Ch3l or ch3cl which is more reactive towards sn1
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Answer:
Explanation:
In an SN1 reaction mechanism, a carbocation must form. In this case, if this rxn was an SN1, there would be a methyl carbocation.
Overall stability for carbocations is as follows:
Methyl<primary<secondary<tertiary
Methyl carbocation (a.k.a. Methenium) is not stable. (The more you can spread the charge around, the more stable your carbocation is. )
This is why the above reaction does not give SN1
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