Final answer:
To calculate the equilibrium constant for the reaction between Zn2+(aq) and Fe(s), we need to use the standard electrode potentials of the two half-reactions. The standard cell potential (E∘ cell) can be calculated by subtracting the potentials of the two half-reactions. Using the Nernst equation, we can then relate E∘ cell to the equilibrium constant (K) by considering the reaction quotient (Q).
Step-by-step explanation:
To calculate the equilibrium constant for the reaction between Zn2+(aq) and Fe(s), we need to use the standard electrode potentials of the two half-reactions. The reduction half-reaction for Zn2+(aq) is Zn2+(aq) + 2e− → Zn(s) with an E∘ of -0.76 V, and the reduction half-reaction for Fe2+(aq) is Fe2+(aq) + 2e− → Fe(s) with an E∘ of -0.45 V. Since the overall reaction involves the reduction of Zn2+(aq) and the oxidation of Fe(s), we can subtract the two half-reaction potentials to calculate the standard cell potential. In this case, the standard cell potential (E∘ cell) would be -0.76 V - (-0.45 V) = -0.31 V.
Next, we can use the Nernst equation to relate the equilibrium constant (K) with the standard cell potential (E∘ cell). The Nernst equation is given by:
E = E∘ - (RT/nF)ln(Q)
Where E is the cell potential under nonstandard conditions, E∘ is the standard cell potential, R is the gas constant (8.314 J/(mol·K)), T is the temperature in Kelvin, n is the number of electrons transferred in the reaction (in this case, 2), F is the Faraday constant (96,485 C/mol), and Q is the reaction quotient.
The reaction quotient (Q) can be calculated using the concentrations of the species involved in the reaction. In this case, it would be Q = [Zn2+(aq)] / ([Fe(s)]^2).
Using the calculated E∘ cell and the given values for the standard electrode potentials of the half-reactions, we can substitute them into the Nernst equation to solve for the equilibrium constant (K).