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chemistry

Answer 1

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Diels-Alder Reaction

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The [4+2]-cycloaddition of a conjugated diene and a dienophile (an alkene or alkyne), an electrocyclic reaction that involves the 4 π-electrons of the diene and 2 π-electrons of the dienophile. The driving force of the reaction is the formation of new σ-bonds, which are energetically more stable than the π-bonds.

In the case of an alkynyl dienophile, the initial adduct can still react as a dienophile if not too sterically hindered. In addition, either the diene or the dienophile can be substituted with cumulated double bonds, such as substituted allenes.

With its broad scope and simplicity of operation, the Diels-Alder is the most powerful synthetic method for unsaturated six-membered rings.

A variant is the hetero-Diels-Alder, in which either the diene or the dienophile contains a heteroatom, most often nitrogen or oxygen. This alternative constitutes a powerful synthesis of six-membered ring heterocycles.

so, your answer is option no. $\bold{A}$

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Answer 2

Hola Mate !

What is the name of the Diels-Alder product of the reaction shown below( In Attachment) ?

Correct Answer: Option A

⇒ 4-chloro-1,2-dimethylcyclohexene

Explanation:

4-chloro-1,2-dimethylcyclohexene is the name of the Diels-Alder product of the reaction shown below( In Attachment).

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