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Solutions
Chapter 13
Properties of Solutions
John D. Bookstaver
St. Charles Community College
St. Peters, MO
 2006, Prentice Hall, Inc.
Chemistry, The Central Science, 10th edition
Theodore L. Brown; H. Eugene LeMay, Jr.;
and Bruce E. Bursten
Solutions
Solutions
• Solutions are homogeneous mixtures of two
or more pure substances.
• In a solution, the solute is dispersed uniformly
throughout the solvent.
Solutions
Solutions
The intermolecular
forces between solute
and solvent particles
must be strong enough
to compete with those
between solute particles
and those between
solvent particles.
Solutions
How Does a Solution Form?
As a solution forms, the solvent pulls solute
particles apart and surrounds, or solvates,
them. Play animation
Solutions
How Does a Solution Form
If an ionic salt is
soluble in water, it is
because the ion-
dipole interactions
are strong enough
to overcome the
lattice energy of the
salt crystal.
Solutions
Energy Changes in Solution
• Simply put, three
processes affect the
energetics of the
process:
Separation of solute
particles
Separation of solvent
particles
New interactions
between solute and
solvent
Solutions
Energy Changes in Solution
The enthalpy
change of the
overall process
depends on H for
each of these steps.
Solutions
Why Do Endothermic
Processes Occur?
Things do not tend to
occur spontaneously
(i.e., without outside
intervention) unless
the energy of the
system is lowered.
Solutions
Why Do Endothermic
Processes Occur?
Yet we know that in
some processes,
like the dissolution
of NH4NO3 in water,
heat is absorbed,
not released.
Solutions
Enthalpy Is Only Part of the Picture
The reason is that
increasing the disorder
or randomness (known
as entropy) of a system
tends to lower the
energy of the system.
Solutions
Enthalpy Is Only Part of the Picture
So even though
enthalpy may increase,
the overall energy of
the system can still
decrease if the system
becomes more
disordered.
Solutions
Answer: The entropy increases because each gas eventually becomes dispersed in twice the volume it originally
occupied.
SAMPLE EXERCISE 13.1 continued
PRACTICE EXERCISE
Does the entropy of the system increase or decrease when the stopcock is opened to allow mixing of the two
gases in this apparatus?
Solutions
Student, Beware!
Just because a substance disappears when it
comes in contact with a solvent, it doesn’t
mean the substance dissolved.
Solutions
Student, Beware!
• Dissolution is a physical change—you can get back the
original solute by evaporating the solvent.
• If you can’t, the substance didn’t dissolve, it reacted.
Solutions
Types of Solutions
• Saturated
Solvent holds as much
solute as is possible at
that temperature.
Dissolved solute is in
dynamic equilibrium
with solid solute
particles.
Solutions
Types of Solutions
• Unsaturated
Less than the
maximum amount of
solute for that
temperature is
dissolved in the
solvent.
Solutions
Types of Solutions
• Supersaturated
Solvent holds more solute than is normally
possible at that temperature.
These solutions are unstable; crystallization can
usually be stimulated by adding a “seed crystal” or
scratching the side of the flask.
Solutions
Factors Affecting Solubility
• Chemists use the axiom
“like dissolves like”:
Polar substances tend to
dissolve in polar solvents.
Nonpolar substances tend
to dissolve in nonpolar
solvents.
Solutions
Factors Affecting Solubility
The more similar the
intermolecular
attractions, the more
likely one substance
is to be soluble in
another.
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Factors Affecting Solubility
Glucose (which has
hydrogen bonding)
is very soluble in
water, while
cyclohexane (which
only has dispersion
forces) is not.
Solutions
Factors Affecting Solubility
• Vitamin A is soluble in nonpolar compounds
(like fats).
• Vitamin C is soluble in water.
Solutions
SAMPLE EXERCISE 13.2 Predicting Solubility Patterns
Predict whether each of the following substances is more likely to dissolve in carbon tetrachloride (CCl4) or in
water: C7H16, Na2SO4, HCl, and I2.
Solve: C7H16 is a hydrocarbon, so it is molecular and nonpolar. Na2SO4, a compound containing a metal and
nonmetals, is ionic; HCl, a diatomic molecule containing two nonmetals that differ in electronegativity, is polar;
and I2, a diatomic molecule with atoms of equal electronegativity, is nonpolar. We would therefore predict that
C7H16 and I2 would be more soluble in the nonpolar CCl4 than in polar H2O, whereas water would be the better
solvent for Na2SO4 and HCl.
Solutions
Answer: C5H12 < C5H11 Cl < C5H11 OH < C5H10(OH)2 (in order of increasing polarity and hydrogen-bonding
ability)
SAMPLE EXERCISE 13.2 continued
PRACTICE EXERCISE
Arrange the following substances in order of increasing solubility in water:
Solutions
Gases in Solution
• In general, the
solubility of gases in
water increases with
increasing mass.
• Larger molecules
have stronger
dispersion forces.
Solutions
Gases in Solution
• The solubility of
liquids and solids
does not change
appreciably with
pressure.
• The solubility of a
gas in a liquid is
directly proportional
to its pressure.
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Henry’s Law
Sg = kPg
where
• Sg is the solubility of
the gas;
• k is the Henry’s law
constant for that gas in
that solvent;
• Pg is the partial
pressure of the gas
above the liquid.play animation
Solutions
SAMPLE EXERCISE 13.3 A Henry’s Law Calculation
Calculate the concentration of CO2 in a soft drink that is bottled with a partial pressure of CO2 of 4.0 atm over
the liquid at 25°C. The Henry’s law constant for CO2 in water at this temperature is 3.1  10–2 mol/L-atm.
PRACTICE EXERCISE
Calculate the concentration of CO2 in a soft drink after the bottle is opened and equilibrates at 25°C under a
CO2 partial pressure of 3.0  10–4 atm.
Solution
Analyze: We are given the partial pressure of CO2, and the Henry’s law constant, k, and asked to
calculate the concentration of CO2 in the solution.
Plan: With the information given, we can use Henry’s law, Equation 13.4, to calculate the solubility,
Solve:
Check: The units are correct for solubility, and the answer has two significant figures consistent with both the
partial pressure of CO2 and the value of Henry’s constant.
2
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Temperature
Generally, the
solubility of solid
solutes in liquid
solvents increases
with increasing
temperature.
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Temperature
• The opposite is true
of gases:
Carbonated soft
drinks are more
“bubbly” if stored in
the refrigerator.
Warm lakes have
less O2 dissolved in
them than cool lakes.
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Ways of
Expressing
Concentrations
of Solutions
Solutions
Mass Percentage
Mass % of A =
mass of A in solution
total mass of solution
 100
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Parts per Million and
Parts per Billion
ppm =
mass of A in solution
total mass of solution
 106
Parts per Million (ppm)
Parts per Billion (ppb)
ppb =
mass of A in solution
total mass of solution
 109
Solutions
SAMPLE EXERCISE 13.4 Calculation of Mass-Related Concentrations
(a) A solution is made by dissolving 13.5 g of glucose (C6H12O6) in 0.100 kg of water. What is the mass
percentage of solute in this solution? (b) A 2.5-g sample of groundwater was found to contain 5.4 g of Zn2+
What is the concentration of Zn2+ in parts per million?
