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NEET • CHEMISTRY • CHEMICAL BONDING & MOLECULAR STRUCTURE

Chemical bonding & molecular structure practice · Easy

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211 Easy
Remembering +4 | -1
Which type of compounds show high melting and boiling points
View answer and explanation
Correct option: A
Electrovalent compounds
Option A (Electrovalent compounds) is correct because electrovalent compounds have strong electrostatic forces of attraction between ions, leading to high melting and boiling points.
Solution approach
  1. Correct Answer + Core Reason: Electrovalent compounds have high melting and boiling points due to strong electrostatic forces.

    Step-by-Step Solution:

    Step 1: Electrovalent compounds (also known as ionic compounds) are formed by the complete transfer of electrons from one atom to another, resulting in the formation of ions.

    Step 2: These ions are held together by strong electrostatic forces of attraction.

    Step 3: Breaking these strong electrostatic forces requires a large amount of energy, hence the high melting and boiling points.

    Why other options are wrong:
    - Option B: Covalent compounds have relatively weaker intermolecular forces (e.g., van der Waals forces) compared to the strong electrostatic forces in electrovalent compounds. Therefore, they have lower melting and boiling points.
    - Option C: Coordinate compounds generally have properties intermediate between ionic and covalent compounds, and their melting and boiling points are usually lower than those of electrovalent compounds.
    - Option D: This is incorrect because the melting and boiling points of these three types of compounds are significantly different.

    Key Concepts:
    - Electrovalent (Ionic) bonding
    - Covalent bonding
    - Intermolecular forces
    - Melting and boiling points

    Memory Aids:
    - Ionic = Ions = Strong attraction = High MP/BP

    Quick Tips:
    - Remember that ionic compounds generally have much higher melting and boiling points than covalent compounds.
212 Easy
Application +4 | -1
Which of the following is diamagnetic?
View answer and explanation
Correct option: C
Li2\mathrm{L}{\mathrm{i}_2}
Option C (Li2\mathrm{L}{\mathrm{i}_2}) is correct because it has all its electrons paired in its molecular orbital configuration, resulting in no net magnetic moment.
Solution approach
  1. Correct Answer + Core Reason: Li2\mathrm{L}{\mathrm{i}_2}. Diamagnetic species have all paired electrons.

    Step-by-Step Solution:

    Step 1: Determine the electronic configuration of each species using molecular orbital theory.

    Step 2: The electronic configurations are:
    H2+\mathrm{H}_2^ +: (σ1s)1(\sigma_{1s})^1
    O2{\mathrm{O}_2}: (σ2s)2(σ2s∗)2(σ2pz)2(π2px)2(π2py)2(π2px∗)1(π2py∗)1(\sigma_{2s})^2(\sigma_{2s}^*)^2(\sigma_{2p_z})^2(\pi_{2p_x})^2(\pi_{2p_y})^2(\pi_{2p_x}^*)^1(\pi_{2p_y}^*)^1
    Li2\mathrm{L}{\mathrm{i}_2}: (σ2s)2(\sigma_{2s})^2
    Fe2+\mathrm{Fe}_2^ +: This is complex and not easily determined by simple MO theory. However, Fe typically has unpaired electrons.

    Step 3: Identify the species with all paired electrons.
    H2+\mathrm{H}_2^ + has one unpaired electron.
    O2{\mathrm{O}_2} has two unpaired electrons.
    Li2\mathrm{L}{\mathrm{i}_2} has all paired electrons.
    Fe2+\mathrm{Fe}_2^ + is likely to have unpaired electrons.

    Step 4: Diamagnetic species have all paired electrons.

    Why other options are wrong:
    - Option A: H2+\mathrm{H}_2^ + is paramagnetic.
    - Option B: O2{\mathrm{O}_2} is paramagnetic.
    - Option D: Fe2+\mathrm{Fe}_2^ + is paramagnetic.

    Key Concepts:
    - Molecular orbital theory
    - Electronic configuration
    - Paramagnetism and diamagnetism

    Memory Aids:
    - Paramagnetic: unpaired electrons; Diamagnetic: all paired electrons.

    Quick Tips:
    - Determine the electronic configuration and check for unpaired electrons.
213 Easy
Application +4 | -1
The bond order in O2+{O}_2^{+}is
View answer and explanation
Correct option: B
2.5
Option B (2.5) is correct because the bond order is calculated using molecular orbital theory, and for O2+O_2^+, it is 2.5.
Solution approach
  1. Correct Answer + Core Reason: 2.5. The bond order is calculated using molecular orbital theory.

