Which of the following correctly describes the known mechanism of the Diels-Alder reaction? Select one: A. A strained 4-member ring intermediate is formed which rearranges to a 6- member ring. B. A di-radical, 6-member ring intermediate is formed. C. The mechanism is a one-step process with bond-making, bond breaking changes occurring simultaneously. D. A zwitterion species (molecule with full +1 and -1 charges) is rapidly formed as an intermediate. Е. A resonance-stabilized carbocation intermediate is formed in a slow step.

Chemistry
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Chapter1: Chemical Foundations
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Which of the following correctly describes the known mechanism of the Diels-Alder
reaction?
Select one:
A. A strained 4-member ring intermediate is formed which rearranges to a 6-
member ring.
B. A di-radical, 6-member ring intermediate is formed.
C. The mechanism is a one-step process with bond-making, bond breaking
changes occurring simultaneously.
D.
A zwitterion species (molecule with full +1 and -1 charges) is rapidly formed
as an intermediate.
E. A resonance-stabilized carbocation intermediate is formed in a slow step.
Transcribed Image Text:Which of the following correctly describes the known mechanism of the Diels-Alder reaction? Select one: A. A strained 4-member ring intermediate is formed which rearranges to a 6- member ring. B. A di-radical, 6-member ring intermediate is formed. C. The mechanism is a one-step process with bond-making, bond breaking changes occurring simultaneously. D. A zwitterion species (molecule with full +1 and -1 charges) is rapidly formed as an intermediate. E. A resonance-stabilized carbocation intermediate is formed in a slow step.
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