Which of the following statements is invalid?

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(C) Statement $A$ is correct because carbocation stability lowers the activation energy of the rate-determining step.Statement $B$ is correct as a pri

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Isopropyl chloride reacts with sodium ethoxide to form $1-$ethoxypropane.

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(C) Statement $A$ is correct because carbocation stability lowers the activation energy of the rate-determining step.Statement $B$ is correct as a primary carbocation rearranges to a more stable secondary carbocation via a $1,2-$hydride shift.Statement $C$ is invalid. Isopropyl chloride $(CH_3CHClCH_3)$ reacting with sodium ethoxide $(NaOCH_2CH_3)$ primarily undergoes an $E2$ elimination reaction to form propene,not $1-$ethoxypropane. Even if substitution occurs,it would form $2-$ethoxypropane,not $1-$ethoxypropane.Statement $D$ is correct as propyl halides $(CH_3CH_2CH_2X)$ react with sodium ethoxide via an $S_N2$ mechanism to form $1-$ethoxypropane $(CH_3CH_2CH_2OCH_2CH_3)$.

Similar Questions

Which one of the following halogen compounds is least reactive towards hydrolysis by $S_{N}1$ mechanism?

Which of the following will most readily give the dehydrohalogenation product?

Which one of the following forms propane nitrile as the major product?

The correct reactivity order of the following compounds towards alkaline hydrolysis is:-
$I. \ p-CH_3O-C_6H_4-CH_2Cl$
$II. \ C_6H_5-CH_2Cl$
$III. \ p-CH_3-C_6H_4-CH_2Cl$
$IV. \ m-CH_3-C_6H_4-CH_2Cl$

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