(4.28 \times 10^{-4} s^{-1})(4.00 \times 10^3 s) $$ $$ \ln\frac{[\mathrm{NH}_{2}\mathrm{CONH}_{2}]_t}{0.500 M} = -1.712 $$ Now, find \([\mathrm{NH}_{2}\mathrm{CONH}_{2}]_t\): $$ [\mathrm{NH}_{2}\mathrm{CONH}_{2}]_t = 0.500 M\, e^{-1.712} = 0.213 M $$
04

Calculate the half-life of the reaction

The half-life (\(t_{1/2}\)) of a first-order reaction can be calculated using the formula: $$ t_{1/2} = \frac{0.693}{k} $$ Using the calculated rate constant \(k = 4.28 \times 10^{-4} s^{-1}\), we can find the half-life: $$ t_{1/2} = \frac{0.693}{4.28 \times 10^{-4} s^{-1}} = 1.62 \times 10^3 s $$ In summary: (a) The rate constant k is \(4.28 \times 10^{-4} s^{-1}\). (b) The concentration of urea after \(4.00 \times 10^3 s\) is \(0.213 M\). (c) The half-life for this reaction at \(61.05^{\circ} C\) is \(1.62 \times 10^3 s\).

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Most popular questions from this chapter

Consider the hypothetical reaction $2 \mathrm{~A}+\mathrm{B} \longrightarrow 2 \mathrm{C}+\mathrm{D}$. The following two-step mechanism is proposed for the reaction: $$ \begin{array}{l} \text { Step } 1: \mathrm{A}+\mathrm{B} \longrightarrow \mathrm{C}+\mathrm{X} \\\ \text { Step } 2: \mathrm{A}+\mathrm{X} \longrightarrow \mathrm{C}+\mathrm{D} \end{array} $$ \(\mathrm{X}\) is an unstable intermediate. (a) What is the predicted rate law expression if Step 1 is rate determining? (b) What is the predicted rate law expression if Step 2 is rate determining? (c) Your result for part (b) might be considered surprising for which of the following reasons: (i) The concentration of a product is in the rate law. (ii) There is a negative reaction order in the rate law. (iii) Both reasons (i) and (ii). (iv) Neither reasons (i) nor (ii).

The reaction between ethyl bromide $\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Br}\right)\( and hydroxide ion in ethyl alcohol at \)330 \mathrm{~K}$, $\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Br}(a l c)+\mathrm{OH}^{-}(a l c) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)+\mathrm{Br}^{-}(a l c),$ is first order each in ethyl bromide and hydroxide ion. When \(\left[\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Br}\right]\) is $0.0477 \mathrm{M}\( and \)\left[\mathrm{OH}^{-}\right]\( is \)0.100 \mathrm{M},$ the rate of disappearance of ethyl bromide is $1.7 \times 10^{-7} \mathrm{M} / \mathrm{s}$. (a) What is the value of the rate constant? (b) What are the units of the rate constant? (c) How would the rate of disappearance of ethyl bromide change if the solution were diluted by adding an equal volume of pure ethyl alcohol to the solution?

Which of the following linear plots do you expect for a reaction $\mathrm{A} \longrightarrow$ products if the kinetics are (a) zero order, (b) first order, or (c) second order?

A certain enzyme catalyzes a biochemical reaction. In water, without the enzyme, the reaction proceeds with a rate constant of $6.50 \times 10^{-4} \mathrm{~min}^{-1}\( at \)37^{\circ} \mathrm{C} .$ In the presence of the enzyme in water, the reaction proceeds with a rate constant of $1.67 \times 10^{4} \mathrm{~min}^{-1}\( at \)37^{\circ} \mathrm{C}$. Assuming the collision factor is the same for both situations, calculate the difference in activation energies for the uncatalyzed versus enzyme-catalyzed reaction.

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}^{-}(\( alc \))\( has an activation energy of \)86.8 \mathrm{~kJ} / \mathrm{mol}\( and a frequency factor of \)2.1 \times 10^{11} \mathrm{M}^{-1} \mathrm{~s}^{-1}$ (a) Predict the rate constant for the reaction at \(30^{\circ} \mathrm{C}\). (b) A solution of KOH in ethanol is made up by dissolving \(0.500 \mathrm{~g} \mathrm{KOH}\) in ethanol to form $500 \mathrm{~mL}\( of solution. Similarly, \)1.500 \mathrm{~g}\( of \)\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{I}\( is dissolved in ethanol to form \)500 \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 \(30^{\circ} \mathrm{C} ?(\mathbf{c})\) Which reagent in the reaction is limiting, assuming the reaction proceeds to completion? ((d) Assuming the frequency factor and activation energy do not change as a function of temperature, calculate the rate constant for the reaction at $40^{\circ} \mathrm{C} .$

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