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CBSE JEE Main & Advanced Chemistry: Chemical Bonding And Molecular Structure Important Questions & Complete Chapter Notes

Published: October 21, 2026 Author: NEET & JEE STUDY HUB
🎯 Curriculum & Exam Overview

Chemical Bonding explains the formation of stable molecules through electrostatic forces and orbital overlaps, forming the bedrock of inorganic and organic chemistry. It carries high weightage because concepts like VSEPR, Hybridization, and MO Theory are fundamental to predicting molecular geometry and reactivity in advanced JEE topics.

1. 📚 Quick Revision Notes & Core Theory

1
Kossel-Lewis Approach: Atoms achieve stability by attaining an octet of electrons in their valence shell via ionic (transfer) or covalent (sharing) bonding.
2
VSEPR Theory: Molecular geometry is determined by the minimization of repulsions between valence shell electron pairs (bonding and lone pairs).
3
Molecular Orbital (MO) Theory: Linear Combination of Atomic Orbitals (LCAO) explains magnetism and bond order by filling molecular orbitals based on energy levels.
⚡ High-Yield Formula & Reaction Sheet
  • Bond Order = 1/2 [Number of bonding electrons (Nb) - Number of antibonding electrons (Na)]
  • Formal Charge = [Total valence electrons in free atom] - [Total non-bonding electrons] - 1/2 [Total bonding electrons]
⚠️ Common Board Trap Alert
Assuming the order of energies in MO diagrams remains constant for all molecules; specifically, for O2 and F2, the sigma-2pz orbital lies lower in energy than pi-2px/pi-2py, whereas for B2, C2, and N2, the pi-2px/pi-2py orbitals lie lower.
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3. 📝 Interactive Chapter DPP & Practice Questions

Question 1 • MCQ
4 Mark(s)
The correct order of the O – O bond length of O$_{2}$, O$_{3}$ and H$_{2}$O$_{2}$  is given as
(A) O$_{2}$ < H$_{2}$O$_{2}$ < O$_{3}$
(B) O$_{3}$ < H$_{2}$O$_{2}$ < O$_{2}$
(C) H$_{2}$O$_{2}$ < O$_{2}$ < O$_{3}$
(D) O$_{2}$ < O$_{3}$ < H$_{2}$O$_{2}$
💡 View Step-by-Step Solution & Answer Key

Correct Answer: d

Explanation: O$_{2}$ < O$_{3}$ < H$_{2}$O$_{2}$ Bond lengths of O – O in O$_{2}$ is 1.21Å , H$_{2}$O$_{2}$ is 1.48Å and O$_{3}$ is 1.28Å. Therefore,correct order of the O – O bond length is H$_{2}$O$_{2}$ > O$_{3}$ > O$_{2}$.

Question 2 • MCQ 🔥 JEE Main (2026)
4 Mark(s)
Among the following, the CORRECT combinations are A. $IF _3 ⟶ T$ -shaped $( sp ^3 d)$ B. $IF _5 ⟶$ Square pyramidal $( sp ^3 d^2)$ C. $IF _7 ⟶$ Pentagonal bipyramidal $( sp ^3 d^3)$ D. $ClO _4{ }^{-} ⟶$ Square planar $( sp ^2 d)$ Choose the correct answer from the options given below:
(A) B, C and D Only
(B) A, B, C and D
(C) A, B and C Only
(D) A and B Only
💡 View Step-by-Step Solution & Answer Key

Correct Answer: (c)

Explanation: Concept: VSEPR theory predicts molecular shapes based on lone pairs and bond pairs. Hybridisation corresponds to the steric number (bond pairs + lone pairs). Explanation: For $\mathrm{IF}_3$ : Iodine has 7 valence electrons. Three bonds and two lone pairs give steric number 5. Thus $sp^3d$ hybridisation and T‑shaped geometry. Correct. For $\mathrm{IF}_5$ : Iodine forms five bonds and has one lone pair. Steric number 6 leads to $sp^3d^2$ hybridisation and square pyramidal shape. Correct. For $\mathrm{IF}_7$ : Iodine forms seven bonds and has no lone pair. Steric number 7 gives $sp^3d^3$ hybridisation and pentagonal bipyramidal shape. Correct. For $\mathrm{ClO}_4^-$ : Chlorine has 7 valence electrons plus one negative charge. Four bonds and no lone pair give steric number 4. Hybridisation is $sp^3$ , geometry is tetrahedral, not square planar. Hence D is incorrect. ![image](https://cdn.qbnexa.com/jeepyqs/img_62b2b3611aa3.png) Answer: A, B and C Only (Option C).

