The product of this hydration is 1-phenylcyclohexanol
Work Step by Step
Draw the structures first and locate the double bond. The product formed is 1-phenylcyclohexanol. Steps: 1) Protonation of the double bond forms a carbocation. 2) Nucleophilic attack by water on the most substituted carbon gives a protonated alcohol. 3) Deprotonation gives the alcohol.