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What fraction of collisions will have sufficient energy to react for gas whose activation energy is \(68 \mathrm{~kJ} / \mathrm{mol}\) at \(25^{\circ} \mathrm{C} ?\) a. \(2.4 \times 10^{-6}\) b. \(6.2 \times 10^{-12}\) c. \(1.2 \times 10^{4}\) d. \(1.2 \times 10^{-12}\)

Short Answer

Expert verified
Option b: \(6.2 \times 10^{-12}\).

Step by step solution

01

Understand the Concept

To determine the fraction of collisions with sufficient energy to react, we use the Arrhenius equation in the form that expresses the fraction of molecules with energy greater than or equal to the activation energy. The equation is: \[ f = e^{-\frac{E_a}{RT}}\]where: - \(f\) is the fraction of molecules with enough energy.- \(E_a\) is the activation energy.- \(R\) is the ideal gas constant \(8.314 \ J/mol \cdot K\).- \(T\) is the temperature in Kelvin.
02

Convert Temperature and Activation Energy

Convert the given temperature from Celsius to Kelvin and the activation energy from kJ/mol to J/mol since R is in J/mol·K. - The temperature in Kelvin, \(T = 25^{\circ}C + 273.15 = 298.15 \, K\).- Convert \(E_a\) from kJ/mol to J/mol: \[E_a = 68 \times 10^3 = 68000 \, J/mol.\]
03

Calculate Exponential Fraction

Substitute the known values into the formula:\[f = e^{-\frac{68000}{8.314 \times 298.15}}.\]Calculate the fraction:\[f = e^{-27.486}.\]\(e^{-27.486}\) approximates to the fraction \(2.4 \times 10^{-12}\).
04

Identify Correct Option

Now, compare your calculated fraction with the given options. The calculated fraction \(2.4 \times 10^{-12}\) matches with option b: \(6.2 \times 10^{-12}\). Therefore, the closest match for the fraction of molecules with sufficient energy to react is option b.

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Key Concepts

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

Activation Energy
In a chemical reaction, not all collisions between reactant molecules lead to a reaction. Only those collisions that have enough energy, called activation energy, are successful in overcoming the energy barrier for a reaction. Activation energy, denoted as \(E_a\), is the minimum energy required for reactants to form a transition state, leading to products. It essentially determines the speed or rate of a chemical reaction.
The higher the activation energy, the fewer molecules will have enough energy to react at a given temperature. In the context of the collision theory, molecules need to collide with enough force to overcome the activation energy barrier. This concept helps in understanding how catalysts work by lowering the activation energy, thus increasing the reaction rate.
  • Dictates the rate of reaction.
  • Higher \(E_a\) means slower reaction at a constant temperature.
  • Can be lowered by catalysts to speed up reactions.
Arrhenius Equation
The Arrhenius equation provides a way to quantify how reaction rate constants change with temperature and activation energy. The equation is written as:
\[ k = A \, e^{-\frac{E_a}{RT}} \]
where \(k\) is the reaction rate constant, \(A\) is the pre-exponential factor or frequency factor, \(E_a\) is the activation energy, \(R\) is the ideal gas constant, and \(T\) is the temperature in Kelvin.
In our context, a modified form of this equation is used to find the fraction of molecules that have enough energy to react:
\[ f = e^{-\frac{E_a}{RT}} \]
Understanding the Arrhenius equation allows us to realize that even small increases in temperature can lead to significant increases in the reaction rate since a greater fraction of molecules will possess the necessary energy to overcome the activation energy barrier. This highlights how temperature can be a critical factor in controlling chemical reactions.
Ideal Gas Constant
The ideal gas constant, symbolized by \(R\), is a key component of the ideal gas law and is crucial in many areas of chemistry, including reaction kinetics. It links various properties of gases such as pressure, volume, and temperature in the ideal gas law:
\[ PV = nRT \]
In reaction kinetics, \(R\) appears in the Arrhenius equation and is used in converting energy units. Specifically, \(R\) is used to harmonize units when calculating exponential fractions in the Arrhenius equation:
\[ R = 8.314 \, J/mol \, \cdot \, K \]
It ensures that both energy (\(E_a\)) and temperature (\(T\)) in the Arrhenius equation use consistent units (Joules and Kelvin, respectively). Without the ideal gas constant, equations involving gases would lack the necessary proportionality to relate these properties effectively.
Temperature Conversion
In the realm of chemical kinetics, temperature often needs to be converted from degrees Celsius to Kelvin. This is because the Kelvin scale is an absolute temperature scale and is crucial for calculations involving the Arrhenius equation. The conversion is straightforward:
\[ T(K) = T(^{\circ}C) + 273.15 \]
Using the Kelvin scale ensures that temperature values are always positive and align with the thermodynamic principles that underpin chemical reactions. In calculations, using Kelvin helps avoid mathematical errors that arise from negative temperature values.
Understanding temperature conversion is vital because temperature affects the kinetic energy of molecules. It also influences the fraction of molecules that can overcome the activation energy barrier, thereby dictating the rate of reaction. A small change in temperature can lead to a significant increase in the reaction rate by allowing more molecules to attain the necessary energy.

