10. The following Diels-Alder cycloaddition was recently performed by Mukherjee et al. CH,Cl, CO,Et + ACN Co,Et ACO,Et CN -78°C, 8h 25% 75% When cyclopentadiene is added in excess, the reaction is pseudo-1s order with respect to the fumaric nitrile ester. If 4 hours represents the time for half of the original amount of ester to be consumed, then calculate the amount of 1 and 2 diastereoisomers that are formed after 90 min if performed with 75.0 mmol of ester.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter30: Orbitals And Organic Chemistry: Pericyclic Reactions
Section30.SE: Something Extra
Problem 21AP
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10.
The following Diels-Alder cycloaddition was recently performed by Mukherjee et al.
CH,Cl,
CO,Et +
ACN
Co,Et
AcO,Et
CN
-78°C, 8h
25%
75%
When cyclopentadiene is added in excess, the reaction is pseudo-1“ order with respect to the fumaric
nitrile ester. If 4 hours represents the time for half of the original amount of ester to be consumed, then
calculate the amount of 1 and 2 diastereoisomers that are formed after 90 min if performed with 75.0 mmol
of ester.
Transcribed Image Text:10. The following Diels-Alder cycloaddition was recently performed by Mukherjee et al. CH,Cl, CO,Et + ACN Co,Et AcO,Et CN -78°C, 8h 25% 75% When cyclopentadiene is added in excess, the reaction is pseudo-1“ order with respect to the fumaric nitrile ester. If 4 hours represents the time for half of the original amount of ester to be consumed, then calculate the amount of 1 and 2 diastereoisomers that are formed after 90 min if performed with 75.0 mmol of ester.
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