Question 12.17:
Explain the terms Inductive and Electromeric effects. Which electron displacement effect

explains the following correct orders of acidity of the carboxylic acids?

(a)Cl3CCOOH > Cl2CHCOOH > ClCH2COOH

(b)CH3CH2COOH > (CH3)2CHCOOH > (CH3)3C.COOH

Inductive effect

The permanent displacement of sigma (σ) electrons along a saturated chain, whenever an

electron withdrawing or electron donating group is present, is called inductive effect.

Inductive effect could be + I effect or – I effect. When an atom or group attracts electrons

towards itself more strongly than hydrogen, it is said to possess – I effect.


For example,

When an atom or group attracts electrons towards itself less strongly than hydrogen, it is

said to possess + I effect.

For example,

Electrometric effect

It involves the complete transfer of the shared pair of π electrons to either of the two

atoms linked by multiple bonds in the presence of an attacking agent. For example,

Electrometric effect could be + E effect or – E effect.

+ E effect: When the electrons are transferred towards the attacking reagent

– E effect: When the electrons are transferred away from the attacking reagent

(a) Cl3CCOOH > Cl2CHCOOH > ClCH2COOH

The order of acidity can be explained on the basis of Inductive effect (– I effect). As the

number of chlorine atoms increases, the – I effect increases. With the increase in – I

effect, the acid strength also increases accordingly.

(b) CH3CH2COOH > (CH3)2 CHCOOH > (CH3)3 C.COOH

The order of acidity can be explained on the basis of inductive effect (+ I effect). As the

number of alkyl groups increases, the + I effect also increases. With the increase in + I

effect, the acid strength also increases accordingly.