PRACTICE EXERCISE
(a) Calculate the mass percentage of NaCl in a solution containing 1.50 g of NaCl in 50.0 g of water. (b) A
commercial bleaching solution contains 3.62 mass % sodium hypochlorite, NaOCl. What is the mass of NaOCl
in a bottle containing 2500 g of bleaching solution?
Answers: (a) 2.91%, (b) 90.5 g of NaOCl
Solution
(a) Analyze: We are given the number of grams of solute (13.5 g) and the number of grams of solvent
(0.100 kg = 100 g). From this we must calculate the mass percentage of solute.
Plan: We can calculate the mass percentage by using Equation 13.5. The mass of the solution is the sum of the
mass of solute (glucose) and the mass of solvent (water).
Solve:
Comment: The mass percentage of water in this solution is (100 – 11.9)% = 88.1%.
(b) Analyze: In this case we are given the number of micrograms of solute. Because 1 g is 1  10–6 g,
5.4 g = 5.4  10–6 g.
Plan: We calculate the parts per million using Equation 13.6.
Solve:
Solutions
moles of A
total moles in solution
XA =
Mole Fraction (X)
• In some applications, one needs the
mole fraction of solvent, not solute—
make sure you find the quantity you
need!
Solutions
mol of solute
L of solution
M =
Molarity (M)
• You will recall this concentration
measure from Chapter 4.
• Because volume is temperature
dependent, molarity can change with
temperature.
Solutions
mol of solute
kg of solvent
m =
Molality (m)
Because both moles and mass do not
change with temperature, molality
(unlike molarity) is not temperature
dependent.
Solutions
SAMPLE EXERCISE 13.5 Calculation of Molality
A solution is made by dissolving 4.35 g glucose (C6H12O6) in 25.0 mL of water at 25°C. Calculate the molality
of glucose in the solution.
PRACTICE EXERCISE
What is the molality of a solution made by dissolving 36.5 g of naphthalene (C10H8) in 425 g of toluene (C7H8)?
Answer: 0.670 m
Solution
Analyze: We are asked to calculate a molality. To do this, we must determine the number of moles of solute
(glucose) and the number of kilograms of solvent (water).
Plan: We use the molar mass of C6H12O6 to convert grams to moles. We use the density of water to convert
milliliters to kilograms. The molality equals the number of moles of solute divided by the number of kilograms
of solvent (Equation 13.9).
Solve: Use the molar mass of glucose, 180.2 g/mol, to convert grams to moles:
Because water has a density of 100 g/mL, the mass of the solvent is
Finally, use Equation 13.9 to obtain the molality:
Solutions
SAMPLE EXERCISE 13.6 Calculation of Mole Fraction and Molality
An aqueous solution of hydrochloric acid contains 36% HCl by mass. (a) Calculate the mole fraction of HCl in
the solution. (b) Calculate the molality of HCl in the solution.
Solution
Analyze: We are asked to calculate the concentration of the solute, HCl, in two related concentration units,
given only the percentage by mass of the solute in the solution.
Plan: In converting concentration units based on the mass or moles of solute and solvent (mass percentage,
mole fraction, and molality), it is useful to assume a certain total mass of solution. Let’s assume that there is
exactly 100 g of solution. Because the solution is 36% HCl, it contains 36 g of HCl and (100 – 36) g = 64 g of
H2O. We must convert grams of solute (HCl) to moles in order to calculate either mole fraction or molality. We
must convert grams of solvent H2O to moles to calculate mole fractions, and to kilograms to calculate molality.
Solve: (a) To calculate the mole fraction of HCl, we convert the masses of HCl and H2O to moles and then use
Equation 13.7:
Solutions
PRACTICE EXERCISE
A commercial bleach solution contains 3.62 mass % NaOCl in water. Calculate (a) the molality and (b) the mole
fraction of NaOCl in the solution.
Answers: (a) 0.505 m, (b) 9.00  10–3
SAMPLE EXERCISE 13.6 continued
(b) To calculate the molality of HCl in the solution, we use Equation 13.9. We calculated the number of moles of
HCl in part (a), and the mass of solvent is 64 g = 0.064 kg:
Solutions
SAMPLE EXERCISE 13.7 Calculation of Molarity
A solution contains 5.0 g of toluene (C7H8) and 225 g of benzene and has a density of 0.876 g/mL. Calculate the
molarity of the solution.
Solution
Analyze: Our goal is to calculate the molarity of a solution, given the masses of solute and solvent and the
density of the solution.
Plan: The molarity of a solution is the number of moles of solute divided by the number of liters of solution
(Equation 13.8). The number of moles of solute (C7H8) is calculated from the number of grams of solute and its
molar mass. The volume of the solution is obtained from the mass of the solution (mass of solute + mass of
solvent = 5.0 g + 225 g = 230 g) and its density.
Solve: The number of moles of solute is
The density of the solution is used to convert the mass of the solution to its volume:
Molarity is moles of solute per liter of solution:
Solutions
PRACTICE EXERCISE
A solution containing equal masses of glycerol (C3H8O3) and water has a density of 1.10 g/mL. Calculate (a)
the molality of glycerol, (b) the mole fraction of glycerol, (c) the molarity of glycerol in the solution.
SAMPLE EXERCISE 13.7 continued
Check: The magnitude of our answer is reasonable. Rounding moles to 0.05 and liters to 0.25 gives a molarity
of
The units for our answer (mol/L) are correct, and the answer, 0.21 M, has two significant figures, corresponding
to the number of significant figures in the mass of solute (2).
Comment: Because the mass of the solvent (0.225 kg) and the volume of the solution (0.263 L) are similar in
magnitude, the molarity and molality are also similar in magnitude:
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Changing Molarity to Molality
If we know the
density of the
solution, we can
calculate the
molality from the
molarity, and vice
versa.
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Colligative Properties
• Changes in colligative properties
depend only on the number of solute
particles present, not on the identity of
the solute particles.
• Among colligative properties are
Vapor pressure lowering
Boiling point elevation
Melting point depression
Osmotic pressure
Solutions
Vapor Pressure
Because of solute-
solvent intermolecular
attraction, higher
concentrations of
nonvolatile solutes
make it harder for
solvent to escape to
the vapor phase.
Solutions
Vapor Pressure
Therefore, the vapor
pressure of a solution
is lower than that of
the pure solvent.
Solutions
Raoult’s Law
PA = XAPA
where
• XA is the mole fraction of compound A
• PA is the normal vapor pressure of A at
that temperature
NOTE: This is one of those times when you
want to make sure you have the vapor
pressure of the solvent.
Solutions
SAMPLE EXERCISE 13.8 Calculation of Vapor-Pressure Lowering
Glycerin (C3H8O3) is a nonvolatile nonelectrolyte with a density of 1.26 g/mL at 25°C. Calculate the vapor
pressure at 25°C of a solution made by adding 50.0 mL of glycerin to 500.0 mL of water. The vapor pressure of
pure water at 25°C is 23.8 torr (Appendix B).
Solution
Analyze: Our goal is to calculate the vapor pressure of a solution, given the volumes of solute and solvent and
the density of the solute.
Plan: We can use Raoult’s law (Equation 13.10) to calculate the vapor pressure of a solution. The mole
fraction of the solvent in the solution, XA, is the ratio of the number of moles of solvent (H2O) to total solution
(moles C3H8O3 + moles H2O).
