Exam 1 True/False Practice Flashcards

1
Q

Which of the following is/are polar?

CH3OCH3

A

Polar

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2
Q

Which of the following is/are polar?

BrF3

A

Polar

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3
Q

Which of the following is/are polar?

SF6

A

Nonpolar

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4
Q

Which of the following is/are polar?

SO3

A

Nonpolar

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5
Q

Which of the following is/are polar?

C3H8

A

Nonpolar

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6
Q

Which of the following is/are polar?

SO2

A

Polar

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7
Q

Intermolecular forces are within molecules; bonds are
between molecules.

A

False

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8
Q

Bonds are generally weaker than intermolecular forces.

A

False

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9
Q

The strongest intermolecular force in a pure substance is hydrogen bonding.

A

True

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10
Q

Dipole-dipole forces are the result of an instantaneous dipole interacting with an induced dipole.

A

False

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11
Q

Dispersion forces are present between all molecules, but are the only intermolecular force between two non-polar molecules.

A

True

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12
Q

The strongest intermolecular force between two CH3CHO molecules is hydrogen bonding

A

False

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13
Q

The strongest intermolecular force between two silicon tetrafluoride molecules is dipole-dipole forces.

A

False

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14
Q

There are only dipole-dipole forces and dispersion forces between two CH2F2 molecules; there is not hydrogen bonding.

A

True

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15
Q

There should be dipole-dipole forces and dispersion forces between two C6H14 molecules

A

False

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16
Q

The strongest intermolecular force between two helium atoms should be dispersion forces.

A

True

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17
Q

Solids have strong intermolecular forces relative to thermal energy

A

True

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18
Q

Solids can be categorized as crystalline or amorphous; amorphous solids have no long-range order.

A

True

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19
Q

We can change from a liquid to a gas by increasing
temperature or increasing pressure.

A

False

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20
Q

In a liquid, the particles can move with respect to one another, so liquids have an indefinite volume, but definite shape.

A

False

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21
Q

The strongest intermolecular force between two CH3CHO molecules is hydrogen bonding

A

False

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22
Q

The strongest intermolecular force between two silicon tetrafluoride molecules is dipole-dipole forces.

A

False

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23
Q

There are only dipole-dipole forces and dispersion forces between two CH2F2 molecules; there is not hydrogen bonding.

A

True

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24
Q

There should be dipole-dipole forces and dispersion forces between two C6H14 molecules

A

False

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25
Q

The strongest intermolecular force between two helium atoms should be dispersion forces.

A

True

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26
Q

Vaporization is the process of changing a substance from a liquid to a gas

A

True

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27
Q

The rate of vaporization increases with increasing temperature and surface area, but decreasing intermolecular forces

A

True

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28
Q

If a liquid is considered volatile, it is explosive

A

False

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29
Q

Vaporization only occurs at the boiling point of a liquid

A

False

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30
Q

The energy change for vaporization is the same magnitude, but opposite sign as the energy change for condensation

A

True

31
Q

The boiling point of a liquid is when the vapor pressure of the liquid is equal to the external pressure

A

True

32
Q

If the pressure above a liquid-vapor system in equilibrium decreases (a disturbance), some of the liquid will evaporate (to minimize the disturbance and restore equilibrium)

A

True

33
Q

Dynamic equilibrium is reached when the condensation and vaporization processes stop

A

False

34
Q

If you bring a pot of water from sea level to La Paz, Bolivia (11,975 ft above sea level), you will increase its boiling point

A

False

35
Q

Another word for fusion is freezing

A

False

36
Q

Fusion is an endothermic process, so the enthalpy of fusion is positive

A

True

37
Q

Heating a liquid in a closed container until its temperature is beyond the critical temperature produces a supercritical fluid

A

True

38
Q

An ice cube slowly disappearing from an ice cube tray in a freezer is an example of sublimation

A

True

39
Q

There is no change in temperature when energy is added to a block of ice at its freezing point until all the ice has melted

A

True

40
Q

Enthalpy of fusion generally decreases with increasing strength of intermolecular forces

A

False

41
Q

solution that contains more dissolved solute than the equilibrium amount is supersaturated

A

True

42
Q

Solubility of most solids decreases with increasing temperature

A

False

43
Q

Solubility of most gases increases with increasing pressure and temperature.

