Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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The rate of a Diels-Alder reaction is favored by
select all that apply
electron withdrawing dienophile
electron donating dienophile
s-cis diene
s-trans diene
sdsdienophile
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Transcribed Image Text:The rate of a Diels-Alder reaction is favored by select all that apply electron withdrawing dienophile electron donating dienophile s-cis diene s-trans diene sdsdienophile
Expert Solution
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Step 1

In Diels Alder reaction mechanism, electrons from dienophile attack on Carbon first of diene , thus there is a single bond formed between Carbon first and sixth. 

Finally cyclic addition product is obtained. 

In this Reaction , when bridge ring is formed, the Substituent bonded to dienophile may be cis or trans in nature. 

Chemistry homework question answer, step 1, image 1

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