    Step-by-Step Solution:

    Step 1: Determine the electronic configuration of O2+O_2^+.
    - O2O_2: (σ2s)2(σ2s∗)2(σ2p)2(π2p)4(π2p∗)2(\sigma_{2s})^2 (\sigma_{2s}^*)^2 (\sigma_{2p})^2 (\pi_{2p})^4 (\pi_{2p}^*)^2
    - O2+O_2^+: (σ2s)2(σ2s∗)2(σ2p)2(π2p)4(π2p∗)1(\sigma_{2s})^2 (\sigma_{2s}^*)^2 (\sigma_{2p})^2 (\pi_{2p})^4 (\pi_{2p}^*)^1

    Step 2: Calculate the bond order.
    - Bond order = Numberofbondingelectrons−Numberofantibondingelectrons2\frac{{Number of bonding electrons - Number of antibonding electrons}}{2}
    - Bond order = 10−52=2.5\frac{{10 - 5}}{2} = 2.5

    Why other options are wrong:
    - Option A (2): This would be the bond order of O22+O_2^{2+}.
    - Option C (1.5): This is not a possible bond order for an oxygen species.
    - Option D (3): This is not a possible bond order for an oxygen species.

    Key Concepts:
    - Molecular orbital theory
    - Electronic configuration
    - Bond order

    Memory Aids:
    - Bond order = (Bonding electrons - Antibonding electrons) / 2

    Quick Tips:
    - Remember the molecular orbital diagrams for diatomic molecules.
214 Easy
Application +4 | -1
The hybridization of phosphorus in POCl3\mathrm{POC}{\mathrm{l}_3} is same as in:
View answer and explanation
Correct option: A
PinPCl3\mathrm{P in PC}{\mathrm{l}_3}
Option A (PinPCl3\mathrm{P in PCl_3}) is correct because both POCl3POCl_3 and PCl3PCl_3 have phosphorus as the central atom with three bonding pairs and one lone pair (or a double bond and two single bonds in POCl3POCl_3), resulting in sp3sp^3 hybridization.
Solution approach
  1. Correct Answer + Core Reason: PinPCl3\mathrm{P in PC}{\mathrm{l}_3}. Both have sp3sp^3 hybridization.

    Step-by-Step Solution:

    Step 1: Determine the hybridization of P in POCl3POCl_3.

    Step 2: P in POCl3POCl_3 has 3 single bonds to Cl and one double bond to O. This is equivalent to 4 sigma bonds. Therefore, the hybridization is sp3sp^3.

    Step 3: Determine the hybridization of P in PCl3PCl_3.

    Step 4: P in PCl3PCl_3 has 3 single bonds to Cl and one lone pair. Therefore, the hybridization is sp3sp^3.

    Step 5: Determine the hybridization of S in SF6SF_6.

    Step 6: S in SF6SF_6 has 6 single bonds to F. Therefore, the hybridization is sp3d2sp^3d^2.

    Step 7: Determine the hybridization of Cl in ClF3ClF_3.

    Step 8: Cl in ClF3ClF_3 has 3 single bonds to F and 2 lone pairs. Therefore, the hybridization is sp3dsp^3d.

    Step 9: Determine the hybridization of B in BCl3BCl_3.

    Step 10: B in BCl3BCl_3 has 3 single bonds to Cl. Therefore, the hybridization is sp2sp^2.

    Why other options are wrong:
    - **Option B (SinSF6\mathrm{S in S}{\mathrm{F}_6}):** The hybridization is sp3d2sp^3d^2.
    - **Option C (ClinClF3\mathrm{Cl in Cl}{\mathrm{F}_3}):** The hybridization is sp3dsp^3d.
    - **Option D (BinBCl3\mathrm{B in BC}{\mathrm{l}_3}):** The hybridization is sp2sp^2.

    Key Concepts:
    - Hybridization
    - VSEPR theory

    Memory Aids:
    - Steric number = number of sigma bonds + number of lone pairs

    Quick Tips:
    - Draw the Lewis structures to determine the number of sigma bonds and lone pairs.
215 Easy
Application +4 | -1
Which of the following species would be expected paramagnetic
View answer and explanation
Correct option: C
Cu++{Cu}^{++}
Option C (Cu++{Cu}^{++}) is correct because Cu++Cu^{++} has an unpaired electron in its electronic configuration, making it paramagnetic.
Solution approach
  1. Correct Answer + Core Reason: Cu++{Cu}^{++}. Paramagnetic species have unpaired electrons.

    Step-by-Step Solution:

    Step 1: Define paramagnetism: Paramagnetism is the property of a substance being attracted to a magnetic field due to the presence of unpaired electrons.

    Step 2: Determine the electronic configuration of each species.

