Consider the acid-catalyzed hydration of propene to yield propan-2-ol. Which of the following statem — Alcohols Phenols and Ethers Chemistry Question

💡 Solution & Explanation

The acid-catalyzed hydration of an alkene is a multi-step electrophilic addition. Step 1 forms the most stable carbocation (secondary in the case of propene, adhering to Markovnikov's rule). Step 2 is the nucleophilic attack of water, creating an oxonium ion. Step 3 is deprotonation to yield the final alcohol.