\[ \ln k = \ln A - \frac{E_a}{R} . \frac{1}{T} \]
Comparing this with the straight-line equation \( y = mx + c \), the slope \( m = -\frac{E_a}{R} \)
\[ \text{Slope} = -\frac{E_a}{R} = -2 \times 10^4 \]
\[ \Rightarrow \frac{E_a}{R} = 2 \times 10^4 \Rightarrow E_a = R . 2 \times 10^4 = 8.3 . 2 \times 10^4 = 1.66 \times 10^5~\text{J mol}^{-1} \]
\[ = \frac{1.66 \times 10^5}{1000} = 166~\text{kJ mol}^{-1} \]
166 kJ mol\(^{-1}\)
Standard electrode potential for \( \text{Sn}^{4+}/\text{Sn}^{2+} \) couple is +0.15 V and that for the \( \text{Cr}^{3+}/\text{Cr} \) couple is -0.74 V. The two couples in their standard states are connected to make a cell. The cell potential will be:
To calculate the cell potential (\( E^\circ_{\text{cell}} \)), we use the standard electrode potentials of the given redox couples.
Given data:
\( E^\circ_{\text{Sn}^{4+}/\text{Sn}^{2+}} = +0.15V \)
\( E^\circ_{\text{Cr}^{3+}/\text{Cr}} = -0.74V \)