Download JEE MCQs for JEE Chemistry: Chemical Bonding and Molecular Structure
Access targeted multiple-choice questions for Chemical Bonding and Molecular Structure designed to align with the latest JEE academic syllabus for JEE Chemistry. These objective practice sets help students evaluate their conceptual understanding and improve exam readiness.
Chapter-wise Objective Questions: Chemical Bonding and Molecular Structure
View or download the dedicated Chemical Bonding and Molecular Structure MCQ resource below. Practicing these 50 objective questions regularly builds familiarity with standard exam patterns and helps secure higher marks in final Chemistry evaluations.
Multiple Choice Questions
(a) \( \ce{BCl3} \)
(b) \( \ce{ICl} \)
(c) \( \ce{NH3} \)
(d) \( \ce{PCl3} \)
Show Answer & Explanation
Answer: (a) \( \ce{BCl3} \)
Explanation:
1. In \( \ce{BCl3} \) boron has only six electrons around it
2. In \( \ce{ICl} \), \( \ce{NH3} \) and \( \ce{PCl3} \) the central atoms have octets.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{CO2} \) only
(b) \( \ce{BCl3} \) only
(c) none of these
(d) both \( \ce{BCl3} \) and \( \ce{PCl5} \)
Show Answer & Explanation
Answer: (d) both \( \ce{BCl3} \) and \( \ce{PCl5} \)
Explanation:
1. \( \ce{BCl3} \) has a sextet on B and \( \ce{PCl5} \) has ten electrons on P (expanded octet)
2. \( \ce{CO2} \) obeys the octet rule.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{N3-} \) only
(b) \( \ce{N3-} \), \( \ce{CNO-} \) and \( \ce{NCN^2-} \) are all isoelectronic with \( \ce{CO2} \)
(c) \( \ce{CNO-} \) only
(d) \( \ce{NCN^2-} \) only
Show Answer & Explanation
Answer: (b) \( \ce{N3-} \), \( \ce{CNO-} \) and \( \ce{NCN^2-} \) are all isoelectronic with \( \ce{CO2} \)
Explanation:
1. \( \ce{CO2} \) has 22 electrons
2. \( \ce{N3-} \): 21+1 = 22; \( \ce{CNO-} \): 6+7+8+1 = 22; \( \ce{NCN^2-} \): 7+6+7+2 = 22
3. All have 22 electrons.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{BrF5} \)
(b) \( \ce{CO2} \)
(c) \( \ce{SF6} \)
(d) \( \ce{IF7} \)
Show Answer & Explanation
Answer: (b) \( \ce{CO2} \)
Explanation:
1. In \( \ce{CO2} \) each atom has eight electrons
2. In \( \ce{BrF5} \), \( \ce{SF6} \) and \( \ce{IF7} \) the central atom has 12, 12 and 14 electrons.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 1.5
(b) 1
(c) 2
(d) 1.33
Show Answer & Explanation
Answer: (a) 1.5
Explanation:
1. Two Kekule structures give one double bond and one single bond for each pair: (2+1)/2 = 1.5.
2. Only option (a) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{CO2} \)
(b) \( \ce{CO} \)
(c) \( \ce{CO3^2-} \)
(d) \( \ce{CH3COO-} \)
Show Answer & Explanation
Answer: (c) \( \ce{CO3^2-} \)
Explanation:
1. Bond orders are about 1.33 in \( \ce{CO3^2-} \), 2 in \( \ce{CO2} \), 3 in \( \ce{CO} \) and 1.5 in \( \ce{CH3COO-} \)
2. The lowest bond order gives the weakest bond.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{CO2} \) < \( \ce{CO3^2-} \) < CO
(b) \( \ce{CO3^2-} \) < \( \ce{CO2} \) < CO
(c) CO < \( \ce{CO2} \) < \( \ce{CO3^2-} \)
(d) CO < \( \ce{CO3^2-} \) < \( \ce{CO2} \)
Show Answer & Explanation
Answer: (c) CO < \( \ce{CO2} \) < \( \ce{CO3^2-} \)
Explanation:
1. Bond order: CO 3, \( \ce{CO2} \) 2, \( \ce{CO3^2-} \) 1.33
2. A higher bond order means a shorter bond.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) p orbitals can only overlap sidewise
(b) A sigma bond is stronger than a pi bond
(c) s orbitals never form pi bonds
(d) Two atoms can have only one sigma bond between them
Show Answer & Explanation
Answer: (a) p orbitals can only overlap sidewise
Explanation:
1. p orbitals can overlap head-on and give sigma bonds (as in \( \ce{F2} \)), so the first statement is false
2. The others are correct.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) A sigma bond is stronger than a pi bond
(b) A sigma bond is weaker than a pi bond
(c) A double bond is stronger than a single bond
(d) A double bond is shorter than a single bond
Show Answer & Explanation
Answer: (b) A sigma bond is weaker than a pi bond
Explanation:
1. End-on overlap (sigma) is better than sidewise overlap (pi), so a sigma bond is stronger than a pi bond
2. The first statement is wrong.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 3
(b) 5
(c) 4
(d) 6
Show Answer & Explanation
Answer: (b) 5
Explanation:
1. \( \ce{CH3OH} \) has three C-H bonds, one C-O bond and one O-H bond
2. All five are sigma bonds.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 3
(b) 5
(c) 2
(d) 4
Show Answer & Explanation
Answer: (d) 4
Explanation:
1. The bonds are H-O, O-N, N-O and N=O. Each has one sigma bond, so 4
2. The pi bond in N=O adds one pi bond.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 7 and 3
(b) 6 and 4
(c) 5 and 5
(d) 8 and 2
Show Answer & Explanation
Answer: (a) 7 and 3
Explanation:
1. The carbon chain has 3 C-C links (3 sigma) and 4 C-H bonds (4 sigma): 7 sigma
2. The three double bonds give 3 pi bonds.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 3 and 1
(b) 2 and 2
(c) 4 and 0
(d) 1 and 3
Show Answer & Explanation
Answer: (c) 4 and 0
Explanation:
1. N has no lone pair in \( \ce{NO3-} \); it forms three sigma bonds and takes part in one delocalised pi bond, so 4 bond pairs and 0 lone pairs.
