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

Product $B$ may be :

Difficult
View Solution

What will be the product $B$ formed in the following reaction sequence?
$CH_3CH_2CH_2OH$ $\xrightarrow{PCl_5} A$ $\xrightarrow{alc. KOH} B$

$A$ benzene derivative did not produce a white precipitate with ammoniacal silver nitrate solution (Tollens' reagent) but decolorized cold dilute alkaline $KMnO_4$ solution (Baeyer's reagent). The compound is:

An alkene gives two moles of $HCHO$,one mole of $CO_2$,and one mole of $CH_3COCHO$ on ozonolysis. What is its structure?

What is the correct order of stability for the following alkenes?

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