Phases Flashcards

How does a dissolved solute affect the vapor pressure of water? When does a gas most closely mimic ideal behavior? Master these topics and much more, and gain that confidence you need for the Chemical & Physical Foundations section of the MCAT.

1
Q

Define:

a phase of matter

A

It is a physically distinct form of a substance that can be separated from another form.

Generally “phase” is used interchangeably with “state of matter.”

Solid, liquid, and gas are the three phases of matter that the MCAT will test. Though plasmas are an additional state of matter, the MCAT does not explicitly test them.

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2
Q

Which two state functions can be used to actively change the phase of a substance?

A
  • Temperature can be added or removed. In general, an increase in temperature drives the phase change solid⇒liquid⇒gas.
  • Pressure (volume) can be increased or decreased. In general, an increase in pressure (or decrease in volume) drives the phase change gas⇒liquid⇒solid.
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3
Q

What name is associated with a phase change from

  1. solid to liquid?
  2. liquid to solid?
A
  1. A change from solid to liquid is melting, or fusion.
  2. A change from liquid to solid is freezing, or solidification.
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4
Q

What name is associated with a phase change from

  1. gas to liquid?
  2. liquid to gas?
A
  1. A change from gas to liquid is condensation.
  2. A change from liquid to gas is boiling, or vaporization.
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5
Q

What name is associated with a phase change from

  1. gas to solid?
  2. solid to gas?
A
  1. A change from gas to solid is deposition.
  2. A change from solid to gas is sublimation.
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6
Q

What phase is the substance in regions A, B, and C in the diagram below?

A

A represents the region of the solid phase, while B is the liquid phase and C is the gas phase.

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7
Q

What phase conversions are being shown with the arrows marked A and B?

A

A is fusion (or melting), while B is freezing (or solidification).

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8
Q

What phase conversions are being shown with the arrows marked A and B?

A

A is vaporization (or boiling), while B is condensation.

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9
Q

What phase conversions are being shown with the arrows marked A and B?

A

A is sublimation, while B is deposition.

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10
Q

What points are the arrows marked A and B pointing to?

A

A is the triple point; B is the critical point.

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11
Q

Explain the significance of the critical point.

A

The critical temperature and critical pressure combine to form the critical point.

  • The critical temperature is the temperature above which a distinct liquid-to-gas vaporization can no longer be accurately determined.
  • The critical pressure is the pressure above which a distinct gas-to-liquid condensation can no longer be accurately determined.
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12
Q

Explain the significance of the triple point.

A

It is the point at which a substance can exist in equilibrium in all three states (solid, liquid, and gas).

For example, water at its triple point exists as ice, liquid water, and steam - all at one temperature and pressure. A substance at its triple point can instantaneously interconvert between any phase.

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13
Q

How does the phase diagram of water differ from the one below?

A

The solid/liquid boundary for water has a slight negative slope.

This occurs because water’s solid phase is less dense than its liquid phase.

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14
Q

Different materials require different amounts of heat in order to transition into a new phase. Why is this?

A

This difference exists due to intermolecular forces.

The attraction of molecules to each other determines the temperature at which a substance will change phase, and subsequently dictates the amount of heat necessary to undergo that transition (termed the heat of vaporization or the heat of fusion, depending on the phase change).

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15
Q

Name three types of intermolecular forces.

A

From strongest to weakest, the intermolecular forces are:
1. hydrogen bonds
2. dipole-dipole forces
3. London dispersion forces

Intermolecular forces are attractive forces between separate molecules, not actual bonds.

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16
Q

Define:

dipole-dipole forces

A

They occur when a molecule has a net dipole moment. The molecule’s dipole is attracted to the dipoles of other molecules in the same sample.

This attraction exists due to Coulombic forces; the positive end of the dipole is attracted to negative charges and vice versa.

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17
Q

Define:

hydrogen bonds

A

They are an extreme form of dipole forces. They occur when a hydrogen atom is covalently bonded to O, N, or F.

The high electronegativity difference between these atoms and hydrogen creates strong dipoles, which result in the strongest dipole-dipole interactions between molecules.

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18
Q

Define:

London dispersion forces

A

They are attractions between nonpolar molecules as a result of instantaneous dipoles.

