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For a first order reaction, the plot of ...

For a first order reaction, the plot of log `k` against 1/T is a straight line. The slope of the line is equal to

A

`(E_(a))/(R)`

B

`(2.303)/(E_(a)xxR)`

C

`(E_(a))/(2.303)`

D

`(-E_(a))/(2.303 R)`

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The correct Answer is:
To solve the question regarding the slope of the plot of log \( k \) against \( \frac{1}{T} \) for a first-order reaction, we will use the Arrhenius equation and the relationship between the rate constant \( k \) and temperature \( T \). ### Step-by-Step Solution: 1. **Understand the Arrhenius Equation**: The Arrhenius equation relates the rate constant \( k \) to the temperature \( T \) as follows: \[ k = A e^{-\frac{E_a}{RT}} \] where: - \( k \) = rate constant - \( A \) = pre-exponential factor (frequency factor) - \( E_a \) = activation energy - \( R \) = universal gas constant - \( T \) = temperature in Kelvin 2. **Take the Natural Logarithm**: To analyze the relationship between \( k \) and \( T \), we take the natural logarithm of both sides: \[ \ln k = \ln A - \frac{E_a}{RT} \] 3. **Convert to Logarithm Base 10**: We can convert the natural logarithm to base 10 using the conversion factor \( \log k = \frac{\ln k}{2.303} \): \[ \log k = \frac{\ln A}{2.303} - \frac{E_a}{2.303RT} \] 4. **Rearranging the Equation**: Rearranging gives us: \[ \log k = \left(-\frac{E_a}{2.303R}\right) \left(\frac{1}{T}\right) + \frac{\ln A}{2.303} \] This is in the form of a linear equation \( y = mx + c \), where: - \( y = \log k \) - \( x = \frac{1}{T} \) - \( m = -\frac{E_a}{2.303R} \) (slope) - \( c = \frac{\ln A}{2.303} \) (y-intercept) 5. **Identify the Slope**: From the above equation, we can see that the slope \( m \) of the plot of \( \log k \) against \( \frac{1}{T} \) is: \[ \text{slope} = -\frac{E_a}{2.303R} \] ### Final Answer: The slope of the line when plotting \( \log k \) against \( \frac{1}{T} \) for a first-order reaction is: \[ -\frac{E_a}{2.303R} \]
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