    Step 3: Copper (Cu) has an electronic configuration of [Ar] 3d¹⁰ 4s¹.

    Step 4: Cu+{Cu}^{+} has an electronic configuration of [Ar] 3d¹⁰. All electrons are paired, so it is diamagnetic.

    Step 5: Cu++{Cu}^{++} has an electronic configuration of [Ar] 3d⁹. There is one unpaired electron, so it is paramagnetic.

    Step 6: H2{H}_2 has a configuration of σ1s2\sigma_{1s}^2. All electrons are paired, so it is diamagnetic.

    Step 7: Copper crystals are metallic and have complex electronic band structures, but the presence of unpaired electrons at the Fermi level makes them paramagnetic.

    Step 8: However, the question asks for a *species*, implying an ion or molecule, not a bulk metal.

    Why other options are wrong:
    - Option A: Copper crystals are paramagnetic, but the question is looking for a *species* (ion or molecule).
    - Option B: Cu+{Cu}^{+} is diamagnetic because it has a filled d-shell (3d¹⁰) with no unpaired electrons.
    - Option D: H2{H}_2 is diamagnetic because all its electrons are paired.

    Key Concepts:
    - Paramagnetism
    - Diamagnetism
    - Electronic configuration

    Memory Aids:
    - Unpaired electrons = paramagnetic
    - Paired electrons = diamagnetic

    Quick Tips:
    - Determine the number of unpaired electrons in each species.
216 Easy
Remembering +4 | -1
Debye is
View answer and explanation
Correct option: C
Unit of dipole momentum
Option C is correct because Debye is the unit used to measure dipole moment.
Solution approach
  1. Correct Answer + Core Reason: Unit of dipole momentum. Debye is the standard unit for measuring dipole moment.

    Step-by-Step Solution:

    Step 1: Recall the definition of Debye. Debye is a unit used to quantify the dipole moment of a molecule.

    Step 2: Conclusion: Debye is the unit of dipole momentum.

    Why other options are wrong:
    - Option A: Unit of radius: This is incorrect because radius is measured in units of length (e.g., meters, angstroms).
    - Option B: Unit of bond order: This is incorrect because bond order is a dimensionless quantity.
    - Option D: Unit of bond length: This is incorrect because bond length is measured in units of length (e.g., meters, angstroms).

    Key Concepts:
    - Dipole Moment
    - Debye Unit

    Memory Aids:
    - Associate Debye with dipole moment.

    Quick Tips:
    - Remember that dipole moment is a measure of the polarity of a molecule.
217 Easy
Application +4 | -1
Bond order of N2−\mathrm{N}_2^ - anion is :
View answer and explanation
Correct option: C
2.5
Option C (2.5) is correct because the bond order is calculated as (bonding electrons - antibonding electrons)/2, and for N2−N_2^- it is (10-5)/2 = 2.5.
Solution approach
  1. Correct Answer + Core Reason: 2.5. The bond order is calculated using the formula (bonding electrons - antibonding electrons) / 2.

    Step-by-Step Solution:

    Step 1: Determine the electronic configuration of N2−\mathrm{N}_2^ - using molecular orbital theory.

    Step 2: The electronic configuration of N2N_2 is (σ2s)2(σ2s∗)2(σ2pz)2(π2px)2(π2py)2(\sigma_{2s})^2(\sigma_{2s}^*)^2(\sigma_{2p_z})^2(\pi_{2p_x})^2(\pi_{2p_y})^2.\nSince N2−\mathrm{N}_2^ - has one extra electron, the electronic configuration is (σ2s)2(σ2s∗)2(σ2pz)2(π2px)2(π2py)2(π2p∗)1(\sigma_{2s})^2(\sigma_{2s}^*)^2(\sigma_{2p_z})^2(\pi_{2p_x})^2(\pi_{2p_y})^2(\pi_{2p}^*)^1.

    Step 3: Count the number of bonding and antibonding electrons.\nBonding electrons: 2 (σ2s\sigma_{2s}) + 2 (σ2pz\sigma_{2p_z}) + 4 (π2px\pi_{2p_x} and π2py\pi_{2p_y}) = 10\nAntibonding electrons: 2 (σ2s∗\sigma_{2s}^*) + 1 (π2p∗\pi_{2p}^*) = 5

    Step 4: Calculate the bond order.\nBond order = (Number of bonding electrons - Number of antibonding electrons) / 2\nBond order = (10 - 5) / 2 = 2.5

    Why other options are wrong:
    - Option A: 3 is the bond order of N2N_2.
    - Option B: 2 is not the correct bond order for N2−\mathrm{N}_2^ -.
    - Option D: 1.5 is not the correct bond order for N2−\mathrm{N}_2^ -.

