Asked by Kim
I just need some clarification regarding SN1 reactions
Okay...so a reaction with a secondary ALKYL HALiDE + CH3OH (Methanal), why is the nucleophile CH3O? why doesn't it dissociate to give CH3 and OH?
Okay...so a reaction with a secondary ALKYL HALiDE + CH3OH (Methanal), why is the nucleophile CH3O? why doesn't it dissociate to give CH3 and OH?
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Kim
methanol*
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