Question:

In which of the below reactions do we find \( \alpha, \beta \)-unsaturated carbonyl compounds undergoing a ring closure reaction with conjugated dienes?

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The Diels-Alder reaction is a type of cycloaddition that involves the reaction between a conjugated diene and a dienophile, forming a six-membered ring.
Updated On: Jan 6, 2026
  • Perkin reaction
  • Diels-Alder reaction
  • Claisen rearrangement
  • Hoffman reaction
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The Correct Option is B

Solution and Explanation


Step 1: Identifying the reaction type.
The Diels-Alder reaction is a cycloaddition reaction between a diene and a dienophile, often involving \( \alpha, \beta \)-unsaturated carbonyl compounds.

Step 2: Conclusion.
Thus, the correct answer is option (B).

Final Answer: \[ \boxed{\text{(B) Diels-Alder reaction}} \]
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