1. Cl2, H20 2. NaOH Another mechanism for the formation of epoxides is through the formationofa chlorohydrin. Alkenes react with chlorine in the presence of H0 to give a chlorohydrin via a cyclic chloronium ion intermec iate. When the chlorohydrin is treated with strong base, HCl is eliminated and the epoxide is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions :OH Hö :CI:

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
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Draw curved arrows to show the movement of electrons in this step of the mechanism. 

1. Cl2, H20
2. NaOH
Another mechanism for the formation of epoxides is through the formation ofa chlorohydrin. Alkenes react with chlorine in the
presence of H0 to give a chlorohydrin via a cyclic chloronium ion intermec iate. When the chlorohydrin is treated with strong base,
HCl is eliminated and the epoxide is formed.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
ci:
CI:
H2O
Transcribed Image Text:1. Cl2, H20 2. NaOH Another mechanism for the formation of epoxides is through the formation ofa chlorohydrin. Alkenes react with chlorine in the presence of H0 to give a chlorohydrin via a cyclic chloronium ion intermec iate. When the chlorohydrin is treated with strong base, HCl is eliminated and the epoxide is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions ci: CI: H2O
1. Cl2, H20
2. NaOH
Another mechanism for the formation of epoxides is through the formation of a c hlorohydrin. Alkenes react with chlorine in the presence
of H,0 to give a chlorohydrin via a cyclic chloronium ion intermediate. When th chlorohydrin is treated with strong base, HCl is
eliminated and the epoxide is formed.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
ci:
CI:
. Hö
H2
Transcribed Image Text:1. Cl2, H20 2. NaOH Another mechanism for the formation of epoxides is through the formation of a c hlorohydrin. Alkenes react with chlorine in the presence of H,0 to give a chlorohydrin via a cyclic chloronium ion intermediate. When th chlorohydrin is treated with strong base, HCl is eliminated and the epoxide is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions ci: CI: . Hö H2
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