Step 1: Recall the S\(_N\)1 mechanism.
The rate-determining step in S\(_N\)1 is ionisation of the substrate to form a carbocation. This step requires stabilisation of both the carbocation intermediate and the leaving group anion.
Step 2: Match the solvent requirement.
Polar protic solvents (e.g., water, alcohols) stabilise ions by hydrogen bonding and electrostatic solvation -- they are ideal for S\(_N\)1. Polar aprotic solvents favour S\(_N\)2 instead. \[ oxed{ ext{Polar protic solvent}} \]