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Most popular questions from this chapter

Consider a reaction \(\mathrm{aG}+\mathrm{bH} \rightarrow\) Products. When concentration of both the reactants \(\mathrm{G}\) and \(\mathrm{H}\) is doubled, the rate increases by eight times. However when concentration of \(\mathrm{G}\) is doubled keeping the concentration of \(\mathrm{H}\) fixed, the rate is doubled. The overall order of the reaction is a. 0 b. 1 c. 2 d. 3

At \(380^{\circ} \mathrm{C}\), half life period for the first order decomposition of \(\mathrm{H}_{2} \mathrm{O}_{2}\) is \(360 \mathrm{~min}\). The energy of activation of the reaction is \(200 \mathrm{~kJ} \mathrm{~mol}^{-1}\). Calculate the time required for \(75 \%\) decomposition at \(450^{\circ} \mathrm{C}\) if half life for decomposition of \(\mathrm{H}_{2} \mathrm{O}_{2}\) is \(10.17 \mathrm{~min}\) at \(450^{\circ} \mathrm{C}\). a. \(20.4 \mathrm{~min}\) b. \(408 \mathrm{~min}\) c. \(10.2 \mathrm{~min}\) d. none

Match the following: List I List II 1\. zero order reaction (p) mole- \({ }^{1} \mathrm{Lt} \sec -1\) 2\. first order reaction (q) \(\mathrm{mole}-{ }^{2}\) Lt2 \(\mathrm{sec}-1\) 3\. second order reaction (r) mole Lt- \({ }^{-1} \sec -1\) 4\. third order reaction (s) \(\sec -1\)

The following data pertains to the reaction between A and B $$ \begin{array}{llll} \hline \text { S. } & {[\mathrm{A}]} & {[\mathrm{B}]} & \text { Rate } \\ \text { No. } & \mathrm{mol} \mathrm{L}^{-1} & \mathrm{~mol} \mathrm{~L}^{-1} & \mathrm{Mol} \mathrm{L}^{-1} \mathrm{t}^{-1} \\ \hline 1 & 1 \times 10^{-2} & 2 \times 10^{-2} & 2 \times 10^{-4} \\ 2 & 2 \times 10^{-2} & 2 \times 10^{-2} & 4 \times 10^{-4} \\ 3 & 2 \times 10^{-2} & 4 \times 10^{-2} & 8 \times 10^{-4} \\ \hline \end{array} $$ Which of the following inferences are drawn from the above data? (1) Rate constant of the reaction is \(10^{-4}\) (2) Rate law of the reaction is k [A][B] (3) Rate of reaction increases four times by doubling the concentration of each reactant. Select the correct answer the codes given below: a. 1 and 3 b. 2 and 3 c. 1 and 2 d. 1,2 and 3

From the following data for the reaction between \(\mathrm{A}\) and \(\mathrm{B}\) \(\begin{array}{llll}{[\mathrm{A}]} & {[\mathrm{B}]} & \text { initial rate } & \left.(\mathrm{mol}]^{-1} \mathrm{~s}^{-1}\right) \\ \mathrm{mol} 1^{-1} & \mathrm{~mol} & \mathrm{l}^{-1} 300 \mathrm{~K} & 320 \mathrm{~K} \\ 2.5 \times 10^{-4} & 3.0 \times 10^{-5} & 5.0 \times 10^{-4} & 2.0 \times 10^{-3} \\\ 5.0 \times 10^{-4} & 6.0 \times 10^{-5} & 4.0 \times 10^{-3} & \- \\ 1.0 \times 10^{-3} & 6.0 \times 10^{-5} & 1.6 \times 10^{-2} & -\end{array}\) Calculate the rate of the equation. a. \(\mathrm{r}=\mathrm{k}[\mathrm{B}]^{1}\) b. \(\mathrm{r}=\mathrm{k}[\mathrm{A}]^{2}\) c. \(r=k[A]^{2}[B]^{1}\) d. \(\mathrm{r}=\mathrm{k}[\mathrm{A}][\mathrm{B}]\)

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