AP Chemistry Unit 3 Cheat Sheet: Intermolecular Forces & Properties
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AP Chemistry Unit 3: Intermolecular Forces & Properties
TLDR
Understand London dispersion, dipole–dipole, hydrogen bonding, and ion–dipole forces.
Stronger IMFs → higher boiling point, melting point, viscosity, and surface tension.
Weaker IMFs → higher vapor pressure and faster evaporation.
Master boiling point trends, solubility rules, phase diagrams, and Clausius–Clapeyron.
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Why This Unit Matters
Many AP Chemistry questions ask you to compare substances or justify why one boils, evaporates, dissolves, or condenses faster than another.
The secret: it all comes down to IMFs.
Intermolecular forces explain real-world behavior — why oil and water don’t mix, why water has unusually high boiling point, why ionic compounds dissolve in water, and even why ice floats.
Master this unit and you gain a powerful lens for predicting physical properties throughout the entire course.
1. The Four Types of Intermolecular Forces
London Dispersion Forces (LDF)
Present in all molecules and atoms.
Weakest IMF; strength increases with molar mass and surface area.
Larger electron clouds → easier to polarize → stronger LDFs.
Examples: I₂ > Br₂ > Cl₂ > F₂ in IMF strength.
Dipole–Dipole Forces
Occur between polar molecules with permanent dipoles.
Stronger dipole moment → stronger interaction.
You must know how to determine molecular polarity from shape.
Hydrogen Bonding
A special, very strong dipole interaction.
Occurs when H is bonded to N, O, or F.
Responsible for water’s high boiling point and ice’s structure.
Ion–Dipole Interactions
Between ions and polar molecules (ex. Na⁺–H₂O).
Key for understanding why ionic compounds dissolve in water.
Mnemonic: “London → Dipole → H-bond → Ionic” (weak to strong).
2. Forces & Properties
Stronger intermolecular forces lead to:
Higher boiling point
Higher melting point
Higher viscosity
Higher surface tension
Lower vapor pressure
Weaker IMFs → liquids evaporate more easily.
Mnemonic: “IMFs climb, vapor pressure dives.”
3. Solubility & Miscibility
“Like dissolves like”:
Polar dissolves polar
Nonpolar dissolves nonpolar
Ion–dipole interactions explain why salts dissolve in water.
Network solids (diamond, SiO₂) do not dissolve because they have covalent bonds, not IMFs.
4. Vapor Pressure, Boiling Point & Phase Changes
Vapor pressure: pressure exerted by molecules escaping liquid surface.
High IMFs → fewer molecules escape → low vapor pressure.
Boiling point = when vapor pressure equals external pressure.
Key Equation (Clausius–Clapeyron):
ln(P₁/P₂) = −(ΔHvap / R)(1/T₁ − 1/T₂)
Used for comparing vapor pressures at different temperatures.
Phase Change Energy:
Heating within a phase: q = mCΔT
Phase change: q = nΔHvap or q = nΔHfus
5. Phase Diagrams
Show relationship between P and T for solid, liquid, gas.
Triple point: all 3 phases coexist.
Critical point: above this, liquid and gas become indistinguishable.
Water’s solid–liquid line slopes backward → ice is less dense than liquid water.
Mnemonic: “Triple touch, Critical climb.”
6. Solids & Crystal Types
Ionic solids: high melting, brittle, conductive when molten.
Molecular solids: low melting, weak IMFs.
Metallic solids: malleable, ductile, conductive.
Network covalent: extremely high melting (C, SiO₂).
Strength order: Network > Ionic > Metallic > Molecular.
7. Chromatography & IMF Application
Chromatography separates based on polarity and IMF strength.
If stationary phase is polar → polar molecules stick more, travel slower.
Rf = distance solute / distance solvent front.
High Rf = weak IMF with stationary phase.
Common Pitfalls
Confusing intermolecular forces (between molecules) and intramolecular bonds (within a molecule).
Thinking hydrogen bonding occurs with any H — it must be H–N, H–O, or H–F.
Assuming strong IMFs → high vapor pressure (it’s the opposite).
Forgetting that network solids have covalent bonds, not IMFs.
Misidentifying molecular polarity because of incorrect geometry.
Tutor Tip
Before answering any property question, ask:
What IMFs does this molecule have, and how strong are they?
This single step accurately predicts boiling point, melting point, vapor pressure, solubility, and even chromatography behavior.
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