Contents
- 1 CHEMICAL BONDING - Resonance Chemistry Notes
- 2 1. Types of Chemical Bonds
- 3 2. Octet Rule & Its Limitations
- 4 3. Valence Bond Theory (VBT) & Hybridization
- 5 4. Molecular Orbital Theory (MOT)
- 6 5. Dipole Moment (μ) and Bond Polarity
- 7 6. Resonance & Formal Charge
- 8 Tips for JEE/NEET/GATE
- 9 Resonance Chemistry Chemical Bonding
- 10 (968)-chemistry-gyan-sutra-jee-main.pdf
- 11 CHEMiCAL BOnDinG AnD MOLECULAR StRUCtURE
- 12 What is Resonance?
- 13 Key Characteristics of Resonance:
- 14 Example: Benzene C6H6C_6H_6C6H6
- 15 Rules for Drawing Resonance Structures:
- 16 Common Compounds Showing Resonance:
- 17 Importance in GATE Chemistry:
- 18 Resonance Chemistry Chemical Bonding
- 19 Unit: 8 Chemical Bonding: Resonance
CHEMICAL BONDING - Resonance Chemistry Notes
Chemical bonding is one of the most important topics in Physical Chemistry for JEE, NEET, and GATE. It explains how atoms combine to form molecules through various types of forces.
1. Types of Chemical Bonds
Bond Type | How It Forms? | Example |
---|---|---|
Ionic Bond | Transfer of electrons | NaCl, KCl, MgO |
Covalent Bond | Sharing of electrons | H₂, O₂, CH₄ |
Coordinate Bond | One atom donates a lone pair | NH₃ → BF₃, H₃O⁺ |
Metallic Bond | Delocalized electron cloud | Cu, Fe, Ag |
Hydrogen Bond | H atom bonded to F, O, N | H₂O, NH₃, HF |
2. Octet Rule & Its Limitations
Octet Rule → Atoms tend to gain, lose, or share electrons to complete 8 valence electrons (stable noble gas configuration).
Limitations:
Incomplete Octet: BeCl₂, BCl₃
Expanded Octet: SF₆, PCl₅
Odd Electron Species: NO, NO₂
3. Valence Bond Theory (VBT) & Hybridization
VBT: Explains bonding in terms of atomic orbitals overlapping to form bonds.
Hybridization: Mixing of orbitals to form new hybrid orbitals of equal energy.
Hybridization | Shape | Example |
---|---|---|
sp | Linear (180°) | BeCl₂, CO₂ |
sp² | Trigonal Planar (120°) | BF₃, SO₃ |
sp³ | Tetrahedral (109.5°) | CH₄, NH₃, H₂O |
sp³d | Trigonal Bipyramidal (90°, 120°) | PCl₅ |
sp³d² | Octahedral (90°) | SF₆, [Ni(CN)₄]²⁻ |
4. Molecular Orbital Theory (MOT)
Atomic orbitals combine to form Molecular Orbitals (MO).
Bond Order = (Bonding e⁻ - Antibonding e⁻) / 2
Higher bond order → Stronger bond & shorter bond length.
MOT Order for O₂, F₂, etc.:
σ(1s) < σ*(1s) < σ(2s) < σ*(2s) < π(2px) = π(2py) < σ(2pz) < π(2px) = π(2py)** < σ*(2pz)
Paramagnetic molecules: O₂, B₂ (Unpaired e⁻)
Diamagnetic molecules: N₂, F₂ (All paired e⁻)
5. Dipole Moment (μ) and Bond Polarity
μ = Charge (q) × Bond Length (d)
Polar molecules: H₂O, NH₃, HF (μ ≠ 0)
Nonpolar molecules: CO₂, BF₃, CH₄ (μ = 0)
6. Resonance & Formal Charge
Resonance: Delocalization of π-electrons, stabilizing the molecule.
Example:
Ozone (O₃)
Benzene (C₆H₆)
Carbonate ion (CO₃²⁻)
Formal Charge = (Valence e⁻ - Nonbonding e⁻ - Bonding e⁻/2)
Used to determine the most stable resonance structure.
Tips for JEE/NEET/GATE
Remember hybridization rules (sp, sp², sp³)
MOT diagrams are important for O₂, N₂, F₂
Practice bond order and dipole moment questions
Know the exceptions of the octet rule
Do you need solved examples or short tricks for Chemical Bonding?
Resonance Chemistry Chemical Bonding
(968)-chemistry-gyan-sutra-jee-main.pdf
CHEMiCAL BOnDinG AnD MOLECULAR StRUCtURE
Resonance in Chemistry is a key concept in chemical bonding, especially in the context of molecular structure and stability. It is commonly asked in GATE and other competitive exams. Here's a quick breakdown:

What is Resonance?
Resonance refers to the delocalization of electrons within molecules that have conjugated double bonds or lone pairs next to π bonds. Instead of existing in a single Lewis structure, such molecules are best represented by multiple resonance structures.
These structures differ only in the arrangement of electrons, not in the position of atoms.

Key Characteristics of Resonance:
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Real structure is a hybrid: The actual structure is a resonance hybrid, more stable than any single contributing structure.
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Resonance energy: The difference in energy between the most stable resonance structure and the hybrid.
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Stabilization: Resonance increases molecular stability.
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No real shifting: Electrons don’t actually move back and forth—they are delocalized.

Example: Benzene C6H6C_6H_6C6H6
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Has two equivalent resonance structures:
Structure 1: \text{Structure 1: } \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ Structure 1: Alternating single and double bonds\text{Alternating single and double bonds}Alternating single and double bonds Structure 2: Double and single bonds reversed\text{Structure 2: } \ \ \text{Double and single bonds reversed}Structure 2: Double and single bonds reversed
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Actual structure: All C–C bonds are equal in length due to π-electron delocalization.

Rules for Drawing Resonance Structures:
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Same molecular formula and position of atoms.
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Only π electrons or lone pairs can move.
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Octet rule must be obeyed (especially for 2nd period elements).
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Overall charge must remain the same.

Common Compounds Showing Resonance:
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Ozone (O₃)
-
Nitrate ion (NO₃⁻)
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Carbonate ion (CO₃²⁻)
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Acetate ion (CH₃COO⁻)

Importance in GATE Chemistry:
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Predicting molecular geometry (via hybridization and resonance).
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Calculating formal charge and stability.
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Understanding acid-base behavior and reactivity.
Let me know if you'd like a diagram of resonance structures, practice GATE questions, or a video explanation to reinforce this topic.