JEE Chemistry Chemical Bonding and Molecular Structure MCQs Set 34

Multiple Choice Questions (MCQs) for JEE Chemistry: Chemical Bonding and Molecular Structure

Review structured MCQ sets for JEE Chemistry Chemical Bonding and Molecular Structure. Built according to official JEE guidelines, these downloadable questions support daily revision and core concept reinforcement.

Practice Chemical Bonding and Molecular Structure MCQs for JEE Chemistry

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Multiple Choice Questions

Question 1: Which statement is true for \( \ce{IO2F2^-} \)?
(a) The electron pairs are at the corners of a trigonal bipyramid with one equatorial pair unshared, and its structure is analogous to \( \ce{SF4} \)
(b) It has sp3d hybridisation and is T-shaped
(c) The electron pairs are tetrahedral
(d) It is square planar with sp3d2 hybridisation
Show Answer & Explanation

Answer: (a) The electron pairs are at the corners of a trigonal bipyramid with one equatorial pair unshared, and its structure is analogous to \( \ce{SF4} \)

Explanation:
1. Iodine has 8 valence electrons here (7 + 1 charge); four sigma bonds use 4 pairs of the 5 sigma-framework positions and one lone pair remains, giving sp3d with the lone pair equatorial
2. The shape is see-saw, like \( \ce{SF4} \), not T-shaped.

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.

Question 2: In which reaction does the electron-pair geometry of the underlined (central) element change?
(a) \( \ce{NH3 + H^+ -> NH4^+} \) (nitrogen)
(b) \( \ce{H2O + H^+ -> H3O^+} \) (oxygen)
(c) \( \ce{2SO2 + O2 -> 2SO3} \) (sulphur)
(d) \( \ce{BF3 + F^- -> BF4^-} \) (boron)
Show Answer & Explanation

Answer: (d) \( \ce{BF3 + F^- -> BF4^-} \) (boron)

Explanation:
1. Boron changes from 3 pairs (trigonal planar, sp2) to 4 pairs (tetrahedral, sp3)
2. In the other cases the electron-pair geometry stays tetrahedral (N, O) or trigonal planar (S in \( \ce{SO2} \) and \( \ce{SO3} \)).

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.

Question 3: In which of the following do the numbers of lone pairs and bond pairs on the central atom differ?
(a) \( \ce{H2O} \)
(b) \( \ce{I3^-} \)
(c) \( \ce{O2F2} \) (each O)
(d) \( \ce{SCl2} \)
Show Answer & Explanation

Answer: (b) \( \ce{I3^-} \)

Explanation:
1. The central I in \( \ce{I3^-} \) has 2 bond pairs and 3 lone pairs
2. In \( \ce{H2O} \), \( \ce{SCl2} \) and each O of \( \ce{O2F2} \), the central atom has 2 bond pairs and 2 lone pairs.

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.

Question 4: The hybridisations of the central atoms of \( \ce{N3^-} \), \( \ce{NOCl} \) and \( \ce{N2O} \) are respectively
(a) sp, sp, sp3
(b) sp, sp2, sp
(c) sp2, sp, sp
(d) sp2, sp2, sp
Show Answer & Explanation

Answer: (b) sp, sp2, sp

Explanation:
1. \( \ce{N3^-} \) (linear, 2 sigma bonds, no lone pair on central N) is sp
2. In \( \ce{NOCl} \) the central N has 2 sigma bonds and 1 lone pair, so sp2 (bent)
3. In \( \ce{N2O} \) (N=N=O) the central N has 2 sigma bonds and no lone pair, so sp.

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.

Question 5: In pent-3-en-1-yne, \( \ce\( \ce{HC#C-CH=CH-CH3} \) \), the terminal carbon atoms are hybridised respectively as
(a) sp and sp2
(b) sp2 and sp3
(c) sp2 and sp
(d) sp and sp3
Show Answer & Explanation

Answer: (d) sp and sp3

Explanation:
1. The first carbon is in a triple bond, so sp
2. The last carbon is the saturated methyl group with four single bonds, so sp3.

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.

Question 6: In the reaction \( \ce{BF3 + F^- -> BF4^-} \), the hybridisation of boron in \( \ce{BF3} \) and \( \ce{BF4^-} \) respectively is
(a) sp2, sp3
(b) sp3, sp3
(c) sp2, sp2
(d) sp3, sp3d
Show Answer & Explanation

Answer: (a) sp2, sp3

Explanation:
1. \( \ce{BF3} \) has 3 sigma bonds and no lone pair, so sp2. \( \ce{BF4^-} \) has 4 sigma bonds, so sp3.
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.

