chapter 13 lecture on solutions & colligative properties

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Chapter 11- Properties of Solutions Sections 13.1 - 13.3 Dissolving Solubility Read pg 529 – 543 pg 564 #1, 2, 3, 4, 6, 12, 13, 17, 19, 22, 25, 27, 29, 31, 84

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Chapter 13 Lecture for AP Chemistry

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Page 1: Chapter 13 Lecture on Solutions & Colligative Properties

Chapter 11- Properties of Solutions

Sections 13.1 - 13.3

Dissolving SolubilityRead pg 529 – 543 pg 564 #1, 2, 3, 4, 6, 12, 13, 17, 19, 22, 25, 27, 29, 31, 84

Page 2: Chapter 13 Lecture on Solutions & Colligative Properties

Solutions

• Solutions are homogeneous mixtures of two or more pure substances.

• In a solution, the solute is dispersed uniformly throughout the solvent.

Page 3: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 4: Chapter 13 Lecture on Solutions & Colligative Properties

How Does a Solution Form?

As a solution forms, the solvent pulls solute particles apart and surrounds, or solvates, them.

Page 5: Chapter 13 Lecture on Solutions & Colligative Properties

QuickTime™ and aSorenson Video decompressorare needed to see this picture.

Page 6: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 7: Chapter 13 Lecture on Solutions & Colligative Properties

From weakest to strongest, rank the following solutions in terms of solvent–solute interactions: NaCl in water, butane (C4H10) in benzene (C6H6), water in ethanol.

1. NaCl in water < C4H10 in C6H6 < water in ethanol2. Water in ethanol < NaCl in water < C4H10 in

C6H6 3. C4H10 in C6H6 < water in ethanol < NaCl in

water

Page 8: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

Butane in benzene will have only weak dispersion force interactions. Water in ethanol will exhibit much stronger hydrogen-bonding interactions. However, NaCl in water will show ion–dipole interactions because NaCl will dissolve into ions.

1. NaCl in water < C4H10 in C6H6 < water in ethanol2. Water in ethanol < NaCl in water < C4H10 in

C6H6 3. C4H10 in C6H6 < water in ethanol < NaCl in

water

Page 9: Chapter 13 Lecture on Solutions & Colligative Properties

Energy Changes in Solution

• Simply put, three processes affect the energetics of the process:Separation of solute

particlesSeparation of solvent

particlesNew interactions between

solute and solvent

Page 10: Chapter 13 Lecture on Solutions & Colligative Properties

Energy Changes in Solution

The enthalpy change of the overall process depends on H for each of these steps.

Page 11: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 12: Chapter 13 Lecture on Solutions & Colligative Properties

Why Do Endothermic Processes Occur?

Yet we know that in some processes, like the dissolution of NH4NO3 in water, heat is absorbed, not released.

Page 13: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 14: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 15: Chapter 13 Lecture on Solutions & Colligative Properties

Water vapor reacts with excess solid sodium sulfate to form the hydrated form of the salt. The chemical reaction is

Does the entropy increase or decrease?

SAMPLE EXERCISE 13.1 Assessing Entropy Change

Page 16: Chapter 13 Lecture on Solutions & Colligative Properties

Answer: The entropy increases because each gas eventually becomes dispersed in twice the volume it originally occupied.

The water vapor becomes less dispersed (more ordered). When a system becomes more ordered, its entropy is decreased.

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?

Page 17: Chapter 13 Lecture on Solutions & Colligative Properties

Student, Beware!

Just because a substance disappears when it comes in contact with a solvent, it doesn’t mean the substance dissolved.

Page 18: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 19: Chapter 13 Lecture on Solutions & Colligative Properties

Types of Solutions

• SaturatedSolvent holds as much

solute as is possible at that temperature.

Dissolved solute is in dynamic equilibrium with solid solute particles.

Page 20: Chapter 13 Lecture on Solutions & Colligative Properties

Types of Solutions

• UnsaturatedLess than the

maximum amount of solute for that temperature is dissolved in the solvent.

Page 21: Chapter 13 Lecture on Solutions & Colligative Properties

Types of Solutions

• SupersaturatedSolvent 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.

Page 22: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 23: Chapter 13 Lecture on Solutions & Colligative Properties

Factors Affecting Solubility

The more similar the intermolecular attractions, the more likely one substance is to be soluble in another.

Page 24: Chapter 13 Lecture on Solutions & Colligative Properties

Factors Affecting Solubility

Glucose (which has hydrogen bonding) is very soluble in water, while cyclohexane (which only has dispersion forces) is not.

Page 25: Chapter 13 Lecture on Solutions & Colligative Properties

Factors Affecting Solubility

• Vitamin A is soluble in nonpolar compounds (like fats).

• Vitamin C is soluble in water.

Page 26: Chapter 13 Lecture on Solutions & Colligative Properties

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. Solution 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.

Page 27: Chapter 13 Lecture on Solutions & Colligative Properties

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:

Page 28: Chapter 13 Lecture on Solutions & Colligative Properties

Gases in Solution

• In general, the solubility of gases in water increases with increasing mass.

• Larger molecules have stronger dispersion forces.

Page 29: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 30: Chapter 13 Lecture on Solutions & Colligative Properties

Henry’s LawSg = 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.

Page 31: Chapter 13 Lecture on Solutions & Colligative Properties

QuickTime™ and aSorenson Video decompressorare needed to see this picture.

Page 32: Chapter 13 Lecture on Solutions & Colligative Properties

At a certain temperature, the Henry’s law constant for N2 is 6.0 104 M/atm. If N2 is present at 3.0 atm, what is the solubility of N2?

1. 6.0 104 M2. 1.8 103 M3. 2.0 104 M4. 5.0 105 M

Page 33: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

Henry’s law,

Sg = kPg

Sg = (6.0 104 M/atm)(3.0 atm)

Sg = 1.8 103 M

1. 6.0 104 M2. 1.8 103 M3. 2.0 104 M4. 5.0 105 M

Page 34: Chapter 13 Lecture on Solutions & Colligative Properties

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.

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

Page 35: Chapter 13 Lecture on Solutions & Colligative Properties

Temperature

Generally, the solubility of solid solutes in liquid solvents increases with increasing temperature.

Page 36: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 37: Chapter 13 Lecture on Solutions & Colligative Properties

Chapter 11- Properties of Solutions

Section 13.4

Ways of Expressing Concentrations of Solutions Read pg 529 – 543 pg 564 #1, 2, 3, 4, 6, 12, 13, 17, 19, 22, 25, 27, 29, 31, 84

Page 38: Chapter 13 Lecture on Solutions & Colligative Properties

Mass Percentage

Mass % of A =mass of A in solutiontotal mass of solution

100

Page 39: Chapter 13 Lecture on Solutions & Colligative Properties

Determine the mass percentage of hexane in a solution containing 11 g of butane in 110 g of hexane.

1.9.0 %2.10. %3.90.%4.91 %

Page 40: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

Thus,

110 g(110 g + 11 g)

100solution of mass total

solution incomponent of masscomponent of % mass

100 = 91%

1. 9.0 %2. 10. %3. 90.%4. 91 %

Page 41: Chapter 13 Lecture on Solutions & Colligative Properties

Parts per Million andParts per Billion

ppm =mass of A in solutiontotal mass of solution

106

Parts per Million (ppm)

Parts per Billion (ppb)

ppb =mass of A in solutiontotal mass of solution

109

Page 42: Chapter 13 Lecture on Solutions & Colligative Properties

If 3.6 mg of Na+ is detected in a 200. g sample of water from Lake Erie, what is its concentration in ppm?

1. 7.2 ppm2. 1.8 ppm3. 18 ppm4. 72 ppm

Page 43: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

610solution of mass total

solution incomponent of masscomponent of ppm

ppm 1810g 200.

g 0.0036

g 200.

mg 3.6 6

1. 7.2 ppm2. 1.8 ppm3. 18 ppm4. 72 ppm

Page 44: Chapter 13 Lecture on Solutions & Colligative Properties

moles of Atotal 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!