While nonpolar molecules do not contain permanent dipoles, their electron clouds can reorganize and lead to partial polarization. The more valence electrons present in a molecule, the larger the instantaneous dipole can be.

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19
Q

How do intermolecular forces affect the boiling point of a substance?

A

The stronger the intermolecular forces present, the higher the boiling point. In other words, the more tightly the molecules are attracted in the liquid phase, the more difficult the substance is to vaporize.

In the absence of other factors, hydrogen bonding correlates with the highest boiling points, followed by dipole-dipole forces. Nonpolar molecules, which only exhibit London dispersion forces, boil the most easily.

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20
Q

List the following forces from weakest to strongest: dipole-dipole forces, hydrogen bonding, London dispersion forces.

A
  1. London dispersion forces (weakest)
  2. dipole-dipole forces
  3. hydrogen bonding (strongest)
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21
Q

Define:

heat of vaporization

(Hvap)

A

It represents the energy necessary to convert one mole of a substance from the liquid phase to the gas phase at constant pressure.

Note that this process takes place at constant temperature, and is represented on a heating curve by a plateau region. ΔHvap is always positive, since vaporization is an endothermic process.

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22
Q

Define:

heat of fusion

A

It represents the energy required to melt one mole of a substance from the solid phase to the liquid phase at constant pressure.

Note that this process also takes place at constant temperature, and is represented on a heating curve by a plateau region. ΔHfus is always positive, since melting is an endothermic process.

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23
Q

What processes are associated with the plateaus labeled A and B on the general heating curve below?

A
  • At A, fusion is occurring.
    Hfusion can used to calculate the heat needed for this process.
  • At B, vaporization is occurring.
    Hvap can be used to calculate the heat needed for this process.
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24
Q

In the diagram below, why are the slopes zero for the plateaus labeled A and B?

A

A slope of zero means that no temperature change is occurring. At these regions, the substance is undergoing a phase change, so any heat input is dedicated to breaking bonds between molecules instead of increasing temperature.

For example, during the vaporization of water, heat is needed to break the hydrogen bonds between liquid water molecules and convert it to gaseous steam.

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25
Q

In the diagram below, what equation determines the heat added in the regions where the temperature is rising?

A

q = mcΔT

Where:

q = heat required (J)
m = mass of the sample (g)
c = specific heat of the substance (J/g*K)
ΔT = temperature change (K)

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26
Q

What is the value of the specific heat (c) of water?

A

1 cal/g*K

In SI units, c ≈ 4.18 J/g*K.

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27
Q

In the diagram below, what equation can be used to calculate the heat required throughout the plateau regions?

A

q = mHL

Where:

q = heat required (J)
m = mass (g)
HL = latent heat of phase change (J/g)

This formula calculates the heat required to change a certain mass of a substance from one phase to another. For the first plateau, HL represents the heat of fusion; for the second plateau, it represents the heat of vaporization.

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28
Q

How much heat is required to increase the temperature of 20 grams of water by 5 degrees, starting at 20 ºC?

A

100 cal

At 20 ºC, water is a liquid and has a specific heat of 1 cal/gºC.

Since temperature is changing within this temperature range but phase is not, use the formula q = mcΔT.

q = 20 (1) (5) = 100 cal

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29
Q

Define:

colligative property

A

In a mixture, it is one that depends only on the number of molecules of solute dissolved in the solvent, not the solute’s chemical nature.

Vapor pressure, boiling point, freezing point, and osmotic pressure are all colligative properties.

30
Q

What relationship exists between a liquid’s vapor pressure and its boiling point?

A

The boiling point is the temperature in which the vapor pressure above a liquid equals the surrounding atmospheric pressure.

To boil a liquid, either its vapor pressure must be increased (usually by heating), or the atmospheric pressure must be decreased.

31
Q

Define:

mole fraction

A

It is the ratio of moles of a particular substance to the total moles of all substances present.

The formula for mole fraction is:

xA = nA / ntotal

Where:

xA = mole fraction of A
nA = number of moles of A
ntotal = total number of moles of all substances present

32
Q

Define:

Raoult’s Law

A

It defines the pressure above a mixture of liquids.

