Draw the product formed when diene and dienophile react in a Diels–Alder reaction.

Explanation:

Diels-Alder reactions are cyclo-additional reactions between conjugated dienes and a dienophile (a substituted alkene compound for example acrylic acid) to produce a ring structure of cyclohexene compounds.

From the image attached below, we will see the reaction between 2,3-dimethylbuta-1,3-diene which is a conjugated diene with acrylic acid to produce a Diel-Alder adduct as the product.  From the reaction, a single new π-bond and two σ-bonds are produced.

answer:

the reaction is type of combination reaction.

explanation:

on the product side, there are 2 molecules of bonded to fe   which means one atom of fe are combined two molecules of . so, balanced chemical equation becomes :

this reaction follows the reaction type of combination reaction. a combination reaction is defined as chemical reaction in which reactants combines together to form a single product.