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For a reaction A (s) + B^(2+) rarr B(s) ...

For a reaction `A (s) + B^(2+) rarr B(s) + A ^(2+) , ` at `25^(@) C E^(o) "" _(cell) = 0.2955 V. ` Hence, `K_(eq)` will be :

A

10

B

`10^(10)`

C

`-10`

D

`10^(-10)`

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To find the equilibrium constant \( K_{eq} \) for the reaction \[ A (s) + B^{2+} \rightleftharpoons B (s) + A^{2+} \] given that the standard cell potential \( E^{\circ}_{cell} = 0.2955 \, V \) at \( 25^{\circ}C \), we can use the Nernst equation. The steps to solve for \( K_{eq} \) are as follows: ### Step 1: Write the Nernst Equation The Nernst equation relates the cell potential to the equilibrium constant: \[ E_{cell} = E^{\circ}_{cell} - \frac{0.0591}{n} \log K_{eq} \] ### Step 2: Identify the Number of Electrons Transferred In the given reaction, \( A \) is oxidized to \( A^{2+} \) and \( B^{2+} \) is reduced to \( B \). Each of these processes involves the transfer of 2 electrons. Thus, \( n = 2 \). ### Step 3: Set Up the Equation at Equilibrium At equilibrium, the cell potential \( E_{cell} = 0 \). Therefore, we can set up the equation: \[ 0 = E^{\circ}_{cell} - \frac{0.0591}{n} \log K_{eq} \] Substituting the known values: \[ 0 = 0.2955 - \frac{0.0591}{2} \log K_{eq} \] ### Step 4: Rearrange the Equation Rearranging the equation gives: \[ \frac{0.0591}{2} \log K_{eq} = 0.2955 \] ### Step 5: Solve for \( \log K_{eq} \) Now, multiply both sides by \( \frac{2}{0.0591} \): \[ \log K_{eq} = \frac{0.2955 \times 2}{0.0591} \] Calculating the right side: \[ \log K_{eq} = \frac{0.5910}{0.0591} \approx 10.00 \] ### Step 6: Calculate \( K_{eq} \) To find \( K_{eq} \), we take the antilogarithm: \[ K_{eq} = 10^{10.00} = 10 \] ### Final Answer Thus, the equilibrium constant \( K_{eq} \) is: \[ \boxed{10} \] ---
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