Some Factors Affecting Solubility Solubility
The amount of solute per unit of solvent needed to form a saturated solution
MiscibleMutually soluble in all proportions
Effect of Temperature on Solubility
1. Most solid substances become more soluble as temperature rises2. Most gases become less soluble as temperature rises
Some Factors Affecting Solubility
Effect of Pressure on Solubility
1. No effect on liquids or solids
2. The solubility of a gas in a liquid at a given temperature is directly proportional to the partial pressure of the gas over the solution, @ 25°C
Henry’s Law solubility = k x P
k = constant characteristic of specific gas, mol/Latm
P = partial pressure of the gas over the sol’n
Some Factors Affecting Solubility
a) Equal numbers of gas molecules escaping liquid and returning to liquid
b) Increase pressure, increase # of gas molecules returning to liquid, solubility increases
c) A new equilibrium is reached, where the #’s of escaping = #
of returning
Example 9
Which of the following will become less soluble in water as the temperature is increased?
1) NaOH(s)
2) CO2(g)
Example 10
The solubility of CO2 in water is 3.2 x 10-2 M @
25°C and 1 atm pressure. What is the Henry’s-Law constant for CO2 in mol/L atm?
solubility = k x P
Physical Behavior of Solutions: Colligative Properties
• H2O b.p. 100.0o C f.p. 0.0o C
• 1.00 m NaCl b.p. 101.0o C f.p. -3.7o C
o
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Colligative properties:
Properties that depend on the amount of a dissolved solute but not on its chemical identity
There are four main colligative properties:1. Vapor pressure lowering2. Freezing point depression3. Boiling point elevation4. Osmosis:
The vapor pressure of a solution is different from the vapor of the pure solvent.
Two different cases:
1. solute is non-volatilesolute has no vapor pressure of its ownexample: dissolving a solidvapor pressure of the solution is always lower than that of the pure solvent
2. solute is volatile solute has its own vapor pressureexample: mixing 2 liquids vapor pressure of the mixture is intermediate between the vapor pressures of the two pure liquids
Vapor-pressure Lowering of Solutions: Raoult’s Law
• Solutions with a Nonvolatile Solute
If the solute is nonvolatile and has no appreciable vapor pressure of its own (solid dissolved) the vapor pressure of the solution is always lower that that of the pure solvent.
Solutions with a Nonvolatile Solute!!!
Raoult’s Law: Psoln = Psolv · Xsolv
Psoln = vapor pressure of the solution
Psolv = vapor pressure of the pure solvent
Xsolv = mole fraction of the solvent in the solution
Vapor pressure lowering is a colligative property (only dependent on amount of solute and not on its chemical identity!) For ionic substances calculate the total moles of solute particles,
1 mol NaCl will result in 1 mol Na+ and 1 mol Cl- = 2 moles of particles
1 mol Na2SO4 will give 3 moles of particles
Raoult’s Law applies to only Ideal solutions
1. Law works best when solute concentrations are low an d when solute and solvent particles have similar intermolecular forces.
2. Further complication is that at higher concentrationsionic compounds are not 100% dissociated.
Example1 mol NaCl is only 90% dissociated
10% is undissociated
resulting in less particles in solution than expected
Example 9
What is the vapor pressure (in mm Hg) of a solution prepared by dissolving 5.00 g of benzoic acid (C7H6O2) in 100.00 g of ethyl alcohol (C2H6O) at
35°C? The vapor pressure of the pure ethyl alcohol at 35°C is 100.5 mm Hg
Psoln = Psolv · Xsolv MM C7H6O2 = 122.12 g/mol
Psolv = 100.5 mm Hg MM C2H6O = 46.07 g/mol
1mol
a) 5 g C7H6O2 x ---------- = 0.0409 mol 122.12g
b) 100 g C2H6O x 1 mol/ 46.07 g = 2.17 mol
c) Xsolv = 2.17 mol / (0.0409 + 2.17 mol) = 0.982
Psoln = Psolv · Xsolv
= 100.5 mm Hg · 0.982 = 98.7 mm Hg
Solutions with a Nonvolatile Solute
Close-up view of part of the vapor pressure curve for a pure solvent and a solution of a nonvolatile solute. Which curve represents the pure solvent, and which the solution?
Why?
Reason for vapor pressure loweringG = Hvap - T S Hvap = positive, disfavored
S = positive, favored
Hvap is (nearly) the same for a pure solvent and a solvent in a solution
S is different solvent in a solution has more disorder than pure solvententropy of a solution is higher than the pure solvententropy of the vapor in both cases the same
Entropy increase for vaporization from a solution is smaller than vaporization from a pure solvent
Less entropy increase means less favored
Solutions with a Volatile Solute!! For a mixture of 2 volatile liquids A and B the overall vapor
pressure is the sum of the vapor pressure of the 2 components (Dalton’s law)
Ptotal = PA + PB
The vapor pressure for each component is calculated byRaoult’s law: vapor pressure is equal to the mole fraction of A
times the vapor pressure of pure A
Ptotal = PA + PB = (P0A · XA) + (P0
B · XB)
P°A = vapor pressure of pure A XA = mole fraction of A
P°B = vapor pressure of pure B XB = mole fraction of B
Solutions with a Volatile Solute
Close-up view of part of the vapor pressure curves for two pure liquids and a mixture of the two. Which curves represent the pure liquids, and which the mixture?
