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.

there is none because earth is stationary and flat.

a 20-cm-long, cylindrical graphite (pure carbon) rod is inserted into an oxidizing atmosphere at 1145 k and 1.013 x 105 pa pressure. the oxidizing process is limited by the diffu- sion of oxygen counterflow to the carbon monoxide that is formed on the cylindrical surface.