Question

Which of the following alkyl halide would undergo SN1 reaction easily
1) CH3Cl
2) CH3-CH2-CH(Cl)-CH3
3) CH3-CH2-Cl
4) (CH3)3C-Cl

Answer 1

Answer:

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Explanation:

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All the given compounds are tertiary alkyl halides but the bond formed between carbon and iodine (C-l) bond is the weakest bond due to large difference in the size of carbon and iodine. So, (CH3)3 C-l aives SN1 reaction most readily.

Answer 2

HYE MATES ✌YOUR ANSWER IS HERE ⬇⬇⬇

➡ALL OPTION IS CORRECT .

➡BUT

➡SN1 REACTION EASILY;

➡CH3- CH2-CH (CL)-CH3

HOPE ITS HELP YOU✌