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vapor pressure
pressure exerted by gas in equilibrium w/ liquid phase at given temp
volatile
having significant vapor pressure at given temp
higher vapor pressure = more volatile
presence of nonvolatile solute
affects rate of evaporation, decreases vapor pressure of solution compared to pure solvent
Raoult’s Law
Psolution = xsolventPsolevent
vapor pressure of volatile solvent lowered by presence of nonvolatile solute
more nonvolatile solute particles = lower vapor pressure of solution
Boiling Point Elevation
decrease in vapor pressure of solution of pure substance at all temperatures corresponds to increase in boiling point
Freezing point depression
solutions freeze at lower temperatures than pure solvents
molality
m=\frac{n_{solute}}{\operatorname{kg}solvent}
used when calculating boiling point elevation/freezing point depression
hypertonic (osmosis)
higher concentration of solutes inside
net osmotic flow out = cell shrinks
isotonic (osmosis)
match in concentration
no net osmotic flow = no change in cell
hypotonic (osmosis)
lower concentration inside cell
net osmotic flow into cell = cell expands
colligative property
characteristics of solutions depending on concentration
osmotic pressure
II = iMRT
M = total molar concentration
R = gas law constant
T = absolue temp
van’t Hoff Factor
ratio of concentrations of solute particles : concentration of potential particles if solute didn’t dissociate
ion pair (van’t Hoff)
cluster formed when cation & anion associate w/ each other
desalination (reverse osmosis)
process involving removing most ions from seawater
Henry’s Law
C_{gas}=k_{H}P_{gas}
Cgas → maximum concentration of gas
kH → constant for gas
Pgas → partial pressure of gas