The value of \(log K_{c}\) for the given cell reaction at 298 K is
\(Cu(s)+2Ag^{+}(aq)\rightarrow Cu^{2+}(aq)+2Ag(s)\).
(Given: \(E^{\circ}_{Cu^{2+}/Cu}=0.34V, E^{\circ}_{Ag^{+}/Ag}=0.80V; \frac{2.303RT}{F}=0.06\))
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When the cell reaction reaches equilibrium, the net potential is zero, allowing us to calculate the equilibrium constant directly from standard electrode potentials.
Step 1: Recall the link at equilibrium. At equilibrium the cell voltage is zero and we use $E^\circ_{cell}=\frac{2.303RT}{nF}\log K_c$. Step 2: Find the standard cell voltage. Copper is oxidised (anode) and silver is reduced (cathode). \[ E^\circ_{cell}=E^\circ_{cathode}-E^\circ_{anode}=0.80-0.34=0.46\ \text{V} \] Step 3: Count electrons. Copper gives 2 electrons and two silver ions take one each, so $n=2$. Step 4: Put values in the formula. Using $\frac{2.303RT}{F}=0.06$: \[ 0.46=\frac{0.06}{2}\log K_c=0.03\log K_c \] Step 5: Solve for log Kc. \[ \log K_c=\frac{0.46}{0.03}\approx15.33 \] Step 6: State the answer. \[ \boxed{\log K_c\approx15.33} \]