Solve: To calculate the mole fraction of water in the solution, we must determine the number of moles of
C3H8O3 and H2O:
Solutions
PRACTICE EXERCISE
The vapor pressure of pure water at 110°C is 1070 torr. A solution of ethylene glycol and water has a vapor
pressure of 1.00 atm at 110°C. Assuming that Raoult’s law is obeyed, what is the mole fraction of ethylene
glycol in the solution?
Answer: 0.290
SAMPLE EXERCISE 13.8 continued
The vapor pressure of the solution has been lowered by 0.6 torr relative to that of pure water.
We now use Raoult’s law to calculate the vapor pressure of water for the solution:
Solutions
Boiling Point Elevation and
Freezing Point Depression
Nonvolatile solute-
solvent interactions
also cause solutions
to have higher boiling
points and lower
freezing points than
the pure solvent.
Solutions
Boiling Point Elevation
The change in boiling
point is proportional to
the molality of the
solution:
Tb = Kb  m
where Kb is the molal
boiling point elevation
constant, a property of
the solvent.
Tb is added to the normal
boiling point of the solvent.
Solutions
Freezing Point Depression
• The change in freezing
point can be found
similarly:
Tf = Kf  m
• Here Kf is the molal
freezing point
depression constant of
the solvent.
Tf is subtracted from the normal
freezing point of the solvent.
Solutions
Boiling Point Elevation and
Freezing Point Depression
Note that in both
equations, T does
not depend on what
the solute is, but
only on how many
particles are
dissolved.
Tb = Kb  m
Tf = Kf  m
Solutions
SAMPLE EXERCISE 13.9 Calculation of Boiling-Point Elevation and
Freezing-Point Lowering
Automotive antifreeze consists of ethylene glycol (C2H6O2), a nonvolatile nonelectrolyte. Calculate the boiling
point and freezing point of a 25.0 mass % solution of ethylene glycol in water.
Solution
Analyze: We are given that a solution contains 25.0 mass % of a nonvolatile, nonelectrolyte solute and asked
to calculate the boiling and freezing points of the solution. To do this, we need to calculate the boiling-point
elevation and freezing-point depression.
Plan: In order to calculate the boiling-point elevation and the freezing-point depression using Equations 13.11
and 13.12, we must express the concentration of the solution as molality. Let’s assume for convenience that we
have 1000 g of solution. Because the solution is 25.0 mass % ethylene glycol, the masses of ethylene glycol and
water in the solution are 250 and 750 g, respectively. Using these quantities, we can calculate the molality of the
solution, which we use with the molal boiling-point-elevation and freezing-point-depression constants
(Table 13.4) to calculate Tb and Tf . We add Tb to the boiling point and subtract Tf from the freezing point
of the solvent to obtain the boiling point and freezing point of the solution.
We can now use Equations 13.11 and 13.12 to calculate the changes in the boiling and freezing points:
Solve: The molality of the solution is calculated as follows:
Solutions
Comment: Notice that the solution is a liquid over a larger temperature range than the pure solvent.
PRACTICE EXERCISE
Calculate the freezing point of a solution containing 0.600 kg of CHCl3 and 42.0 g of eucalyptol (C10H18O), a
fragrant substance found in the leaves of eucalyptus trees. (See Table 13.4.)
Answer: –65.6ºC
SAMPLE EXERCISE 13.9 continued
Hence, the boiling and freezing points of the solution are
Solutions
Colligative Properties of
Electrolytes
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.
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Colligative Properties of
Electrolytes
However, a 1 M solution of NaCl does not show
twice the change in freezing point that a 1 M
solution of methanol does.
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van’t Hoff Factor
One mole of NaCl in
water does not
really give rise to
two moles of ions.
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van’t Hoff Factor
Some Na+ and Cl−
reassociate for a
short time, so the
true concentration of
particles is
somewhat less than
two times the
concentration of
NaCl.
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The van’t Hoff Factor
• Reassociation is
more likely at higher
concentration.
• Therefore, the
number of particles
present is
concentration
dependent.
Solutions
The van’t Hoff Factor
We modify the
previous equations
by multiplying by the
van’t Hoff factor, i
Tf = Kf  m  i
Solutions
Osmosis
• Some substances form semipermeable
membranes, allowing some smaller
particles to pass through, but blocking
other larger particles.
• In biological systems, most
semipermeable membranes allow water
to pass through, but solutes are not free
to do so.
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Osmosis
In osmosis, there is net movement of solvent from
the area of higher solvent concentration (lower
solute concentration) to the are of lower solvent
concentration (higher solute concentration).
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Osmotic Pressure
• The pressure required to stop osmosis,
known as osmotic pressure, , is
n
V
 = ( )RT = MRT
where M is the molarity of the solution
If the osmotic pressure is the same on both sides
of a membrane (i.e., the concentrations are the
same), the solutions are isotonic.play animation
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Osmosis in Blood Cells
• If the solute
concentration outside
the cell is greater than
that inside the cell, the
solution is hypertonic.
• Water will flow out of
the cell, and crenation
results.
Solutions
Osmosis in Cells
• If the solute
concentration outside
the cell is less than
that inside the cell, the
solution is hypotonic.
• Water will flow into the
cell, and hemolysis
results.
Solutions
SAMPLE EXERCISE 13.11 Calculations Involving Osmotic Pressure
The average osmotic pressure of blood is 7.7 atm at 25°C. What concentration of glucose (C6H12O6) will be
isotonic with blood?
Comment: In clinical situations the concentrations of solutions are generally expressed as mass percentages.
The mass percentage of a 0.31 M solution of glucose is 5.3%. The concentration of NaCl that is isotonic with
blood is 0.16 M because NaCl ionizes to form two particles, Na+ and Cl– (a 0.155 M solution of NaCl is 0.310
M in particles). A 0.16 M solution of NaCl is 0.9 mass % in NaCl. This kind of solution is known as a
physiological saline solution.
PRACTICE EXERCISE
What is the osmotic pressure at 20°C of a 0.0020 M sucrose (C12H22O11) solution?
Answer: 0.048 atm, or 37 torr
Solution
Analyze: We are asked to calculate the concentration of glucose in water that would be isotonic with blood,
given that the osmotic pressure of blood at 25°C is 7.7 atm.
Plan: Because we are given the osmotic pressure and temperature, we can solve for the concentration, using
Equation 13.13.
Solve:
Solutions
Molar Mass from
Colligative Properties
We can use the
effects of a colligative
property such as
osmotic pressure to
determine the molar
mass of a compound.
Solutions
SAMPLE EXERCISE 13.10 Freezing-Point Depression in Aqueous Solutions
List the following aqueous solutions in order of their expected freezing point: 0.050 m CaCl2, 0.15 m NaCl, 0.10
m HCl, 0.050 m HC2H3O2, 0.10 m C12H22O11.
Solution
Analyze: We must order five aqueous solutions according to expected freezing points, based on molalities and
the solute formulas.
Plan: The lowest freezing point will correspond to the solution with the greatest concentration of solute
particles. To determine the total concentration of solute particles in each case, we must determine whether the
substance is a nonelectrolyte or an electrolyte and consider the number of ions formed when it ionizes.
Solve: CaCl2, NaCl, and HCl are strong electrolytes, HC2H3O2, is a weak electrolyte, and C12H22O11 is a
nonelectrolyte. The molality of each solution in total particles is as follows:
Because the freezing points depend on the total molality of particles in solution, the expected ordering is 0.15 m
NaCl (lowest freezing point), 0.10 m HCl, 0.050 m CaCl2, 0.10 m C12H22O11, and 0.050 m HC2H3O2, (highest
freezing point).
