(ii) Irradiation of diene A at 254 nm affords a photostationary mixture of A with triene B. Provide a mechanism for the formation of B and define the stereochemistry of the alkenes, explaining this stereochemical outcome by reference to the interacting frontier molecular orbitals. hv

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
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Problem 73AP: Use your knowledge of directing effects, along with the following data, to deduce the directions of...
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Irradiation of diene A at 254 nm affords a photostationary mixture of A
with triene B. Provide a mechanism for the formation of B and define the
stereochemistry of the alkenes, explaining this stereochemical outcome by
reference to the interacting frontier molecular orbitals.
H.
hv
H
B
Transcribed Image Text:Irradiation of diene A at 254 nm affords a photostationary mixture of A with triene B. Provide a mechanism for the formation of B and define the stereochemistry of the alkenes, explaining this stereochemical outcome by reference to the interacting frontier molecular orbitals. H. hv H B
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