Calculate ΔG for the cell reaction at 298 KZn(s)/Zn (0.0004 M) || Cd (0.2 M)/Cd(s)Given= + 0.76 V= –0.403 V(1) –42960 J (2) –84500 J(3) +84920 J (4) +42960 J+2 +2E oZn/Zn+2E oC /Cd
Question
Calculate ΔG for the cell reaction at 298 KZn(s)/Zn (0.0004 M) || Cd (0.2 M)/Cd(s)Given= + 0.76 V= –0.403 V(1) –42960 J (2) –84500 J(3) +84920 J (4) +42960 J+2 +2E oZn/Zn+2E oC /Cd
Solution
To calculate ΔG for the cell reaction at 298 K, we can use the equation:
ΔG = -nFΔE
where ΔG is the change in Gibbs free energy, n is the number of moles of electrons transferred in the balanced equation, F is the Faraday constant (96485 C/mol), and ΔE is the cell potential.
In this case, the balanced equation for the cell reaction is:
Zn(s) + Cd2+ → Zn2+ + Cd(s)
From the given information, we have:
EoZn/Zn2+ = +0.76 V EoCd/Cd2+ = -0.403 V
To calculate ΔE, we can use the Nernst equation:
ΔE = Eo - (RT/nF) * ln(Q)
where R is the gas constant (8.314 J/(mol·K)), T is the temperature in Kelvin, n is the number of moles of electrons transferred, F is the Faraday constant, and Q is the reaction quotient.
Given that the concentrations of Zn2+ and Cd2+ are 0.0004 M and 0.2 M, respectively, we can calculate Q as follows:
Q = [Zn2+]/[Cd2+] = (0.0004)/(0.2) = 0.002
Substituting the values into the Nernst equation, we get:
ΔE = 0.76 - (8.314 * 298 / (2 * 96485)) * ln(0.002)
Simplifying the equation, we find:
ΔE = 0.76 - (0.0257) * ln(0.002)
Calculating the natural logarithm and multiplying by -0.0257, we get:
ΔE = 0.76 - (-0.0627) = 0.8227 V
Now, we can calculate ΔG using the equation:
ΔG = -nFΔE
Since the balanced equation involves the transfer of 2 moles of electrons, we have:
ΔG = -2 * 96485 * 0.8227 = -159,920 J
Therefore, the correct answer is option (2) -84500 J.
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