PSEB / NCERT CLASS 11 CHEMISTRY CEP 2 CHAPTER 3 AND 4 MCQS, 2 MARKS ,3 MARKS QUESTIONS WITH ANSWERS

key points and definitions from Chapter 3 and Chapter 4 


Chapter 3 – Classification of Elements and Periodicity of Properties

Key Points / Definitions

  1. Mendeleev’s Periodic Table:
    Dimitri Mendeleev arranged elements in the increasing order of their atomic weights.
    Mendeleev’s Periodic Law: The properties of elements are the periodic functions of their atomic weights.

  2. Merits of Mendeleev’s Periodic Table:

    • First systematic classification of elements.

    • Corrected atomic weights of some elements.

    • Left gaps for undiscovered elements and predicted their properties.

    • Placed elements with similar properties in the same group.

  3. Drawbacks of Mendeleev’s Periodic Table:

    • Some elements with dissimilar properties were placed in the same group.

    • Position of hydrogen, lanthanoids, and actinoids was uncertain.

    • Could not explain isotopes.

    • Did not strictly follow the increasing order of atomic weights.

  4. Modern Periodic Law:
    Proposed by Moseley.
    It states that “The physical and chemical properties of elements are the periodic functions of their atomic numbers.”

  5. Modern Periodic Table:
    Elements are classified into s, p, d, and f blocks based on their electronic configurations.

    • s-block: General configuration ns¹–ns²

    • p-block: ns²np¹–ns²np⁶

    • d-block: (n–1)d¹–(n–1)d¹⁰ns⁰–ns²

    • f-block: (n–2)f¹–(n–2)f¹⁴(n–1)d⁰–(n–1)d¹ns²

  6. Periodic Trends:

    • Atomic Radius: Decreases across a period, increases down a group.

    • Ionization Energy: Increases across a period, decreases down a group.

    • Electron Affinity: Increases across a period, decreases down a group.

    • Electronegativity: Increases across a period, decreases down a group.

    • Metallic Character: Decreases across a period, increases down a group.

  7. Diagonal Relationship:
    Elements of second period show similarity with elements of third period diagonally (e.g., Li–Mg, Be–Al).

  8. Effective Nuclear Charge (Zeff):
    The net positive charge experienced by valence electrons.
    Increases across a period and decreases down a group.

  9. Periodic Table Blocks:

    • s-block: Alkali and alkaline earth metals.

    • p-block: Includes metals, nonmetals, and metalloids.

    • d-block: Transition elements.

    • f-block: Inner transition elements (lanthanoids and actinoids).


Competency enhancement Plan Class 6 to 12 Solution

Chapter 4 – Chemical Bonding

Key Points / Definitions

  1. Need for Chemical Bonding:
    Atoms combine to achieve stability by completing their octet (or duplet for H, He).
    Stable molecules form when energy is lowered through bonding.

  2. Types of Chemical Bonds:

    (a) Ionic (Electrovalent) Bond:
    Formed by transfer of electrons from a metal to a nonmetal.
    Example: NaCl, CaF₂
    Properties: Hard, brittle, high melting points, conduct electricity in molten or aqueous states.

    (b) Covalent Bond:
    Formed by sharing of electrons between nonmetal atoms.
    Example: H₂, Cl₂, CH₄
    Properties: Directional, low melting and boiling points, poor conductors.

    • Coordinate (Dative) Bond: Shared pair donated by one atom. Example: NH₄⁺, CO

    (c) Metallic Bond:
    Positive metal ions surrounded by a sea of delocalized electrons.
    Explains malleability, ductility, and conductivity.

  3. Important Theories of Bonding:

    (a) Octet Rule:
    Atoms tend to have 8 electrons in their outermost shell.
    Exceptions: H, He, Be, B, and elements with expanded octet (P, S, Xe).

    (b) VSEPR Theory (Valence Shell Electron Pair Repulsion):
    Shape of molecule depends on repulsion between electron pairs.
    Examples:

    • BeCl₂ – Linear

    • BF₃ – Trigonal planar

    • CH₄ – Tetrahedral

    • NH₃ – Pyramidal

    • H₂O – Bent

    (c) Valence Bond Theory (VBT):
    Bond forms due to overlap of half-filled orbitals.
    Explains hybridization types:

    • sp (linear)

    • sp² (trigonal planar)

    • sp³ (tetrahedral)

    • sp³d (trigonal bipyramidal)

    • sp³d² (octahedral)

    (d) Molecular Orbital Theory (MOT):
    Describes bonding in terms of molecular orbitals formed from atomic orbitals.

    • Bond order = (Nb – Na)/2
      Example: O₂ is paramagnetic.

  4. Bond Parameters:

    • Bond Length: Distance between nuclei of bonded atoms.

    • Bond Energy: Energy required to break one mole of bonds.

    • Bond Order: Indicates strength and length of bond.

    • Bond Angle: Angle between two bonds from the same atom.

  5. Polarity of Bonds:
    When two atoms have different electronegativities, the bond becomes polar (e.g., H–Cl).
    If the molecule is symmetric, overall dipole moment may be zero (e.g., CO₂).

  6. Hydrogen Bonding:
    Formed between H atom attached to N, O, or F and another electronegative atom.
    Example: H₂O, HF, NH₃.
    Responsible for high boiling points and unique properties of water.

  7. Resonance:
    When a molecule cannot be represented by a single structure.
    Example: CO₃²⁻, NO₃⁻, benzene.

  8. Hybridization Examples:

    • sp: BeCl₂

    • sp²: BF₃

    • sp³: CH₄

    • sp³d: PCl₅

    • sp³d²: SF₆

  9. Difference between Ionic and Covalent Bonds:

    Property Ionic Bond Covalent Bond
    Formation Transfer of electrons Sharing of electrons
    Type of elements Metal + Nonmetal Nonmetal + Nonmetal
    Nature Hard, brittle Soft
    Conductivity In molten/aqueous form Poor conductors
    Example NaCl CH₄
  10. Metallic Bond:
    Metal atoms release electrons to form a pool of delocalized electrons — gives rise to electrical conductivity, malleability, and metallic lustre.



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