    Key Concepts:
    - Molecular orbital theory
    - Electronic configuration
    - Bond order

    Memory Aids:
    - Remember the formula for calculating bond order.

    Quick Tips:
    - Determine the electronic configuration first, then calculate the bond order.
218 Easy
Remembering +4 | -1
Electrolytes are compound containing
View answer and explanation
Correct option: A
Electrovalent bond
Option A (Electrovalent bond) is correct because electrolytes are compounds that dissociate into ions in solution, which is characteristic of electrovalent or ionic bonds.
Solution approach
  1. Correct Answer + Core Reason: Electrovalent bond. Electrolytes dissociate into ions due to the presence of electrovalent bonds.

    Step-by-Step Solution:

    Step 1: Define Electrolytes: Electrolytes are substances that produce ions when dissolved in a polar solvent like water, making the solution electrically conductive.

    Step 2: Identify Bond Types: Consider the different types of chemical bonds: electrovalent (ionic), covalent, coordinate, and hydrogen bonds.

    Step 3: Relate Bond Type to Electrolytic Behavior: Electrovalent bonds involve the complete transfer of electrons, resulting in ions. These ions are responsible for the electrolytic behavior.

    Step 4: Conclusion: Electrolytes contain electrovalent bonds because these bonds lead to the formation of ions when dissolved.

    Why other options are wrong:
    - Option B: Covalent bonds involve sharing of electrons and do not typically result in the formation of ions in solution.
    - Option C: Coordinate bonds are a type of covalent bond where one atom provides both electrons, but they don't necessarily lead to ion formation in solution.
    - Option D: Hydrogen bonds are intermolecular forces, not intramolecular bonds, and do not lead to ion formation.

    Key Concepts:
    - Electrolytes
    - Electrovalent (Ionic) Bonds
    - Covalent Bonds
    - Ionization

    Memory Aids:
    - Electrolytes = Ions (think of \"electro\" relating to ions)

    Quick Tips:
    - Remember that electrolytes conduct electricity due to the presence of ions, which are formed by ionic compounds.
219 Easy
Remembering +4 | -1
The value of one debye unit is equal to :
View answer and explanation
Correct option: C
3.33×10−30 Cm3.33 \times 10^{-30} \mathrm{~Cm}
Option C (3.33×10−30 Cm3.33 \times 10^{-30} \mathrm{~Cm}) is correct because one debye unit is defined as 3.33×10−303.33 \times 10^{-30} Coulomb-meters.
Solution approach
  1. Correct Answer + Core Reason: 3.33×10−30 Cm3.33 \times 10^{-30} \mathrm{~Cm}. This is the definition of a Debye unit.

    Step-by-Step Solution:

    Step 1: Recall the definition of a Debye unit.
    1 Debye (D) = 3.33564×10−303.33564 \times 10^{-30} Coulomb-meters (Cm).

    Step 2: Identify the closest value among the options.
    3.33×10−30 Cm3.33 \times 10^{-30} \mathrm{~Cm} is the closest value.

    Why other options are wrong:
    - Option A: Incorrect value for Debye unit.
    - Option B: Incorrect value for Debye unit.
    - Option D: Incorrect value for Debye unit.

    Key Concepts:
    - Debye unit
    - Dipole moment

    Memory Aids:
    - Remember the value of 1 Debye in Coulomb-meters.

    Quick Tips:
    - Know the definition of common units.
220 Easy
Remembering +4 | -1
Molecular orbitals theory was proposed by:
View answer and explanation
Correct option: D
Mullikan
Option D (Mullikan) is correct because Robert S. Mulliken is one of the primary developers of the molecular orbital theory.
Solution approach
  1. Correct Answer + Core Reason: Mullikan. Robert S. Mulliken is known for his contributions to the molecular orbital theory.

    Step-by-Step Solution:

    Step 1: Recall the scientists associated with different bonding theories.

    Step 2: Molecular orbital theory is attributed to Robert S. Mulliken and Friedrich Hund.

    Why other options are wrong:
    - Option A: Werner is known for coordination chemistry.
    - Option B: Kossel is known for his theory of ionic bonding.
    - Option C: Moseley is known for his work on atomic numbers and X-ray spectra.

    Key Concepts:
    - Molecular orbital theory
    - Chemical bonding
    - History of chemistry

    Memory Aids:
    - Mullikan = Molecular Orbital Theory

    Quick Tips:
    - Associate specific scientists with their key contributions to bonding theories.
Revision notes and key takeaways

Review CHEMICAL BONDING & MOLECULAR STRUCTURE in your textbook or class notes, then use this set to check your understanding.

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