1. Cl2, H20 2. NaOH Another mechanism for the formation of epoxides is through the formation of a chlorohydrin. Alkenes react with chlorine in the presence of H2O to give a chlorohydrin via a cyclic chloronium ion intermediate. 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

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Chapter1: Chemical Foundations
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1. Cl2, H20
2. NaOH
Another mechanism for the formation of epoxides is through the formation of a chlorohydrin. Alkenes react with chlorine in the presence of H,O to give a chlorohydrin via a cyclic chloronium ion
intermediate. 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
+
Transcribed Image Text:1. Cl2, H20 2. NaOH Another mechanism for the formation of epoxides is through the formation of a chlorohydrin. Alkenes react with chlorine in the presence of H,O to give a chlorohydrin via a cyclic chloronium ion intermediate. 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 +
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