Homogeneous mixture of a solute dissolved in a solvent
Molarity
Moles of solute per liters of solution
Mass by percent
Common for dilute aqueous solutions
Mole fraction
Moles of one substance per total moles of a mixture, commonly used for gas mixtures
Molality
Doesn't change with temperature, unlike molarity
Like dissolves like
A polar solvent must be used to dissolve a polar or ionic solute
Solute-solute
Breaks bonds/IMF and is endothermic
Solvent-solvent
Breaks bonds/IMF and is endothermic
Solute-solvent
Breaks bonds/IMF and is exothermic
Oil and water don't mix
Oil has weak IMF and is non polar so the solute-solvent interactions are very weak, therefore they can't overcome solvent-solvent interactions of water
Enthalpy change
Associated with the dispersal of a solute in water
Factors that affect solubility
Structure- size, shape, polarity
Pressure-especially for gases
Temperature
Molecular structure
Determines polarity
If solute and solvent are similar
Solubility is favored
Pressure has little effect on solubility of solids or liquids
But significantly increases solubility of a gas
If pressure is increased
Gas concentration increases
Henry's law
The amount of gas dissolved is directly proportional to the pressure of gas above solution
Most solids increase solubility in water with increasing temperature
(some are opposite)
Temperature dependence of a solid's solubility can be determined only with experiment
Liquid solutions
Have different physical properties than pure solvents
Colligative property
The fact that identity of a solute is irrelevant, only how much is present matters
Colligative properties
Vapor pressure lowering
Freezing point depression
Boiling point elevation
Osmotic pressure
Vapor pressure lowering
The presence of a nonvolatile solute lowers the vapor pressure of a solvent
Raoult's law
The solute lowers the vapor pressure of a solvent
Ideal solution
A liquid-liquid solution that obeys Raoult's law
For ideal solutions, the identity of solute doesn't matter, only moles of particles matter
Solute-solute, solvent-solvent, and solute-solvent interactions are similar and not extremely strong in ideal solutions
When solvent and solute strongly attract
Solvent molecules cannot turn to vapor as easily
When solvent and solute very weakly attract
Solvent molecules can turn to vapor more easily
Colligative properties want to be as dilute as possible
Boiling point elevation
A nonvolatile solute lowers vapor pressure of solvent, increasing boiling point
Freezing point depression
Freezing point of solutions are lower than that of pure solvent
Osmotic pressure
Excess pressure on solution arises because of difference in liquid levels
Osmosis
The flow of solvent into a solution through semi-permeable membrane that separates them
Small concentrations of solution produce relatively large osmotic pressures and can characterize solutions and determine molar mass
Isotonic solutions
Have ideal osmotic pressures
Van't Hoff Factor (i)
The number of particles a solute breaks into
To determine I, count the number of ions in a salt's formula (expected value)