Question 3 • MCQ 🔥 AP EAPCET (2024)
4 Mark(s)
In which of the following sets the sum of bond orders of three species is maximum ?
(A) $\mathrm{B}_2, \mathrm{CN}^{-}, \mathrm{O}_2^{2-}$
(B) $\mathrm{O}_2, \mathrm{~F}_2, \mathrm{O}_2^{2+}$
(C) $\mathrm{O}_2^{-}, \mathrm{N}_2, \mathrm{O}_2^{+}$
(D) $\mathrm{C}_2, \mathrm{O}_2, \mathrm{He}_2^{2+}$
💡 View Step-by-Step Solution & Answer Key

Correct Answer: (c)

Explanation: Explanation of Bond Order Calculation **Bond Order (B.O.)** is calculated using the formula: $ \text{Bond Order} = \frac{1}{2} (\text{number of electrons in bonding orbitals} - \text{number of electrons in antibonding orbitals}) $ Let's analyze each set: Set (a): $\mathrm{B}_2, \mathrm{CN}^-, \mathrm{O}_2^{2-}$ **$\mathrm{B}_2$**: $ \text{Number of bonding electrons} = 4, \text{Number of antibonding electrons} = 2 $ $ \text{B.O.} = \frac{1}{2}(4-2) = 1 $ **$\mathrm{CN}^-$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 4 $ $ \text{B.O.} = \frac{1}{2}(10-4) = 3 $ **$\mathrm{O}_2^{2-}$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 8 $ $ \text{B.O.} = \frac{1}{2}(10-8) = 1 $ Total Bond Order for Set (a): $ 1 + 3 + 1 = 5 $ Set (b): $\mathrm{O}_2, \mathrm{F}_2, \mathrm{O}_2^{2+}$ **$\mathrm{O}_2$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 6 $ $ \text{B.O.} = \frac{1}{2}(10-6) = 2 $ **$\mathrm{F}_2$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 8 $ $ \text{B.O.} = \frac{1}{2}(10-8) = 1 $ **$\mathrm{O}_2^{2+}$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 4 $ $ \text{B.O.} = \frac{1}{2}(10-4) = 3 $ Total Bond Order for Set (b): $ 2 + 1 + 3 = 6 $ Set (c): $\mathrm{O}_2^-, \mathrm{N}_2, \mathrm{O}_2^+$ **$\mathrm{O}_2^-$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 7 $ $ \text{B.O.} = \frac{1}{2}(10-7) = 1.5 $ **$\mathrm{N}_2$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 4 $ $ \text{B.O.} = \frac{1}{2}(10-4) = 3 $ **$\mathrm{O}_2^+$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 5 $ $ \text{B.O.} = \frac{1}{2}(10-5) = 2.5 $ Total Bond Order for Set (c): $ 1.5 + 3 + 2.5 = 7 $ Set (d): $\mathrm{C}_2, \mathrm{O}_2, \mathrm{He}_2^{2+}$ **$\mathrm{C}_2$**: $ \text{Number of bonding electrons} = 8, \text{Number of antibonding electrons} = 4 $ $ \text{B.O.} = \frac{1}{2}(8-4) = 2 $ **$\mathrm{O}_2$**: $ \text{Number of bonding electrons} = 10, \text{Number of antibonding electrons} = 6 $ $ \text{B.O.} = \frac{1}{2}(10-6) = 2 $ **$\mathrm{He}_2^{2+}$**: $ \text{Number of bonding electrons} = 2, \text{Number of antibonding electrons} = 0 $ $ \text{B.O.} = \frac{1}{2}(2-0) = 1 $ Total Bond Order for Set (d): $ 2 + 2 + 1 = 5 $ Conclusion Set (c) has the maximum total bond order sum of $7$.

Question 4 • MCQ
4 Mark(s)
Which statement is correct?
(A) Melting Point of H$_{2}$O, NH$_{3}$ are maximum in their respective group due to intermolecular H-bonding.
(B) oiling Point of CH$_{4}$ out of CH$_{4}$, SiH$_{4}$, GeH$_{4}$, and SnH$_{4}$ is least due to weak intermolecular force of attraction
(C) Formic acid forms dimer by H-bonding.
(D) ll are correct
💡 View Step-by-Step Solution & Answer Key

Correct Answer: d

Explanation: All are correct Hydrogen bonding is a special type of dipole-dipole attraction between molecules, not a covalent bond to a hydrogen atom. It results from the attractive force between a hydrogen atom covalently bonded to a very electronegative atom such as a N, O, or F atom and another very electronegative atom.  At high pressure or in the vapor phase, formic acid consists of hydrogen bonded dimers rather than individual molecules.

Question 5 • MCQ 🔥 MHT CET (2025)
4 Mark(s)
Which of the following compounds has high lattice enthalpy?
(A) LiCl
(B) NaCl
(C) $\mathrm{BeF}_2$
(D) $\mathrm{CaCl}_2$
💡 View Step-by-Step Solution & Answer Key

Correct Answer: (c)

Explanation: As the size of the cation decrease, lattice enthalpy increases. Hence, $\mathrm{BeF}_2$ exhibits the highest lattice enthalpy among the given.

4. ❓ Frequently Asked Questions (Exam Strategy)

❓ Why does H2O have a bent geometry instead of linear?
H2O has two bonding pairs and two lone pairs on the central Oxygen atom. According to VSEPR theory, the strong repulsion between lone pairs forces the bond angle to decrease from 180° to approximately 104.5°.
❓ What is the significance of Hybridization in bonding?
Hybridization involves the mixing of atomic orbitals of similar energies to form new hybrid orbitals of equivalent energy. This process explains the equivalence of bond lengths and bond angles in symmetric molecules like CH4.
❓ Can a molecule have a fractional bond order?
Yes, bond order is defined by the MO theory as half the difference between bonding and antibonding electrons. Molecules like the superoxide ion (O2-) have a bond order of 1.5, which is physically valid.
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