Addition of HCI to 1-methoxycyclohexene yields 1-chloro-1-methoxycyclo- hexane as the sole product. Use resonance structures to explain why none of the other regioisomer is formed.
Addition of HCI to 1-methoxycyclohexene yields 1-chloro-1-methoxycyclo- hexane as the sole product. Use resonance structures to explain why none of the other regioisomer is formed.
Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy
Section14.SE: Something Extra
Problem 54AP
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![14.45 Addition of HCl to 1-methoxycyclohexene yields 1-chloro-1-methoxycyclo-
hexane as the sole product. Use resonance structures to explain why none of
the other regioisomer is formed.
OCH3
-CI
LOCH3
HCI](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F424c00fa-abe3-4dd7-b4b2-d7eb889716f3%2Fa28e52aa-a13d-43b3-8257-5e0cf85df769%2Fvm9evev_processed.jpeg&w=3840&q=75)
Transcribed Image Text:14.45 Addition of HCl to 1-methoxycyclohexene yields 1-chloro-1-methoxycyclo-
hexane as the sole product. Use resonance structures to explain why none of
the other regioisomer is formed.
OCH3
-CI
LOCH3
HCI
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