The reactivity of ethyl chloride towards nucl | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(D) The reactivity of alkyl halides towards nucleophilic substitution depends on the stability of the carbocation intermediate (in $S_N1$) or steric h

Vedclass · Accepted Answer

Less than that of chlorobenzene

Vedclass · Answer

(D) The reactivity of alkyl halides towards nucleophilic substitution depends on the stability of the carbocation intermediate (in $S_N1$) or steric hindrance (in $S_N2$).Benzyl chloride $(C_6H_5CH_2Cl)$ is highly reactive due to the resonance stabilization of the benzyl carbocation.Ethyl chloride $(C_2H_5Cl)$ is a primary alkyl halide and is less reactive than benzyl chloride.Chlorobenzene $(C_6H_5Cl)$ is the least reactive due to the partial double bond character of the $C-Cl$ bond caused by resonance.Therefore,the correct order of reactivity is $C_6H_5CH_2Cl > C_2H_5Cl > C_6H_5Cl$.Thus,the reactivity of ethyl chloride is less than that of benzyl chloride.

The reactivity of ethyl chloride towards nucleophilic substitution is:

Similar Questions

Dehydrohalogenation of an alkyl halide is a/an

The reactivity order of the following molecules towards $S_N1$ reaction is:
$(I)$ Allyl chloride
$(II)$ Chlorobenzene
$(III)$ Ethyl chloride

Ethyl acetate is obtained when methyl magnesium iodide reacts with

Identify the chiral molecule from the following.

What is the correct order of leaving group ability for the following groups?
$I. -OAc$
$II. -OMe$
$III. -OSO_2Me$
$IV. -OSO_2CF_3$

Vedclass Test Series

Exam Paper Generator

Online Exam Module