Solutions
SAMPLE EXERCISE 13.10 continued
PRACTICE EXERCISE
Which of the following solutes will produce the largest increase in boiling point upon addition to 1 kg of water:
1 mol of Co(NO3)2, 2 mol of KCl, 3 mol of ethylene glycol (C2H6O2)?
Answer: 2 mol of KCl because it contains the highest concentration of particles, 2 m K+ and 2 m Cl–, giving 4 m
in all
Solutions
SAMPLE EXERCISE 13.12 Molar Mass from Freezing-Point Depression
A solution of an unknown nonvolatile electrolyte was prepared by dissolving 0.250 g of the substance in 40.0 g
of CCl4. The boiling point of the resultant solution was 0.357°C higher than that of the pure solvent. Calculate
the molar mass of the solute.
Solution
Analyze: Our goal is to calculate the molar mass of a solute based on knowledge of the boiling-point
elevation of its solution in CCl4, Tb = 0.357ºC, and the masses of solute and solvent. Table 13.4 gives Kb for the
solvent (CCl4), Kb = 5.02ºC/m.
Plan: We can use Equation 13.11, Tb = Kbm, to calculate the molality of the solution. Then we can use
molality and the quantity of solvent (40.0 g CCl4) to calculate the number of moles of solute. Finally, the molar
mass of the solute equals the number of grams per mole, so we divide the number of grams of solute (0.250 g)
by the number of moles we have just calculated.
Solve: From Equation 13.11 we have
Thus, the solution contains 0.0711 mol of solute per kilogram of solvent. The solution was prepared using
40.0 g = 0.0400 kg of solvent (CCl4). The number of moles of solute in the solution is therefore
Solutions
PRACTICE EXERCISE
Camphor (C10H16O) melts at 179.8°C, and it has a particularly large freezing-point-depression constant, Kf =
40.0ºC/m. When 0.186 g of an organic substance of unknown molar mass is dissolved in 22.01 g of liquid
camphor, the freezing point of the mixture is found to be 176.7°C. What is the molar mass of the solute?
Answer: 110 g/mol
SAMPLE EXERCISE 13.12 continued
The molar mass of the solute is the number of grams per mole of the substance:
Solutions
SAMPLE EXERCISE 13.13 Molar Mass from Osmotic Pressure
The osmotic pressure of an aqueous solution of a certain protein was measured in order to determine the
protein’s molar mass. The solution contained 3.50 mg of protein dissolved in sufficient water to form 5.00 mL of
solution. The osmotic pressure of the solution at 25°C was found to be 1.54 torr. Calculate the molar mass of
the protein.
Solution
Analyze: Our goal is to calculate the molar mass of a high-molecular-mass protein, based on its osmotic
pressure and a knowledge of the mass of protein and solution volume.
Plan: The temperature (T = 25ºC) and osmotic pressure ( = 1.54 torr) are given, and we know the value of R
so we can use Equation 13.13 to calculate the molarity of the solution, M. In doing so, we must convert
temperature from °C to K and the osmotic pressure from torr to atm. We then use the molarity and the volume
of the solution (5.00 mL) to determine the number of moles of solute. Finally, we obtain the molar mass by
dividing the mass of the solute (3.50 mg) by the number of moles of solute.
Solve: Solving Equation 13.13 for molarity gives
Because the volume of the solution is 5.00 ml = 5.00  10–3 L, the number of moles of protein must be
Solutions
Comment: Because small pressures can be measured easily and accurately, osmotic pressure measurements
provide a useful way to determine the molar masses of large molecules.
PRACTICE EXERCISE
A sample of 2.05 g of polystyrene of uniform polymer chain length was dissolved in enough toluene to form
0.100 L of solution. The osmotic pressure of this solution was found to be 1.21 kPa at 25°C. Calculate the
molar mass of the polystyrene.
Answer: 4.20  104 g/mol
SAMPLE EXERCISE 13.13 continued
The molar mass is the number of grams per mole of the substance. The sample has a mass of
3.50 mg = 3.50  10–3g. The molar mass is the number of grams divided by the number of moles:
Solutions
Colloids:
Suspensions of particles larger than
individual ions or molecules, but too small to
be settled out by gravity.
Solutions
Tyndall Effect
• Colloidal suspensions
can scatter rays of light.
• This phenomenon is
known as the Tyndall
effect.
Solutions
Colloids in Biological Systems
Some molecules have
a polar, hydrophilic
(water-loving) end and
a nonpolar,
hydrophobic (water-
hating) end.
Solutions
Colloids in Biological Systems
Sodium stearate
is one example
of such a
molecule.
Solutions
Colloids in Biological Systems
These molecules
can aid in the
emulsification of fats
and oils in aqueous
solutions.
Solutions
SAMPLE INTEGRATIVE EXERCISE Putting Concepts Together
A 0.100-L solution is made by dissolving 0.441 g of CaCl2(s) in water. (a) Calculate the osmotic pressure of this
solution at 27°C, assuming that it is completely dissociated into its component ions. (b) The measured osmotic
pressure of this solution is 2.56 atm at 27°C. Explain why it is less than the value calculated in (a), and
calculate the van’t Hoff factor, i, for the solute in this solution. (See the “Closer Look” box in Section 13.5 on
page 557.) (c) The enthalpy of solution for CaCl2 is H = –81.3 kJ/mol. If the final temperature of the solution
was 27.0°C, what was its initial temperature? (Assume that the density of the solution is 1.00 g /mL, that its
specific heat is 4.18 J/g-K, and that the solution loses no heat to its surroundings.)
Solution
(a) The osmotic pressure is given by Equation 13.13, π = MRT. We know the temperature, T = 27ºC = 300
K and the gas constant, R = 0.0821 L-atm/mol-K. We can calculate the molarity of the solution from the mass of
CaCl2 and the volume of the solution:
Soluble ionic compounds are strong electrolytes. • (Sections 4.1 and 4.3) Thus, CaCl2 consists of metal cations
(Ca2+) and nonmetal anions (Cl–). When completely dissociated, each CaCl2 unit forms three ions (one (Ca2+)
and two Cl–). Hence the total concentration of ions in the solution is (3)(0.0397 M) = 0.119 M, and the osmotic
pressure is
Solutions
A kelvin has the same size as a degree Celsius. • (Section 1.4) Because the solution temperature increases by
0.773°C, the initial temperature was 27.0ºC – 0.773ºC = 26.2°C.
The heat absorbed by the solution is q = +0.323 kJ = 323 J. The mass of the 0.100 L of solution is (100 mL)(1.00
g/mL) = 100 g (to 3 significant figures). Thus the temperature change is
Thus, the solution behaves as if the CaCl2 has dissociated into 2.62 particles instead of the ideal 3.
(c) If the solution is 0.0397 M in CaCl2 and has a total volume of 0.100 L, the number of moles of solute is
(0.100 L)(0.0397 mol/L) = 0.00397 mol. Hence the quantity of heat generated in forming the solution is
(0.00397 mol)(–81.3 kJ/mol) = –0.323 kJ. The solution absorbs this heat, causing its temperature to increase.
