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For a diene to undergo a Diels-Alder reaction it must a. be substituted with electron-withdrawing groups b. be able to adopt an s-trans conformation c. be substituted with electron-donating groups d. be able to adopt an s-cis conformation For Diels-Alder cycloaddition reactions to take place most rapidly and in highest yield the dienophile must a. be substituted with electron-withdrawing groups b. be able to adopt an s-trans conformation c. be substituted with electron-donating groups d. be able to adopt an s-cis conformation Draw the mechanism of the bromination of 2-ethyl-1.3-cyclopentadiene.
For a diene to undergo a Diels-Alder reaction it must a. be substituted with electron-withdrawing groups b. be able to adopt an s-trans conformation c. be substituted with electron-donating groups d. be able to adopt an s-cis conformation For Diels-Alder cycloaddition reactions to take place most rapidly and in highest yield the dienophile must a. be substituted with electron-withdrawing groups b. be able to adopt an s-trans conformation c. be substituted with electron-donating groups d. be able to adopt an s-cis conformation Draw the mechanism of the bromination of 2-ethyl-1.3-cyclopentadiene.
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Casey DurganLv2
13 Apr 2019
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