The formula for Raoult’s Law is:

Ptotal = P0AxA + P0BxB + …

Where:

Ptotal = total pressure above the mixture
P0A = vapor pressure of pure substance A
xA = mole fraction of substance A in the mixture

Each term represents the partial pressure above the mixture of one of the components.

33
Q

What is the partial pressure of acetone above a 50/50 molar mixture of water and acetone at STP, if the pure vapor pressure of acetone at STP is 100 torr?

A

50 torr

Raoult’s Law: Ptotal = P0AxA + P0BxB + …

The partial pressure of a liquid above a mixture is equal to the vapor pressure of the pure liquid times its mole fraction in the mixture. In a 50/50 mixture of water and acetone, each substance will only contribute half of the vapor pressure of the pure compound; for that reason, acetone’s partial pressure will be half of its pure vapor pressure.

34
Q

Define:

non-ideal solution

A

It is one that does not follow Raoult’s Law. Non-ideal solutions can have pressures either greater or less than those predicted by Raoult’s Law.

For example, a solution with large attractive forces between solute and solvent, such as salt water, will have a lower vapor pressure than that predicted by Raoult’s Law.

35
Q

Define:

van’t Hoff factor

(i)

A

It is the number of particles that an ionic solute yields upon dissociation.

For example, NaCl dissociates into Na+ and Cl- ions, a total of 2 per equivalent of NaCl. The van’t Hoff factor for NaCl is i = 2.

36
Q

What are the values of the van’t Hoff factor for:

  1. KOH
  2. C6H12O6
  3. H2SO4
  4. CaCl2
A
  1. KOH: i = 2 (K+ and OH-)
  2. C6H12O6: i = 1
  3. H2SO4: i = 3 (2H+ and SO42-)
  4. CaCl2: i = 3 (2Cl- and Ca2+)

Note that glucose, like other covalent compounds, does not dissociate.

37
Q

Define:

molality

(m)

A

It represents the number of moles of solute dissolved into one kilogram of solvent.

Molality uses the lowercase letter “m” in equations; be careful not to confuse this with mass. Also, note that the molality is measured per kilogram of solvent, not total solution.

38
Q

What equation can be used to find the boiling point elevation of a solvent after solute has been added?

A

ΔTb = Kbmi

Where:

Kb= a solvent-specific constant (kg*K/mol)
m = the molality of the solution (mol/kg)
i = the van’t Hoff factor of the solute
ΔTb = the temperature change of the solvent’s boiling point (K)

39
Q

Which will have a higher boiling point: a 1 m NaCl solution or a 1 m glucose solution?

A

NaCl solution

Remember that ΔTb = Kbmi. The i value for NaCl is 2, while the value for glucose is 1. The equimolar NaCl solution will thus have twice the boiling point elevation.

40
Q

When can the equation for boiling point elevation not be used?

A
  • the mixture is volatile
  • the solute does not fully dissolve or dissociate
  • a significant density difference exists between the mixture components, causing one to sit on top of the other
41
Q

How does addition of a solute affect the freezing point of a liquid?

A

The freezing point of a liquid will be lowered, as the solute hinders proper crystallization of the solvent molecules.

Freezing point depression is a colligative property.

42
Q

What equation can be used to find the freezing point depression of a solvent after solute has been added?

A

ΔTf = Kfmi

Where:

Kf = a solvent-specific constant (kg*K/mol)
m = the molality of the solution (mol/kg)
i = the van’t Hoff factor of the solvent
ΔTf = the temperature change of the solvent’s freezing point (K)

43
Q

Which will have a lower freezing point, a 1 m CaCl2 solution or a 2 m CaCl2 solution?

A

2 m solution

Based on the equation ΔTf = Kfmi, the 2 m solution will have twice the drop in freezing point of the 1 m solution.

44
Q

A chemist wants to melt the ice on her driveway on a very cold day, and has equal moles of each of the following substances to add to the ice. Based on colligative properties, which would work the best?

  1. H3PO4
  2. MgCl2
  3. C12H22O11
A

H3PO4

Assuming equimolal addition, H3PO4 will yield the largest decrease in the water’s freezing point because it has the highest van’t Hoff factor.

  1. The i value of H3PO4, or phosphoric acid, is 4.
  2. The i value of MgCl2, or magnesium chloride, is 3.
  3. The i value of C12H22O11, or sucrose, is 1.
45
Q

Which of the following aqueous solutions will have the lowest freezing point?