The relationship between temperature change and heat is given by Equation 5.19:
SAMPLE INTEGRATIVE EXERCISE continued
(b) The actual values of colligative properties of electrolytes are less than those calculated, because the
electrostatic interactions between ions limit their independent movements. In this case the van’t Hoff factor,
which measures the extent to which electrolytes actually dissociate into ions, is given by

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chapter_13au.ppt

  • 1. Solutions Chapter 13 Properties of Solutions John D. Bookstaver St. Charles Community College St. Peters, MO  2006, Prentice Hall, Inc. Chemistry, The Central Science, 10th edition Theodore L. Brown; H. Eugene LeMay, Jr.; and Bruce E. Bursten
  • 2. Solutions Solutions • Solutions are homogeneous mixtures of two or more pure substances. • In a solution, the solute is dispersed uniformly throughout the solvent.
  • 3. Solutions Solutions The intermolecular forces between solute and solvent particles must be strong enough to compete with those between solute particles and those between solvent particles.
  • 4. Solutions How Does a Solution Form? As a solution forms, the solvent pulls solute particles apart and surrounds, or solvates, them. Play animation
  • 5. Solutions How Does a Solution Form If an ionic salt is soluble in water, it is because the ion- dipole interactions are strong enough to overcome the lattice energy of the salt crystal.
  • 6. Solutions Energy Changes in Solution • Simply put, three processes affect the energetics of the process: Separation of solute particles Separation of solvent particles New interactions between solute and solvent
  • 7. Solutions Energy Changes in Solution The enthalpy change of the overall process depends on H for each of these steps.
  • 8. Solutions Why Do Endothermic Processes Occur? Things do not tend to occur spontaneously (i.e., without outside intervention) unless the energy of the system is lowered.
  • 9. Solutions Why Do Endothermic Processes Occur? Yet we know that in some processes, like the dissolution of NH4NO3 in water, heat is absorbed, not released.
  • 10. Solutions Enthalpy Is Only Part of the Picture The reason is that increasing the disorder or randomness (known as entropy) of a system tends to lower the energy of the system.
  • 11. Solutions Enthalpy Is Only Part of the Picture So even though enthalpy may increase, the overall energy of the system can still decrease if the system becomes more disordered.
  • 12. Solutions Answer: The entropy increases because each gas eventually becomes dispersed in twice the volume it originally occupied. SAMPLE EXERCISE 13.1 continued PRACTICE EXERCISE Does the entropy of the system increase or decrease when the stopcock is opened to allow mixing of the two gases in this apparatus?
  • 13. Solutions Student, Beware! Just because a substance disappears when it comes in contact with a solvent, it doesn’t mean the substance dissolved.
  • 14. Solutions Student, Beware! • Dissolution is a physical change—you can get back the original solute by evaporating the solvent. • If you can’t, the substance didn’t dissolve, it reacted.
  • 15. Solutions Types of Solutions • Saturated Solvent holds as much solute as is possible at that temperature. Dissolved solute is in dynamic equilibrium with solid solute particles.
  • 16. Solutions Types of Solutions • Unsaturated Less than the maximum amount of solute for that temperature is dissolved in the solvent.
  • 17. Solutions Types of Solutions • Supersaturated Solvent holds more solute than is normally possible at that temperature. These solutions are unstable; crystallization can usually be stimulated by adding a “seed crystal” or scratching the side of the flask.
  • 18. Solutions Factors Affecting Solubility • Chemists use the axiom “like dissolves like”: Polar substances tend to dissolve in polar solvents. Nonpolar substances tend to dissolve in nonpolar solvents.
  • 19. Solutions Factors Affecting Solubility The more similar the intermolecular attractions, the more likely one substance is to be soluble in another.
  • 20. Solutions Factors Affecting Solubility Glucose (which has hydrogen bonding) is very soluble in water, while cyclohexane (which only has dispersion forces) is not.
  • 21. Solutions Factors Affecting Solubility • Vitamin A is soluble in nonpolar compounds (like fats). • Vitamin C is soluble in water.
  • 22. Solutions SAMPLE EXERCISE 13.2 Predicting Solubility Patterns Predict whether each of the following substances is more likely to dissolve in carbon tetrachloride (CCl4) or in water: C7H16, Na2SO4, HCl, and I2. Solve: C7H16 is a hydrocarbon, so it is molecular and nonpolar. Na2SO4, a compound containing a metal and nonmetals, is ionic; HCl, a diatomic molecule containing two nonmetals that differ in electronegativity, is polar; and I2, a diatomic molecule with atoms of equal electronegativity, is nonpolar. We would therefore predict that C7H16 and I2 would be more soluble in the nonpolar CCl4 than in polar H2O, whereas water would be the better solvent for Na2SO4 and HCl.
  • 23. Solutions Answer: C5H12 < C5H11 Cl < C5H11 OH < C5H10(OH)2 (in order of increasing polarity and hydrogen-bonding ability) SAMPLE EXERCISE 13.2 continued PRACTICE EXERCISE Arrange the following substances in order of increasing solubility in water:
  • 24. Solutions Gases in Solution • In general, the solubility of gases in water increases with increasing mass. • Larger molecules have stronger dispersion forces.
  • 25. Solutions Gases in Solution • The solubility of liquids and solids does not change appreciably with pressure. • The solubility of a gas in a liquid is directly proportional to its pressure.
  • 26. Solutions Henry’s Law Sg = kPg where • Sg is the solubility of the gas; • k is the Henry’s law constant for that gas in that solvent; • Pg is the partial pressure of the gas above the liquid.play animation
  • 27. Solutions SAMPLE EXERCISE 13.3 A Henry’s Law Calculation Calculate the concentration of CO2 in a soft drink that is bottled with a partial pressure of CO2 of 4.0 atm over the liquid at 25°C. The Henry’s law constant for CO2 in water at this temperature is 3.1  10–2 mol/L-atm. PRACTICE EXERCISE Calculate the concentration of CO2 in a soft drink after the bottle is opened and equilibrates at 25°C under a CO2 partial pressure of 3.0  10–4 atm. Solution Analyze: We are given the partial pressure of CO2, and the Henry’s law constant, k, and asked to calculate the concentration of CO2 in the solution. Plan: With the information given, we can use Henry’s law, Equation 13.4, to calculate the solubility, Solve: Check: The units are correct for solubility, and the answer has two significant figures consistent with both the partial pressure of CO2 and the value of Henry’s constant. 2
  • 28. Solutions Temperature Generally, the solubility of solid solutes in liquid solvents increases with increasing temperature.
  • 29. Solutions Temperature • The opposite is true of gases: Carbonated soft drinks are more “bubbly” if stored in the refrigerator. Warm lakes have less O2 dissolved in them than cool lakes.
