Step 1: The Arrhenius equation.
The Arrhenius equation, \( k = A e^{\frac{-E_a}{RT}} \), links the rate constant \( k \) to temperature \( T \) and activation energy \( E_a \). Rearranging by taking the natural logarithm of both sides yields \( \ln k = \ln A - \frac{E_a}{RT} \). This linear form \( y = mx + b \) indicates that the slope \( m \) equals \( -\frac{E_a}{R} \), allowing determination of activation energy from the slope.
Step 2: Calculating activation energy from the slope.
Given the slope \( m = -2.55 \times 10^4 \, \text{K} \), and the universal gas constant \( R = 8.314 \, \text{J/mol·K} \), activation energy \( E_a \) can be calculated. Using the relation \( E_a = -mR \), we get \( E_a = 2.55 \times 10^4 \times 8.314 = 2.12 \times 10^5 \, \text{J/mol} \).
Step 3: Conclusion.
The calculated activation energy is \( 2.12 \times 10^5 \, \text{J/mol} \), corresponding to option (1).
Consider the following compounds. Arrange these compounds in a n increasing order of reactivity with nitrating mixture. The correct order is : 