  1. 1 m BrCl
  2. 0.5 m Na2SO3
  3. 1.5 m KCl
A

1.5 m KCl (aq)

Freezing point depression is dependent on molality and the number of solute atoms per kilogram of water.

  1. BrCl = 1 m x 2 ions = 2
  2. Na2SO3 = 0.5 m x 3 ions = 1.5
  3. KCl = 1.5 m x 2 ions = 3
46
Q

How are hypertonic, isotonic, and hypotonic solutions defined?

A

A solution’s tonicity is defined relative to another solution, often referred to as the “standard.”

  • A hypertonic solution has a higher solute concentration than the standard.
  • An isotonic solution has the same solute concentration as the standard.
  • A hypotonic solution has a lower solute concentration than the standard.
47
Q

Define:

osmotic pressure

A

It is the pressure that results from a tonicity difference across a semipermeable membrane.

Water molecules will be drawn across the membrane toward the hypertonic side, in an attempt to promote isotonicity. For example, if red blood cells are placed in a hypotonic environment, water will flow into the cells and cause them to expand.

48
Q

What equation can be used to calculate osmotic pressure?

A

π = nRTi
V

Where:

Π = osmotic pressure (atm)
n = number of moles of solute
R = ideal gas constant (L-atm/K*mol)
T = temperature (K)
i = the van’t Hoff factor of the solute
V = volume (L)

49
Q

At a constant temperature, how will the osmotic pressure of a 1 M NaCl solution compare to that of a 1 M CaCl2 solution?

A

The osmotic pressure of the CaCl2 solution will be higher.

CaCl2 has a van’t Hoff factor of 3 (Ca+2, 2 Cl-) compared to 2 for NaCl (Na+, Cl-). Since Π = iMRT, and M,R,T are all constant, the van’t Hoff factors determine the osmotic pressure difference.

50
Q

How will the osmotic pressure of a solution change when its temperature is increased?

A

The osmotic pressure will be greater at a higher temperature.

Since Π = iMRT, and i,M,R are all constant, the difference between the new and old temperatures determines the osmotic pressure difference. Osmotic pressure and temperature are directly proportional.

51
Q

Define:

colloid

A

It is a system in which one substance is microscopically dispersed evenly throughout another substance.

Colloidal particles will not settle to the bottom due to gravity and time. Colloids can occur in any of the three phases of matter.

For example, air is a gaseous colloid composed of many gases, milk is a colloid of liquid butter fat in aqueous solution, and colored glass is a solid colloid of metal oxides in a silica matrix.

52
Q

What common characteristics distinguish colloids?

A
  • Colloids have a continuous phase, or dispersion medium, and an internal phase, or dispersed medium.
  • The internal phase particles are too small to easily extract physically, though it is possible to extract them chemically.
  • Liquid and solid colloids scatter light; in other words, they are opaque or translucent. Only gas colloids can be colorless.
53
Q

What values define Standard Temperature and Pressure (STP)?

A

They require a temperature of 0ºC (273 K) and a pressure of 1 atm.

The MCAT occasionally refers to standard state conditions, which (among other stipulations) require a temperature of 25ºC and a pressure of 1 atm.

54
Q

List the assumptions of the kinetic molecular theory of gases.

A

This theory assumes that gases act in an ideal fashion. Assumptions of this theory include:

  1. A gas molecule has no volume of its own.
  2. The collisions between gas molecules are completely elastic, so molecules do not lose energy due to dissipative forces.
  3. The average kinetic energy of gas molecules is directly proportional to the temperature of the gas.
55
Q

Define:

absolute temperature

A

It is any temperature that is given in Kelvin (K).

Absolute zero, or 0 K, is the temperature at which all molecules cease movement completely. To convert Kelvin to Celsius:

TK = TC + 273.15

56
Q

Define:

Charles’ Law

A

It states that the volume of a gas is directly proportional to its temperature at constant pressure.

Shown above is the equation for Charles’ Law.

57
Q

If the pressure of an ideal gas system is held constant but the temperature is doubled, what does Charles’ Law predict will happen to the volume?

