Download JEE MCQs for JEE Chemistry: Chemical Bonding and Molecular Structure
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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) \( \ce{OF2} \)
(b) \( \ce{SF2} \)
(c) \( \ce{SF4} \)
(d) \( \ce{OF4} \)
Show Answer & Explanation
Answer: (d) \( \ce{OF4} \)
Explanation:
1. Oxygen is in period 2 and has no d orbitals, so it cannot expand its octet to form \( \ce{OF4} \)
2. Sulphur can (period 3), so \( \ce{SF4} \) is possible
3. \( \ce{OF2} \) and \( \ce{SF2} \) obey the octet rule.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{NH3} \)
(b) \( \ce{CO2} \)
(c) \( \ce{CH4} \)
(d) \( \ce{NF3} \)
Show Answer & Explanation
Answer: (a) \( \ce{NH3} \)
Explanation:
1. \( \ce{CO2} \) and \( \ce{CH4} \) are symmetric with zero dipole
2. In \( \ce{NH3} \) the N-H bond dipoles and the lone pair point the same way
3. In \( \ce{NF3} \) the lone pair opposes the N-F dipoles, so its moment is small
4. So \( \ce{NH3} \) has the highest.
Teacher's Note:
1. Net polarity needs both polar bonds and an asymmetric shape; for ionic versus covalent character apply Fajans' rules (small, highly charged cation, large anion means more covalent).
(a) \( \ce{Li2} \) < \( \ce{He2^+} \) < \( \ce{O2^+} \) < \( \ce{C2} \)
(b) \( \ce{C2} \) < \( \ce{O2^+} \) < \( \ce{Li2} \) < \( \ce{He2^+} \)
(c) \( \ce{He2^+} \) < \( \ce{Li2} \) < \( \ce{C2} \) < \( \ce{O2^+} \)
(d) \( \ce{O2^+} \) < \( \ce{C2} \) < \( \ce{Li2} \) < \( \ce{He2^+} \)
Show Answer & Explanation
Answer: (c) \( \ce{He2^+} \) < \( \ce{Li2} \) < \( \ce{C2} \) < \( \ce{O2^+} \)
Explanation:
1. Bond orders: \( \ce{He2^+} \) 0.5, \( \ce{Li2} \) 1, \( \ce{C2} \) 2, \( \ce{O2^+} \) 2.5
2. Stability increases with bond order, so He2+ < Li2 < C2 < O2+.
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) sp2
(b) sp
(c) sp3
(d) sp3d
Show Answer & Explanation
Answer: (c) sp3
Explanation:
1. The simplest stable borane is diborane \( \ce{B2H6} \)
2. Each boron forms four bonds: two terminal B-H and two bridging B-H-B. So boron is sp3 hybridised.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) see-saw, sp3d
(b) square planar, sp3d
(c) tetrahedral, sp3
(d) square pyramidal, sp3d
Show Answer & Explanation
Answer: (a) see-saw, sp3d
Explanation:
1. \( \ce{SF4} \) has 4 bond pairs and 1 lone pair, so 5 electron pairs and sp3d hybridisation
2. With the lone pair equatorial, the shape is see-saw.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{O2} \)
(b) \( \ce{O2^+} \)
(c) \( \ce{O2^-} \)
(d) \( \ce{O2^2-} \)
Show Answer & Explanation
Answer: (b) \( \ce{O2^+} \)
Explanation:
