Final answer:
According to the information provided, the reaction in question will proceed through the SN1 mechanism, which is a unimolecular substitution process. In SN1 reactions, the nucleophile attacks the carbonation intermediate from either side, resulting in retention and inversion of configuration. SN1 reactions are commonly observed with tertiary alkyl halides.
Step-by-step explanation:
The provided information suggests that the reaction will proceed through the SN1 mechanism. In an SN1 mechanism, the reaction proceeds through a unimolecular substitution process, where the rate of the reaction is proportional to the concentration of the substrate.
The reaction involves a carbonation intermediate and the nucleophile attacks from either side, resulting in both retention and inversion of configuration. SN1 reactions occur primarily with tertiary alkyl halides.