A

The system’s volume will also double.

Charles’ Law indicates that at a constant pressure, the temperature and volume of a gas are directly proportional. Remember that you must use temperature in Kelvin, not Celsius, for Charles’ Law calculations.

58
Q

Define:

Boyle’s Law

A

It states that the volume of a gas is inversely proportional to its pressure at a constant temperature.

Shown above is the equation for Boyle’s Law.

59
Q

If the temperature of an ideal gas system is held constant but the pressure is reduced by 1/2, what does Boyle’s Law predict will happen to the volume?

A

The system’s volume will double.

Boyle’s Law indicates that at a constant temperature, the pressure and volume of a gas are inversely proportional. Remember that you must use temperature in Kelvin, not Celsius, for Boyle’s Law calculations.

60
Q

Define:

Avogadro’s Law

A

It states that the volume of a gas is directly proportional to its number of moles at a constant temperature and pressure.

V / n = constant

Where:

V = volume in L
n = number of moles

61
Q

If the pressure and temperature of an ideal gas system are held constant but the number of moles is decreased to 1/3 of the original value, what does Avogadro’s Law predict will happen to the system’s volume?

A

The system’s volume will also decrease to 1/3 of its original value.

Avogadro’s Law indicates that at a constant pressure and temperature, the number of moles and the volume of a gas are directly proportional.

62
Q

Define:

ideal gas law

A

It combines Charles’, Boyle’s, and Avogadro’s Laws into one.

PV = nRT

Where:

P = pressure (atm or Pa)
V = volume (L)
n = number of moles
R = the ideal gas constant: 0.082 L(atm)/mol(K) or 8.31 J/mol(K)
T = temperature (K)

63
Q

What is the volume of 1 mole of gas molecules at STP?

A

22.4 L

This is called the standard molar volume, and is true for a mole of any ideal gas at STP. While this value can be calculated using the ideal gas law, it is worth memorizing.

64
Q

How is the partial pressure of a gas in a mixture calculated?

A

PA = xAPtotal

Where:

PA = pressure from gas A
xA = mole fraction of A (a ratio of the moles of A to the total moles of gas)
Ptotal = total pressure of the sytem due to all gases present

65
Q

Define:

Dalton’s Law

A

Ptotal = PA + PB + PC + …

It states that the total pressure of a system of ideal gases is equal to the sum of the partial pressures of all gases in the mixture.

66
Q

How is the average kinetic energy of an ideal gas calculated?

A

KEavg = (3/2)nRT

Where:

KEavg = average kinetic energy (J)
n = number of moles of gas
R = ideal gas constant: 0.082 L(atm)/mol(K) or 8.31 J/mol(K)
T = temperature (K)

67
Q

When do gases deviate most from ideal behavior?

A
  1. low temperatures
  2. high pressures (low volume)
68
Q

Why do low temperatures and high pressures cause a gas to deviate from ideal behavior?

A

Gases deviate from ideal at low temperatures because the molecules have very low kinetic energy and their motion will be affected by intermolecular attractive forces.

Gases deviate from ideal at high pressures, or very low volumes, because the molecules get forced closer together, and will start to exhibit characteristics more like a liquid than a gas.

69
Q

What does the van der Waals equation of state measure?

A

It can be used to calculate the degree of deviation from ideal gas behavior.

(P + a(n/V)2)(V - nb) = nRT

Where:

P = pressure (atm or Pa)
V = volume (L)
n = number of moles
R = ideal gas constant: 0.082 L(atm)/mol(K) or 8.31 J/mol(K)
T = temperature (K)
a = attraction between molecules due to intermolecular forces
b = actual volume taken up by gas molecules

Note that you do not need to have this equation memorized, but you should know what it measures.

70
Q

Which will deviate more from ideal behavior: a polar or a nonpolar gas?

A

polar gases

The larger the attractive forces, the more a gas will demonstrate real, or nonideal, behavior. If attractive forces are large enough under certain conditions, the gas can condense into a liquid.

71
Q

Which will deviate more from ideal behavior: a real gas made up of small molecules, or a real gas made up of large molecules?

A

gases made up of larger molecules

An ideal gas is assumed to have particles with no volume of their own. The larger the particles of a real gas, the less ideal its behavior can be.