Step 1: General rule with inert Pt electrodes.
At the cathode, the ion with the highest reduction potential is preferentially reduced. At the anode, the most easily oxidised species is discharged (concentration also plays a role).
Step 2: Aqueous $CuCl_2$ (i).
Cathode: $Cu^{2+}$ has a higher reduction potential than $H^+$, so copper deposits. Anode: high $Cl^-$ concentration drives chloride oxidation over water, releasing $Cl_2$. \[ \text{Cathode: }Cu^{2+}+2e^-\rightarrow Cu \quad \text{Anode: }2Cl^-\rightarrow Cl_2+2e^- \]
Step 3: Concentrated $H_2SO_4$ (ii).
Cathode: $2H^++2e^-\rightarrow H_2$. Anode: $SO_4^{2-}$ is extremely difficult to oxidise, so water is oxidised to $O_2$: $2H_2O\rightarrow O_2+4H^++4e^-$. \[ \boxed{(i)\;Cu\text{ and }Cl_2;\quad(ii)\;H_2\text{ and }O_2} \]