Why does bromine add faster to a disubstituted double bond
Why does bromine add faster to a disubstituted double bond than a monosubstituted double bond to produce dibromides?
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Why does bromine add faster to a disubstituted double bond than a monosubstituted double bond to produce dibromides
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If one reacts a double bond with bromine in chloroform a dibromide is obtained. However, if one reacts bromine in water with a double bond, a vicinal halohydrin is formed. Provide an explanation for this result and show a mechanism for the reactio
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