Worked solution
Step 1: Set up the rule for feasibility
For a reaction written as (metal X is oxidised) + (metal ion Y\textsuperscript{n+} is reduced) → (metal X ion) + (metal Y), the metal ion couple that is reduced is the cathode and the metal couple that is oxidised is the anode:
Ecell⊖=E⊖(cathode, species reduced)−E⊖(anode, species oxidised)
The reaction is feasible under standard conditions only if Ecell⊖>0.
Step 2: Test each option
A: Cu(s)+Fe2+(aq)→Cu2+(aq)+Fe(s). Here Fe2+ is reduced (cathode, −0.44 V) and Cu is oxidised (anode, +0.34 V):
Ecell⊖=(−0.44)−(+0.34)=−0.78 V(not feasible)
B: Fe(s)+Mg2+(aq)→Fe2+(aq)+Mg(s). Here Mg2+ is reduced (cathode, −2.37 V) and Fe is oxidised (anode, −0.44 V):
Ecell⊖=(−2.37)−(−0.44)=−1.93 V(not feasible)
C: Zn(s)+Fe2+(aq)→Zn2+(aq)+Fe(s). Here Fe2+ is reduced (cathode, −0.44 V) and Zn is oxidised (anode, −0.76 V):
Ecell⊖=(−0.44)−(−0.76)=+0.32 V(feasible, Ecell⊖>0)
D: Cu(s)+Zn2+(aq)→Cu2+(aq)+Zn(s). Here Zn2+ is reduced (cathode, −0.76 V) and Cu is oxidised (anode, +0.34 V):
Ecell⊖=(−0.76)−(+0.34)=−1.10 V(not feasible)
Step 3: Interpret the result
Only reaction C gives a positive Ecell⊖. This matches the electrochemical series: zinc lies below iron in the table (more negative E⊖), meaning zinc is a stronger reducing agent than iron and readily loses electrons to Fe2+(aq), displacing iron from solution. In every other option, the metal being oxidised is actually the weaker reducing agent of the pair (i.e. it lies above, or has a more positive E⊖ than, the ion it is supposedly reducing), so those reactions run in the thermodynamically unfavourable direction.
Final answer
- The only feasible reaction under standard conditions is Zn(s)+Fe2+(aq)→Zn2+(aq)+Fe(s), with Ecell⊖=+0.32 V, option C.