which one show faster SN2 reaction between benzyl cloride and clorobenze? explain it.
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I would have to write it out but since a Sn1 reaction goes from reactant to product in one step with no intermediates, and I guess the benzyl chloride has a ring I think and methyl chloride is just CH3 attached to the carbon chain we call that has a methyl molecule attached to it already, and no closed ring with its double bones
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