a-explain-why-sn2-and-sn1-reactions-are-both-not-feasible-for-1-chloromethyl-1-m

Question

a. Explain why both S_N2 and S_N1 reactions are not feasible for 1-(chloromethyl)-1-isopropylcyclohexane.

b. Are E2 and E1 reactions feasible for it?

Accepted Answer

a. The S_N1 reaction is not feasible due to the formation of an unstable primary carbocation. The S_N2 reaction is not feasible due to the steric hindrance for the backside attack.

b. E2 and E1 reactions are also not feasible.

Answer

a. S_N1 and S_N2 reactions are not feasible due to the steric hindrance for the backside attack.

b. E2 and E1 reactions are also not feasible.

Answer

a. S_N1 and S_N2 reactions are not feasible due to the steric hindrance for the backside attack.

b. E2 and E1 reactions are both feasible.

Answer

a. The S_N1 reaction is not feasible due to the formation of an unstable primary carbocation. The S_N2 reaction is not feasible due to the steric hindrance for the backside attack.

b. E2 and E1 reactions are both feasible.

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a. Explain why both S_N2 and S_N1 reactions are not feasible for 1-(chloromethyl)-1-isopropylcyclohexane.
b. Are E2 and E1 reactions feasible for it?