Isn't the mechanism of aqueous sodium hydroxide and 1-bromobutane involves both heterolytic bond fission and attacking by a nucleophile?
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attack by a nucleophile on a carbon atom with a partial positive charge
heterolytic bond fission and attack by a nucleophile on a carbocation
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Explanation:
Well your thinking is absolutely right but only for tertiary halogenoalkane as this is a prinary halogenoalkane it will follow SN2 mechamism. In which necleophile attacks on a partial positive carbon
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