NEET PG /Chemistry

Chemical bonding

Inorganic Chemistry · free study notes · Updated

Chemical Bonding – NEET PG Study Notes

(Chemistry – 10 th‑12 th & Pre‑Clinical)

Goal: Understand the nature, types, and characteristics of chemical bonds.
Why it matters: All medicines, biochemistry, and pharmacology rely on the way atoms hold together.


1. Simple Explanation

A chemical bond is a force of attraction that holds atoms together in a molecule or crystal lattice.

  • Electrons (negative) are shared, transferred, or delocalised among atoms.
  • The balance of electron density determines whether a bond is ionic (full transfer), covalent (sharing), or metallic (delocalised sea of electrons).
  • Additional interactions – hydrogen bonds, van der Waals forces, coordinate (dative) bonds – fine‑tune molecular structure and reactivity.

2. Key Points

Concept What it is How it appears in molecules Key Take‑Aways
Electronegativity (χ) Ability of an atom to attract electrons Determines bond polarity χ difference > 1.7 → ionic; 0.4–1.7 → polar covalent; < 0.4 → non‑polar covalent
Bond Polarity Unequal sharing of electrons Creates dipole moments (e.g., H₂O) Dipole–dipole, hydrogen bonding
Octet Rule Atoms seek 8 valence electrons Forms ionic/covalent bonds Exceptions: H (2), d‑block, expanded octet
Hybridization Mixing of atomic orbitals Predicts molecular shape (sp, sp², sp³) Key for VSEPR geometry
VSEPR Theory Repulsion of electron pairs dictates shape Predicts bond angles (e.g., 104.5° in H₂O) Good for simple molecules
Resonance Delocalised electrons over multiple structures Stabilises molecules (e.g., benzene) Resonance energy > 0
Molecular Orbital (MO) Theory Combines atomic orbitals into MOs (bonding/antibonding) Explains bond order, magnetism Bond order = (n_bonding – n_antibonding)/2
Ionic vs. Covalent Transfer vs. sharing of electrons NaCl (ionic), H₂O (covalent) Ionic: high lattice energy; Covalent: bond dissociation energy
Metallic Bonding Delocalised “sea” of electrons Conductivity, malleability Bond energy ≈ 1–3 eV per atom
Coordinate (Dative) Bond One atom donates both electrons Complexes (e.g., NH₃·BH₃) Often in Lewis acid–base reactions
Hydrogen Bond H–X (X = N, O, F) with lone pair on another atom Stabilises DNA, water structure Strength: 5–30 kJ mol⁻¹
Van der Waals Forces London dispersion, dipole–dipole Weak, short‑range Important in polymer physics

3. Worked Example – Formation of a Water Molecule (H₂O)

  1. Electron Count & Octet Rule

    • H: 1 electron → needs 1 more (2e⁻ total)
    • O: 6 valence electrons → needs 2 more (8e⁻ total)
  2. Lewis Structure

         H
         |
    H : O : H
    
    • Two lone pairs on O (4 e⁻).
    • Two O–H σ bonds (2 e⁻ each).
  3. Bond Polarity

    • χ(O)=3.44, χ(H)=2.20 → Δχ≈1.24 → polar covalent
    • O has partial negative (δ⁻), H partial positive (δ⁺).
  4. Hybridization & Geometry

    • O uses sp³ hybrid orbitals → tetrahedral electron geometry.
    • Two lone pairs occupy 2 positions → bent molecular shape.
    • Bond angle ≈ 104.5° (slightly less than tetrahedral 109.5° due to lone‑pair repulsion).
  5. Dipole Moment

    • Vector addition of two O–H dipoles → net dipole ≈ 1.85 D (dipole moment of water).
  6. Bond Dissociation Energy (BDE)

    • O–H BDE ≈ 463 kJ mol⁻¹.
  7. Hydrogen Bonding (optional)

    • H₂O can donate two H bonds (via H atoms) and accept two (via lone pairs).

Key Take‑Aways from Example

  • Octet rule guides Lewis structure.
  • Electronegativity difference → bond polarity.
  • Hybridization predicts shape and bond angles.
  • Dipole moment arises from arrangement of polar bonds.

4. Quick Revision Summary

Topic Remember Quick Check
Electronegativity χ = 0 (F) → 4.0 (O) χ diff > 1.7 → ionic
Bond Types Ionic, covalent (polar/non‑polar), metallic Identify by χ diff
Octet Rule 8 valence e⁻

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