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When an unsymmetrical alkene such as propene is treated with N-bromosuc- cinimide 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.

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Step-by-step explanation:

kindly check the file below to show the explanation . Thanks

When an unsymmetrical alkene such as propene is treated with N-bromosuc- cinimide-example-1
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