To calculate the overall standard reduction potential for a series of redox reac tions, use the relationship \(∆G = −nFE^◦\) and combine the contributions from all steps.
The reactions are as follows:
The total Gibbs free energy for the combined reaction is:
\[ \Delta G_3 = \Delta G_1 + \Delta G_2 \]
Substitute \( \Delta G = -nFE^\circ \):
\[ -4FE^\circ_3 = -3F(2.2) + (-1F)(0.7) \]
Simplify the equation:
\[ 4E^\circ_3 = 6.6 + 0.7 = 7.3 \]
Divide by 4:
\[ E^\circ_3 = \frac{7.3}{4} = 1.825 \, \text{V} \]
Express in millivolts:
\[ E^\circ_3 = 1.825 \times 10^3 \, \text{mV} \]
The value of \( x \) is 1825.
For the reaction A(g) $\rightleftharpoons$ 2B(g), the backward reaction rate constant is higher than the forward reaction rate constant by a factor of 2500, at 1000 K.
[Given: R = 0.0831 atm $mol^{–1} K^{–1}$]
$K_p$ for the reaction at 1000 K is:
A square loop of sides \( a = 1 \, {m} \) is held normally in front of a point charge \( q = 1 \, {C} \). The flux of the electric field through the shaded region is \( \frac{5}{p} \times \frac{1}{\varepsilon_0} \, {Nm}^2/{C} \), where the value of \( p \) is: