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Core Chemistry Concepts

Sep 28, 2025

Overview

This lecture reviews core topics from AP Chemistry Unit 2: Compound Structure and Properties, focusing on chemical bonding, molecular structure, polarity, Lewis diagrams, lattice energy, and related trends for the summative assessment.

Types of Chemical Bonds and Polarity

  • Electronegativity increases left to right and decreases top to bottom in the periodic table.
  • Polar covalent bonds form when atoms with unequal electronegativity share electrons; the more electronegative atom gets a partial negative charge.
  • The bond with the largest electronegativity difference (e.g., Ge–O) has the greatest dipole moment.
  • Bonds between identical atoms (e.g., C–C) have no dipole moment (zero polarity).

Potential Energy Curves and Bond Strength

  • Bond length corresponds to the minimum potential energy between two atoms.
  • Bond energy is the energy required to break the bond, always reported as a positive value.
  • Shorter bonds (smaller atoms or higher bond order) have higher bond energies.
  • If two atoms are closer (smaller atomic radius), more energy is needed to break their bond.

Ionic vs. Covalent Compounds

  • Ionic compounds form between metals and nonmetals, have high melting points, are solid at room temp, and conduct electricity when molten or dissolved.
  • Covalent (molecular) compounds form between nonmetals, often have lower melting points, and do not conduct electricity.

Lewis Structures, Bond Order, and Resonance

  • Lewis diagrams require correct valence electron counts, bonds, and lone pairs to satisfy octets when possible.
  • Multiple bonds (double/triple) may be needed when there are not enough electrons for octets.
  • Higher bond order correlates with higher bond energy (triple > double > single bond).
  • Resonance structures share electron pairs among multiple positions; bond order may be fractional (e.g., 1.5).

Lattice Energy and Coulomb’s Law

  • Lattice energy increases with higher ionic charge and decreases with increased ionic radius.
  • Stronger attractions (smaller ions, higher charge) mean higher lattice energies and more difficult separation.

Molecular Geometry and Polarity

  • Electron domains determine geometry: 4 domains = tetrahedral (109.5°), 3 = trigonal planar (120°), 2 = linear (180°).
  • Lone pairs increase repulsion, reducing bond angles (e.g., NH3 bond angle < CH4).
  • Polar molecules have asymmetric electron distributions or different terminal atoms; nonpolar molecules are symmetric and have identical outer atoms.

Alloys and Steel Structure

  • Interstitial alloys form when small atoms fit between larger atoms; steel (Fe and C) is interstitial.
  • Higher carbon content in steel increases rigidity by obstructing atom movement.

Formal Charge and Preferred Lewis Structures

  • Assign formal charge: valence electrons – (dots + bonds).
  • Most preferred structure has the smallest charges and places negative charge on the most electronegative atom.

Counting Sigma and Pi Bonds

  • Single bond: 1 sigma.
  • Double bond: 1 sigma, 1 pi.
  • Triple bond: 1 sigma, 2 pi.

Key Terms & Definitions

  • Electronegativity — measure of an atom’s ability to attract electrons.
  • Dipole Moment — separation of charges in a bond or molecule.
  • Bond Order — number of shared electron pairs between atoms.
  • Lattice Energy — energy required to separate one mole of an ionic solid into gaseous ions.
  • Resonance — delocalization of electrons across multiple structures.
  • Sigma Bond — the first covalent bond between two atoms.
  • Pi Bond — additional bonds in double/triple bond situations.
  • Interstitial Alloy — alloy with smaller atoms filling spaces between larger atoms.
  • Formal Charge — calculated charge on atoms in a Lewis structure.

Action Items / Next Steps

  • Review periodic trends and how they affect bonding.
  • Practice drawing Lewis structures and identifying molecular shapes.
  • Study resonance and formal charge to determine preferred Lewis structures.
  • Complete and check assigned packet problems for Unit 2.