Draw the products of the Diels–Alder reaction of 1,3-butadiene with cis-1,2-dibromoethene. Use wedge-and-dash bonds to show the stereochemistry of the products. Hydrogens must be shown on chirality centers. Refer to the hint for advice about drawing molecules that contain a chirality center. Select Draw Rings More Erase cH Br Br `Br

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Chapter1: Chemical Foundations
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Draw the products of the Diels-Alder reaction of 1,3-butadiene with cis-1,2-dibromoethene. Use wedge-and-dash bonds to show
the stereochemistry of the products. Hydrogens must be shown on chirality centers.
Refer to the hint for advice about drawing molecules that contain a chirality center.
Select
Draw
Rings
More
Erase
H
Br
Br
Br
Transcribed Image Text:Draw the products of the Diels-Alder reaction of 1,3-butadiene with cis-1,2-dibromoethene. Use wedge-and-dash bonds to show the stereochemistry of the products. Hydrogens must be shown on chirality centers. Refer to the hint for advice about drawing molecules that contain a chirality center. Select Draw Rings More Erase H Br Br Br
Expert Solution
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Diels-Alder reaction:

The Diels–Alder reaction is a pericyclic reaction (cycloaddition) between a conjugated diene and a substituted alkene, 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.

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