Predict the product of the diels-alder reaction of this compound with cyclopentadiene. draw your product in the window below.

Among the compounds occurs a Diels-Alder reaction, which is a pericyclic cycloaddition reaction between a ciclic conjugated diene and an unsaturated compound commonly called dienophile, to form a substituted derivative.

Through the simultaneous construction of two new carbon-carbon bonds, the Diels-Alder reaction provides a reliable way to form rings with good control over regal and stereochemical results.

Explanation:

the answer is a! (2.9 x 10^-18 j) hope i could someone. : )