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Notes on Relative Strengths of Interparticle Forces (Unit 10 Part 2)

Covalent Bonds

  • The strongest interparticle forces among common types. They hold atoms together in networks or within molecules.
  • Evidence of strength: water boils after covalent bonds within water break; hydrogen bonds break before O–H covalent bonds do.
  • We will not rank covalent bonds across different covalent-network substances.

Relative Strengths – Quick Summary

  • Covalent bonds → strongest
  • Ionic bonds
  • Metallic bonds
  • Strong hydrogen bonds
  • Dipole-dipole forces (DDF)
  • London dispersion forces (LDF)
  • Weakest overall
  • Reminder: "charge" and "distance" are recurring themes in comparing strengths.

Ionic Bonds – Key Rules

  • Strength grows with higher ion charges: strength ∝ product of charges |q{ ext{cation}}| imes|q{ ext{anion}}|.
    • Example: Na⁺–NO₃⁻: $(1)(1)=1$; Ca²⁺–S²⁻: $(2)(2)=4$; Fe²⁺–S²⁻: $(2)(2)=4$; Al³⁺–O²⁻: $(3)(2)=6$.
  • When charges are the same in two compounds, the bond is stronger for the compound with smaller ions (shorter distance).
    • Compare radii of cations and anions; smaller radii → ions closer together → stronger ionic bond.
  • Polyatomic ions: sketch likely structure to estimate sizes for comparison.

Example #1: CaS vs MgO

  • Charges: both have +2 and -2 → product = 4 (same).
  • Cation radii: Ca²⁺ larger than Mg²⁺; Anion radii: S²⁻ larger than O²⁻.
  • Result: MgO ions are smaller → ionic bond stronger in MgO.
  • Evidence: MgO mp = 2852^\circ\mathrm{C} vs CaS mp = 2525^\circ\mathrm{C}.

Example #2: KCl vs KClO₃

  • Charges: +1 and -1 → product = 1 (same).
  • Cations: same (K⁺).
  • Anions: Cl⁻ vs ClO₃⁻; Cl⁻ is smaller.
  • Predicted strength: KCl stronger than KClO₃.
  • Evidence: mp(KCl) = 770^\circ\mathrm{C}; mp(KClO_3) = 356^\circ\mathrm{C}.

Metallic Bonds – Key Rules

  • Forces arise from cations in a sea of delocalized electrons.
  • What differs among metals: cation charge, number of delocalized electrons, and cation radius.
  • General trend: higher cation charges and more delocalized electrons → stronger metallic bonding; smaller cation radii can contribute.
  • Common charges (example set):
    • K: +1
    • Ca: +2
    • Cr: +3
  • Predicted metallic bond strength (relative): K < Ca < Cr.

London Dispersion Forces (LDF) – Key Rules

  • Strength increases with size of atoms/molecules (more electrons → larger electron cloud → stronger instantaneous dipoles).
  • Shape/surface area matters: more surface area → stronger LDF.
  • For a set of nonpolar molecules with the same formula, larger molecules have stronger LDF and higher mp/bp.
  • Typical ranking for a group like H₂, F₂, Cl₂, Br₂, I₂: H₂ < F₂ < Cl₂ < Br₂ < I₂ (weakest to strongest LDF).
  • Physical state at room temperature often follows size: H₂, F₂, Cl₂: gas; Br₂: liquid; I₂: solid (as size increases).

London Dispersion vs Polarity in Polar Molecules

  • Dipole-dipole forces (DDF) are stronger for more polar molecules.
  • Polar molecules also have LDF; the dominant interaction depends on size and polarity.
  • Rules of thumb:
    • If two molecules are similar in size (LDF similar) but differ in polarity, DDF can dominate.
    • If molecule sizes differ (one much larger) and polarity differs, LDF often dominates.
  • Example: NF₃ vs CHF₃
    • Molar masses: NF₃ (71) vs CHF₃ (70); LDF strength similar; CHF₃ is more polar (DDF stronger); Boiling points reflect this (CHF₃ bp higher).
  • Example: PF₃ vs PCl₃
    • PF₃ is smaller and more polar (DDF stronger); PCl₃ is larger (LDF stronger); Boiling point data show LDF can dominate when size difference is significant.
  • Example: HF vs HCl/HBr/HI
    • HF forms hydrogen bonds, which are much stronger than typical DDF or LDF, yielding a much higher boiling point (HF bp ≈ 19 °C, much higher than the others).

Practical Takeaways for Quick Recall

  • Strength order (strongest to weakest): Covalent bonds > Ionic bonds > Metallic bonds > Hydrogen bonds > Dipole-dipole forces > London dispersion forces.
  • For ionic compounds: higher charges and smaller ion radii generally yield stronger bonds; use charge product and ion sizes to compare.
  • For metallic bonds: higher cation charges and more delocalized electrons strengthen the bond; cation radius also plays a role.
  • For nonpolar molecules: larger size and greater surface area → stronger LDF and higher mp/bp.
  • For polar molecules: compare DDF vs LDF by size and polarity; hydrogen bonding can override other forces (HF example).

Flow Chart and Practice Context (Study Aid)

  • A flow chart exists to determine whether a substance is metallic, ionic, covalent-network, or molecular, and to identify the IPF (LDF, DDF, H-bonding, etc.).
  • Practice problems help apply these rules to rank seven substances from strongest to weakest IPF.

What’s Next

  • Next presentation covers Properties Related to Interparticle Force Strength.
  • For extra practice: Unit 10 – Part 3: Properties Related to Interparticle Force Strength and Q&A Sheet #17, problems 16-33.