Question:
In this reaction, we get types of substituted alcohols (stereoisomers not considered)
In this reaction, we get types of substituted alcohols (stereoisomers not considered)
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Epoxide ring opening: acid-catalysed gives attack at more substituted carbon; base-catalysed gives attack at less substituted carbon.
Updated On: Apr 23, 2026
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The Correct Option is C
Solution and Explanation
Step 1: Understanding the Concept:
The reaction involves addition of nucleophile to epoxide. Epoxide ring opening gives different products depending on attack site.
Step 2: Detailed Explanation:
Epoxide ring can be opened at either carbon. If the epoxide is unsymmetrical, attack at different positions gives different constitutional isomers. Three distinct substituted alcohols are possible.
Step 3: Final Answer:
Thus, three types of alcohols are obtained.
The reaction involves addition of nucleophile to epoxide. Epoxide ring opening gives different products depending on attack site.
Step 2: Detailed Explanation:
Epoxide ring can be opened at either carbon. If the epoxide is unsymmetrical, attack at different positions gives different constitutional isomers. Three distinct substituted alcohols are possible.
Step 3: Final Answer:
Thus, three types of alcohols are obtained.
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