Covalent character of ionic bond increases with: small cation, large anion, high charge on either ion, cation with d-electrons (pseudo-noble-gas configuration).
-- NCERT Class 11 Chemistry, Ch. 4, p. 8Electronegativity Fajan
Lesson
Electronegativity is the tendency of a bonded atom to attract shared electron pairs toward itself. Pauling's scale (NCERT Class 11 Chemistry Chapter 4, page 8) assigns fluorine the highest value (4.0). Across a period, electronegativity increases (rising nuclear charge, shrinking radius); down a group, it decreases (more shielding, larger radius).
A common confusion: treating electronegativity and electron affinity as interchangeable. Electronegativity is a bond property — it describes pull on shared electrons within a molecule. Electron affinity is an isolated-atom property — the energy change when a gaseous atom gains an electron.
Fajan's rules predict when an ionic bond develops covalent character. The central idea: a small, highly charged cation polarises a large, highly charged anion, distorting its electron cloud toward the cation. This polarisation introduces covalent character into what would otherwise be a purely ionic bond.
Conditions favouring covalent character (Fajan's rules):
- Small cation with high charge (high charge density → strong polarising power).
- Large anion with high charge (easily polarisable electron cloud).
- Cation with pseudo-noble-gas configuration (e.g., Cu⁺, Ag⁺ with 18-electron core) polarises more than a noble-gas-configuration cation of similar size and charge.
The dipole moment formula μ = q × d (NCERT Class 11 Chemistry Chapter 4) connects here: the greater the electronegativity difference in a diatomic bond, the larger the partial charge q and hence the larger μ. For polyatomic molecules, individual bond dipoles are summed as vectors — symmetric molecules like CO₂ and BF₃ have zero net dipole despite having polar bonds.
Watch out: NEET questions frequently test whether you can distinguish polarising power (cation property) from polarisability (anion property), and whether you remember that pseudo-noble-gas cations polarise more than noble-gas cations of comparable size.
Practice MCQs
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
Which of the following elements has the highest electronegativity on the Pauling scale?
Electronegativity of elements generally increases:
Fajan's rules predict the degree of:
Among LiF, LiCl, LiBr, and LiI, which lithium halide has the most covalent character according to Fajan's rules?
Which of the following cations has the greatest polarising power?
The dipole moment of CO₂ is zero despite C=O bonds being polar. This is because:
Cu⁺ (ionic radius 77 pm) and Na⁺ (ionic radius 102 pm) both have a +1 charge. According to Fajan's rules, CuCl is expected to have more covalent character than NaCl. What is the additional reason beyond size?
Arrange the following in order of increasing covalent character: NaCl, MgCl₂, AlCl₃.
Quick recall before you leave
Worked Example
- 1
Given
HF has a bond length of 0.92 Å (9.2 × 10⁻¹¹ m) and an observed dipole moment of 1.91 D. HCl has a bond length of 1.27 Å (1.27 × 10⁻¹⁰ m) and an observed dipole moment of 1.03 D.
- 2
Required
Explain why HF has a larger dipole moment than HCl despite having a shorter bond length d.
- 3
Concept
Dipole moment μ = q × d. A larger d alone would increase μ, yet HF (shorter d) has a larger μ than HCl. This means the partial charge q on HF must be significantly larger, overriding the shorter distance.
- 4
Formula
μ = q × d, therefore q = μ / d.
- 5
Substitution
For HF: q = 1.91 D / 0.92 Å (in relative terms) For HCl: q = 1.03 D / 1.27 Å (in relative terms)
- 6
Calculation
Relative charge density comparison: - HF: 1.91 / 0.92 ≈ 2.08 D/Å - HCl: 1.03 / 1.27 ≈ 0.81 D/Å The ratio q(HF)/q(HCl) ≈ 2.08/0.81 ≈ 2.6. Fluorine's much higher electronegativity (4.0 vs chlorine's 3.0) pulls electron density far more strongly, creating a partial charge roughly 2.6 times larger in HF. Note: The bond lengths and dipole moments are given data — they are treated as exact for this comparison. The ratio calculation uses them directly.
- 7
Final answer
HF has a larger dipole moment than HCl because fluorine's greater electronegativity (4.0 vs 3.0) creates a much larger partial charge q, which more than compensates for the shorter bond length. The electronegativity difference dominates the μ = q × d product.
- 8
Common trap
Students sometimes assume that longer bond length automatically means larger dipole moment (since d appears in μ = qd). This ignores the charge term. When electronegativity difference changes significantly between two molecules, q can dominate over d.
- 9
Similar NEET-style question
"Among HF, HCl, HBr, and HI, which has the highest dipole moment? Justify using electronegativity and the dipole moment formula." Answer: HF — highest electronegativity difference (F = 4.0, H = 2.1) produces the largest partial charge, outweighing the effect of bond length. ---
Before solving, remember these
Formulas
Bond order from MO theory
Higher bond order: shorter, stronger bond. N₂: BO=3, O₂: BO=2, F₂: BO=1.
| Symbol | Quantity | SI Unit |
|---|---|---|
| N_b | bonding electrons | - |
| N_a | antibonding electrons | - |
| BO | bond order | - |
Valid when
- MO theory framework
- Closed-shell molecule (or with appropriate treatment)
Dipole moment
Product of charge magnitude and bond length. SI: C·m. Common: Debye (1 D = 3.336e-30 C·m).
| Symbol | Quantity | SI Unit |
|---|---|---|
| q | charge | C |
| d | bond length | m |
| mu | dipole moment | C*m or D |
Valid when
- Diatomic or vector-summed for polyatomic
- Polar bond
Exam Traps & Common Mistakes
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Inorganic Exception
Student counts only bonded atoms when assigning hybridization. Lone pairs count toward steric number too. Steric number = bond pairs + lone pairs → hybridization.
When it triggers
Molecule with central atom having lone pairs (e.g., NH₃: 3 bonds + 1 lp = 4 = sp³; H₂O: 2+2 = 4 = sp³).
How to avoid
Steric number formula: SN = (bond pairs) + (lone pairs). SN=2: sp; SN=3: sp²; SN=4: sp³; SN=5: sp³d; SN=6: sp³d². Lone pairs distort but still count.
Root cause: concept gap
Correction
Steric number = bond pairs + lone pairs. NH3: SN=4 → sp³ (despite trigonal pyramidal shape).
Root cause: concept gap
Correction
Memorise the ordering switch at N2/O2 boundary. Affects bond order and magnetic property predictions.
Root cause: formula misuse
Correction
BO = (Nb - Na)/2. Antibonding electrons subtract. F2: 8 bonding, 6 antibonding → BO = 1.
Past Year Questions
14 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
The element expected to form largest ion to achieve the nearest noble gas configuration is
Which statement regarding polymers is not correct?
Amongst the following which one will have maximum ‘lone pair - lone pair’ electron repulsions?
In one molal solution that contains 0.5 mole of a solute, there is
Which of the following molecules is non-polar in nature?
How NEET usually asks this
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
Determine hybridization of central atom from molecular formula or geometry.
Common distractors
ignores lone pairs
Counts only bonding pairs
From MO configuration of homonuclear diatomic, compute bond order and predict magnetic property.
Common distractors
forgets anti bonding
Counts only bonding electrons
Predict molecular geometry (linear, bent, trigonal pyramidal, etc.) from VSEPR steric number and lone pairs.
Common distractors
ignores lp bp distortion
Doesn't adjust for lone-pair repulsion
Sources
Test yourself on this topic with real past-paper questions:
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