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Given : Hg(2)^(2+) rightarrow 2Hg, E^(...

Given :
`Hg_(2)^(2+) rightarrow 2Hg`, `E^(@) = 0.789 V` and `Hg^(2+) + 2e^(-) rightarrow Hg`, `E^(@) = 0.854V`
Calculate the equilibrium consant for `Hg_(2)^(2+) rightarrow Hg + Hg^(2+)`.

A

`3.13xx10^(-3)`

B

`3.13xx10^(-4)`

C

`6.26xx10^(-3)`

D

`6.26xx10^(-4)`

Text Solution

AI Generated Solution

The correct Answer is:
To calculate the equilibrium constant for the reaction \( \text{Hg}_2^{2+} \rightleftharpoons \text{Hg} + \text{Hg}^{2+} \), we will follow these steps: ### Step 1: Write the half-reactions and their standard reduction potentials. 1. The first half-reaction is: \[ \text{Hg}_2^{2+} + 2e^- \rightarrow 2\text{Hg} \quad E^\circ = 0.789 \, \text{V} \] 2. The second half-reaction is: \[ \text{Hg}^{2+} + 2e^- \rightarrow \text{Hg} \quad E^\circ = 0.854 \, \text{V} \] ### Step 2: Reverse the second half-reaction to represent oxidation. To find the overall reaction, we need to reverse the second half-reaction because we want to obtain \(\text{Hg}^{2+}\) on the product side: \[ \text{Hg} \rightarrow \text{Hg}^{2+} + 2e^- \quad E^\circ = -0.854 \, \text{V} \] ### Step 3: Add the half-reactions. Now, we can add the two half-reactions together: 1. From the first half-reaction: \[ \text{Hg}_2^{2+} + 2e^- \rightarrow 2\text{Hg} \] 2. From the reversed second half-reaction: \[ \text{Hg} \rightarrow \text{Hg}^{2+} + 2e^- \] Adding these gives: \[ \text{Hg}_2^{2+} \rightarrow \text{Hg} + \text{Hg}^{2+} \] ### Step 4: Calculate the standard cell potential \(E^\circ\). The standard cell potential for the overall reaction is calculated by adding the potentials of the half-reactions: \[ E^\circ_{\text{cell}} = E^\circ_{\text{reduction}} + E^\circ_{\text{oxidation}} = 0.789 \, \text{V} + (-0.854 \, \text{V}) = -0.065 \, \text{V} \] ### Step 5: Relate \(E^\circ\) to the equilibrium constant \(K\). The relationship between the standard cell potential and the equilibrium constant is given by the equation: \[ \Delta G^\circ = -nFE^\circ \] and \[ \Delta G^\circ = -RT \ln K \] Setting these equal gives: \[ -nFE^\circ = -RT \ln K \] ### Step 6: Solve for \(K\). Rearranging the equation gives: \[ \ln K = \frac{nFE^\circ}{RT} \] Where: - \(n = 2\) (number of electrons transferred) - \(F = 96485 \, \text{C/mol}\) (Faraday's constant) - \(R = 8.314 \, \text{J/(mol K)}\) - \(T = 298 \, \text{K}\) Substituting the values: \[ \ln K = \frac{2 \times 96485 \times (-0.065)}{8.314 \times 298} \] Calculating this gives: \[ \ln K \approx -6.3 \] Thus: \[ K \approx e^{-6.3} \approx 6.3 \times 10^{-3} \] ### Final Answer: The equilibrium constant \(K\) for the reaction \( \text{Hg}_2^{2+} \rightleftharpoons \text{Hg} + \text{Hg}^{2+} \) is approximately \( 6.3 \times 10^{-3} \). ---

To calculate the equilibrium constant for the reaction \( \text{Hg}_2^{2+} \rightleftharpoons \text{Hg} + \text{Hg}^{2+} \), we will follow these steps: ### Step 1: Write the half-reactions and their standard reduction potentials. 1. The first half-reaction is: \[ \text{Hg}_2^{2+} + 2e^- \rightarrow 2\text{Hg} \quad E^\circ = 0.789 \, \text{V} \] ...
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