Ptotal should be intermediate to A & B
Raoult’s law applies only to ideal solutions
Most real solutions show deviations
Example 10
What is the vapor pressure ( in mm Hg) of a sol’n prepared by dissolving 25.0 g of ethyl alcohol (C2H5OH) in 100.0 g of water at 25°C? The vapor
pressure of pure water is 23.8 mm Hg and the vapor pressure of ethyl alcohol is 61.2 mm Hg at 25°C
Example 10
P°H2O = 23.8 mm Hg P°C2H5OH = 61.2 mm Hg XH2O = mole fraction of A
25 g C2H5OH x 1 mol / 46.07 g = 0.543 mol C2H5OH100.0 g H2O x 1 mol/ 18 g = 5.56 mol H2OXH2O = 5.56 /(5.56 + 0.543) = 0.91
XC2H5OH = mole fraction of BXC2H5OH = 0.543 / (0.543 + 5.56) = 0.09
Ptot = (23.8 x 0.91) + (61.2 x 0.09) = 27.2 mm Hg
Boiling Point Elevation and Freezing Point Depression of Solutions
A solution has a lower vapor pressure than the pure liquid. To reach the atmospheric pressure (boiling point) the temperature must be higher.
Tb = Kb · m Boiling point elevation Tf = Kf · m Freezing point depression
Kb = molal boiling-point elevation constant
Kf = molal freezing-point depression constantm = molality
Example 11
What is the normal boiling point in °C of a solution prepared by dissolving 1.50 g of aspirin (C9H8O4)
in 75.00 g of chloroform (CHCl3)? The normal
boiling point of chloroform is 61.7 °C and Kb of
chloroform is 3.63 °C kg/mol
Example 11
Tb = Kb · m
m = mole solute / kg solvent
MM C9H8O4 = 180.16 g/mol
1.50 g C9H8O4 x 1 mol / 180.16 g = 0.00833 mol C9H8O4
75.00 g CHCl3 = 0.07500 kg CHCl3
m =0 .00833 mol C9H8O4 / 0.07500 kg CHCl3 = 0.111 m
Tb = 3.63 °C kg/mol · 0.111 mol/kg = 0.403 °C
Boiling point = 0.403 °C + 61.7 °C = 62.1 °C
Osmosis and Osmotic Pressure
Membranes are semipermeable materials
They allow water and other small molecules to
pass through, but they block the passage of
larger molecules or ions.
All living cells contain membranesand osmosis is important in biological systems
Osmosis provides the primary means by whichwater is transported into and out of cells
Osmosis is responsible for the ability of plant roots to suck up water from the soil
Thermodynamic explanation
Every system wants to balance out the concentration
One side pure solventOther side solution ordered system
The system tries to get into a more disorderedmore randomness state
The entropy will increase
Osmosis is similar to diffusion
Osmosis Pressure
1. The amount of pressure necessary to achieve equilibrium
2. = MRT = osmotic pressureM = molarityR = gas constant, .08206 L atm/K mol
T = temperature in Kelvin
Isotonic sodium chloride solution
The total concentration of dissolved particles insidered blood cells is 0.30 M.
What is the osmotic pressure at body temp (310 k) ?
Isotonic sodium chloride solution
The total concentration of dissolved particles insidered blood cells is 0.30 M.
What is the osmotic pressure at body temp (310 k) ?
All medical infusions must have the same osmotic pressureOtherwise the blood cells would burst!Therefore isotonic NaCl solutions are injected
Q: What is the mass% of an isotonic NaCl solution?
Since the molarity in blood cells is 0.3 M, we need 0.15 MNaCl (0.15 M Na+ and 0.15 M Cl-)
Na = 23.0 amuCl = 35.5 amu NaCl = 58.5 amu
0.15 M NaCl = 58.5 x 0.15 = 9 g/L ; 0.9 mass%
Example 12
What osmotic pressure in atm would you expect for a solution of 0.125 M C6H12O6 that is separated from pure water by a semipermeable membrane at 310 K?
= MRT
= (0.125 mol/L)(.08206 L atm/K mol)(310 K) = 3.18 atm
Example 13
A solution of unknown substance in water at 300 K gives rise to an osmotic pressure of 3.85 atm. What is the molarity of the solution?
= MRT
M = /RT
M = 3.85 atm / [(.08206 L atm/K mol)(300 K)]
M = .156 mol/L
Some uses of colligative properties
1 Freezing-point depression - sprinkling of salt to melt snow - antifreeze in automobile cooling system - de-icing of airplane wings
2 Osmosis - desalination of seawater with reverse osmosis
3 Molar mass determination can use any four colligative properties most accurate is osmotic pressure, since the magnitude of osmosis effect is so great
Example 14
• What is the molar mass of sucrose if a solution prepared by dissolving 0.822 g of sucrose in water and diluting to a volume of 300.0 mL has an osmotic pressure of 149 mm Hg at 298 K?
= MRT
149 mm Hg x 1 atm / 760 mm Hg = 0 .196 atm
M = /RT
= 0.196 atm / [(0.08206 L atm/K mol)(298 K)]
= 0.00802 mol/L
0.00802 mol/L x 1 L/1000 mL x 300 mL = 0.00241 mol
MM = mass of sucrose / moles of sucrose
= 0.822 g / 0.00241 mol = 341.08 g/mol