Question 7: In which of the following is the bond angle maximum?
(a) \( \ce{NH3} \)
(b) \( \ce{PCl3} \)
(c) \( \ce{NH4^+} \)
(d) \( \ce{SCl2} \)
Show Answer & Explanation

Answer: (c) \( \ce{NH4^+} \)

Explanation:
1. \( \ce{NH4^+} \) has no lone pair and is tetrahedral (109.5 degrees)
2. \( \ce{NH3} \) is about 107, \( \ce{SCl2} \) about 103 and \( \ce{PCl3} \) about 100 degrees.

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.

Question 8: The number of S-O-S bonds in the trimer of \( \ce{SO3} \) is
(a) 3
(b) 1
(c) 2
(d) 6
Show Answer & Explanation

Answer: (a) 3

Explanation:
1. The cyclic trimer \( \ce{(SO3)3} \) has a six-membered ring of alternating S and O atoms with each S carrying two terminal oxygens
2. The ring contains three S-O-S bridges.

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.

Question 9: Which of the following does NOT contain an S-S linkage?
(a) \( \ce{H2S2O5} \)
(b) \( \ce{H2S2O3} \)
(c) \( \ce{H2S4O6} \)
(d) \( \ce{H2S2O7} \)
Show Answer & Explanation

Answer: (d) \( \ce{H2S2O7} \)

Explanation:
1. \( \ce{H2S2O7} \) (pyrosulphuric acid) has the two S atoms bridged through oxygen (S-O-S)
2. \( \ce{H2S2O5} \), \( \ce{H2S2O3} \) and the polythionic acid \( \ce{H2S4O6} \) each have S-S 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.

Question 10: Which statement is INCORRECT about the pyrosilicate ion \( \ce{Si2O7^6-} \)?
(a) The silicon atoms are sp3 hybridised
(b) There is one Si-Si bond
(c) One oxygen atom is shared between two tetrahedra
(d) There are eight Si-O bonds
Show Answer & Explanation

Answer: (b) There is one Si-Si bond

Explanation:
1. Two \( \ce{SiO4} \) tetrahedra share one bridging oxygen
2. Each Si has four Si-O bonds, giving 8 in all, and each Si is sp3. There is no Si-Si bond; the units are linked through oxygen.

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.

Question 11: Which statement is correct for the cyclic silicate \( \ce{[Si6O18]^n-} \)?
(a) each Si is bonded to three oxygen atoms
(b) the value of n is 12
(c) each oxygen is bonded to two Si atoms
(d) all of the other statements are correct
Show Answer & Explanation

Answer: (b) the value of n is 12

Explanation:
1. Each Si is bonded to four oxygens (two bridging and two terminal), so statement B is false
2. Of the 18 oxygens, 6 are bridging and 12 are terminal, so C is false
3. The charge is 6(+4) + 18(-2) = -12, so n = 12.

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.

Question 12: Choose the molecules in which hybridisation occurs without needing promotion of an electron (that is, in the ground state): (a) \( \ce{BCl3} \), (b) \( \ce{NH3} \), (c) \( \ce{PCl3} \), (d) \( \ce{BeF2} \)
(a) a, b and d
(b) a, b and c
(c) c and d
(d) b and c
Show Answer & Explanation

Answer: (d) b and c

Explanation:
1. In \( \ce{NH3} \) and \( \ce{PCl3} \) the central atoms already have lone pairs and three unpaired p electrons, so they hybridise from the ground state
2. For \( \ce{BCl3} \) and \( \ce{BeF2} \) one s electron must first be promoted to a p orbital to give the required unpaired electrons.

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.

Question 13: In sp3d hybridisation, if the equatorial plane is the x-y plane, the orbitals involved in the p-d hybridisation (the axial pair) are
(a) px and dxy
(b) py and dyz
(c) pz and dz2
(d) dx2-y2 and pz
Show Answer & Explanation

Answer: (c) pz and dz2

Explanation:
1. The sp3d set can be viewed as sp2 (s, px, py) forming the equatorial plane, plus pz and dz2 forming the two axial bonds.
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.

Question 14: A sigma-bonded molecule \( \ce{MX3} \) is T-shaped. The number of lone pairs on the central atom M is
(a) 0
(b) 1
(c) 2
(d) 3
Show Answer & Explanation

Answer: (c) 2

Explanation:
1. A T-shape comes from a trigonal bipyramid with 3 bond pairs and 2 lone pairs in the equatorial plane, as in \( \ce{ClF3} \).
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.

