) For the two dienes shown, shade in the lobes of the four molecular orbitals (on the left) and then populate the appropriate orbitals with pi electrons. Next, in the middle diagram, shade in the lobes of the highest occupied molecular orbital that is used in part a) for thermal electrocyclization. Draw the expected product in the box and explain briefly, using terms such as conrotatory and/or disrotatory, why that particular stereoisomer is formed under thermal conditions. Repeat this process in part b) for the photolytic situation. 8888 8888 8888 a) & CH3 CH3 - - ff 28 H₂C A
) For the two dienes shown, shade in the lobes of the four molecular orbitals (on the left) and then populate the appropriate orbitals with pi electrons. Next, in the middle diagram, shade in the lobes of the highest occupied molecular orbital that is used in part a) for thermal electrocyclization. Draw the expected product in the box and explain briefly, using terms such as conrotatory and/or disrotatory, why that particular stereoisomer is formed under thermal conditions. Repeat this process in part b) for the photolytic situation. 8888 8888 8888 a) & CH3 CH3 - - ff 28 H₂C A
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions
Section: Chapter Questions
Problem 20.28P: Write the frontier molecular orbital analysis for the cycloaddition of butadiene with butadiene when...
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Question
![) For the two dienes shown, shade in the lobes of the four molecular orbitals (on the left) and then
populate the appropriate orbitals with pi electrons. Next, in the middle diagram, shade in the lobes of the
highest occupied molecular orbital that is used in part a) for thermal electrocyclization. Draw the expected
product in the box and explain briefly, using terms such as conrotatory and/or disrotatory, why that
particular stereoisomer is formed under thermal conditions. Repeat this process in part b) for the photolytic
situation.
8888
a)
b)
CH3
CH3
8888
Energy 8888 -
CH3
8888
8888
CH3
8888
Energy 8888
| | |
| | | I
88 вон
8
H₂C
88 дона
H₂C
2
A
hv](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F18057168-5c09-4b49-9474-3873a7f885f6%2F9a47a4bd-2254-42a3-bde9-ae8f70f326a8%2Fe50s3wf_processed.jpeg&w=3840&q=75)
Transcribed Image Text:) For the two dienes shown, shade in the lobes of the four molecular orbitals (on the left) and then
populate the appropriate orbitals with pi electrons. Next, in the middle diagram, shade in the lobes of the
highest occupied molecular orbital that is used in part a) for thermal electrocyclization. Draw the expected
product in the box and explain briefly, using terms such as conrotatory and/or disrotatory, why that
particular stereoisomer is formed under thermal conditions. Repeat this process in part b) for the photolytic
situation.
8888
a)
b)
CH3
CH3
8888
Energy 8888 -
CH3
8888
8888
CH3
8888
Energy 8888
| | |
| | | I
88 вон
8
H₂C
88 дона
H₂C
2
A
hv
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