Since these properties depend on the number of particles dissolved, solutions of electrolytes (which dissociate in solution) should show greater changes than those of nonelectrolytes.
However, a 1 M solution of NaCl does not show twice the change in freezing point that a 1 M solution of methanol does.
(a) A cell placed in an isotonic solution. The net movement of water in and out of the cell is zero because the concentration of solutes inside and outside the cell is the same.
Colligative Properties
1. Boiling Point Elevation – The increase in boiling point of a solution relative to that of the pure solvent is directly proportional to the number of solute particles per mole of solvent molecules. That is,
DTb = i Kb m
where DTb = increase in boiling point relative to that of the pure solvent, Kb is called the molal boiling point elevation constant, and m = molality of the solution.
2. Freezing Point Depression – Like the boiling point elevation, the decrease in freezing point of a solution relative to that of the pure solvent is directly proportional to the molality of the solute. That is, DTf = iKf m
where DTf = decrease in freezing point relative to that of the pure solvent, Kf is called the molal freezing point depression constant, and m = molality of the solution.
Nonvolatile solute-solvent interactions also cause solutions to have higher boiling points and lower freezing points than the pure solvent.
DTb = (Tb -Tb°) = i ·m ·kb
Where, DTb = BP. Elevation
Tb = BP of solvent in solution
Tb° = BP of pure solvent
m = molality , kb = BP Constant
PA = XAP°A
where
NOTE: This is one of those times when you want to make sure you have the vapor pressure of the solvent.
PA = cAP°A
PA = vapour pressure of solvent A above the solution
cA = mole fraction of the solvent A in the solution
P°A = vapour pressure of pure solvent A
Because of solute-solvent intermolecular attraction, higher concentrations of nonvolatile solutes make it harder for solvent to escape to the vapor phase.
Therefore, the vapor pressure of a solution is lower than that of the pure solvent.
Colligative properties depend on the number of particles rather than their nature