Colligative properties depend only on the number of solute particles and not their identity. They include vapor pressure lowering, boiling point elevation, and freezing point depression. Electrolytes produce a greater effect than nonelectrolytes of the same concentration due to dissociation into ions. To determine molar mass, use the colligative property change to calculate molality and then moles of solute.
Colligative properties depend only on the number of solute particles and not their identity. They include vapor pressure lowering, boiling point elevation, and freezing point depression. Electrolytes produce a greater effect than nonelectrolytes of the same concentration due to dissociation into ions. To determine molar mass, use the colligative property change to calculate molality and then moles of solute.
Colligative properties depend only on the number of solute particles and not their identity. They include vapor pressure lowering, boiling point elevation, and freezing point depression. Electrolytes produce a greater effect than nonelectrolytes of the same concentration due to dissociation into ions. To determine molar mass, use the colligative property change to calculate molality and then moles of solute.
on the number and not on the identity of the solute particles. • Thus, these depend on the collective effect of the concentration of solute particles present in an ideal solution. Colligative Properties
• Because of their direct relationship to the
number of solute particles, the colligative properties are very useful for characterizing the nature of a solute after it is dissolved in a solvent and for determining the molar masses of substances Effect of solute concentration on the colligative properties of solutions
• The effect would depend on the ratio of the number of
particles of solute and solvent in the solution and not on the identity of the solute. • However, it is necessary to take into account whether the solute is an electrolyte or a nonelectrolyte. NONVOLATILE SOLUTE • Vapor pressure is a direct measure of escaping tendency of molecules. • A pure liquid (solvent) in a closed container will establish equilibrium with 1) VAPOR PRESSURE its vapor. And when that equilibrium is LOWERING reached, the pressure exerted by the vapor is called the vapor pressure. • A substance that has no measurable vapor pressure is nonvolatile, while one that exhibits a vapor pressure is volatile. NOTE:
• The addition of a nonvolatile solute resulted to a lowering of the
vapor pressure of the solvent. • The lowering of the vapor pressure depends on the number of solute particles that have been dissolved. The chemical nature of the solute is not considered because vapor pressure is merely a physical property of the solvent and does not undergo a chemical reaction with the solvent and does not itself escape into the gas phase. When a liquid evaporates easily, it will have a large number of its molecules in the gas phase resulting to a high vapor pressure. MOLE FRACTION SAMPLE PROBLEM 1:
Calculate the vapor pressure of a
solution made by dissolving 50.0 g glucose, C6H12O6, in 500 g of water. The vapor pressure of pure water is 47.1 torr at 37°C SAMPLE PROBLEM 2:
The vapor pressure of an aqueous solution
is found to be 24.90 mmHg at 25 °C. What is the mole fraction of solute in this solution? The vapor pressure of water is 25.756 mm Hg at 25 °C. ELECTROLYTE VS. NONELECTROLYTE While the chemical nature of the solute is not a factor to consider, it is important to take into consideration whether the solute is an electrolyte or nonelectrolyte. STRONG ELECTROLYTES
• Ionic compounds like sodium chloride, NaCl,
are strong electrolytes that dissociate into ions when they dissolve in solution results in a larger number of dissolved particles. Consider two different solutions of equal concentration: one is made from ionic compound NaCl, while the other is made from the molecular compound glucose (C6H12O6). The equations below show what happens when these solutions dissolve : • The sodium chloride, NaCl dissociates into 2 ions, while glucose does not dissociate. Thus, equal concentrations of each solution will result in twice as many dissolved particles as in the case of NaCl. • The vapor pressure of the solvent in NaCl solution (electrolyte) will be lowered twice as much as that of the solvent in the glucose (nonelectrolyte) solution. • Since the surface now of salt solution is covered by more solute particles, there is less room for solvent molecules to evaporate lowering the vapor pressure of the solvent, water. 2) BOILING POINT ELEVATION
The addition of a nonvolatile solute
lowers the vapor pressure of the solution; consequently the temperature must be raised to restore the vapor pressure of the solution to the value conforming to the pure solvent. Specifically, the temperature at which the vapor pressure is 1 atm will be higher than the normal boiling point by an amount known as the boiling point elevation. The figure shows the phase diagram of a solution and the effect that the lowered vapor pressure has on the boiling point of the solution compared to the solvent. In this case the sucrose solution has a higher boiling point than the pure solvent. Since the vapor of the solution is lower, more heat must be supplied to the solution to bring its vapor pressure up to the pressure of the external atmosphere. The boiling point elevation is the difference in temperature between the boiling point of the pure solvent and that of the solution. BOILING POINT ELEVATION SAMPLE PROBLEM 1:
Calculate the boiling point of a solution
containing 5g sucrose C12H22O11 dissolved in 180 g of water H2O. The mass of solute (5g) is given which is dissolved in 180 g of solvent, water H2O. (Kb of H2O= 0.512°C/m, Normal boiling point of water = 100°C) SAMPLE PROBLEM 2:
What is the new boiling point of a
solution prepared by adding 85.0 g of sodium chloride (NaCl) to 356 g of water? The boiling point constant for water is 0.52 °C kg/mol. The freezing point of a substance is the temperature at which the solid and liquid forms can coexist indefinitely, at 3) FREEZING POINT equilibrium. Under these conditions DEPRESSION molecules pass between the 2 phases at equal rates because their escaping tendencies from the two phases are identical. The figure shows the phase diagram for a pure solvent and how it changes when a solute is added to it. The solute lowers the vapor pressure of the solvent resulting in a lower freezing point for the solution compared to the pure solvent. The freezing point depression is the difference in temperature between the freezing point of a pure solvent and that of a solution. On the graph, Tf represents the freezing point depression. SAMPLE PROBLEM 1:
What is the freezing point depression
when 62.5 g of toluene (C7H8) is dissolved in 477 g of naphthalene (C10H8)? The freezing point constant for naphthalene is 7.00 °C/m. SAMPLE PROBLEM 2:
Determine the freezing point of a
solution of 10.0g Urea, CO(NH2)2, in 2.50 x 102 g of water. The normal freezing point of water is 0°C and Kf = 1.86°C/m HOW TO CALCULATE THE MOLAR MASS OF A SOLUTE FROM FREEZING POINT DEPRESSION OR BOILING POINT ELEVATION DATA STEPS
Step 1: Calculate molality from m= ΔTf/Kf or m = ΔTb/Kb.
Express as mol solute/kg solvent. Step 2: Using molality as a conversion factor between moles of solute and kilograms of solvent, find the number of moles of solute. Step 3: Use the defining equation for molar mass, MM ≡ g/mol, to calculate the molar mass of the solute. SAMPLE PROBLEM 1
What is the molecular mass of an organic
compound if 15.0 g of the compound is dissolved in 220.0 g of carbon tetrachloride (CCl4) raising the boiling point to 84.36˚C? Boiling point of carbon tetrachloride is 76.72˚C, Kb for CCl4 = 5.02˚C/m. SAMPLE PROBLEM 2
How many grams of Pyrazine (C4H4N2)
would have to be dissolved in 2 kg of carbon tetrachloride (CCl4) to lower the freezing point by 5.6°C? The freezing point constant for carbon tetrachloride is 30.0°C/m.