Page 45: Chapter 13 Lecture on Solutions & Colligative Properties

mol of soluteL of solution

M =

Molarity (M)

• You will recall this concentration measure from Chapter 4.

• Because volume is temperature dependent, molarity can change with temperature.

Page 46: Chapter 13 Lecture on Solutions & Colligative Properties

mol of solutekg of solvent

m =

Molality (m)

Because both moles and mass do not change with temperature, molality (unlike molarity) is not temperature dependent.

Page 47: Chapter 13 Lecture on Solutions & Colligative Properties

What is the molality of 6.4 g of methanol (CH3OH) dissolved in 50.

moles of water?

1. 0.040 m2. 0.22 m3. 0.064 m4. 0.11 m

Page 48: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

kg/1000g) g/mol)(1 .0 water)(18mol (50

g/mol) (32.0methanol)/ g (6.4=m

mm 0.22kg) (0.90

mol) (0.20==

1. 0.040 m2. 0.22 m3. 0.064 m4. 0.11 m

Page 49: Chapter 13 Lecture on Solutions & Colligative Properties

Changing Molarity to Molality

If we know the density of the solution, we can calculate the molality from the molarity, and vice versa.

Page 50: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Solution molar mass of glucose, 180.2 g/mol

water has a density of 1.00 g/mL, so the mass of the solvent is

Page 51: Chapter 13 Lecture on Solutions & Colligative Properties

Chapter 11- Properties of Solutions

Section 13.5 & 13.6

Colligative Properties &ColloidsRead pg 529 – 543 pg 564 #1, 2, 3, 4, 6, 12, 13, 17, 19, 22, 25, 27, 29, 31, 84

Page 52: Chapter 13 Lecture on Solutions & Colligative Properties

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 areVapor pressure lowering Boiling point elevationMelting point depressionOsmotic pressure

Page 53: Chapter 13 Lecture on Solutions & Colligative Properties

Vapor Pressure

Because of solute-solvent intermolecular attraction, higher concentrations of nonvolatile solutes make it harder for solvent to escape to the vapor phase.

Page 54: Chapter 13 Lecture on Solutions & Colligative Properties

Vapor Pressure

Therefore, the vapor pressure of a solution is lower than that of the pure solvent.

Page 55: Chapter 13 Lecture on Solutions & Colligative Properties

Raoult’s Law

PA = XAPAwhere• XA is the mole fraction of compound A

• PA 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.

Page 56: Chapter 13 Lecture on Solutions & Colligative Properties

At a certain temperature, water has a vapor pressure of 90.0 torr. Calculate the vapor pressure of a water solution containing 0.080 mole sucrose and 0.72 mole water.

1. 9.0 torr2. 10. torr3. 80. torr

4. 81. torr5. 90. torr

Page 57: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

totali PP i

Pi = XiPtotal

Pi = (0.72 mol/[0.72 + 0.080 mol])(90.0 torr)

Pi = (0.90)(90.0 torr) = 81. torr

1. 9.0 torr2. 10. torr3. 80. torr4. 81. torr5. 90. torr

Page 58: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 59: Chapter 13 Lecture on Solutions & Colligative Properties

Boiling Point ElevationThe 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.

Page 60: Chapter 13 Lecture on Solutions & Colligative Properties

Ethanol normally boils at 78.4°C. The boiling point elevation constant for ethanol is 1.22°C/m. What is the boiling point of a 1.0 m solution of CaCl2 in ethanol?

1. 77.2°C2. 79.6°C3. 80.8°C

4. 82.1°C5. 83.3°C

Page 61: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

The increase in boiling point is determined by the molality of total particles in the solution. Thus, a 1.0 m solution of CaCl2 contains 1.0 m Ca2+ and

2.0 m Cl for a total of 3.0 m. Thus, the boiling point is elevated 3.7°C, so it is 78.4°C + 3.7°C = 82.1°C.

mKT bb

1. 77.2°C2. 79.6°C3. 80.8°C4. 82.1°C5. 83.3°C

Page 62: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 63: Chapter 13 Lecture on Solutions & Colligative Properties

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

Page 64: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 65: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 66: Chapter 13 Lecture on Solutions & Colligative Properties

van’t Hoff Factor

One mole of NaCl in water does not really give rise to two moles of ions.

