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:

You use the atomic number to find out how many protons and neutrons there are in the atom. you use the atomic mass to find out how many protons and electrons there are in the atom. 

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