Identify the nucleophile that attacks the carbocation in the second step of acid catalysed hydration of alkenes?(a) OH^–(b) H2O(c) H^+(d) H3O^+I got this question by my school teacher while I was bunking the class.My doubt is from Alcohols and Phenols topic in section Alcohols, Phenols and Ethers of Chemistry – Class 12

Identify the nucleophile that attacks the carbocation in the second st

1.	Identify the nucleophile that attacks the carbocation in the second step of acid catalysed hydration of alkenes?(a) OH^–(b) H2O(c) H^+(d) H3O^+I got this question by my school teacher while I was bunking the class.My doubt is from Alcohols and Phenols topic in section Alcohols, Phenols and Ethers of Chemistry – Class 12
Answer» CORRECT option is (B) H2O To elaborate: Nucleophiles are electron RICH species that attack the part of the structure that is electron deficient. In this step, the H2O nucleophile attacks the carbocation FORMING a protonated alcohol.

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