QUESTION 9 Why would the compound below not react with a dienophile in a Diels-Alder reaction? The compound cannot adopt the s-cis conformation. There are no electron withdrawing groups on the compound. There are no electron donating groups on the compound. The compound is not a conjugated diene. 0000 QUESTION 10 Which of the following is not a feature of the Diels-Alder reaction? They form new six-membered rings. They are initiated by peroxides. Three TT bonds break. They are concerted.

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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QUESTION 9
Why would the compound below not react with a dienophile in a Diels-Alder reaction?
The compound cannot adopt the s-cis conformation.
There are no electron withdrawing groups on the compound.
There are no electron donating groups on the compound.
The compound is not a conjugated diene.
0000
QUESTION 10
Which of the following is not a feature of the Diels-Alder reaction?
They form new six-membered rings.
They are initiated by peroxides.
Three TT bonds break.
They are concerted.
Transcribed Image Text:QUESTION 9 Why would the compound below not react with a dienophile in a Diels-Alder reaction? The compound cannot adopt the s-cis conformation. There are no electron withdrawing groups on the compound. There are no electron donating groups on the compound. The compound is not a conjugated diene. 0000 QUESTION 10 Which of the following is not a feature of the Diels-Alder reaction? They form new six-membered rings. They are initiated by peroxides. Three TT bonds break. They are concerted.
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