Explain the reactivity of alkenes towards electrophilic reagents.

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) Alkenes contain a carbon-carbon double bond consisting of one strong $\sigma$-bond and one weak $\pi$-bond.
The $\pi$-electrons are loosely held and are available as a source of electron density,making the alkene molecule electron-rich.
Electrophiles $(E^+)$ are electron-deficient species that are attracted to this electron-rich $\pi$-electron cloud.
Upon attack by an electrophile,the weak $\pi$-bond breaks easily,leading to the formation of a more stable saturated compound through an addition reaction.
Therefore,alkenes are more reactive towards electrophilic addition reactions compared to alkanes,which only contain strong $\sigma$-bonds.

Explore More

Similar Questions

Ethylene reacts with Baeyer's reagent to give

The major products $P$ and $Q$ from the below reactions are :
$CH_3CH=CH_2 \xrightarrow{HBr} P$
$CH_3CH=CH_2 \xrightarrow[(BH_3)_2]{H_2O, H_2O_2 / OH^-} Q$

For the preparation of alkenes,an aqueous concentrated solution of sodium or potassium salts of carboxylic acids is subjected to ........

The major product of the reaction is:

The product obtained when $2-$methylpropan$-2-$ol is treated with alumina $(Al_2O_3)$ at $423 \ K$ is

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