1. Bond energy increases with bond order: \( \ce{O2^+} \) 2.5, \( \ce{O2} \) 2, \( \ce{O2^-} \) 1.5, \( \ce{O2^2-} \) 1
2. So \( \ce{O2^+} \) has the highest bond energy.
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) pyramidal with angle close to 110 degrees
(b) trigonal planar with a bond angle close to 120 degrees
(c) T-shaped with angle 90 degrees
(d) bent T-shaped with angle close to 89 degrees
Show Answer & Explanation
Answer: (b) trigonal planar with a bond angle close to 120 degrees
Explanation:
1. The lone pair on nitrogen is delocalised into the empty d orbitals of silicon (p-pi to d-pi bonding)
2. The nitrogen becomes sp2-like, so the molecule is planar with about 120 degrees, unlike \( \ce{NMe3} \).
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) P > Si > Cl > S
(b) S < Cl < P < Si
(c) Si > P > S > Cl
(d) Si < P < S < Cl
Show Answer & Explanation
Answer: (d) Si < P < S < Cl
Explanation:
1. The d orbitals contract and become more effective for overlap as the effective nuclear charge rises across the period
2. So the p-pi to d-pi interaction increases from Si to P to S to Cl.
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) \( \ce{BF4^-} \) and \( \ce{NH4^+} \)
(b) \( \ce{NF3} \) and \( \ce{BF3} \)
(c) \( \ce{BCl3} \) and \( \ce{BrCl3} \)
(d) \( \ce{NH3} \) and \( \ce{NO3^-} \)
Show Answer & Explanation
Answer: (a) \( \ce{BF4^-} \) and \( \ce{NH4^+} \)
Explanation:
1. \( \ce{BF4^-} \) and \( \ce{NH4^+} \) both have four bond pairs and no lone pair, so both are sp3 and tetrahedral
2. \( \ce{NF3} \) is pyramidal and \( \ce{BF3} \) planar
3. \( \ce{BCl3} \) is planar and \( \ce{BrCl3} \) T-shaped
4. \( \ce{NH3} \) is pyramidal and \( \ce{NO3^-} \) planar.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) 10 and 6
(b) 16 and 0
(c) 12 and 4
(d) 14 and 2
Show Answer & Explanation
Answer: (c) 12 and 4
Explanation:
1. \( \ce{P4S10} \) has the adamantane-like \( \ce{P4} \) cage structure
2. Six bridging S atoms give 12 P-S single bonds, and four terminal S atoms give 4 P=S bonds
3. Total sulphur = 6 + 4 = 10.
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) -1
(c) 0
(d) -2
Show Answer & Explanation
Answer: (a) +1
Explanation:
1. The central oxygen has one double bond, one single bond and one lone pair: 3 bonds
2. Formal charge = 6 - 2 - 3 = +1.
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) \( \ce{NH3} \) > \( \ce{H2O} \) > \( \ce{NF3} \)
(b) \( \ce{NH3} \) > \( \ce{NF3} \) > \( \ce{H2O} \)
(c) \( \ce{H2O} \) > \( \ce{NF3} \) > \( \ce{NH3} \)
(d) \( \ce{H2O} \) > \( \ce{NH3} \) > \( \ce{NF3} \)
Show Answer & Explanation
Answer: (d) \( \ce{H2O} \) > \( \ce{NH3} \) > \( \ce{NF3} \)
Explanation:
1. The observed dipole moments are \( \ce{H2O} \) about 1.85 D, \( \ce{NH3} \) about 1.47 D and \( \ce{NF3} \) about 0.24 D. In \( \ce{NF3} \) the lone pair moment opposes the N-F bond moments
2. Hence H2O > NH3 > NF3.
Teacher's Note:
1. Net polarity needs both polar bonds and an asymmetric shape; for ionic versus covalent character apply Fajans' rules (small, highly charged cation, large anion means more covalent).
