Chemical Bonding and Molecular Structure
📐 Formula & Cheat Sheet (English)
MP Board Class 11 Chemistry
Chapter 4: Chemical Bonding and Molecular Structure
Quick Revision Notes & Formula Sheet
1. Kössel-Lewis Approach & Octet Rule (अष्टक नियम)
- Octet Rule: Atoms combine either by transfer of valence electrons (gaining or losing) or by sharing of valence electrons in order to attain a stable octet (8 electrons in their valence shell).
- Exceptions to Octet Rule:
- Incomplete octet of central atom: $LiCl$, $BeH_2$, $BF_3$ (Central atom has $< 8$ electrons).
- Odd-electron molecules: $NO$, $NO_2$ (Contain unpaired electrons).
- Expanded octet: $PF_5$, $SF_6$, $H_2SO_4$ (Central atom has $> 8$ electrons due to presence of vacant d-orbitals).
2. Formal Charge (फॉर्मल आवेश)
Formal charge helps in selecting the lowest energy (most stable) structure among different Lewis structures.
$$\text{Formal Charge (FC)} = V - L - \frac{1}{2} S$$
Where:
- $V$ = Total number of valence electrons in free atom
- $L$ = Total number of non-bonding electrons (lone pair electrons)
- $S$ = Total number of bonding (shared) electrons
3. Ionic or Electrovalent Bond
Formed by complete transfer of electrons from one atom to another.
- Factors favoring Ionic Bond formation:
- Low Ionization Enthalpy of cation-forming metal.
- High negative Electron Gain Enthalpy of anion-forming non-metal.
- High Lattice Enthalpy ($\Delta_{lattice}H$) of formed ionic compound.
4. Bond Parameters
- Bond Length: Equilibrium distance between nuclei of two bonded atoms.
- Bond Angle: Angle between orbitals containing bonding electron pairs around central atom.
- Bond Enthalpy: Amount of energy required to break one mole of bonds of a particular type between two atoms in a gaseous state.
- $\text{Bond Enthalpy} \propto \text{Bond Order} \propto \frac{1}{\text{Bond Length}}$
- Bond Order (आबंध कोटि): Number of bonds between two atoms in a molecule.
- Isoelectronic molecules/ions have same bond order (e.g., $F_2$ and $O_2^{2-}$ have Bond Order = 1).
5. Dipole Moment ($\mu$) & Fajan's Rule
Dipole Moment (द्विध्रुव आघूर्ण)
Measures the polarity of a covalent bond. $$\mu = q \times d$$
Where:
- $q$ = Magnitude of charge
- $d$ = Distance of separation
- Unit: Debye ($D$). ($1 \text{ D} = 3.3356 \times 10^{-30} \text{ C}\cdot\text{m}$)
- Net Dipole Moment ($\mu_{net}$) for polyatomic molecules:
- Non-polar molecules (Symmetrical): $\mu_{net} = 0$ (e.g., $CO_2, BF_3, CCl_4$)
- Polar molecules (Asymmetrical): $\mu_{net} \neq 0$ (e.g., $H_2O, NH_3$)
- Note: Dipole moment of $NH_3 > NF_3$ because orbital dipole of lone pair in $NF_3$ opposes the resultant dipole of $N-F$ bonds.
Fajan's Rules (Covalent character in Ionic Bonds)
- Covalent Character is maximum when:
- Size of Cation is small.
- Size of Anion is large.
- Charge on Cation or Anion is high.
- Pseudo-noble gas configuration of cation ($ns^2 np^6 nd^{10}$).
6. VSEPR Theory (Valence Shell Electron Pair Repulsion)
Predicts the 3D shape of molecules based on electron pair repulsions.
