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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.
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
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.
Solutions
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
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.
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.
Solutions
Temperature
Generally, the
solubility of solid
solutes in liquid
solvents increases
with increasing
temperature.
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.
Solutions
Ways of
Expressing
Concentrations
of Solutions
Solutions
Mass Percentage
Mass % of A =
mass of A in solution
total mass of solution
× 100
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
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
Changing Molarity to Molality
If we know the
density of the
solution, we can
calculate the
molality from the
molarity, and vice
versa.
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
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
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
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.
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.
Solutions
van’t Hoff Factor
One mole of NaCl in
water does not really
give rise to two
moles of ions.
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.
Solutions
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.
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).
Solutions
Osmotic Pressure
• The pressure required to stop osmosis,
known as osmotic pressure, π, is
n
V
π = ( )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.
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.
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
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
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.

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Chapter 13

  • 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.
  • 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 Student, Beware! Just because a substance disappears when it comes in contact with a solvent, it doesn’t mean the substance dissolved.
  • 13. 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.
  • 14. 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.
  • 15. Solutions Types of Solutions • Unsaturated Less than the maximum amount of solute for that temperature is dissolved in the solvent.
  • 16. 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.
  • 17. 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.
  • 18. Solutions Factors Affecting Solubility The more similar the intermolecular attractions, the more likely one substance is to be soluble in another.
  • 19. Solutions Factors Affecting Solubility Glucose (which has hydrogen bonding) is very soluble in water, while cyclohexane (which only has dispersion forces) is not.
  • 20. Solutions Factors Affecting Solubility • Vitamin A is soluble in nonpolar compounds (like fats). • Vitamin C is soluble in water.
  • 21. Solutions Gases in Solution • In general, the solubility of gases in water increases with increasing mass. • Larger molecules have stronger dispersion forces.
  • 22. 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.
  • 23. 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.
  • 24. Solutions Temperature Generally, the solubility of solid solutes in liquid solvents increases with increasing temperature.
  • 25. 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.
  • 27. Solutions Mass Percentage Mass % of A = mass of A in solution total mass of solution × 100
  • 28. 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
  • 29. 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!
  • 30. 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.
  • 31. 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.
  • 32. Solutions Changing Molarity to Molality If we know the density of the solution, we can calculate the molality from the molarity, and vice versa.
  • 33. 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
  • 34. 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.
  • 35. Solutions Vapor Pressure Therefore, the vapor pressure of a solution is lower than that of the pure solvent.
  • 36. 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.
  • 37. 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.
  • 38. 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.
  • 39. 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.
  • 40. 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
  • 41. 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.
  • 42. 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.
  • 43. Solutions van’t Hoff Factor One mole of NaCl in water does not really give rise to two moles of ions.
  • 44. 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.
  • 45. Solutions The van’t Hoff Factor • Reassociation is more likely at higher concentration. • Therefore, the number of particles present is concentration dependent.
  • 46. Solutions The van’t Hoff Factor We modify the previous equations by multiplying by the van’t Hoff factor, i ∆Tf = Kf  m  i
  • 47. 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.
  • 48. 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).
  • 49. Solutions Osmotic Pressure • The pressure required to stop osmosis, known as osmotic pressure, π, is n V π = ( )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.
  • 50. 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.
  • 51. 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.
  • 52. 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.
  • 53. Solutions Colloids: Suspensions of particles larger than individual ions or molecules, but too small to be settled out by gravity.
  • 54. Solutions Tyndall Effect • Colloidal suspensions can scatter rays of light. • This phenomenon is known as the Tyndall effect.
  • 55. Solutions Colloids in Biological Systems Some molecules have a polar, hydrophilic (water-loving) end and a nonpolar, hydrophobic (water- hating) end.
  • 56. Solutions Colloids in Biological Systems Sodium stearate is one example of such a molecule.
  • 57. Solutions Colloids in Biological Systems These molecules can aid in the emulsification of fats and oils in aqueous solutions.