Question 15: The correct order of bond angle is
(a) \( \ce{H2S} \) < \( \ce{NH3} \) < \( \ce{CH4} \) < \( \ce{BF3} \)
(b) \( \ce{NH3} \) < \( \ce{H2S} \) < \( \ce{CH4} \) < \( \ce{BF3} \)
(c) \( \ce{H2S} \) < \( \ce{NH3} \) < \( \ce{BF3} \) < \( \ce{CH4} \)
(d) \( \ce{H2S} \) < \( \ce{CH4} \) < \( \ce{NH3} \) < \( \ce{BF3} \)
Show Answer & Explanation

Answer: (a) \( \ce{H2S} \) < \( \ce{NH3} \) < \( \ce{CH4} \) < \( \ce{BF3} \)

Explanation:
1. The angles are \( \ce{H2S} \) about 92, \( \ce{NH3} \) 107, \( \ce{CH4} \) 109.5 and \( \ce{BF3} \) 120 degrees.
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.

Question 16: In which of the following molecules are all the bonds NOT equal?
(a) \( \ce{NF3} \)
(b) \( \ce{BF3} \)
(c) \( \ce{AlF3} \) (in the gas phase, monomer)
(d) \( \ce{ClF3} \)
Show Answer & Explanation

Answer: (d) \( \ce{ClF3} \)

Explanation:
1. \( \ce{ClF3} \) is T-shaped, with two axial Cl-F bonds that are longer than the single equatorial bond
2. In \( \ce{NF3} \) and \( \ce{BF3} \) all bonds are equivalent.

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.

Question 17: Which of the following is the correct order of bond length?
(a) \( \ce{BF4^-} \) < \( \ce{BF3} \)
(b) \( \ce{NO2^+} \) < \( \ce{NO2^-} \)
(c) \( \ce{CCl4} \) < \( \ce{CF4} \)
(d) \( \ce{CH3^+} \) > \( \ce{CH4} \)
Show Answer & Explanation

Answer: (b) \( \ce{NO2^+} \) < \( \ce{NO2^-} \)

Explanation:
1. \( \ce{NO2^+} \) has N-O bond order 2 (115 pm) and \( \ce{NO2^-} \) has bond order 1.5 (124 pm), so the first is shorter
2. \( \ce{BF3} \) has partial pi bonding, so its B-F is shorter than that in \( \ce{BF4^-} \)
3. C-F is shorter than C-Cl, and \( \ce{CH3^+} \) (sp2) has shorter C-H bonds than \( \ce{CH4} \).

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.

Question 18: Identify the correct statement.
(a) A single N-N bond is stronger than a single P-P bond
(b) A single N-N bond is weaker than a single P-P bond
(c) The N triple bond N is weaker than P triple bond P
(d) All three statements are false
Show Answer & Explanation

Answer: (b) A single N-N bond is weaker than a single P-P bond

Explanation:
1. The N-N single bond is weak (about 160 kJ per mole) because of lone pair-lone pair repulsion between the small N atoms, while P-P is about 200 kJ per mole
2. Triple bonds show the reverse, \( \ce{N2} \) (945 kJ per mole) being much stronger than \( \ce{P2} \).

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.

Question 19: Which of the following is correct?
(a) \( \ce{S3O9} \) contains no S-S linkage
(b) \( \ce{S2O6^2-} \) contains an O-O linkage
(c) \( \ce{(HPO3)3} \) contains a P-P linkage
(d) \( \ce{S2O8^2-} \) contains an S-S linkage
Show Answer & Explanation

Answer: (a) \( \ce{S3O9} \) contains no S-S linkage

Explanation:
1. The \( \ce{S3O9} \) trimer is a ring of S-O-S links
2. In dithionate \( \ce{S2O6^2-} \) the S atoms are directly bonded (S-S) with no O-O. \( \ce{(HPO3)3} \) has P-O-P ring links
3. \( \ce{S2O8^2-} \) has an O-O peroxide link between two sulphate units.

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.

Question 20: Which is the INCORRECT statement?
(a) The number of hybrid orbitals formed equals the number of atomic orbitals mixed
(b) Effective hybridisation is not possible between orbitals of widely different energies
(c) The 2px and 2py orbitals of carbon can hybridise to give two new, more stable orbitals
(d) Hybridisation is more significant in valence bond theory of localised bonds than in molecular orbital theory
Show Answer & Explanation

Answer: (c) The 2px and 2py orbitals of carbon can hybridise to give two new, more stable orbitals

Explanation:
1. Mixing two p orbitals gives no gain in stability, because hybrids are stabilised by including s-character
2. The other three statements are standard facts about hybridisation.

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.

Chemical Bonding and Molecular Structure Objective Questions & Solutions for JEE Chemistry

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