The Diels-Alder reaction between butadiene and dimethyl maleate yields a ring structure, as shown in the product. Complete the structure by drawing any missing bonds and indicating the stereochemistry of the new stereocenters. Select Draw Rings More Erase H 160 °C 24h
The Diels-Alder reaction between butadiene and dimethyl maleate yields a ring structure, as shown in the product. Complete the structure by drawing any missing bonds and indicating the stereochemistry of the new stereocenters. Select Draw Rings More Erase H 160 °C 24h
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Diels-Alder reaction:
The Diels–Alder reaction is a reaction between a conjugated diene and a substituted alkene, commonly termed the to form a substituted cyclohexene derivative. The reaction is a pericyclic reaction with a concerted mechanism. The reaction is classified as a thermally-allowed [4+2] cycloaddition.
The reaction follows the concerted mechanism hence the stereochemistry of the reactant will remain in the products.
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