Practice MCQs for JEE Chemistry Chemical Bonding and Molecular Structure
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Multiple Choice Questions
(a) \( \ce{BeCl2} \) < \( \ce{MgCl2} \) < \( \ce{CaCl2} \) < \( \ce{SrCl2} \)
(b) \( \ce{BeCl2} \) < \( \ce{CaCl2} \) < \( \ce{SrCl2} \) < \( \ce{MgCl2} \)
(c) \( \ce{BeCl2} \) > \( \ce{MgCl2} \) > \( \ce{CaCl2} \) > \( \ce{SrCl2} \)
(d) \( \ce{SrCl2} \) > \( \ce{BeCl2} \) > \( \ce{CaCl2} \) > \( \ce{MgCl2} \)
Show Answer & Explanation
Answer: (c) \( \ce{BeCl2} \) > \( \ce{MgCl2} \) > \( \ce{CaCl2} \) > \( \ce{SrCl2} \)
Explanation:
1. The smaller the cation, the higher the polarising power, so the covalent character falls down the group.
Teacher's Note:
1. Be2+ is the smallest.
(a) AgF
(b) AgCl
(c) AgBr
(d) AgI
Show Answer & Explanation
Answer: (d) AgI
Explanation:
1. AgI is the most covalent and least soluble. AgF is quite soluble.
Teacher's Note:
1. Solubility: AgF > AgCl > AgBr > AgI.
(a) There is more charge on \( \ce{Sn^4+} \)
(b) The size of \( \ce{Sn^4+} \) is small
(c) The ionic potential of \( \ce{Sn^4+} \) is high
(d) The shape of \( \ce{SnCl4} \) is tetrahedral
Show Answer & Explanation
Answer: (a) There is more charge on \( \ce{Sn^4+} \)
Explanation:
1. Sn4+ has a high charge and strongly polarises Cl-, making SnCl4 covalent (molecular) with a low melting point.
Teacher's Note:
1. Fajans' rules.
(a) \( \ce{Li+} \) > \( \ce{Na+} \) > \( \ce{K+} \) > \( \ce{Rb+} \) > \( \ce{Cs+} \)
(b) \( \ce{Li+} \) < \( \ce{Na+} \) < \( \ce{K+} \) < \( \ce{Rb+} \) < \( \ce{Cs+} \)
(c) \( \ce{Li+} \) > \( \ce{Na+} \) > \( \ce{K+} \) < \( \ce{Rb+} \)
(d) \( \ce{Li+} \) < \( \ce{Na+} \) < \( \ce{K+} \) > \( \ce{Rb+} \)
Show Answer & Explanation
Answer: (b) \( \ce{Li+} \) < \( \ce{Na+} \) < \( \ce{K+} \) < \( \ce{Rb+} \) < \( \ce{Cs+} \)
Explanation:
1. Li+ is the most heavily hydrated, so its hydrated size is the largest and its mobility the lowest.
2. Conductance rises from Li+ to Cs+.
Teacher's Note:
1. The hydrated radius, not the bare radius, determines mobility.
(a) NaCl
(b) KCl
(c) NaBr
(d) NaF
Show Answer & Explanation
Answer: (d) NaF
Explanation:
1. NaF has the smallest ions and the highest lattice energy (m.p. 993 C).
Teacher's Note:
1. Smaller ions mean a larger lattice energy.
(a) \( \ce{MgCO3} \)
(b) \( \ce{Li2CO3} \)
(c) \( \ce{ZnCO3} \)
(d) \( \ce{K2CO3} \)
Show Answer & Explanation
Answer: (d) \( \ce{K2CO3} \)
Explanation:
1. K2CO3 is thermally stable up to its melting point; the others decompose to oxide and CO2.
Teacher's Note:
1. Alkali carbonates (except Li) are stable.
(a) \( \ce{Na2CO3} \)
(b) \( \ce{Li2CO3} \)
(c) \( \ce{K2SO4} \)
(d) \( \ce{NaHCO3} \)
Show Answer & Explanation
Answer: (b) \( \ce{Li2CO3} \)
Explanation:
1. \( \ce{Li2CO3 -> Li2O + CO2} \). NaHCO3 gives Na2CO3 and not an oxide.
