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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?

Short Answer

Expert verified
The rate constant (a) is approximately 3.57 × 10⁻⁶ M⁻¹s⁻¹. The units of the rate constant (b) are M⁻¹s⁻¹. After diluting the solution by adding an equal volume of pure ethyl alcohol (c), the rate of disappearance of ethyl bromide would decrease to approximately 4.25 × 10⁻⁷ M/s.

Step by step solution

01

Write the rate law

For a reaction that is first order with respect to both ethyl bromide and hydroxide ion, we can write the rate law as: Rate = k * [C2H5Br] * [OH-] We are given the rate of disappearance of ethyl bromide, which is 1.7 × 10⁻⁷ M/s, and the initial concentrations of C2H5Br and OH- as 0.0477 M and 0.100 M, respectively.
02

Solve for the rate constant (k)

We have all the information required to solve for k. Using the rate law: k = Rate / ([C2H5Br] * [OH-]) k = (1.7 × 10⁻⁷ M/s) / (0.0477 M * 0.100 M) k ≈ 3.57 × 10⁻⁶ M⁻¹s⁻¹ So, the value of the rate constant is approximately 3.57 × 10⁻⁶ M⁻¹s⁻¹. #b) Units of the rate constant# The units of the rate constant can be derived from the rate law: Rate = k * [C2H5Br] * [OH-] Since Rate has units of M/s and concentrations have units of M, we can find the units for k as follows: M/s = k * (M * M) => k = (M/s) / (M * M) => k = M⁻¹s⁻¹ Therefore, the units of the rate constant are M⁻¹s⁻¹. #c) Change in the rate of disappearance of ethyl bromide if the solution is diluted#
03

Calculate the new concentrations after dilution

If we dilute the solution by adding an equal volume of pure ethyl alcohol, the concentrations of both C2H5Br and OH- will be halved: [C2H5Br'] = [C2H5Br] / 2 = 0.0477 M / 2 = 0.02385 M [OH-'] = [OH-] / 2 = 0.100 M / 2 = 0.050 M
04

Determine the new rate of disappearance of ethyl bromide

Using the rate law and the new concentrations, we can calculate the new rate of disappearance of ethyl bromide: Rate' = k * [C2H5Br'] * [OH-'] Rate' = (3.57 × 10⁻⁶ M⁻¹s⁻¹) * (0.02385 M) * (0.050 M) Rate' ≈ 4.25 × 10⁻⁷ M/s After dilution, the rate of disappearance of ethyl bromide would be approximately 4.25 × 10⁻⁷ M/s.

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Most popular questions from this chapter

The oxidation of \(\mathrm{SO}_{2}\) to \(\mathrm{SO}_{3}\) is catalyzed by \(\mathrm{NO}_{2}\). Thereaction proceeds as follows: $$ \begin{aligned} &\mathrm{NO}_{2}(g)+\mathrm{SO}_{2}(g) \longrightarrow \mathrm{NO}(g)+\mathrm{SO}_{3}(g) \\ &2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g) \end{aligned} $$ (a) Show that the two reactions can be summed to give the overall oxidation of \(\mathrm{SO}_{2}\) by \(\mathrm{O}_{2}\) to give \(\mathrm{SO}_{3}\). (Hint: The top reaction must be multiplied by a factor so the \(\mathrm{NO}\) and \(\mathrm{NO}_{2}\) cancel out.) (b) Why do we consider \(\mathrm{NO}_{2}\) a catalyst and not an intermediate in this reaction? (c) Is this an example of homogeneous catalysis or heterogeneous catalysis?

The following data were measured for the reaction $\mathrm{BF}_{3}(g)+\mathrm{NH}_{3}(g) \longrightarrow \mathrm{F}_{3} \mathrm{BNH}_{3}(g)$ \begin{tabular}{lccl} \hline Experiment & {\(\left[\mathrm{BF}_{3}\right](M)\)} & {\(\left[\mathrm{NH}_{3}\right](M)\)} & Initial Rate \((M / \mathrm{s})\) \\ \hline 1 & \(0.250\) & \(0.250\) & \(0.2130\) \\ 2 & \(0.250\) & \(0.125\) & \(0.1065\) \\ 3 & \(0.200\) & \(0.100\) & \(0.0682\) \\ 4 & \(0.350\) & \(0.100\) & \(0.1193\) \\ 5 & \(0.175\) & \(0.100\) & \(0.0596\) \\ \hline \end{tabular} (a) What is the rate law for the reaction? (b) What is the overall order of the reaction? (c) What is the value of the rate constant for the reaction? (d) What is the rate when \(\left[\mathrm{BF}_{3}\right]=0.100 \mathrm{M}\) and \(\left[\mathrm{NH}_{3}\right]=0.500 \mathrm{M} ?\)

Dinitrogen pentoxide \(\left(\mathrm{N}_{2} \mathrm{O}_{5}\right)\) decomposes in chloroform as a solvent to yield \(\mathrm{NO}_{2}\) and \(\mathrm{O}_{2}\). The decomposition is first order with a rate constant at \(45^{\circ} \mathrm{C}\) of \(1.0 \times 10^{-5} \mathrm{~s}^{-1}\). Calculate the partial pressure of \(\mathrm{O}_{2}\) produced from \(1.00\) L of \(0.600 \mathrm{M} \mathrm{N}_{2} \mathrm{O}_{5}\) solution at \(45^{\circ} \mathrm{C}\) over a period of \(20.0 \mathrm{~h}\) if the gas is collected in a 10.0-L container. (Assume that the products do not dissolve in chloroform.)

The isomerization of methyl isonitrile \(\left(\mathrm{CH}_{3} \mathrm{NC}\right)\) to acetonitrile \(\left(\mathrm{CH}_{3} \mathrm{CN}\right)\) was studied in the gas phase at \(215^{\circ} \mathrm{C}\), and the following data were obtained: $$ \begin{array}{ll} \hline \text { Time (s) } & \text { [CH }_{3} \text { NC] (M) } \\ \hline 0 & 0.0165 \\ 2,000 & 0.0110 \\ 5,000 & 0.00591 \\ 8,000 & 0.00314 \\ 12,000 & 0.00137 \\ 15,000 & 0.00074 \\ \hline \end{array} $$ (a) Calculate theaverage rate of reaction, in \(M / \mathrm{s}\), for the time interval between each measurement. (b) Graph \(\left[\mathrm{CH}_{3} \mathrm{NC}\right]\) versus time, and determine the instantaneous rates in \(\mathrm{M} / \mathrm{s}\) at \(t=5000 \mathrm{~s}\) and \(t=8000 \mathrm{~s}\).

Based on their activation energies and energy changes and assuming that all collision factors are the same, which of the following reactions would be fastest and which would be slowest? Explain your answer. (a) \(E_{a}=45 \mathrm{~kJ} / \mathrm{mol} ; \Delta E=-25 \mathrm{~kJ} / \mathrm{mol}\) (b) \(E_{a}=35 \mathrm{~kJ} / \mathrm{mol} ; \Delta E=-10 \mathrm{~kJ} / \mathrm{mol}\) (c) \(E_{a}=55 \mathrm{~kJ} / \mathrm{mol} ; \Delta E=10 \mathrm{~kJ} / \mathrm{mol}\)

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