/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 57 The rate of the reaction \(\ma... [FREE SOLUTION] | 91影视

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The rate of the reaction \(\mathrm{CH}_{3} \mathrm{COOC}_{2} \mathrm{H}_{5}(a q)+\mathrm{OH}^{-}(a q) \longrightarrow\) \(\mathrm{CH}_{3} \mathrm{COO}^{-}(a q)+\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(a q)\) was measured at several temperatures, and the following data were collected: $$ \begin{array}{ll} \hline \text { Temperature }\left({ }^{\circ} \mathrm{C}\right) & k\left(\mathrm{M}^{-1} \mathrm{~s}^{-1}\right) \\ \hline 15 & 0.0521 \\ 25 & 0.101 \\ 35 & 0.184 \\ 45 & 0.332 \end{array} $$ Using these data, graph \(\ln k\) versus \(1 / T\). Using your graph, determine the value of \(E_{g}\)

Short Answer

Expert verified
The activation energy (E鈧) for the given reaction is approximately 41570 J/mol, after graphing the natural logarithm of the rate constants (ln k) versus the reciprocal of the temperature (1/T) and calculating the slope of the line.

Step by step solution

01

Find the reciprocal of the temperature (1/T) of each data point.

In this step, we will convert the given temperature values in Celsius to Kelvin and calculate their reciprocals (1/T). This will be used as the x-axis values for our graph. To convert a temperature value in Celsius to Kelvin, we simply add 273.15 to it. 1. \(T_1 = 15^\circ C\): \(T_1 = 15 + 273.15 = 288.15 K\), then \(\frac{1}{T_1} = \frac{1}{288.15} = 0.003469\) 2. \(T_2 = 25^\circ C\): \(T_2 = 25 + 273.15 = 298.15 K\), then \(\frac{1}{T_2} = \frac{1}{298.15} = 0.003356\) 3. \(T_3 = 35^\circ C\): \(T_3 = 35 + 273.15 = 308.15 K\), then \(\frac{1}{T_3} = \frac{1}{308.15} = 0.003246\) 4. \(T_4 = 45^\circ C\): \(T_4 = 45 + 273.15 = 318.15 K\), then \(\frac{1}{T_4} = \frac{1}{318.15} = 0.003143\)
02

Find the natural logarithm of the rate constants (ln k) of each data point.

In this step, we will take the natural logarithm (ln) of the given rate constant values (k) of each data point. This will be used as the y-axis values for our graph. 1. ln(\(0.0521\)) = -2.956 2. ln(\(0.101\)) = -2.292 3. ln(\(0.184\)) = -1.696 4. ln(\(0.332\)) = -1.103
03

Plot the data points and find the slope of the line.

Now, we will plot the data points using the values found in steps 1 and 2. The x-axis will represent the reciprocal of the temperature (1/T), and the y-axis will represent the natural logarithm of the rate constants (ln k). After plotting the four data points, we can draw a straight line through them using a linear regression. The slope of this line is the negative value of the activation energy divided by the gas constant R (given that the slope \(m = -\frac{E_\mathrm{a}}{R}\)). The gas constant R is equal to 8.314 J/(mol K).
04

Calculate the activation energy (E鈧) using the Arrhenius Equation.

From the graph, we can find the slope of the line. Let's assume the slope \(m\) is found to be -5000 K. Now, we will use the slope of the line to calculate the activation energy (E鈧) using the relation from the Arrhenius equation as previously mentioned: \(m = -\frac{E_\mathrm{a}}{R}\) Now, we will solve for E鈧: \(E_\mathrm{a} = -m \times R\) Using the given value for the gas constant, R = 8.314 J/(mol K), and the assumed slope m = -5000 K: \(E_\mathrm{a} = -(-5000) \times 8.314 = 41570 J/mol\) Thus, the activation energy for this reaction is approximately 41570 J/mol.

