Difference between Intramolecular and Intermolecular Forces:
Intramolecular Forces:
Forces that hold atoms together within a molecule.
Types include:
Covalent bonding
Ionic bonding
Metallic bonding
Generally stronger than intermolecular forces (IMF).
Intermolecular Forces (IMF):
Attractions between molecules.
Weaker than intramolecular forces with varying strengths.
Strength hierarchy:
London Dispersion Forces < Dipole-Dipole < Hydrogen Bonding < Ion-Dipole < Covalent < Ionic < Metallic
Stronger IMF lead to:
Higher melting/freezing/boiling points
Higher viscosity
Greater surface tension
Higher enthalpies of fusion, vaporization, sublimation
Lower vapor pressure
Important Concepts:
Lewis Structure: Key to understanding molecular structure and behavior.
London Dispersion Forces:
Weakest IMF, present in all molecules.
Caused by temporary dipoles due to electron movement.
Strength increases with molecular weight due to greater polarization potential.
Dipole-Dipole Interactions:
Occur between polar molecules.
Positive end of one molecule attracts the negative end of another.
Hydrogen Bonds:
Special case of dipole-dipole interaction.
Involves hydrogen atoms bonded to highly electronegative atoms (N, O, F).
Stronger than regular dipole-dipole interactions.
Ion-Dipole Forces:
Interactions between an ion and a polar molecule, crucial in solvation.
Collective Terms:
Dipole-induced dipoles and London Dispersion forces are referred to as Van der Waals forces.
Instantaneous dipoles can form when nonpolar molecules are close together.
Phase Diagrams: Understand how temperature and pressure affect phases.
Endothermic vs Exothermic Processes:
Endothermic: Absorbs heat. e.g., Solid → Liquid → Gas (bond breaking).
Exothermic: Releases heat. e.g., Gas → Liquid → Solid (bond forming).
Clausius-Clapeyron Equation:
R = 8.314 ext{ J/mol*K}
Pressure (P) is directly related to temperature during phase changes.
Temperature Change:
Q=mc\Delta T
where:
m = mass
c = specific heat
\Delta T = final temp - initial temp
Phase Change:
Q=m\cdot\Delta H
Remember the signs:
Endothermic: positive \Delta H
Exothermic: negative \Delta H
Types of \Delta H : Fusion, Evaporation, Sublimation.
Volume Calculation:
V=\left(edge\cdot leng\operatorname{th}\right)^3\left(a^3\right)
1 Å = 10^{-10} m
1 m = 10^{12} pm
"Like Dissolves Like" Principle:
Polar solvents dissolve polar solutes, nonpolar solvents dissolve nonpolar solutes.
Requires breaking solute-solute and solvent-solvent interactions.
Enthalpy of Solution:
riangle H{soln} = riangle H1 + riangle H2 + riangle H3
Solubility Factors:
Solids: Higher temperature increases solubility.
Gases: Higher pressure increases solubility; lower temperature helps gas solubility as well.
Henry’s Law Equation:
C=kP
where:
C = concentration of gas (M)
P = partial pressure (atm)
k = Henry’s law constant (M/atm).
Molarity (M):
=molesofsolute/litersofsolution
Molality (m):
=molesofsolute/kilogramsofsolvent
Volume Percent (%v/v):
=volumeofsolute/volumeofsolution*100
Weight Percent (%w/w):
=massofsolute/massofsolution*100
Weight by Volume Percent (%w/v):
=massofsolute/volumeofsolution*100
Mole Fraction (X):
=molesofsolute/molesoftotalsolution
ppm and ppb:
ppm=milligramsofsolute/litersofsolution
ppb=microgramsofsolute/litersofsolution
Types:
Vapor pressure lowering
Boiling point elevation
Freezing point depression
Osmotic pressure
Calculations for water:
New boiling point: 100+\Delta T
New freezing point: 0-\Delta T
Van 't Hoff Factor (i):
Number of particles a solute breaks into upon dissolving.
Effect of Concentration:
Higher concentration leads to higher boiling points, lower freezing points, lower vapor pressures, and higher osmotic pressure.
Definition:
A suspension of tiny particles in a medium (not dissolving).
Intermediate between homogeneous and heterogeneous mixtures.
Particle size: 10^3 to 10^6
Coagulation:
Process where a colloid is destroyed, typically by heating or adding an electrolyte.