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AP Chemistry Speed Review
Jul 11, 2024
AP Chemistry Speed Review
Introduction
Presenter:
Jeremy Krug
Goal:
Quick review of major AP Chemistry topics in under 20 minutes
Resources:
Ultimate Review Packet offers more detailed study guides, longer review videos, and practice exams for $24.99 with potential discounts for classroom purchases
Unit 1: Atoms
Mole Concept:
Counts atoms/molecules; 1 mole = 6.022 x 10^23 particles
Example: 1 mole of iron is 55.85 grams, 1 mole of water is 18.02 grams
Electron Configurations:
Atoms are most stable with 8 valence electrons
Example: Neon - 1s2, 2s2, 2p6
Coulomb’s Law:
Attraction strength between opposite charges
Greater magnitude of charge and closer distance increase attraction
Applications in photoelectron spectroscopy
Periodic Table Patterns:
Atomic radius: larger at the bottom/left
First ionization energy: higher at top/right
Formation of anions/cations: Anions (gain e-) get larger, cations (lose e-) get smaller
Unit 2: Chemical Compounds
Bonds:
Ionic: Metal + Nonmetal, electrostatic forces
Covalent: Nonmetals share electrons
Polar: Unequal sharing
Nonpolar: Equal sharing
Metallic: Electrons move freely in metals/alloys
Lewis Dot Diagrams:
Visualize shapes and electron distribution
Examples: Tetrahedral (109.5°), Linear (180°), Trigonal planar (120°)
Unit 3: Intermolecular Forces
Dispersion Forces:
Weak, increase with molecule size/polarizability
Dipole-Dipole Forces:
Stronger than dispersion, in polar molecules
Hydrogen Bonding:
Strong, in molecules with O-H, N-H, F-H bonds
States of Matter:
Solids: Fixed shape/volume
Liquids: Flow, fixed volume
Gases: Expand/compress easily
Ideal Gas Law:
PV=nRT; approximates gas behavior
Real gases deviate under certain conditions
Kinetic Energy & Temperature:
Higher temperature = higher average kinetic energy
Concentration Measurement:
Molarity (moles/solute divided by liters/solution)
Light and Matter:
Interaction used in spectrophotometry for concentration analysis
Unit 4: Chemical Reactions
Net Ionic Equations:
Exclude spectator ions
Balancing Equations:
Ensure atom count consistency using coefficients
Types of Reactions:
Precipitation: Formation of solid in solution
Redox: Electron transfer (oxidation/reduction)
Acid-Base: Proton transfer, acid donates H+, base accepts H+
Stoichiometry:
Mole ratio from balanced equations to calculate quantities
Unit 5: Kinetics
Relative Rates:
Based on balanced equation coefficients
Rate Law:
Experimentally determined, Rate = k[Reactant1]^order[Reactant2]^order...
Zero/First/Second-Order Relationships
Integrated Rate Law:
Calculate concentration over time
Reaction Mechanisms:
Multi-step processes with a rate-determining slow step
Collision Theory:
Reactions depend on energy/orientation of collisions
Catalysts:
Lower activation energy, speed up reactions
Unit 6: Thermodynamics
Endothermic vs Exothermic:
Absorb/release heat
Heat Transfer:
Q = MC∆T
Q (Joules), M (mass), C (specific heat capacity), ∆T (temperature change)
Enthalpy Change (∆H):
Reaction heat change, estimated using bond enthalpies or formation enthalpies
Hess’s Law:
Summing individual reaction enthalpies for overall reaction
Unit 7: Equilibrium
Dynamic Equilibrium:
Forward and reverse reactions at equal rates
Reaction Quotient (Q) & Equilibrium Constant (K):
Determines reaction direction
Large K: More product; Small K: More reactant
ICE Charts:
Initial, Change, Equilibrium concentrations for solving equilibrium problems
Le Chatelier’s Principle:
Predicts reaction shift due to changes; only temperature changes K
Unit 8: Acids and Bases
pH and pOH:
pH = -log[H+], pOH = -log[OH-]
pH + pOH = 14 at 25°C
[H+][OH-] = 1 x 10^-14 at 25°C (Kw)
Strong vs Weak Acids/Bases:
Complete vs partial ionization
Acid-Base Titrations:
Find unknown concentration, endpoints identified by indicator
Titration curve inflection point = equivalence point
Buffers:
Resist pH changes, use Henderson-Hasselbalch equation for pH calculation
Unit 9: Applications of Thermodynamics
Entropy (S):
Disorder measurement, increases from solid to gas
Gibbs Free Energy (ΔG):
Determines thermodynamic favorability
ΔG = ΔH - T∆S; negative ΔG is favorable
ΔG related to equilibrium constant K: ΔG = -RTlnK
Electrochemistry:
Galvanic cells, electron flow, salt bridges
Anode (oxidation) and Cathode (reduction)
Calculate cell voltage using standard reduction potentials
Use Nernst Equation for non-standard conditions
Electrolysis:
Uses external electricity to drive non-spontaneous reactions
I = Q/t; relate coulombs to quantity of material plated
Conclusion:
Comprehensive overview of AP Chemistry major topics
For detailed resources, visit Ultimate Review Packet
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