Consider the acid-catalyzed dehydration of alcohols to form alkenes. Which of the following statemen β Alcohols Phenols and Ethers Chemistry Question
Question
Consider the acid-catalyzed dehydration of alcohols to form alkenes. Which of the following statements concerning this specific reaction mechanism are correct?
Answer: A,B,C
π‘ Solution & Explanation
The ease of dehydration ($3^\circ > 2^\circ > 1^\circ$) corresponds to carbocation stability. Secondary and tertiary alcohols undergo E1 elimination via a carbocation. Primary alcohols typically undergo E2 elimination to avoid highly unstable primary carbocations. Statement D is incorrect; the protonation step is fast, while the loss of water to form the carbocation is the slow, rate-determining step.
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