Give the Structure of the Diene and Dienophile That Would

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The Answer is In a Diels-Alder reaction, the two carbons of the double bond and the two adjacent carbons came from the diene. None of these carbons are substituted, so the diene must have been 1,3-butadiene. The remaining carbons of the ring came from the dienophile. The dienophile must have been a trans alkene, since the stereochemistry of the alkene is retained in the product.
In a Diels-Alder reaction, the two carbons of the double bond and the two adjacent carbons came from the diene. None of these carbons are substituted, so the diene must have been 1,3-butadiene. The remaining carbons of the ring came from the dienophile. The dienophile must have been a trans alkene, since the stereochemistry of the alkene is retained in the product.

In a Diels-Alder reaction, the two carbons of the double bond and the two adjacent carbons came from the diene. None of these carbons are substituted, so the diene must have been 1,3-butadiene. The remaining carbons of the ring came from the dienophile. The dienophile must have been a trans alkene, since the stereochemistry of the alkene is retained in the product.

Give the Structure of the Diene and Dienophile That Would

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Give the Structure of the Diene and Dienophile That Would

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Correct Answer:
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