Identify the reaction mechanisms for steps I | vedclass

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(C) The starting material is a chiral secondary alkyl chloride,$CH(Me)(Et)Cl$.Step $I$ leads to product $A$,which shows retention of configuration rel

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$I$ is $S_N1$ and $II$ is $S_N2$

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(C) The starting material is a chiral secondary alkyl chloride,$CH(Me)(Et)Cl$.Step $I$ leads to product $A$,which shows retention of configuration relative to the starting material. This is characteristic of an $S_N1$ mechanism where the nucleophile can attack from the same side as the leaving group due to the formation of a planar carbocation intermediate.Step $II$ leads to product $B$,which shows inversion of configuration. This is characteristic of an $S_N2$ mechanism,where the nucleophile attacks from the side opposite to the leaving group.Therefore,step $I$ is $S_N1$ and step $II$ is $S_N2$.

Identify the reaction mechanisms for steps $I$ and $II$ in the given transformation:
$CH(Me)(Et)Cl + OH^- \rightarrow CH(Me)(Et)OH$
(Refer to the provided image for stereochemical outcomes $A$ and $B$)

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Identify the reaction mechanisms for steps $I$ and $II$ in the given transformation:$CH(Me)(Et)Cl + OH^- \rightarrow CH(Me)(Et)OH$(Refer to the provided image for stereochemical outcomes $A$ and $B$)