Chemists commonly use a rule of thumb that an increase of \(10 \space\mathrm{K}\) in temperature doubles the rate of a reaction. What must the activation energy be for this statement to be true for a temperature increase from 25 to \(35^{\circ} \mathrm{C} ?\)

Short Answer

Expert verified
For the rule of thumb to be true for a temperature increase from 25 to \(35^{\circ} \mathrm{C}\), the activation energy must be approximately \(5284.4 \space\mathrm{J\;mol^{-1}}\).

Step by step solution

01

Convert temperatures to Kelvin scale

First, we need to convert the given temperatures from Celsius to Kelvin. To do this, we will add 273.15 to each temperature: \( T_1 = 25^{\circ} \mathrm{C} + 273.15 = 298.15 \space\mathrm{K} \) \( T_2 = 35^{\circ} \mathrm{C} + 273.15 = 308.15 \space\mathrm{K} \)
02

Write the rule of thumb as a mathematical expression

The rule of thumb states that an increase of 10 K in temperature doubles the rate of the reaction. We can write this as: \( \frac{rate_2}{rate_1} = 2 \)
03

Apply the Arrhenius equation

The Arrhenius equation states that the rate constant k of a reaction depends upon the activation energy E and temperature T as follows: \( k = A \times e^{\frac{-E}{RT}} \) Here, A is the pre-exponential or frequency factor, E is the activation energy, R is the gas constant (\(8.314 \space\mathrm{J\;mol^{-1}K^{-1}}\)), and T is the temperature.
04

Write the equation for the ratio of rate constants

Now, we can write the equation for the ratio of rate constants at the two different temperatures: \( \frac{k_2}{k_1} = \frac{A \times e^{\frac{-E}{R \times 308.15}}}{A \times e^{\frac{-E}{R \times 298.15}}} \) We know that \( \frac{rate_2}{rate_1} = 2 \), and since the rate constant is directly proportional to the rate of reaction, we can substitute it in: \( 2 = \frac{A \times e^{\frac{-E}{R \times 308.15}}}{A \times e^{\frac{-E}{R \times 298.15}}} \)
05

Solve for the activation energy (E)

Now, we need to solve the equation for E. First, we can simplify the equation by canceling the pre-exponential factor A: \( 2 = \frac{e^{\frac{-E}{R \times 308.15}}}{e^{\frac{-E}{R \times 298.15}}} \) Next, we take the natural logarithm of both sides: \( \ln{2} = \ln{\left(\frac{e^{\frac{-E}{R \times 308.15}}}{e^{\frac{-E}{R \times 298.15}}}\right)} \) \( \ln{2} = \frac{-E}{R \times 308.15} + \frac{E}{R \times 298.15} \) Multiplying the whole equation by \(R \times 308.15 \times 298.15\) to get rid of the fractions: \( \ln{2} \times R \times 308.15 \times 298.15 = -E \times 298.15 + E \times 308.15 \) Now, combining the terms with E: \( E(308.15 - 298.15) = \ln{2} \times R \times 308.15 \times 298.15 \) Finally, we can solve for the activation energy E: \( E = \frac{\ln{2} \times R \times 308.15 \times 298.15}{10} \) Inserting the value of R (\(8.314 \space\mathrm{J\;mol^{-1}K^{-1}}\)) and calculating the result: \( E \approx 5284.4 \space\mathrm{J\;mol^{-1}} \) So, the activation energy must be approximately \(5284.4 \space\mathrm{J\;mol^{-1}}\) for the rule of thumb to be true for a temperature increase from 25 to \(35^{\circ} \mathrm{C}\).

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Most popular questions from this chapter

The decomposition of ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) on an alumina \(\left(\mathrm{Al}_{2} \mathrm{O}_{3}\right)\) surface$$\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2} \mathrm{O}(g)$$was studied at 600 K. Concentration versus time data were collected for this reaction, and a plot of \([\mathrm{A}]\) versus time resulted in a straight line with a slope of \(-4.00 \times 10^{-5} \mathrm{mol} / \mathrm{L} \cdot \mathrm{s}\) a. Determine the rate law, the integrated rate law, and the value of the rate constant for this reaction. b. If the initial concentration of \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\) was \(1.25 \times 10^{-2}\) \(M,\) calculate the half-life for this reaction. c. How much time is required for all the \(1.25 \times 10^{-2} M\) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\) to decompose?

Provide a conceptual rationale for the differences in the half-lives of zero-, first-, and second-order reactions.

The reaction $$\mathrm{NO}(g)+\mathrm{O}_{3}(g) \longrightarrow \mathrm{NO}_{2}(g)+\mathrm{O}_{2}(g)$$ was studied by performing two experiments. In the first experiment the rate of disappearance of NO was followed in the presence of a large excess of \(\mathrm{O}_{3}\). The results were as follows \(\left(\left[\mathrm{O}_{3}\right]\right.\) remains effectively constant at \(1.0 \times 10^{14}\) molecules/cm \(^{3}\) ): In the second experiment [NO] was held constant at \(2.0 \times 10^{14}\) molecules/cm \(^{3}\). The data for the disappearance of \(\mathbf{O}_{3}\) are as follows: a. What is the order with respect to each reactant? b. What is the overall rate law? c. What is the value of the rate constant from each set of experiments? $$\text { Rate }=k^{\prime}[\mathrm{NO}]^{x} \quad \text { Rate }=k^{\prime \prime}\left[\mathrm{O}_{3}\right]^{y}$$ d. What is the value of the rate constant for the overall rate law? $$\text { Rate }=k[\mathrm{NO}]^{\mathrm{x}}\left[\mathrm{O}_{3}\right]^y$$

Consider two reaction vessels, one containing A and the other containing \(\mathrm{B},\) with equal concentrations at \(t=0 .\) If both substances decompose by first-order kinetics, where $$\begin{aligned} &k_{A}=4.50 \times 10^{-4} \mathrm{s}^{-1}\\\ &k_{\mathrm{B}}=3.70 \times 10^{-3} \mathrm{s}^{-1} \end{aligned}$$how much time must pass to reach a condition such that \([\mathrm{A}]=\) \(4.00[\mathrm{B}] ?\)

A first-order reaction has rate constants of \(4.6 \times 10^{-2} \mathrm{s}^{-1}\) and \(8.1 \times 10^{-2} \mathrm{s}^{-1}\) at \(0^{\circ} \mathrm{C}\) and \(20 .^{\circ} \mathrm{C},\) respectively. What is the value of the activation energy?

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