Teacher's Note:
1. Lithium is anomalous.
(a) I < II < III
(b) II < III < I
(c) II < I < III
(d) I < III < II
Show Answer & Explanation
Answer: (b) II < III < I
Explanation:
1. Thermal stability increases with the electropositivity of the metal: MgCO3 < Na2CO3 < K2CO3.
Teacher's Note:
1. Group 1 carbonates are more stable than group 2.
(a) \( \ce{BaCO3} \)
(b) \( \ce{ZnCO3} \)
(c) \( \ce{Na2CO3} \)
(d) \( \ce{Li2CO3} \)
Show Answer & Explanation
Answer: (c) \( \ce{Na2CO3} \)
Explanation:
1. Na2CO3 melts without decomposition.
Teacher's Note:
1. BaCO3 decomposes only at very high temperature.
(a) \( \ce{BeCO3} \)
(b) \( \ce{CaCO3} \)
(c) \( \ce{K2CO3} \)
(d) \( \ce{Li2CO3} \)
Show Answer & Explanation
Answer: (c) \( \ce{K2CO3} \)
Explanation:
1. K2CO3 is stable to a very high temperature.
Teacher's Note:
1. The less polarising the cation, the more stable the carbonate.
(a) \( \ce{O3} \)
(b) \( \ce{NO2^-} \)
(c) \( \ce{SO2} \)
(d) \( \ce{NO2+} \)
Show Answer & Explanation
Answer: (d) \( \ce{NO2+} \)
Explanation:
1. NO2+ has 2 bond pairs and no lone pair (sp): linear. The others are bent.
Teacher's Note:
1. 16-valence-electron triatomics are linear.
(a) \( \ce{NH4+} \)
(b) \( \ce{SCl4} \)
(c) \( \ce{SO4^2-} \)
(d) \( \ce{PO4^3-} \)
Show Answer & Explanation
Answer: (b) \( \ce{SCl4} \)
Explanation:
1. SCl4 is see-saw (sp3d). The others are tetrahedral.
Teacher's Note:
1. SiCl4 is tetrahedral.
(a) In NH3 the atomic dipole and bond dipole are in opposite directions, whereas in NF3 they are in the same direction
(b) In NH3 as well as in NF3 the atomic dipole and bond dipole are in the same direction
(c) In NH3 the atomic dipole and bond dipole are in the same direction whereas in NF3 these are in opposite directions
(d) In NH3 as well as NF3 the atomic dipole and bond dipole are in opposite directions
Show Answer & Explanation
Answer: (c) In NH3 the atomic dipole and bond dipole are in the same direction whereas in NF3 these are in opposite directions
Explanation:
1. In NH3, N is negative with the lone pair pointing the same way as the N-H bond dipoles (adding).
2. In NF3, the N-F dipoles point towards F and oppose the lone pair dipole.
Teacher's Note:
1. Vector addition decides the net dipole.
(a) \( \ce{NF3} \)
(b) \( \ce{ClF3} \)
(c) \( \ce{BF3} \)
(d) \( \ce{AlF3} \)
Show Answer & Explanation
Answer: (b) \( \ce{ClF3} \)
Explanation:
1. ClF3 is T-shaped with two axial bonds longer than the equatorial one.
Teacher's Note:
1. The others have identical bonds.
(a) \( \ce{SO3^2-} \) and \( \ce{NO3^-} \)
(b) \( \ce{BF3} \) and \( \ce{NF3} \)
(c) \( \ce{BrO3^-} \) and \( \ce{XeO3} \)
(d) \( \ce{SF4} \) and \( \ce{XeF4} \)
Show Answer & Explanation
Answer: (c) \( \ce{BrO3^-} \) and \( \ce{XeO3} \)
Explanation:
1. BrO3^- and XeO3 are pyramidal (sp3, 1 lone pair).
2. SO3(2-) is pyramidal but NO3- is planar; BF3 planar, NF3 pyramidal; SF4 see-saw, XeF4 square planar.
Teacher's Note:
1. Compare the number of lone pairs.
(a) CO < \( \ce{CO3^2-} \) < \( \ce{CO2} \)
(b) \( \ce{CO3^2-} \) < \( \ce{CO2} \) < CO
(c) CO < \( \ce{CO2} \) < \( \ce{CO3^2-} \)
(d) \( \ce{CO2} \) < CO < \( \ce{CO3^2-} \)
Show Answer & Explanation
Answer: (c) CO < \( \ce{CO2} \) < \( \ce{CO3^2-} \)
Explanation:
1. Bond orders: CO 3, CO2 2, CO3(2-) 1.33. The longer the bond, the lower the order: CO < CO2 < CO3(2-).
Teacher's Note:
1. Bond length is inversely related to bond order.
(a) \( \ce{MgSO4} \)
(b) \( \ce{CaSO4} \)
(c) \( \ce{BaSO4} \)
(d) \( \ce{SrSO4} \)
Show Answer & Explanation
Answer: (a) \( \ce{MgSO4} \)
Explanation:
