Which of the following represents the integrated rate law for a fırst-order reaction? k = Ae( Ea/RT) k1 In Ea + InA %3D k2 R 1 = kt [A]o [A]t [A]t "TAL - kt O IAl - (A), = = -kt

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### Integrated Rate Law for a First-Order Reaction

**Which of the following represents the integrated rate law for a first-order reaction?**
1. \( k = Ae^{(Ea/RT)} \)
2. \( \ln \left( \frac{k_1}{k_2} \right) = \frac{E_a}{R} \left( \frac{1}{T} \right) + \ln A \)
3. \( \frac{1}{[A]_0} - \frac{1}{[A]_t} = kt \)
4. \( \ln \left( \frac{[A]_t}{[A]_0} \right) = -kt \)
5. \( [A]_t - [A]_0 = -kt \)

### Explanation of Diagrams and Equations:

1. **Equation 1**:
   - Represents the Arrhenius equation which describes the temperature dependence of reaction rates.
   - \( k \) is the rate constant.
   - \( A \) is the pre-exponential factor.
   - \( E_a \) is the activation energy.
   - \( R \) is the gas constant.
   - \( T \) is the temperature in Kelvin.
   
2. **Equation 2**:
   - Represents a form of the Arrhenius equation.
   - \( k_1 \) and \( k_2 \) are rate constants at different temperatures.
   - \( \ln \) represents the natural logarithm function.
   - \( E_a \) is activation energy.
   - \( R \) is the gas constant.
   - \( T \) is the temperature.
   
3. **Equation 3**:
   - Represents the integrated rate law for a second-order reaction.
   - \( [A]_0 \) is the initial concentration of reactant A.
   - \( [A]_t \) is the concentration of reactant A at time \( t \).
   - \( k \) is the rate constant.
   - \( t \) is the time.

4. **Equation 4**:
   - Represents the integrated rate law for a first-order reaction.
   - \( [A]_0 \) is the initial concentration of reactant A.
   - \( [A]_t \) is the concentration of reactant A at time \( t \).
   - \( k \) is the rate
Transcribed Image Text:### Integrated Rate Law for a First-Order Reaction **Which of the following represents the integrated rate law for a first-order reaction?** 1. \( k = Ae^{(Ea/RT)} \) 2. \( \ln \left( \frac{k_1}{k_2} \right) = \frac{E_a}{R} \left( \frac{1}{T} \right) + \ln A \) 3. \( \frac{1}{[A]_0} - \frac{1}{[A]_t} = kt \) 4. \( \ln \left( \frac{[A]_t}{[A]_0} \right) = -kt \) 5. \( [A]_t - [A]_0 = -kt \) ### Explanation of Diagrams and Equations: 1. **Equation 1**: - Represents the Arrhenius equation which describes the temperature dependence of reaction rates. - \( k \) is the rate constant. - \( A \) is the pre-exponential factor. - \( E_a \) is the activation energy. - \( R \) is the gas constant. - \( T \) is the temperature in Kelvin. 2. **Equation 2**: - Represents a form of the Arrhenius equation. - \( k_1 \) and \( k_2 \) are rate constants at different temperatures. - \( \ln \) represents the natural logarithm function. - \( E_a \) is activation energy. - \( R \) is the gas constant. - \( T \) is the temperature. 3. **Equation 3**: - Represents the integrated rate law for a second-order reaction. - \( [A]_0 \) is the initial concentration of reactant A. - \( [A]_t \) is the concentration of reactant A at time \( t \). - \( k \) is the rate constant. - \( t \) is the time. 4. **Equation 4**: - Represents the integrated rate law for a first-order reaction. - \( [A]_0 \) is the initial concentration of reactant A. - \( [A]_t \) is the concentration of reactant A at time \( t \). - \( k \) is the rate
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