Which of the following compounds is most reac | vedclass

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

Question

(D) The reactivity of a compound towards $S_{N^1}$ reaction depends on the stability of the carbocation intermediate formed after the departure of the

Vedclass · Accepted Answer

$1-$Methyl$-3-$chlorocyclohexene

Vedclass · Answer

(D) The reactivity of a compound towards $S_{N^1}$ reaction depends on the stability of the carbocation intermediate formed after the departure of the leaving group $(Cl^-)$.$A$: Chlorocyclohexane forms a secondary $(2^{\circ})$ carbocation.$B$: $3-$Chlorocyclohexene forms an allylic carbocation,which is stabilized by resonance.$C$: $1-$Methyl$-1-$chlorocyclohexane forms a tertiary $(3^{\circ})$ carbocation.$D$: $1-$Methyl$-3-$chlorocyclohexene forms an allylic carbocation that is also tertiary $(3^{\circ})$,making it the most stable carbocation among the given options due to both resonance stabilization and the inductive effect of the methyl group.Therefore,the compound in option $D$ is the most reactive towards $S_{N^1}$ reaction.

Which of the following compounds is most reactive towards $S_{N^1}$ reaction?

Similar Questions

The major product $(A)$ is:

Arrange the following alkyl halides in the increasing order of their reactivity towards nucleophilic substitution reaction:
$(I)$ $CH_3CH_2CH(Cl)CH_3$
$(II)$ $CH_2=CHCH(Br)CH_3$
$(III)$ $CH_2=CHCH(Cl)CH_3$
$(IV)$ $CH_3CH=C(Br)CH_3$

Identify '$X$' and '$Y$' in the following sequence of transformations: $CH_3-CH_2-CH_2Br$ $\xrightarrow{X} \text{Product}$ $\xrightarrow{Y} CH_3-CH(Br)-CH_3$.

Ethyl orthoformate is formed by heating which of the following compounds with sodium ethoxide?

The order of reactivity of the given haloalkanes towards nucleophiles is:

Vedclass Test Series

Exam Paper Generator

Online Exam Module