When an unsymmetrical alkene such as propene is treated with N-Bromosuccinimide in aqueous dimethyl sulfoxide, the major
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When an unsymmetrical alkene such as propene is treated with N-Bromosuccinimide in aqueous dimethyl sulfoxide, the major product has the bromine atom bonded to the less highly substituted carbon atom. Is this Markovnikov or non-Markovnikov orientation? Explain.
Transcribed Image Text:
Он Br2, H20 CH3CH=CH2 CHзснCH2Br
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Reaction of the alkene with Br2 formed from NBS produces a cyclic bromonium ion When ...View the full answer
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