$X$ is an isomer of $C_6H_{14}$. It has four primary carbons and two tertiary carbons. '$X$' can be prepared from which of the following reactions?

  • A
    Hydrogenation of $2$-methylpent-$2$-ene
  • B
    Wurtz reaction of $1$-bromopropane
  • C
    Reduction of $2$-chloro-$3$-methylpentane
  • D
    Wurtz reaction of $2$-bromopropane

Explore More

Similar Questions

In alkanes,the bond angle is $...^o$.

In the given reaction,product $B$ is:
Cyclohexane $\xrightarrow{Br_2, h\nu}$ $(A) \xrightarrow{Na, \text{dry ether}}$ $(B)$

Which one gives only one monosubstitution product on chlorination?

Which of the following conditions will give the maximum yield of $C_2H_5Cl$?

Difficult
View Solution

The number of possible monobromo products for the reaction of methylcyclohexane with $Br_2/hv$ is (excluding stereoisomers):

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