(a) \( \ce{N3^-} \)
(b) \( \ce{BrCl2^+} \)
(c) \( \ce{ClF2^-} \)
(d) \( \ce{Br3^-} \)
Show Answer & Explanation
Answer: (b) \( \ce{BrCl2^+} \)
Explanation:
1. \( \ce{N3^-} \) has 16 valence electrons and is linear (sp)
2. \( \ce{ClF2^-} \) and \( \ce{Br3^-} \) have 3 lone pairs on the central halogen, giving a linear shape
3. \( \ce{BrCl2^+} \) has 2 lone pairs and 2 bond pairs on Br, so it is bent.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{SF6} \) only
(b) all of \( \ce{SF6} \), \( \ce{PCl5} \) and \( \ce{IF7} \)
(c) \( \ce{PCl5} \) only
(d) \( \ce{IF7} \) only
Show Answer & Explanation
Answer: (b) all of \( \ce{SF6} \), \( \ce{PCl5} \) and \( \ce{IF7} \)
Explanation:
1. In \( \ce{SF6} \) sulphur has 12 electrons, in \( \ce{PCl5} \) phosphorus has 10 and in \( \ce{IF7} \) iodine has 14
2. Each exceeds the octet, so all three are hypervalent.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{CO3^2-} \) > \( \ce{CO2} \) > \( \ce{CO} \)
(b) \( \ce{CO2} \) > \( \ce{CO} \) > \( \ce{CO3^2-} \)
(c) \( \ce{CO2} \) > \( \ce{CO3^2-} \) > \( \ce{CO} \)
(d) \( \ce{CO} \) > \( \ce{CO2} \) > \( \ce{CO3^2-} \)
Show Answer & Explanation
Answer: (d) \( \ce{CO} \) > \( \ce{CO2} \) > \( \ce{CO3^2-} \)
Explanation:
1. Bond energy rises with bond order
2. The C-O bond order is 3 in \( \ce{CO} \), 2 in \( \ce{CO2} \) and 1.33 in \( \ce{CO3^2-} \)
3. So the order is CO > CO2 > CO3 2-.
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) \( \ce{SO3} \) only
(b) \( \ce{ClO3^-} \) only
(c) both \( \ce{ClO3^-} \) and \( \ce{XeO3} \)
(d) \( \ce{XeO3} \) only
Show Answer & Explanation
Answer: (c) both \( \ce{ClO3^-} \) and \( \ce{XeO3} \)
Explanation:
1. \( \ce{F2SeO} \) has 3 sigma bonds and one lone pair on selenium, giving a pyramidal shape
2. \( \ce{ClO3^-} \) and \( \ce{XeO3} \) are also pyramidal with 3 bond pairs and 1 lone pair, while \( \ce{SO3} \) is planar with no lone pair.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{(CH3)3N} \)
(b) \( \ce{CH3CN} \)
(c) \( \ce{CH2=NH} \)
(d) \( \ce{NO2^+} \)
Show Answer & Explanation
Answer: (c) \( \ce{CH2=NH} \)
Explanation:
1. In \( \ce{CH2=NH} \) nitrogen has 2 sigma bonds (one to C and one to H) and a lone pair, so sp2. \( \ce{(CH3)3N} \) is sp3. \( \ce{CH3CN} \) and \( \ce{NO2^+} \) have nitrogen with 2 sigma bonds and no lone pair, so sp.
2. Only option (c) agrees with this working.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) S is sp3 hybridised and there are 8 lone pairs on the oxygen atoms
(b) S is sp3d2 hybridised and there are 4 lone pairs on the oxygen atoms
(c) S is sp3 hybridised and there is no lone pair in the molecule
(d) S is sp2 hybridised and there are 8 lone pairs on the oxygen atoms
Show Answer & Explanation
Answer: (a) S is sp3 hybridised and there are 8 lone pairs on the oxygen atoms
Explanation:
1. Sulphur has 4 sigma bonds (two S=O and two S-OH) and no lone pair, so sp3. Counting lone pairs: each of the two terminal O atoms has 2 and each of the two OH oxygens has 2, giving 8 in all.