  • 31. Solutions Mass Percentage Mass % of A = mass of A in solution total mass of solution  100
  • 32. Solutions Parts per Million and Parts per Billion ppm = mass of A in solution total mass of solution  106 Parts per Million (ppm) Parts per Billion (ppb) ppb = mass of A in solution total mass of solution  109
  • 33. Solutions SAMPLE EXERCISE 13.4 Calculation of Mass-Related Concentrations (a) A solution is made by dissolving 13.5 g of glucose (C6H12O6) in 0.100 kg of water. What is the mass percentage of solute in this solution? (b) A 2.5-g sample of groundwater was found to contain 5.4 g of Zn2+ What is the concentration of Zn2+ in parts per million? PRACTICE EXERCISE (a) Calculate the mass percentage of NaCl in a solution containing 1.50 g of NaCl in 50.0 g of water. (b) A commercial bleaching solution contains 3.62 mass % sodium hypochlorite, NaOCl. What is the mass of NaOCl in a bottle containing 2500 g of bleaching solution? Answers: (a) 2.91%, (b) 90.5 g of NaOCl Solution (a) Analyze: We are given the number of grams of solute (13.5 g) and the number of grams of solvent (0.100 kg = 100 g). From this we must calculate the mass percentage of solute. Plan: We can calculate the mass percentage by using Equation 13.5. The mass of the solution is the sum of the mass of solute (glucose) and the mass of solvent (water). Solve: Comment: The mass percentage of water in this solution is (100 – 11.9)% = 88.1%. (b) Analyze: In this case we are given the number of micrograms of solute. Because 1 g is 1  10–6 g, 5.4 g = 5.4  10–6 g. Plan: We calculate the parts per million using Equation 13.6. Solve:
  • 34. Solutions moles of A total moles in solution XA = Mole Fraction (X) • In some applications, one needs the mole fraction of solvent, not solute— make sure you find the quantity you need!
  • 35. Solutions mol of solute L of solution M = Molarity (M) • You will recall this concentration measure from Chapter 4. • Because volume is temperature dependent, molarity can change with temperature.
  • 36. Solutions mol of solute kg of solvent m = Molality (m) Because both moles and mass do not change with temperature, molality (unlike molarity) is not temperature dependent.
  • 37. Solutions SAMPLE EXERCISE 13.5 Calculation of Molality A solution is made by dissolving 4.35 g glucose (C6H12O6) in 25.0 mL of water at 25°C. Calculate the molality of glucose in the solution. PRACTICE EXERCISE What is the molality of a solution made by dissolving 36.5 g of naphthalene (C10H8) in 425 g of toluene (C7H8)? Answer: 0.670 m Solution Analyze: We are asked to calculate a molality. To do this, we must determine the number of moles of solute (glucose) and the number of kilograms of solvent (water). Plan: We use the molar mass of C6H12O6 to convert grams to moles. We use the density of water to convert milliliters to kilograms. The molality equals the number of moles of solute divided by the number of kilograms of solvent (Equation 13.9). Solve: Use the molar mass of glucose, 180.2 g/mol, to convert grams to moles: Because water has a density of 100 g/mL, the mass of the solvent is Finally, use Equation 13.9 to obtain the molality:
  • 38. Solutions SAMPLE EXERCISE 13.6 Calculation of Mole Fraction and Molality An aqueous solution of hydrochloric acid contains 36% HCl by mass. (a) Calculate the mole fraction of HCl in the solution. (b) Calculate the molality of HCl in the solution. Solution Analyze: We are asked to calculate the concentration of the solute, HCl, in two related concentration units, given only the percentage by mass of the solute in the solution. Plan: In converting concentration units based on the mass or moles of solute and solvent (mass percentage, mole fraction, and molality), it is useful to assume a certain total mass of solution. Let’s assume that there is exactly 100 g of solution. Because the solution is 36% HCl, it contains 36 g of HCl and (100 – 36) g = 64 g of H2O. We must convert grams of solute (HCl) to moles in order to calculate either mole fraction or molality. We must convert grams of solvent H2O to moles to calculate mole fractions, and to kilograms to calculate molality. Solve: (a) To calculate the mole fraction of HCl, we convert the masses of HCl and H2O to moles and then use Equation 13.7:
  • 39. Solutions PRACTICE EXERCISE A commercial bleach solution contains 3.62 mass % NaOCl in water. Calculate (a) the molality and (b) the mole fraction of NaOCl in the solution. Answers: (a) 0.505 m, (b) 9.00  10–3 SAMPLE EXERCISE 13.6 continued (b) To calculate the molality of HCl in the solution, we use Equation 13.9. We calculated the number of moles of HCl in part (a), and the mass of solvent is 64 g = 0.064 kg:
  • 40. Solutions SAMPLE EXERCISE 13.7 Calculation of Molarity A solution contains 5.0 g of toluene (C7H8) and 225 g of benzene and has a density of 0.876 g/mL. Calculate the molarity of the solution. Solution Analyze: Our goal is to calculate the molarity of a solution, given the masses of solute and solvent and the density of the solution. Plan: The molarity of a solution is the number of moles of solute divided by the number of liters of solution (Equation 13.8). The number of moles of solute (C7H8) is calculated from the number of grams of solute and its molar mass. The volume of the solution is obtained from the mass of the solution (mass of solute + mass of solvent = 5.0 g + 225 g = 230 g) and its density. Solve: The number of moles of solute is The density of the solution is used to convert the mass of the solution to its volume: Molarity is moles of solute per liter of solution:
  • 41. Solutions PRACTICE EXERCISE A solution containing equal masses of glycerol (C3H8O3) and water has a density of 1.10 g/mL. Calculate (a) the molality of glycerol, (b) the mole fraction of glycerol, (c) the molarity of glycerol in the solution. SAMPLE EXERCISE 13.7 continued Check: The magnitude of our answer is reasonable. Rounding moles to 0.05 and liters to 0.25 gives a molarity of The units for our answer (mol/L) are correct, and the answer, 0.21 M, has two significant figures, corresponding to the number of significant figures in the mass of solute (2). Comment: Because the mass of the solvent (0.225 kg) and the volume of the solution (0.263 L) are similar in magnitude, the molarity and molality are also similar in magnitude:
  • 42. Solutions Changing Molarity to Molality If we know the density of the solution, we can calculate the molality from the molarity, and vice versa.
  • 43. Solutions Colligative Properties • Changes in colligative properties depend only on the number of solute particles present, not on the identity of the solute particles. • Among colligative properties are Vapor pressure lowering Boiling point elevation Melting point depression Osmotic pressure
  • 44. Solutions Vapor Pressure Because of solute- solvent intermolecular attraction, higher concentrations of nonvolatile solutes make it harder for solvent to escape to the vapor phase.
  • 45. Solutions Vapor Pressure Therefore, the vapor pressure of a solution is lower than that of the pure solvent.
  • 46. Solutions Raoult’s Law PA = XAPA where • XA is the mole fraction of compound A • PA is the normal vapor pressure of A at that temperature NOTE: This is one of those times when you want to make sure you have the vapor pressure of the solvent.
  • 47. Solutions SAMPLE EXERCISE 13.8 Calculation of Vapor-Pressure Lowering Glycerin (C3H8O3) is a nonvolatile nonelectrolyte with a density of 1.26 g/mL at 25°C. Calculate the vapor pressure at 25°C of a solution made by adding 50.0 mL of glycerin to 500.0 mL of water. The vapor pressure of pure water at 25°C is 23.8 torr (Appendix B). Solution Analyze: Our goal is to calculate the vapor pressure of a solution, given the volumes of solute and solvent and the density of the solute. Plan: We can use Raoult’s law (Equation 13.10) to calculate the vapor pressure of a solution. The mole fraction of the solvent in the solution, XA, is the ratio of the number of moles of solvent (H2O) to total solution (moles C3H8O3 + moles H2O). Solve: To calculate the mole fraction of water in the solution, we must determine the number of moles of C3H8O3 and H2O:
  • 48. Solutions PRACTICE EXERCISE The vapor pressure of pure water at 110°C is 1070 torr. A solution of ethylene glycol and water has a vapor pressure of 1.00 atm at 110°C. Assuming that Raoult’s law is obeyed, what is the mole fraction of ethylene glycol in the solution? Answer: 0.290 SAMPLE EXERCISE 13.8 continued The vapor pressure of the solution has been lowered by 0.6 torr relative to that of pure water. We now use Raoult’s law to calculate the vapor pressure of water for the solution:
  • 49. Solutions Boiling Point Elevation and Freezing Point Depression Nonvolatile solute- solvent interactions also cause solutions to have higher boiling points and lower freezing points than the pure solvent.
