Explain the inductive effect with a suitable example.

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) The inductive effect is the permanent displacement of shared electron pairs along a carbon chain due to the difference in electronegativity between the carbon atom and an attached atom or group.
$1$. It is a permanent effect and operates through $\sigma$-bonds.
$2$. It decreases rapidly as the distance from the source of the effect increases.
$3$. Groups that withdraw electrons are called $-I$ groups (e.g.,$-Cl, -NO_2$),while groups that donate electrons are called $+I$ groups (e.g.,$-CH_3, -C_2H_5$).
Example: In $CH_3-CH_2-CH_2-Cl$,the chlorine atom is more electronegative than carbon. It pulls the shared electron pair of the $C-Cl$ bond towards itself,creating a partial negative charge $(\delta^-)$ on $Cl$ and a partial positive charge $(\delta^+)$ on the $C_1$ atom. This polarization is transmitted to $C_2$ $(\delta\delta^+)$ and $C_3$ $(\delta\delta\delta^+)$,but the effect weakens significantly with distance.

Explore More

Similar Questions

The increasing order of the electron-withdrawing power of the following functional groups is:
a. $-CN$
b. $-COOH$
c. $-NO_2$
d. $-I$

Which of the following groups exhibits $(+)R$ effect?

The effect that makes $2,3-$dimethyl$-2-$butene more stable than $2-$butene is

Orbital interaction between the $\sigma$ bonds of a substituent group and a neighbouring $\pi$ orbital is known as

Which of the following is not correct?

Difficult
View Solution

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