Write in brief about the preparation of alkene from vicinal dihalide.

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) Vicinal dihalides are compounds in which two halogen atoms are attached to two adjacent carbon atoms.
Dehalogenation: When vicinal dihalides are treated with zinc metal,they lose a molecule of $ZnX_2$ to form an alkene. This reaction is known as dehalogenation.
Examples:
$(i) \ CH_2Br-CH_2Br + Zn \xrightarrow{\Delta, \text{Ethanol}} CH_2=CH_2 + ZnBr_2 \ (\text{Ethene})$
$(ii) \ CH_3-CHBr-CH_2Br + Zn \xrightarrow{\Delta, \text{Ethanol}} CH_3CH=CH_2 + ZnBr_2 \ (\text{Propene})$

Explore More

Similar Questions

The reaction of $1-$ethylcyclopentene with $BH_3 / THF$ followed by treatment with $H_2O_2 / NaOH$ produces:

What is the product formed when one molecule of $HBr$ reacts with one molecule of $1,3$-butadiene at $40^{\circ}C$?

Difficult
View Solution

The stereochemistry of the product formed in the following reaction is:

Addition of $HCl$ to propene in the presence of peroxides gives:

Peroxide effect is observed with the addition of $HBr$ but not with the addition of $HI$ to unsymmetrical alkene because

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