Addition of HCI to 1-methoxycyclohexene unexpectedly yields 1-chloro-1-methoxycyclohexane as the sole product. Draw the mechanism of the reaction leading to this single product. Briefly explain why none of the other regioisomer(s) is formed. LOCH3 HCI OCH3 1-methoxycyclohexene 1-chloro-1-methoxycyclohexane

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Chapter1: Chemical Foundations
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Addition of HCI to 1-methoxycyclohexene unexpectedly yields 1-chloro-1-methoxycyclohexane as the sole product. Draw the mechanism of the reaction leading to this
single product. Briefly explain why none of the other regioisomer(s) is formed.
LOCH3
HCl
OCH3
1-methoxycyclohexene
1-chloro-1-methoxycyclohexane
Transcribed Image Text:Addition of HCI to 1-methoxycyclohexene unexpectedly yields 1-chloro-1-methoxycyclohexane as the sole product. Draw the mechanism of the reaction leading to this single product. Briefly explain why none of the other regioisomer(s) is formed. LOCH3 HCl OCH3 1-methoxycyclohexene 1-chloro-1-methoxycyclohexane
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