Given below are two statements:
Statement $(I)$: Benzyl chloride reacts faster in $S_N1$ mechanism than ethyl chloride.
Statement $(II)$: Ethyl carbocation intermediate is less stabilized by hyperconjugation than benzyl carbocation by resonance.
In the light of the above statements, choose the correct answer from the options given below:

  • A
    Both Statement $I$ and Statement $II$ are true
  • B
    Both Statement $I$ and Statement $II$ are false
  • C
    Statement $I$ is true but Statement $II$ is false
  • D
    Statement $I$ is false but Statement $II$ is true

Explore More

Similar Questions

What is the decreasing order of nucleophilicity for the following nucleophiles?
$1. CH_3COO^-$
$2. CH_3O^-$
$3. CN^-$
$4. CH_3-C_6H_4-SO_3^-$ (tosylate ion)

Difficult
View Solution

Which compound might be synthesized by the $S_N2$ displacement of an alkyl-halide?

The major product obtained in the following reaction is $:$

Identify the correct reactivity order for $E_2$ reaction with alc. $KOH$ for the following compounds:
$(i)$ $8$-chlorocycloocta-$1,3,5$-triene
(ii) $3$-chlorocyclohexa-$1,4$-diene
(iii) $3$-chlorocyclobutene

Difficult
View Solution

The reaction of $n$-propyl bromide with ethanolic potassium hydroxide $(KOH)$ produces ...... .

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo