EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
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Chapter 15, Problem 15.35SP

Furan and malemide undergo a Diels-Alder reaction at 25 °C to give the endo isomer of the product. When the reaction takes place at 90 °C, however, the major product is the exo isomer. Further study shows that the endo isomer of the product isomenzes to the exo isomer at 90 °C.

Chapter 15, Problem 15.35SP, Furan and malemide undergo a Diels-Alder reaction at 25 C to give the endo isomer of the product.

  1. a. Draw and label the endo and exo isomers of the Dieis-Alder adduct of furan and maleimide.
  2. b. Which isomer of the product would you usually expect from this reaction? Explain why this isomer is usually favored.
  3. c. Examine your answer to (b) and determine whether this answer applies to a reaction that is kinetic ally controlled or one that is thermodynamically controlled, or both.
  4. d. Explain why the endo isomer predominates when the reaction takes place at 25 °C and why the exo isomer predominates at 90 °C.
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Students have asked these similar questions
9. Determine the product of the following Diels-Alder reaction. CO₂Et 206°C
True or False: Acetylene is a naturally occurring conjugated diene   True or False: The Diels-Alder reaction has the stereochemistry of the dienophile is retained in the product.     True or False: When looking at kinetic vs. thermodynamic products the kinetic product predominates at low temperature.   True or False: the mechanism of the Diels-Alder reaction is three π bonds break; one σ bond and two π bonds form.
Is the following true or false? To catalyse a Diels-Alder reaction a common approach involves the use of a Lewis acid capable of lowering the LUMO of the dienophile.

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EP ORGANIC CHEMISTRY -MOD.MASTERING 18W

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