  • 50. Solutions Boiling Point Elevation The change in boiling point is proportional to the molality of the solution: Tb = Kb  m where Kb is the molal boiling point elevation constant, a property of the solvent. Tb is added to the normal boiling point of the solvent.
  • 51. Solutions Freezing Point Depression • The change in freezing point can be found similarly: Tf = Kf  m • Here Kf is the molal freezing point depression constant of the solvent. Tf is subtracted from the normal freezing point of the solvent.
  • 52. Solutions Boiling Point Elevation and Freezing Point Depression Note that in both equations, T does not depend on what the solute is, but only on how many particles are dissolved. Tb = Kb  m Tf = Kf  m
  • 53. Solutions SAMPLE EXERCISE 13.9 Calculation of Boiling-Point Elevation and Freezing-Point Lowering Automotive antifreeze consists of ethylene glycol (C2H6O2), a nonvolatile nonelectrolyte. Calculate the boiling point and freezing point of a 25.0 mass % solution of ethylene glycol in water. Solution Analyze: We are given that a solution contains 25.0 mass % of a nonvolatile, nonelectrolyte solute and asked to calculate the boiling and freezing points of the solution. To do this, we need to calculate the boiling-point elevation and freezing-point depression. Plan: In order to calculate the boiling-point elevation and the freezing-point depression using Equations 13.11 and 13.12, we must express the concentration of the solution as molality. Let’s assume for convenience that we have 1000 g of solution. Because the solution is 25.0 mass % ethylene glycol, the masses of ethylene glycol and water in the solution are 250 and 750 g, respectively. Using these quantities, we can calculate the molality of the solution, which we use with the molal boiling-point-elevation and freezing-point-depression constants (Table 13.4) to calculate Tb and Tf . We add Tb to the boiling point and subtract Tf from the freezing point of the solvent to obtain the boiling point and freezing point of the solution. We can now use Equations 13.11 and 13.12 to calculate the changes in the boiling and freezing points: Solve: The molality of the solution is calculated as follows:
  • 54. Solutions Comment: Notice that the solution is a liquid over a larger temperature range than the pure solvent. PRACTICE EXERCISE Calculate the freezing point of a solution containing 0.600 kg of CHCl3 and 42.0 g of eucalyptol (C10H18O), a fragrant substance found in the leaves of eucalyptus trees. (See Table 13.4.) Answer: –65.6ºC SAMPLE EXERCISE 13.9 continued Hence, the boiling and freezing points of the solution are
  • 55. Solutions Colligative Properties of Electrolytes 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.
  • 56. Solutions Colligative Properties of Electrolytes However, a 1 M solution of NaCl does not show twice the change in freezing point that a 1 M solution of methanol does.
  • 57. Solutions van’t Hoff Factor One mole of NaCl in water does not really give rise to two moles of ions.
  • 58. Solutions van’t Hoff Factor Some Na+ and Cl− reassociate for a short time, so the true concentration of particles is somewhat less than two times the concentration of NaCl.
  • 59. Solutions The van’t Hoff Factor • Reassociation is more likely at higher concentration. • Therefore, the number of particles present is concentration dependent.
  • 60. Solutions The van’t Hoff Factor We modify the previous equations by multiplying by the van’t Hoff factor, i Tf = Kf  m  i
  • 61. Solutions Osmosis • Some substances form semipermeable membranes, allowing some smaller particles to pass through, but blocking other larger particles. • In biological systems, most semipermeable membranes allow water to pass through, but solutes are not free to do so.
  • 62. Solutions Osmosis In osmosis, there is net movement of solvent from the area of higher solvent concentration (lower solute concentration) to the are of lower solvent concentration (higher solute concentration).
  • 63. Solutions Osmotic Pressure • The pressure required to stop osmosis, known as osmotic pressure, , is n V  = ( )RT = MRT where M is the molarity of the solution If the osmotic pressure is the same on both sides of a membrane (i.e., the concentrations are the same), the solutions are isotonic.play animation
  • 64. Solutions Osmosis in Blood Cells • If the solute concentration outside the cell is greater than that inside the cell, the solution is hypertonic. • Water will flow out of the cell, and crenation results.
  • 65. Solutions Osmosis in Cells • If the solute concentration outside the cell is less than that inside the cell, the solution is hypotonic. • Water will flow into the cell, and hemolysis results.
  • 66. Solutions SAMPLE EXERCISE 13.11 Calculations Involving Osmotic Pressure The average osmotic pressure of blood is 7.7 atm at 25°C. What concentration of glucose (C6H12O6) will be isotonic with blood? Comment: In clinical situations the concentrations of solutions are generally expressed as mass percentages. The mass percentage of a 0.31 M solution of glucose is 5.3%. The concentration of NaCl that is isotonic with blood is 0.16 M because NaCl ionizes to form two particles, Na+ and Cl– (a 0.155 M solution of NaCl is 0.310 M in particles). A 0.16 M solution of NaCl is 0.9 mass % in NaCl. This kind of solution is known as a physiological saline solution. PRACTICE EXERCISE What is the osmotic pressure at 20°C of a 0.0020 M sucrose (C12H22O11) solution? Answer: 0.048 atm, or 37 torr Solution Analyze: We are asked to calculate the concentration of glucose in water that would be isotonic with blood, given that the osmotic pressure of blood at 25°C is 7.7 atm. Plan: Because we are given the osmotic pressure and temperature, we can solve for the concentration, using Equation 13.13. Solve:
  • 67. Solutions Molar Mass from Colligative Properties We can use the effects of a colligative property such as osmotic pressure to determine the molar mass of a compound.
  • 68. Solutions SAMPLE EXERCISE 13.10 Freezing-Point Depression in Aqueous Solutions List the following aqueous solutions in order of their expected freezing point: 0.050 m CaCl2, 0.15 m NaCl, 0.10 m HCl, 0.050 m HC2H3O2, 0.10 m C12H22O11. Solution Analyze: We must order five aqueous solutions according to expected freezing points, based on molalities and the solute formulas. Plan: The lowest freezing point will correspond to the solution with the greatest concentration of solute particles. To determine the total concentration of solute particles in each case, we must determine whether the substance is a nonelectrolyte or an electrolyte and consider the number of ions formed when it ionizes. Solve: CaCl2, NaCl, and HCl are strong electrolytes, HC2H3O2, is a weak electrolyte, and C12H22O11 is a nonelectrolyte. The molality of each solution in total particles is as follows: Because the freezing points depend on the total molality of particles in solution, the expected ordering is 0.15 m NaCl (lowest freezing point), 0.10 m HCl, 0.050 m CaCl2, 0.10 m C12H22O11, and 0.050 m HC2H3O2, (highest freezing point).