1. Small Mg2+ has a very high hydration energy, which exceeds the lattice energy, so MgSO4 is soluble.
Teacher's Note:
1. Solubility of group 2 sulphates falls down the group.
(a) \( \ce{C2^2-} \) < \( \ce{He2+} \) < NO < \( \ce{O2^-} \)
(b) \( \ce{He2+} \) < \( \ce{O2^-} \) < NO < \( \ce{C2^2-} \)
(c) \( \ce{O2^-} \) < NO < \( \ce{C2^2-} \) < \( \ce{He2+} \)
(d) NO < \( \ce{C2^2-} \) < \( \ce{O2^-} \) < \( \ce{He2+} \)
Show Answer & Explanation
Answer: (b) \( \ce{He2+} \) < \( \ce{O2^-} \) < NO < \( \ce{C2^2-} \)
Explanation:
1. Bond orders: He2+ 0.5, O2- 1.5, NO 2.5, C2(2-) 3.
Teacher's Note:
1. Compute (Nb - Na)/2.
(a) 1 sigma and 1 pi bond
(b) 2 sigma and 1 pi bond
(c) 1 sigma and 2 pi bonds
(d) 2 sigma and 2 pi bonds
Show Answer & Explanation
Answer: (b) 2 sigma and 1 pi bond
Explanation:
1. In O3, the central O forms two sigma bonds and there is one pi bond delocalised over the two O-O bonds.
Teacher's Note:
1. Resonance gives equal O-O bonds of order 1.5.
(a) \( \ce{NO2+} \) < \( \ce{NO2} \) < \( \ce{NO2^-} \)
(b) \( \ce{NO2+} \) < \( \ce{NO2^-} \) < \( \ce{NO2} \)
(c) \( \ce{NO2^-} \) < \( \ce{NO2+} \) < \( \ce{NO2} \)
(d) \( \ce{NO2^-} \) < \( \ce{NO2} \) < \( \ce{NO2+} \)
Show Answer & Explanation
Answer: (d) \( \ce{NO2^-} \) < \( \ce{NO2} \) < \( \ce{NO2+} \)
Explanation:
1. NO2- (115 degrees, lone pair repels more) < NO2 (134, single electron) < NO2+ (180, linear).
Teacher's Note:
1. Fewer non-bonding electrons give a larger angle.
(a) \( \ce{BF3} \) and \( \ce{NO2^-} \)
(b) \( \ce{NO2^-} \) and \( \ce{NH2^-} \)
(c) \( \ce{NH2^-} \) and \( \ce{H2O} \)
(d) \( \ce{NO2^-} \) and \( \ce{H2O} \)
Show Answer & Explanation
Answer: (a) \( \ce{BF3} \) and \( \ce{NO2^-} \)
Explanation:
1. BF3: 3 bond pairs (sp2). NO2^-: 2 bond pairs + 1 lone pair (sp2). NH2^- and H2O are sp3.
Teacher's Note:
1. Count sigma bonds plus lone pairs.
(a) MI > MBr > MCl > MF
(b) MCl > MI > MBr > MF
(c) MF > MCl > MBr > MI
(d) MF > MCl > MI > MBr
Show Answer & Explanation
Answer: (a) MI > MBr > MCl > MF
Explanation:
1. Larger anions are more polarisable, so the covalent character increases from F to I.
2. The order is MI > MBr > MCl > MF.
Teacher's Note:
1. Fajans: large anion, small cation, high charge raise covalent character.
(a) London dispersion force
(b) Hydrogen bonding
(c) Dipole-dipole interaction
(d) Covalent bonds
Show Answer & Explanation
Answer: (b) Hydrogen bonding
Explanation:
1. Methanol molecules are held together mainly by O-H...O hydrogen bonds.
Teacher's Note:
1. Hydrogen bonding is the strongest intermolecular force in alcohols.
(a) Isostructural with the same hybridisation for the central atom
(b) Isostructural with different hybridisation
(c) Similar hybridisation for the central atom with different structures
(d) Dissimilar hybridisation for the central atom with different structures
Show Answer & Explanation
Answer: (d) Dissimilar hybridisation for the central atom with different structures
Explanation:
1. NO3^- is trigonal planar (N sp2) and H3O+ is pyramidal (O sp3).
Teacher's Note:
1. Different hybridisation leads to different shapes.
(a) \( \ce{SF4} \)
(b) \( \ce{BF4^-} \)
(c) \( \ce{NH4+} \)
(d) \( \ce{CH4} \)
Show Answer & Explanation
Answer: (a) \( \ce{SF4} \)
Explanation:
1. SF4 is sp3d (5 electron pairs).
Teacher's Note:
1. BF4-, NH4+ and CH4 have 4 electron pairs.
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Chemical Bonding and Molecular Structure Objective Questions & Solutions for JEE Chemistry
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