(Jeremy Krug) AP Chem Unit 3 Review | Properties of Substances and Mixtures
Intermolecular Forces
London Dispersion Forces
Present in all molecules, typically the weakest forces.
Strength increases with larger molecules due to more electrons.
Only intermolecular force in nonpolar molecules.
Dipole-Dipole Forces
Occur between polar molecules, where the positive pole of one molecule attracts the negative pole of another.
Stronger than London dispersion forces.
Hydrogen Bonding
A special case of dipole-dipole forces, occurs when hydrogen is bonded to oxygen, nitrogen, or fluorine.
Strongest type of intermolecular force.
Ion-Dipole Forces
Occur in solutions where polar molecules (like water) interact with ions in ionic compounds.
Can cause ionic compounds to dissolve in polar solvents if the ion-dipole forces are stronger than ionic forces.
Properties of Solids
Ionic Solids
High melting points, brittle, conduct electricity when dissolved in water due to attraction between charged ions.
Covalent Network Solids
Extremely strong due to extensive covalent bonding in all directions (e.g., diamond and silicon dioxide).
Molecular Solids
Made of individual molecules with relatively weak forces, leading to lower melting points (e.g., sugar).
Metallic Solids
Composed of metals or alloys, malleable, ductile, and good conductors of electricity due to a 'sea of electrons'.
Crystalline Solids
Definition: Have a well-defined, orderly structure.
Characteristics:
Regular arrangement of particles.
Sharp melting points.
Examples: Salt, diamonds, ice
Amorphous Solids
Definition: Lack a regular arrangement of particles.
Characteristics:
No defined melting point, deform gradually when heated.
Examples: Glass, plastics, gels.
States of Matter
Solids: Particles are close together, with limited motion (only vibrational).
Liquids: Particles are further apart, allowing them to flow and slide past each other.
Gases: Particles are far apart and move independently, allowing them to expand and be compressed.
Ideal Gas Law
Formula: PV = nRT
P = pressure (atm), V = volume (L), n = number of moles, R = Universal Gas Constant (0.08206 L atm K⁻¹ mol⁻¹), T = temperature (K).
Use this equation to solve for unknown variables using provided constants.
Gas Mixtures
Partial Pressure: The total pressure is the sum of individual gas pressures; calculate the partial pressure using the mole fraction.
Temperature and Kinetic Energy
Temperature reflects the average kinetic energy of molecules; higher temperature indicates faster-moving molecules.
Use the Boltzmann distribution to visualize the range of molecular speeds at different temperatures.
Ideal vs. Real Gases
Ideal gases: No intermolecular attractions, negligible volume.
Real gases, such as helium, behave ideally under high temperature and low pressure where particle interaction is minimized.
Mixture Types
Heterogeneous Mixtures: Visible individual components.
Homogeneous Mixtures (Solutions): Uniformly distributed components; focus on molarity (M = moles of solute/L of solution).
Separating Solutions
Distillation: Capitalizes on differing boiling points to separate components by boiling and condensing.
Chromatography: Involves separation based on different adherence rates to a stationary phase, producing faster or slower passage through a mobile phase.
Solubility Principles
Rule of Thumb: "Like dissolves like"; polar vs. nonpolar solvents and solutes.
Electromagnetic Spectrum and Molecules
Different portions of the spectrum affect molecules differently:
UV/Visible Light: Causes electronic transitions.
Infrared Radiation: Causes vibrational energy changes.
Microwave Radiation: Induces rotational transitions.
Light and Photons
Dual Nature of Light: Can behave as waves and particles (photons).
Photonic Calculations:
Use c = λν (speed of light = wavelength x frequency) to relate wavelength and frequency.
Use E = hν (energy = Planck’s constant x frequency) to find energy of a photon (h = 6.626 x 10⁻³⁴ J s).
Spectrophotometry and Beer-Lambert Law
Beer-Lambert Law: A = εbc
A = absorbance, ε = molar absorptivity, b = path length, c = concentration.
Construct calibration curves to determine unknown concentrations from absorbance measurements.
Outliers: Possible contamination or dilution can lead to data points straying from the expected curve.