- Order of Repulsion: $$\text{Lone Pair - Lone Pair (LP-LP)} > \text{Lone Pair - Bond Pair (LP-BP)} > \text{Bond Pair - Bond Pair (BP-BP)}$$
Geometry vs. Shape Table:
| Electron Pairs | Bond Pairs | Lone Pairs | Hybridization | Geometry | Shape | Examples |
|---|---|---|---|---|---|---|
| 2 | 2 | 0 | $sp$ | Linear | Linear | $BeCl_2, CO_2$ |
| 3 | 3 | 0 | $sp^2$ | Trigonal Planar | Trigonal Planar | $BF_3, BCl_3$ |
| 3 | 2 | 1 | $sp^2$ | Trigonal Planar | Bent / V-shape | $SO_2, PbCl_2$ |
| 4 | 4 | 0 | $sp^3$ | Tetrahedral | Tetrahedral | $CH_4, NH_4^+$ |
| 4 | 3 | 1 | $sp^3$ | Tetrahedral | Trigonal Pyramidal | $NH_3, H_3O^+$ |
| 4 | 2 | 2 | $sp^3$ | Tetrahedral | Bent / V-shape | $H_2O$ |
| 5 | 5 | 0 | $sp^3d$ | Trigonal Bipyramidal | Trigonal Bipyramidal | $PCl_5$ |
| 5 | 4 | 1 | $sp^3d$ | Trigonal Bipyramidal | See-Saw | $SF_4$ |
| 5 | 3 | 2 | $sp^3d$ | Trigonal Bipyramidal | T-shaped | $ClF_3$ |
| 5 | 2 | 3 | $sp^3d$ | Trigonal Bipyramidal | Linear | $XeF_2$ |
| 6 | 6 | 0 | $sp^3d^2$ | Octahedral | Octahedral | $SF_6$ |
| 6 | 5 | 1 | $sp^3d^2$ | Octahedral | Square Pyramidal | $BrF_5$ |
| 6 | 4 | 2 | $sp^3d^2$ | Octahedral | Square Planar | $XeF_4$ |
7. Valence Bond Theory (VBT) & Hybridization
Types of Covalent Bonds:
- Sigma ($\sigma$) Bond: Formed by end-to-end (axial) overlap of atomic orbitals. Stronger bond.
- Pi ($\pi$) Bond: Formed by lateral (sideways) overlap of atomic orbitals. Weaker bond.
- Single bond = $1\sigma$
- Double bond = $1\sigma + 1\pi$
- Triple bond = $1\sigma + 2\pi$
Shortcut Formula to find Hybridization Number ($H$):
$$H = \frac{1}{2} \left[ V + M - C + A \right]$$
Where:
-
$V$ = Valence electrons on central atom
-
$M$ = Number of monovalent atoms attached (H, F, Cl, Br, I)
-
$C$ = Positive charge on cation
-
$A$ = Negative charge on anion
-
Hybridization Determination:
- $H = 2 \rightarrow sp$
- $H = 3 \rightarrow sp^2$
- $H = 4 \rightarrow sp^3$
- $H = 5 \rightarrow sp^3d$
- $H = 6 \rightarrow sp^3d^2$
- $H = 7 \rightarrow sp^3d^3$
8. Molecular Orbital Theory (MOT)
1. Energy Level Diagrams:
-
For molecules with $\le 14$ electrons ($B_2, C_2, N_2$): $$\sigma 1s < \sigma^* 1s < \sigma 2s < \sigma^* 2s < (\pi 2p_x = \pi 2p_y) < \sigma 2p_z < (\pi^* 2p_x = \pi^* 2p_y) < \sigma^* 2p_z$$
-
For molecules with $> 14$ electrons ($O_2, F_2, Ne_2$): $$\sigma 1s < \sigma^* 1s < \sigma 2s < \sigma^* 2s < \sigma 2p_z < (\pi 2p_x = \pi 2p_y) < (\pi^* 2p_x = \pi^* 2p_y) < \sigma^* 2p_z$$
2. Key Formulas in MOT:
-
Bond Order (BO): $$\text{Bond Order} = \frac{1}{2} (N_b - N_a)$$ (where $N_b$ = Bonding electrons, $N_a$ = Anti-bonding electrons)
-
Stability Criteria:
- If $N_b > N_a \rightarrow$ Molecule is Stable ($\text{BO} > 0$)
- If $N_b \le N_a \rightarrow$ Molecule is Unstable ($\text{BO} \le 0$)
-
Magnetic Character:
- If all MOs have paired electrons $\rightarrow$ Diamagnetic (प्रतिचुंबकीय)
- If one or more MOs have unpaired electrons $\rightarrow$ Paramagnetic (अनुचुंबकीय) (e.g., $O_2, B_2$ are paramagnetic)
9. Hydrogen Bonding (हाइड्रोजन आबंध)
Formed when $H$ atom is covalently bonded to a highly electronegative atom ($F, O, N$).
- Intermolecular H-Bonding: Formed between two different molecules of same or different compounds.
- Examples: $H_2O, HF, NH_3$, alcohol in water.
- Effect: Increases Boiling Point and Viscosity.
- Intramolecular H-Bonding: Formed within the same molecule.
- Examples: o-Nitrophenol, Salicylaldehyde.
- Effect: Lowers Boiling Point compared to Intermolecular counterpart (e.g., o-nitrophenol has lower B.P. than p-nitrophenol).