2. Only option (a) agrees with this working.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{ClF3} \) and \( \ce{ClF3O} \)
(b) \( \ce{ClF3O} \) and \( \ce{ClF3O2} \)
(c) \( \ce{[ClF4O]^-} \) and \( \ce{XeOF4} \)
(d) \( \ce{[ClF2O]^+} \) and \( \ce{[ClF4O]^-} \)
Show Answer & Explanation
Answer: (d) \( \ce{[ClF2O]^+} \) and \( \ce{[ClF4O]^-} \)
Explanation:
1. Count sigma bonds plus lone pairs
2. \( \ce{ClF3} \) has 3+2 = 5 and \( \ce{ClF3O} \) 4+1 = 5 (sp3d)
3. \( \ce{ClF3O2} \) has 5+0 = 5 (sp3d)
4. \( \ce{[ClF2O]^+} \) has 3+1 = 4 (sp3) while \( \ce{[ClF4O]^-} \) has 5+1 = 6 (sp3d2)
5. \( \ce{XeOF4} \) has 5+1 = 6, same as \( \ce{[ClF4O]^-} \).
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{NH3} \)
(b) \( \ce{CH4} \)
(c) \( \ce{PH3} \)
(d) \( \ce{H2O} \)
Show Answer & Explanation
Answer: (b) \( \ce{CH4} \)
Explanation:
1. The angles are \( \ce{CH4} \) 109.5 degrees, \( \ce{NH3} \) about 107, \( \ce{H2O} \) about 104.5 and \( \ce{PH3} \) about 93.5
2. So \( \ce{CH4} \) has the highest.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) sp3d, sp3d2
(b) sp3d2, sp3d
(c) sp3, sp3d
(d) sp3, sp3d2
Show Answer & Explanation
Answer: (d) sp3, sp3d2
Explanation:
1. \( \ce{PCl4^+} \) has 4 bond pairs and no lone pair (sp3, tetrahedral)
2. \( \ce{PCl6^-} \) has 6 bond pairs (sp3d2, octahedral).
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{H2O} \) < \( \ce{PH3} \) < \( \ce{P4} \)
(b) \( \ce{P4} \) < \( \ce{PH3} \) < \( \ce{H2O} \)
(c) \( \ce{PH3} \) < \( \ce{H2O} \) < \( \ce{P4} \)
(d) \( \ce{P4} \) < \( \ce{H2O} \) < \( \ce{PH3} \)
Show Answer & Explanation
Answer: (a) \( \ce{H2O} \) < \( \ce{PH3} \) < \( \ce{P4} \)
Explanation:
1. The tetrahedral angle is 109.5 degrees
2. \( \ce{H2O} \) (104.5) deviates by 5, \( \ce{PH3} \) (93.5) by 16 and \( \ce{P4} \) (60) by 49.5 degrees
3. So the order is H2O < PH3 < P4.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) \( \ce{BF3} \)
(b) \( \ce{(AlCl3)2} \)
(c) \( \ce{(BeH2)_n} \)
(d) \( \ce{(BeCl2)_n} \)
Show Answer & Explanation
Answer: (c) \( \ce{(BeH2)_n} \)
Explanation:
1. In polymeric \( \ce{BeH2} \) the hydrogens bridge two Be atoms using only 2 electrons for 3 centres, which is a banana bond
2. In \( \ce{Al2Cl6} \) and \( \ce{(BeCl2)_n} \) the chlorine bridges use lone pairs (3-centre 4-electron)
3. \( \ce{BF3} \) has no bridge.
Teacher's Note:
1. Find the number of bond pairs and lone pairs on the central atom to get the electron geometry and hybridisation, then the shape. Bond energy and magnetism follow from the bond order and unpaired electrons.
(a) ionic
(b) purely covalent (normal)
(c) coordinate covalent
(d) banana-shaped
Show Answer & Explanation
Answer: (c) coordinate covalent
Explanation:
1. The oxygen of the ether donates a lone pair to the empty orbital of boron in \( \ce{BH3} \)
2. This is a coordinate (dative) covalent 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.
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Chemical Bonding and Molecular Structure Objective Questions & Solutions for JEE Chemistry
Download Multiple Choice Questions: Chemical Bonding and Molecular Structure (JEE Chemistry)
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FAQs
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