Organic Chemistry
Organic Chemistry
11th Edition
ISBN: 9781118133576
Author: T. W. Graham Solomons, Craig Fryhle
Publisher: Wiley, John & Sons, Incorporated
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Chapter 13, Problem 51P

Explain the product distribution below based on the polarity of the diene and dienophile, as predicted by contributing resonance structures for each.

Chapter 13, Problem 51P, Explain the product distribution below based on the polarity of the diene and dienophile, as

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2) Rank the following dienes by how rapidly they will undergo Diel-Alder reactions with ethylene.
Suggest a reason why wittig reactions usually give mixtures of cis and trans isomers. which of the cis or trans isomer is the. major product? explain.
Dimethyl azodicarboxylate takes part in a DielsAlder reaction as a dienophile. Write the structure of the cycloaddition product of this molecule with 1,2-dimethylenecyclohexane. Knowing that this compound is formed under mild conditions, explain what favors reactivity in a Diels-Alder reaction over diene and dienophile structures.

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