Page 67: Chapter 13 Lecture on Solutions & Colligative Properties

van’t Hoff Factor

Some Na+ and Cl− reassociate for a short time, so the true concentration of particles is a little less than two times the concentration of NaCl.

Page 68: Chapter 13 Lecture on Solutions & Colligative Properties

The van’t Hoff Factor

• Reassociation is more likely at higher concentration.

• Therefore, the number of particles present is concentration dependent.

Page 69: Chapter 13 Lecture on Solutions & Colligative Properties

The van’t Hoff Factor

We modify the previous equations by multiplying by the van’t Hoff factor, i

Tf = Kf m i

Page 70: Chapter 13 Lecture on Solutions & Colligative Properties

PRACTICE EXERCISEWhich 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

Page 71: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 72: Chapter 13 Lecture on Solutions & Colligative Properties

OsmosisIn 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).

Page 73: Chapter 13 Lecture on Solutions & Colligative Properties

Osmotic Pressure

• The pressure required to stop osmosis, known as osmotic pressure, , is

nV

= ( )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.

Page 74: Chapter 13 Lecture on Solutions & Colligative Properties

QuickTime™ and aSorenson Video 3 decompressorare needed to see this picture.

Page 75: Chapter 13 Lecture on Solutions & Colligative Properties

At 300 K, the osmotic pressure of a solution is 0.246 atm. What is its concentration of the solute?

1. 1.0 M2. 0.50 M3. 0.25 M4. 0.10 M

Page 76: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

M = /RT

M = (0.246 atm)/[(0.0821 L-atm/mol-K)(300K)]

M = (0.246 atm)/(0.2463 L-atm/mol) = 1.0 M

MRTRTV

n

1. 1.0 M2. 0.50 M3. 0.25 M4. 0.10 M

( )

Page 77: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 78: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 79: Chapter 13 Lecture on Solutions & Colligative Properties

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?

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

SolutionPlan: Given the osmotic pressure and temperature, we can solve for the concentration, using Equation 13.13.

Solve:

Page 80: Chapter 13 Lecture on Solutions & Colligative Properties

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.

Page 81: Chapter 13 Lecture on Solutions & Colligative Properties

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.SolutionPlan: Kb for the solvent (CCl4)= 5.02ºC/m. Tb = Kbm.

Solve:

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

Page 82: Chapter 13 Lecture on Solutions & Colligative Properties

PRACTICE EXERCISECamphor (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

Page 83: Chapter 13 Lecture on Solutions & Colligative Properties

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 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

Page 84: Chapter 13 Lecture on Solutions & Colligative Properties

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 EXERCISEA 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:

Page 85: Chapter 13 Lecture on Solutions & Colligative Properties

Colloids:

Suspensions of particles larger than individual ions or molecules, but too small to be settled out by gravity.

Page 86: Chapter 13 Lecture on Solutions & Colligative Properties

Tyndall Effect

• Colloidal suspensions can scatter rays of light.

• This phenomenon is known as the Tyndall effect.

Page 87: Chapter 13 Lecture on Solutions & Colligative Properties

Which of the following is not an example of a colloid?

1. Fog2. Smoke3. Paint4. Milk5. Carbonated water

Page 88: Chapter 13 Lecture on Solutions & Colligative Properties

Correct Answer:

Carbonated water is a solution; all the other substances in the list are excellent examples of colloids.

1. Fog2. Smoke3. Paint4. Milk5. Carbonated water

Page 89: Chapter 13 Lecture on Solutions & Colligative Properties

Colloids in Biological Systems

Some molecules have a polar, hydrophilic (water-loving) end and a nonpolar, hydrophobic (water-hating) end.

Page 90: Chapter 13 Lecture on Solutions & Colligative Properties

Colloids in Biological Systems

Sodium stearate is one example of such a molecule.

Page 91: Chapter 13 Lecture on Solutions & Colligative Properties

Colloids in Biological Systems

These molecules can aid in the emulsification of fats and oils in aqueous solutions.