The Diels-Alder reaction between butadiene and dimethyl maleate yields a ring structure, as shown in the…
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Question “The Diels-Alder reaction between butadiene and dimethyl maleate yields a ring structure, as shown in the…”
Answer
The [4 + 2] Diels-alder reaction is a cycloaddition reaction of conjugated diene with dienophile to form substitutedcyclohexene. This reaction is performed in one step and requires no intermediates.
Diene is a compound that has a conjugated double bonds in a system.
Dienophile is a substituted alkene/alkyne.
Example:
Stereochemistry says that
Cis reactants can lead to Cis products, and Trans reactants can lead to Trans products.
Take a look at the following:
As follows is the product of the reaction:
Ans:
Conclusion
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