AP Chemistry Notes
Atoms and Molecular Geometry
- Basic Geometries
- Tetrahedral: 4 bonding pairs, 0 lone pairs, bond angle 109.5°
- Trigonal Pyramidal: 3 bonding pairs, 1 lone pair, bond angle ~109.5°
- Bent: 2 bonding pairs, 2 lone pairs, bond angle ~109.5°
- Trigonal Planar: 3 bonding pairs, 0 lone pairs, bond angle 120°
- Bent/Angular: 2 bonding pairs, 1 lone pair, bond angle ~120°
- Linear: 2 bonding pairs, 0 lone pairs, bond angle 180°
- Trigonal Bipyramidal: 5 bonding pairs, 0 lone pairs, bond angles 90° & 120°
- See-saw: 4 bonding pairs, 1 lone pair, bond angles ~90° & 120°
- T-shaped: 3 bonding pairs, 2 lone pairs
- Octahedral: 6 bonding pairs, 0 lone pairs, bond angle 90°
- Square Pyramidal: 5 bonding pairs, 1 lone pair, bond angle ~90°
- Square Planar: 4 bonding pairs, 2 lone pairs, bond angle 90°
Intermolecular Forces and Radiation
- Hydrogen Bonding: Occurs in molecules containing O-H, N-H, or F-H bonds.
- Microwave Radiation: Causes rotation of molecules.
- Infrared Radiation: Causes vibration of molecules.
- UV / Visible Radiation: Causes electrons to transition to different energy levels.
Solubility Rules
- Compounds containing Na^+, K^+, or NH_4^+ ions are always soluble in water.
- Compounds containing NO_3^- ions are always soluble in water.
Bond Enthalpies
- The change in enthalpy (\Delta H) is calculated as the sum of the enthalpies of bonds broken minus the sum of the enthalpies of bonds formed.
- \Delta H = \Sigma H{\text{bonds broken}} - \Sigma H{\text{bonds formed}}
- (LEFT SIDE - RIGHT SIDE)
Atomic Structure and Properties
- Electronegativity: The force attracting electrons (F highest).
- Ionization Energy: The energy required to lose an electron (F highest).
- Electron Affinity: The energy change after adding an electron (F-).
Bonding
- Intramolecular Bonding
- Ionic: Between metal & non-metal (e.g., Na^+Cl^-, Na^+ Cl^-).
- Covalent: Between two non-metals.
- Metallic: Between two metals (alloys). Electrons are not associated with a single atom but are "delocalized electrons" forming a "sea of electrons".
- Substitutional: Atoms of compatible radii.
- Interstitial: Atoms of different radii where smaller atoms fill spaces.
- Polar Covalent: Difference in electronegativity forms partial charges.
Intermolecular Forces and Properties
- London Dispersion Forces (LDF): Induced dipole forces due to temporary imbalances.
- Polarizability: How easy it is to polarize a molecule. Higher polarizability with larger electron cloud.
- Stronger LDF leads to higher boiling point, longer molecules/surface area, or larger molar mass.
- Dipole-Dipole: Permanent dipole.
- Hydrogen Bonds: H bonded to F, O, or N - Strongest IMFs - Highest B.P.
- Ion-Dipole
Vapor Pressure
- Lower boiling point results in higher vapor pressure.
Gas Laws
- Ideal Gas Law: (not specified in provided text)
- Molarity equation: M1V1 = M2V2
- Solubility: Like dissolves like.
- Beer-Lambert Law:
- A = \epsilon \cdot l \cdot c
- A: Absorbance, l: length, c: concentration
- Partial Pressure: P{\text{total}} = PA + PB + … = n{\text{total}} \frac{RT}{V}
Chemical Reactions
- General form: NaCl{(aq)} + AgNO{3(aq)} \rightarrow NaNO{3(aq)} + AgCl{(s)}
- Limiting Reactant
- OIL RIG (Oxidation Is Loss, Reduction Is Gain)
- Spectator Ions
- Example: Cl^-{(aq)} + Ag^+{(aq)} \rightarrow AgCl_{(s)}
- Brønsted-Lowry: Acid = H^+ donor (proton), Base = proton / H^+ acceptor.
Kinetics
- Rate Law: Rate = k[A]^x[B]^y
- Half-life follows first-order rate law.
- Use coefficients as orders only in elementary steps.
- Intermediate - created then used up.
- The rate-determining step is the slow step.
- Don't use intermediates in the rate law.
Thermodynamics
- 1 \text{ Cal} = 1 \text{ kcal} = 1000 \text{ calories}
- Calorie (food)= Cal
- Phase Changes:
- \Delta H{\text{vap}} (vaporization), \Delta H{\text{cond}} (condensation), \Delta H{\text{fus}} (fusion = melting), \Delta H{\text{freezing}} in kJ/mol - calculate mass.
- Hess's Law: \Delta H{\text{rxn}} = \Sigma \Delta H{\text{products}} - \Sigma \Delta H_{\text{reactants}}
- Bond Energy: How much energy it takes to break a bond.
- \Delta H{\text{rxn}} = \Sigma BE{\text{broken}} - \Sigma BE_{\text{formed}}
- Divide by mol of rxn if needed.
Equilibrium
- K_{eq} only changes with temperature.
- Q can be calculated at any moment to find direction.
- Le Châtelier's Principle: (not specified in provided text)
- If pressure moves away from the most gaseous side, the system equilibrates.
- If Q > K_{eq}, the reaction is oversaturated.
- Equilibrium shifts in the opposite direction.
- Common Ion Effect: Adding concentration of a common ion.
Acids and Bases
- Polyprotic acids - focus on the first equation.
- Strong acids and bases dissolve in H_2O.
- KaKb = K_w
- Don't need ICE table with acids (use concentration of strong acid).
- pKa = -\log(Ka)
- pH = pK_a @ half equivalence point = [weak acid] = [conjugate base].
- Buffer:
- pH = pK_a + \log \frac{[A^-]}{[HA]}
- Favorable at low temps if -\Delta H and +\Delta S. Unfavorable +\Delta H and -\Delta S.
- Buffers: [weak acid] & [conjugate base]