How do polar protic solvents, such as a water-alcohol mixture, affect the rate of an SN1 reaction of a tertiary alkyl halide?
Q1. How do polar protic solvents, such as a water-alcohol mixture, affect the rate of an SN1 reaction of a tertiary alkyl halide?
Answer: They accelerate the reaction by stabilizing the carbocation
Explanation: Polar protic solvents stabilize the carbocation and leaving group, accelerating SN1; aprotic solvents are wrong because they favor the SN2 pathway.