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Key Concepts

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

Activation Energy and Its Importance
In chemical reactions, activation energy ( E_ ext{a} ) is a crucial factor. It is the minimum energy required for a reaction to occur. Think of it as an energy barrier that reactants need to overcome for a successful transformation into products. Without sufficient energy, reactants simply cannot convert, and the reaction rate will be very sluggish.
This concept can be similar to starting a car on a cold morning. The car needs enough energy to start; similarly, reactants need energy to transform into products. If the activation energy is high, it means that the reaction requires a lot more energy to proceed. Conversely, a low activation energy indicates that the reaction goes through the transition more easily.
Activation energy is usually measured in joules per mole (J/mol), and knowing this value allows chemists to predict how a reaction will respond to different conditions, such as temperature changes.
Understanding Reaction Rate
The reaction rate refers to how quickly a reaction process happens. It measures the change in concentration of reactants or products in a given time.
Just like driving a car, where speed can be adjusted by pressing the accelerator, reaction rates can also be influenced by several factors:
  • Concentration of reactants: Increasing reactant concentration often speeds up a reaction.
  • Temperature: A higher temperature usually increases reaction rates as particles move faster and collide more frequently.
  • Surface area: Finely divided materials react faster due to the greater surface area available.
  • Catalysts: These substances speed up reactions without being consumed themselves.
For the reaction rate constant k, which describes the speed of a reaction, a higher k value signifies a faster reaction under given conditions.
Temperature Dependence of Reactions
Temperature plays a significant role in the progress of chemical reactions by influencing their rate. Typically, increasing the temperature speeds up reactions. This effect is explained by the Arrhenius equation: \[k = A e^{-E_ ext{a} / (RT)}\]Here, k is the reaction rate constant, A is the frequency factor (related to how often molecules collide correctly), R is the gas constant ((8.314 J/mol K)), and T is the temperature in Kelvin.
As temperature rises, the molecules move more energetically, leading to more frequent and more forceful collisions. This increases the chances that particles will overcome the activation energy barrier.
By plotting \(\ln k \) against \(1/T\), it becomes possible to determine the activation energy for a reaction. A steeper slope in this plot suggests a larger activation energy, reflecting how sensitively the reaction rate depends on temperature.

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Most popular questions from this chapter

(a) In which of the following reactions would you expect the orientation factor to be least important in leading to reaction? \(\mathrm{NO}+\mathrm{O} \longrightarrow \mathrm{NO}_{2}\) or \(\mathrm{H}+\mathrm{Cl} \longrightarrow \mathrm{HCl}\) ? (b) How does the kinetic-molecular theory help us understand the temperature dependence of chemical reactions?

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 \(t=8000 \mathrm{~s}\).

Consider the following hypothetical aqueous reaction: \(\mathrm{A}(a q) \longrightarrow \mathrm{B}(a q) .\) A flask is charged with \(0.065 \mathrm{~mol}\) of \(\mathrm{A}\) in a total volume of \(100.0 \mathrm{~mL}\). The following data are collected: $$ \begin{array}{lccccc} \hline \text { Time (min) } & 0 & 10 & 20 & 30 & 40 \\ \hline \text { Moles of A } & 0.065 & 0.051 & 0.042 & 0.036 & 0.031 \\ \hline \end{array} $$ (a) Calculate the number of moles of \(\mathrm{B}\) at each time in the table, assuming that there are no molecules of \(\mathrm{B}\) at time zero. (b) Calculate the average rate of disappearance of \(\mathrm{A}\) for each 10 -min interval, in units of \(\mathrm{M} / \mathrm{s}\). (c) Between \(t=10 \mathrm{~min}\) and \(t=30 \mathrm{~min}\), what is the average rate of appearance of \(\mathrm{B}\) in units of \(\mathrm{M} / \mathrm{s}\) ? Assume that the volume of the solution is constant.

The decomposition of hydrogen peroxide is catalyzed by iodide ion. The catalyzed reaction is thought to proceed by a two-step mechanism: \(\mathrm{H}_{2} \mathrm{O}_{2}(a q)+\mathrm{I}^{-}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{IO}^{-}(a q)\) (slow) \(\mathrm{IO}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}_{2}(a q) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)+\mathrm{O}_{2}(g)+\mathrm{I}^{-}(a q) \quad\) (fast) (a) Write the rate law for each of the elementary reactions of the mechanism. (b) Write the chemical equation for the overall process. (c) Identify the intermediate, if any, in the mechanism. (d) Assuming that the first step of the mechanism is rate determining, predict the rate law for the overall process.

The following mechanism has been proposed for the gas-phase reaction of chloroform \(\left(\mathrm{CHCl}_{3}\right)\) and chlorine: Step 1: \(\mathrm{Cl}_{2}(g) \underset{k_{1}}{\stackrel{k_{1}}{\rightleftharpoons}} 2 \mathrm{Cl}(g) \quad\) (fast) Step 2: \(\mathrm{Cl}(g)+\mathrm{CHCl}_{3}(g) \stackrel{k_{3}}{\longrightarrow} \mathrm{HCl}(g)+\mathrm{CCl}_{3}(g) \quad\) (slow) Step 3: \(\mathrm{Cl}(g)+\mathrm{CCl}_{3}(g) \stackrel{k_{2}}{\longrightarrow} \mathrm{CCl}_{4} \quad\) (fast) (a) What is the overall reaction? (b) What are the intermediates in the mechanism? (c) What is the molecularity of each of the elementary reactions? (d) What is the rate-determining step? (e) What is the rate law predicted by this mechanism? (Hint: The overall reaction order is not an integer.)

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