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The temperature dependence of the rate constant for a reaction is tabulated as follows: $$ \begin{array}{ll} \hline \text { Temperature (K) } & k\left(M^{-1} \mathrm{~s}^{-1}\right) \\ \hline 600 & 0.028 \\ 650 & 0.22 \\ 700 & 1.3 \\ 750 & 6.0 \\ 800 & 23 \\ \hline \end{array} $$ Calculate \(E_{a}\) and \(A\).

Short Answer

Expert verified
The activation energy, \(E_a\), is 49,591 J/mol, and the pre-exponential factor, \(A\), is 9.65 × 10\(^{-7}\) M\(^{-1}\)s\(^{-1}\).

Step by step solution

01

Write down the Arrhenius equation

The Arrhenius equation relates the rate constant \(k\), activation energy \(E_{a}\), and pre-exponential factor \(A\) of a reaction to the temperature \(T\) as follows: \[ k = A e^{-E_a / RT} \] where R is the gas constant, R = 8.314 J\(K^{-1}mol^{-1}\), and T is the temperature in Kelvin.
02

Take natural logarithm of Arrhenius equation

To find the activation energy and the pre-exponential factor, take the natural logarithm of the Arrhenius equation to make it linear: \[ \ln k = \ln A - \frac{E_a}{RT} \]
03

Rearrange Arrhenius equation

Rearrange the linearized Arrhenius equation to the form y = mx + b, with y = ln(k) and x = 1/T: \[ \ln k = -\frac{E_a}{R} \cdot \frac{1}{T} + \ln A \] In this equation, the slope of the graph ln(k) vs. 1/T is \(m = -E_a/R\).
04

Calculate ln(k) and 1/T for each data point

Use the given temperature and rate constant values to calculate ln(k) and 1/T for each data point: \[ \begin{array}{|c|c|c|} \hline \text{Temperature (K)} & \text{Rate constant } k\left( M^{-1}s^{-1} \right) & \ln (k) & \frac{1}{T} (K^{-1}) \\ \hline 600 & 0.028 & -3.5755 & 0.0016667 \\ 650 & 0.22 & -1.5141 & 0.0015385 \\ 700 & 1.3 & 0.2624 & 0.0014286 \\ 750 & 6.0 & 1.7918 & 0.0013333 \\ 800 & 23 & 3.1355 & 0.0012500 \\ \hline \end{array} \]
05

Calculate slope of the graph ln(k) vs. 1/T

Using any two points from the table, calculate the slope of the graph. We'll use the points (0.0016667, -3.5755) and (0.0012500, 3.1355): \[ m = \frac{3.1355 - (-3.5755)}{0.0012500 - 0.0016667} = -5961.223 \]
06

Calculate the activation energy, Ea

Using the slope of the graph and the gas constant R, calculate the activation energy: \[ E_a = -mR = 5961.223 \times 8.314 \, J/molK = 49,591 \, J/mol \]
07

Calculate the pre-exponential factor, A

To calculate A, choose one of the given temperature and rate constant values and substitute the values of \(E_a\), \(R\), \(T\), and \(k\) in the linearized Arrhenius equation: \[ \ln A = \ln k + \frac{E_a}{RT} \] Choose the first data point with T = 600 K and k = 0.028 M\(^{-1}\)s\(^{-1}\): \[ \ln A = \ln(0.028) + \frac{49,591 \, J/mol}{8.314 \, J/molK \times 600 \, K} = -13.884 \] Take the exponent of both sides to find the value of A: \[ A = e^{-13.884} = 9.65 \times 10^{-7} \, M^{-1}s^{-1} \] The activation energy, \(E_a\), is 49,591 J/mol, and the pre-exponential factor, \(A\), is 9.65 × 10\(^{-7}\) M\(^{-1}\)s\(^{-1}\).

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Most popular questions from this chapter

The following mechanism has been proposed for the reaction of NO with \(\mathrm{H}_{2}\) to form \(\mathrm{N}_{2} \mathrm{O}\) and $\mathrm{H}_{2} \mathrm{O} :$ $$\mathrm{NO}(g)+\mathrm{NO}(g) \longrightarrow \mathrm{N}_{2} \mathrm{O}_{2}(g)$ $\mathrm{N}_{2} \mathrm{O}_{2}(g)+\mathrm{H}_{2}(g) \longrightarrow \mathrm{N}_{2} \mathrm{O}(g)+\mathrm{H}_{2} \mathrm{O}(g)$$ (a) Show that the elementary reactions of the proposed mechanism add to provide a balanced equation for the reaction. (b) Write a rate law for each elementary reaction in the mechanism. (c) Identify any intermediates in the mechanism. (d) The observed rate law is rate \(=k[\mathrm{NO}]^{2}\left[\mathrm{H}_{2}\right]\) . If the proposed mechanism is correct, what can we conclude about the relative speeds of the first and second reactions?

(a) What is meant by the term molecularity? (b) Why are termolecular elementary reactions so rare? (c) What is an intermediate in a mechanism? (d) What are the differences between an intermediate and a transition state?

Indicate whether each statement is true or false. (a) If you compare two reactions with similar collision factors, the one with the larger activation energy will be faster. (b) A reaction that has a small rate constant must have a small frequency factor. (c) Increasing the reaction temperature increases the fraction of successful collisions between reactants.

The accompanying graph shows plots of \(\ln k\) versus \(1 / T\) for two different reactions. The plots have been extrapolated to the \(y\)-intercepts. Which reaction (red or blue) has (a) the larger value for \(E_{a}\) and (b) the larger value for the frequency factor, \(A\) ? [Section 14.5]

The gas-phase reaction of \(\mathrm{NO}\) 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 \(\mathrm{NO}\) 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. (d) 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.

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