Analyzing the Setup
Let's visualize the electrochemical cell for this reaction. We are given the chemical equation:
Cu(s)+Sn2+(aq)⟶Cu2+(aq)+Sn(s)
By looking closely at the oxidation states, we can see that solid copper (Cu) is turning into copper ions (Cu2+). This means it is losing electrons, which is the definition of oxidation. Therefore, copper acts as our anode.
Meanwhile, the tin ions (Sn2+) are gaining electrons to become solid tin (Sn). This process is reduction, making tin our cathode.
The Master Equation
To find the Gibbs free energy change (ΔG), we first need to determine the standard cell potential (Ecell∘). The formula is beautifully simple:
Ecell∘=Ecathode∘−Eanode∘
We know tin is the cathode and copper is the anode. Let's substitute their given standard reduction potentials into our equation.
Ecell∘=ESn2+/Sn∘−ECu2+/Cu∘
Calculating this, we find the standard cell potential is −0.50 V. Notice the negative sign? It hints that this reaction isn't going to happen spontaneously on its own.
Final Calculation
Now, since the concentrations of both ions are exactly 1 M, the reaction quotient Q is 1, and the Nernst equation tells us that the cell potential equals the standard cell potential (Ecell=Ecell∘).
To find the Gibbs free energy change, we use the master equation:
How many electrons are transferred? Copper goes from 0 to +2, so n is 2. Let's plug in 2 for n, 96500 for Faraday's constant (F), and −0.50 V for the cell potential.
Multiply these together. The two negative signs cancel out, and 2×0.50 is exactly 1. So, we are left with exactly 96500 Joules.
And there we have it! The Gibbs energy change for this reaction is 96500 J. A positive ΔG confirms our earlier suspicion: this reaction is non-spontaneous. If we wanted this reaction to actually happen, we would need to supply external electrical energy, turning this into an electrolytic cell.