2. Only option (c) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{BeCl2} \) (gas phase)
(b) \( \ce{C2H6} \)
(c) \( \ce{SiH4} \)
(d) \( \ce{PH3} \)
Show Answer & Explanation
Answer: (a) \( \ce{BeCl2} \) (gas phase)
Explanation:
1. Be in monomeric \( \ce{BeCl2} \) has only four electrons in its valence shell
2. The others have complete octets.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{BF3} \)
(b) \( \ce{XeF6} \)
(c) \( \ce{ClO3} \)
(d) \( \ce{SnCl4} \)
Show Answer & Explanation
Answer: (d) \( \ce{SnCl4} \)
Explanation:
1. \( \ce{SnCl4} \) follows the octet rule (4 bonds, 8 electrons)
2. \( \ce{BF3} \) is electron-deficient, \( \ce{XeF6} \) is expanded and \( \ce{ClO3} \) has an odd number of electrons.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) \( \ce{ClO-} \) > \( \ce{ClO2-} \) > \( \ce{ClO3-} \) > \( \ce{ClO4-} \)
(b) \( \ce{ClO4-} \) > \( \ce{ClO3-} \) > \( \ce{ClO2-} \) > \( \ce{ClO-} \)
(c) \( \ce{ClO2-} \) > \( \ce{ClO3-} \) > \( \ce{ClO4-} \) > \( \ce{ClO-} \)
(d) \( \ce{ClO3-} \) > \( \ce{ClO-} \) > \( \ce{ClO2-} \) > \( \ce{ClO4-} \)
Show Answer & Explanation
Answer: (b) \( \ce{ClO4-} \) > \( \ce{ClO3-} \) > \( \ce{ClO2-} \) > \( \ce{ClO-} \)
Explanation:
1. Chlorine uses all its valence bonds spread over the oxygens: +7/4 = 1.75, +5/3 = 1.67, +3/2 = 1.5 and +1/1 = 1.
2. Only option (b) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) Free rotation is possible about a sigma bond but not a pi bond
(b) The sigma bond energy is about 264 kJ/mol and the pi bond energy about 347 kJ/mol
(c) The sigma bond fixes the direction between the carbons
(d) A sigma bond is stronger than a pi bond
Show Answer & Explanation
Answer: (b) The sigma bond energy is about 264 kJ/mol and the pi bond energy about 347 kJ/mol
Explanation:
1. The sigma bond energy (about 347 kJ/mol) is greater than that of a pi bond (about 264 kJ/mol), so the first statement has the values reversed.
2. Only option (b) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 3 and 4
(b) 2 and 3
(c) 3 and 2
(d) 4 and 3
Show Answer & Explanation
Answer: (a) 3 and 4
Explanation:
1. \( \ce{N#C-C#N} \) has three sigma bonds (two C-N and one C-C) and two triple bonds that give 4 pi bonds.
2. Only option (a) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 1
(b) 3
(c) 2
(d) 4
Show Answer & Explanation
Answer: (c) 2
Explanation:
1. Oxygen forms two single bonds to fluorine, so there are 2 bond pairs and 2 lone pairs.
2. Only option (c) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 2, 4, 6
(b) 1, 2, 3
(c) 3, 2, 1
(d) 6, 4, 2
Show Answer & Explanation
Answer: (c) 3, 2, 1
Explanation:
1. Xe has 8 valence electrons: 2, 4 and 6 are used in bonds, leaving 6, 4 and 2 electrons, i.e. 3, 2 and 1 lone pairs.
2. Only option (c) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) different, with 1, 0 and 2 lone pairs on the central atom
(b) the same, with 2, 0 and 1 lone pair
(c) the same, with 1, 1 and 1 lone pair
(d) different, with 0, 1 and 2 lone pairs
Show Answer & Explanation
Answer: (a) different, with 1, 0 and 2 lone pairs on the central atom
Explanation:
1. \( \ce{SF4} \) is see-saw (1 lp), \( \ce{CF4} \) tetrahedral (0 lp) and \( \ce{XeF4} \) square planar (2 lp).
2. Only option (a) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
(a) 2
(b) 3
(c) 0
(d) 1
Show Answer & Explanation
Answer: (d) 1
Explanation:
1. Xe has 8 valence electrons; four electrons go to the four Xe-F bonds and two to the Xe-O bond, leaving 2 electrons, i.e. 1 lone pair.
2. Only option (d) agrees with this working.
Teacher's Note:
1. Draw the Lewis structure first: count valence electrons, join atoms, fill octets, then use multiple bonds. Bond order in resonance hybrids is the total number of bonds divided by the number of equivalent positions.
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Multiple Choice Questions (MCQs) for JEE Chemistry Chemical Bonding and Molecular Structure
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FAQs
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