• Comment on the reactivity of N-methylmaleimide specifically why it is such a reactive dienophile. . ● Comment on the reactivity of 9-anthracenemethanol specifically why it is such an unreactive diene. As the reaction proceeds, the TLC analysis shows a reduction in fluorescence in going from the 9-anthracenemethanol starting material (fluorescent) to the cycloaddition product (non- fluorescent). Explain this observation.

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Chapter1: Chemical Foundations
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Can i have some help on this 3 questions with clear wroting based on the diels alder reaction 

 

• Comment on the reactivity of N-methylmaleimide specifically why it is such a reactive
dienophile.
• Comment on the reactivity of 9-anthracenemethanol specifically why it is such an unreactive
diene.
•
As the reaction proceeds, the TLC analysis shows a reduction in fluorescence in going from
the 9-anthracenemethanol starting material (fluorescent) to the cycloaddition product (non-
fluorescent). Explain this observation.
Transcribed Image Text:• Comment on the reactivity of N-methylmaleimide specifically why it is such a reactive dienophile. • Comment on the reactivity of 9-anthracenemethanol specifically why it is such an unreactive diene. • As the reaction proceeds, the TLC analysis shows a reduction in fluorescence in going from the 9-anthracenemethanol starting material (fluorescent) to the cycloaddition product (non- fluorescent). Explain this observation.
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