  • 69. Solutions SAMPLE EXERCISE 13.10 continued PRACTICE EXERCISE Which of the following solutes will produce the largest increase in boiling point upon addition to 1 kg of water: 1 mol of Co(NO3)2, 2 mol of KCl, 3 mol of ethylene glycol (C2H6O2)? Answer: 2 mol of KCl because it contains the highest concentration of particles, 2 m K+ and 2 m Cl–, giving 4 m in all
  • 70. Solutions SAMPLE EXERCISE 13.12 Molar Mass from Freezing-Point Depression A solution of an unknown nonvolatile electrolyte was prepared by dissolving 0.250 g of the substance in 40.0 g of CCl4. The boiling point of the resultant solution was 0.357°C higher than that of the pure solvent. Calculate the molar mass of the solute. Solution Analyze: Our goal is to calculate the molar mass of a solute based on knowledge of the boiling-point elevation of its solution in CCl4, Tb = 0.357ºC, and the masses of solute and solvent. Table 13.4 gives Kb for the solvent (CCl4), Kb = 5.02ºC/m. Plan: We can use Equation 13.11, Tb = Kbm, to calculate the molality of the solution. Then we can use molality and the quantity of solvent (40.0 g CCl4) to calculate the number of moles of solute. Finally, the molar mass of the solute equals the number of grams per mole, so we divide the number of grams of solute (0.250 g) by the number of moles we have just calculated. Solve: From Equation 13.11 we have Thus, the solution contains 0.0711 mol of solute per kilogram of solvent. The solution was prepared using 40.0 g = 0.0400 kg of solvent (CCl4). The number of moles of solute in the solution is therefore
  • 71. Solutions PRACTICE EXERCISE Camphor (C10H16O) melts at 179.8°C, and it has a particularly large freezing-point-depression constant, Kf = 40.0ºC/m. When 0.186 g of an organic substance of unknown molar mass is dissolved in 22.01 g of liquid camphor, the freezing point of the mixture is found to be 176.7°C. What is the molar mass of the solute? Answer: 110 g/mol SAMPLE EXERCISE 13.12 continued The molar mass of the solute is the number of grams per mole of the substance:
  • 72. Solutions SAMPLE EXERCISE 13.13 Molar Mass from Osmotic Pressure The osmotic pressure of an aqueous solution of a certain protein was measured in order to determine the protein’s molar mass. The solution contained 3.50 mg of protein dissolved in sufficient water to form 5.00 mL of solution. The osmotic pressure of the solution at 25°C was found to be 1.54 torr. Calculate the molar mass of the protein. Solution Analyze: Our goal is to calculate the molar mass of a high-molecular-mass protein, based on its osmotic pressure and a knowledge of the mass of protein and solution volume. Plan: The temperature (T = 25ºC) and osmotic pressure ( = 1.54 torr) are given, and we know the value of R so we can use Equation 13.13 to calculate the molarity of the solution, M. In doing so, we must convert temperature from °C to K and the osmotic pressure from torr to atm. We then use the molarity and the volume of the solution (5.00 mL) to determine the number of moles of solute. Finally, we obtain the molar mass by dividing the mass of the solute (3.50 mg) by the number of moles of solute. Solve: Solving Equation 13.13 for molarity gives Because the volume of the solution is 5.00 ml = 5.00  10–3 L, the number of moles of protein must be
  • 73. Solutions Comment: Because small pressures can be measured easily and accurately, osmotic pressure measurements provide a useful way to determine the molar masses of large molecules. PRACTICE EXERCISE A sample of 2.05 g of polystyrene of uniform polymer chain length was dissolved in enough toluene to form 0.100 L of solution. The osmotic pressure of this solution was found to be 1.21 kPa at 25°C. Calculate the molar mass of the polystyrene. Answer: 4.20  104 g/mol SAMPLE EXERCISE 13.13 continued The molar mass is the number of grams per mole of the substance. The sample has a mass of 3.50 mg = 3.50  10–3g. The molar mass is the number of grams divided by the number of moles:
  • 74. Solutions Colloids: Suspensions of particles larger than individual ions or molecules, but too small to be settled out by gravity.
  • 75. Solutions Tyndall Effect • Colloidal suspensions can scatter rays of light. • This phenomenon is known as the Tyndall effect.
  • 76. Solutions Colloids in Biological Systems Some molecules have a polar, hydrophilic (water-loving) end and a nonpolar, hydrophobic (water- hating) end.
  • 77. Solutions Colloids in Biological Systems Sodium stearate is one example of such a molecule.
  • 78. Solutions Colloids in Biological Systems These molecules can aid in the emulsification of fats and oils in aqueous solutions.
  • 79. Solutions SAMPLE INTEGRATIVE EXERCISE Putting Concepts Together A 0.100-L solution is made by dissolving 0.441 g of CaCl2(s) in water. (a) Calculate the osmotic pressure of this solution at 27°C, assuming that it is completely dissociated into its component ions. (b) The measured osmotic pressure of this solution is 2.56 atm at 27°C. Explain why it is less than the value calculated in (a), and calculate the van’t Hoff factor, i, for the solute in this solution. (See the “Closer Look” box in Section 13.5 on page 557.) (c) The enthalpy of solution for CaCl2 is H = –81.3 kJ/mol. If the final temperature of the solution was 27.0°C, what was its initial temperature? (Assume that the density of the solution is 1.00 g /mL, that its specific heat is 4.18 J/g-K, and that the solution loses no heat to its surroundings.) Solution (a) The osmotic pressure is given by Equation 13.13, π = MRT. We know the temperature, T = 27ºC = 300 K and the gas constant, R = 0.0821 L-atm/mol-K. We can calculate the molarity of the solution from the mass of CaCl2 and the volume of the solution: Soluble ionic compounds are strong electrolytes. • (Sections 4.1 and 4.3) Thus, CaCl2 consists of metal cations (Ca2+) and nonmetal anions (Cl–). When completely dissociated, each CaCl2 unit forms three ions (one (Ca2+) and two Cl–). Hence the total concentration of ions in the solution is (3)(0.0397 M) = 0.119 M, and the osmotic pressure is
  • 80. Solutions A kelvin has the same size as a degree Celsius. • (Section 1.4) Because the solution temperature increases by 0.773°C, the initial temperature was 27.0ºC – 0.773ºC = 26.2°C. The heat absorbed by the solution is q = +0.323 kJ = 323 J. The mass of the 0.100 L of solution is (100 mL)(1.00 g/mL) = 100 g (to 3 significant figures). Thus the temperature change is Thus, the solution behaves as if the CaCl2 has dissociated into 2.62 particles instead of the ideal 3. (c) If the solution is 0.0397 M in CaCl2 and has a total volume of 0.100 L, the number of moles of solute is (0.100 L)(0.0397 mol/L) = 0.00397 mol. Hence the quantity of heat generated in forming the solution is (0.00397 mol)(–81.3 kJ/mol) = –0.323 kJ. The solution absorbs this heat, causing its temperature to increase. The relationship between temperature change and heat is given by Equation 5.19: SAMPLE INTEGRATIVE EXERCISE continued (b) The actual values of colligative properties of electrolytes are less than those calculated, because the electrostatic interactions between ions limit their independent movements. In this case the van’t Hoff factor, which measures the extent to which electrolytes actually dissociate into ions, is given by