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Chemistry Question 63 – JEE-MAIN 2026

Increasing order of electron withdrawing power of following functional groups is: a. - CN b. - COOH c. - NO2 d. - I

Electron-withdrawing groups decrease electron density in a molecule, primarily through inductive (-I) and resonance (-M) effects.

Step 1: Identify Electron-Withdrawing Effects for Each Group✦ Active

The electron-withdrawing power of functional groups is determined by their inductive (I) and mesomeric (M) effects. Let's analyze each group:

a. -CN (Cyano group): Exhibits a strong I effect due to the electronegative nitrogen and a moderate M effect due to the triple bond.

b. -COOH (Carboxyl group): Exhibits a moderate I effect due to the electronegative oxygen atoms and a weak M effect due to the carbonyl group.

c. -NO2 (Nitro group): Exhibits a strong I effect due to the electronegative oxygen atoms and a very strong M effect where it withdraws electrons through resonance.

d. -I (Iodo group): Exhibits a weak I effect due to its electronegativity. Halogens also have a +M effect, but their I effect is considered for EWG comparison, and it's the weakest among the given options.

Step 2: Compare Relative Strengths of Electron-Withdrawing Groups○ Expand

Based on the combined inductive and mesomeric effects, the general order of electron-withdrawing strength is:

NO2>CN>COOH>I

The nitro group (NO2) is generally considered one of the strongest electron-withdrawing groups due to its powerful resonance and inductive effects. The cyano group (CN) is also strong, followed by the carboxyl group (COOH). The iodo group (I) is the weakest among these due to its relatively weak inductive effect.

💡 Teacher's Secret Hint

Remember that resonance effects often dominate over inductive effects when both are present and significant.

Step 3: Arrange in Increasing Order○ Expand

Arranging the functional groups in increasing order of their electron-withdrawing power:

I<COOH<CN<NO2

Translating this to the given labels (a, b, c, d):

d<b<a<c

This order matches option 3.

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