A

False

44
Q

An unsaturated solution contains less than the equilibrium amount of solute

A

True

45
Q

solution in which the dissolved solute is in dynamic equilibrium with the solid (undissolved) solute is a saturated solution

A

True

46
Q

When a solution forms, the solute-solute interactions must be overcome, so ΔHsolute is endothermic

A

True

47
Q

When a solution forms, the solvent-solvent interactions must be overcome, so ΔHsolvent is endothermic

A

True

48
Q

ΔHmix is endothermic

A

False

49
Q

The heat of hydration is the enthalpy change that occurs when 1 mole of the gaseous solute ions are dissolved in water; it is always largely negative (exothermic) for ionic compounds

A

True

50
Q

Colligative properties depend on the number of particles dissolved in solution, not on the type of particles

A

True

51
Q

Vapor pressure increases as the mol fraction of solute dissolved in the solvent increases

A

False

52
Q

Dissolving a nonvolatile solute into a solvent decreases its vapor pressure

A

True

53
Q

If the solute is volatile, it also contributes to the overall vapor pressure of the solution

A

True

54
Q

0.02 M FeBr3 solution will have the same osmotic pressure as a 0.02 M AlCl3 solution, assuming ideal Van Hoff factors.

A

True

55
Q

An aqueous 0.03 m NaCl solution will have a higher boiling point than an aqueous 0.04 m C6H12O6 (glucose) solution, assuming ideal Van Hoff factors.

A

True

56
Q

The measured Van Hoff factor can be larger than the ideal when there is ion pairing.

A

False

57
Q

An aqueous 0.02 m HCl solution will have a higher boiling point than an aqueous 0.02 m HF (a weak acid) solution.

A

True

58
Q

According to collision theory, rate of reaction increases with decreasing temperature because more particles have enough energy to overcome the activation energy

A

False

59
Q

According to collision theory, rate of reaction increases with increasing concentration because particles are more likely to collide with one another

A

True

60
Q

For the reaction 2 A + B + C –> 3 D + E, if the rate at an instant in time is –0.12 M/s for A, then the rate for D is +0.08 M/s.

A

False

61
Q

Rate of reaction generally decreases with time.

A

True

62
Q

For the reaction A –> B + 2C where the reaction is determined to be first order, if the initial rate is 0.01 M/s when [A] = 0.10 M, then the initial rate will be 0.02 M/s when [A] = 0.20 M.

A

True

63
Q

For the reaction A –> 2 B where the reaction is determined to be second order, if the initial rate is 0.001 M/s when [A] = 0.10 M, then the initial rate will be 0.016 M/s when [A] = 0.40 M.

A

True

64
Q

For the reaction A –> B where the reaction is determined to be zero order, if the initial rate is 0.1 M/s when [A] = 2.0 M, then the initial rate will be 0.2 M/s when [A] = 4.0 M.

A

False

65
Q

For the reaction A + B + 2 C –> 3 D + E, if the rate law is Rate = k [A][C], then the overall order of the reaction is 4.

A

False

66
Q

The integrated rate law shows how the rate depends on concentration; the differential rate law shows how concentration depends on time

A

False

67
Q

In the integrated rate law, k is the same rate constant as in the differential rate law

A

True

68
Q

The rate law (differential rate law) must be determined experimentally; the integrated rate law is derived from the rate law mathematically

A

True

69
Q

When the inverse of the concentration of reactant X is plotted vs time, a straight line will result if the reaction is zero-order in X

A

False

70
Q

When the natural log of the concentration of a reactant X is plotted vs time, a straight line will result if the reaction is first-order in X

A

True

71
Q

The first half-life for the reaction 2A -> A2 is 20 seconds. The second half-life is 10 seconds. This reaction is second order.

A

False

72
Q

The first half-life for the reaction 2B -> B2 is 20 seconds. The second half-life is 40 seconds. This reaction is zero order.

A

False

73
Q

The first half-life for the reaction 2C -> C2 is 15 seconds. Each half-life thereafter is 15 seconds. This reaction is first order.

A

True