Ch. 7: Thermochemistry Flashcards

1
Q

What is the difference between an isolated, closed, and open system?

A

Isolated: cannot exchange energy (heat, work) or matter with surroundings

Closed: can exchange energy (heat, work) but cannot exchanged matter

Open: can exchange energy (heat, work) AND matter

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2
Q

What is the first law of thermodynamics?

A

The change in internal energy of a system will be equal to the energy added as heat minus the work done BY the system.

∆U = Q - W

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3
Q

How do isothermal processes affect the total internal energy of a system?

A

Isothermal: constant temperature

Constant temperature implies that the ∆U of the system is constant throughout the process. Therefore Q = W (the heat added to the system is equal to the work done by the system)

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4
Q

What does isothermal expansion look like on a P-V graph?

A

Appears hyperbolic. The area under the curve is equal to work done by the system (which is also equal to the heat that entered the system because Q = W)

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5
Q

What is an adiabatic process and how does it affect the total internal energy of a system?

A

Adiabatic: no heat exchange, Q = 0

Since thermal energy is constant, ∆U = -W meaning that the total internal energy is equal to the work done ON the system by the surroundings (as apposed to the work done by the system on the surroundings)

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6
Q

What does adiabatic expansion look like on a P-V graph?

A

Appear hyperbolic. Temperature changes but there is no heat exchange. The area under the curve is equal to work.

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7
Q

How do isobaric processes affect the total internal energy of the system?

A

Isobaric: constant pressure

This does NOT alter the first law of thermodynamics.

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8
Q

What does isobaric expansion look like on a P-V graph?

A

Appears as a flat line. Slope is zero and the area under the curve equals work.

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9
Q

How do isovolumetric processes affect the total internal energy of the system?

A

Isovolumetric: constant volume

Since volume does not change, there is no work done by or on the system. Thus, ∆U = Q (the change in internal energy is equal to the heat added).

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10
Q

What does isovolumetric expansion look like on a P-V graph?

A

Vertical line, no slope, and there is no area under the curve

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11
Q

What is the difference between a state and process function?

A

State functions are independent of the path taken to reach equilibrium. They cannot describe how a system got to its current equilibrium.

Process functions are dependent on the pathway taken from one equilibrium state to another (heat, work).

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12
Q

List the 8 state functions?

A
Pressure
Density
Temperature
Volume
Enthalpy
Internal Energy
Gibbs Free Energy
Entropy

When I’m under PRESSURE and feeling DENSE, all I want to do is watch TV and get HUGS

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13
Q

What is the difference between standard conditions and STP?

A

Standard conditions are used to for kinetics, equilibrium, and thermodynamics problems = 298K, 25°C, 1 atm, 1 M concentrations

STP is standard temperature and pressure used for gas law calculations = 273 K, 0°C, 1 atm

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14
Q

What is the difference between ∆H°, ∆S°, ∆G° and ∆H, ∆S, ∆G?

A

∆H°, ∆S°, ∆G° represent changes in enthalpy, entropy, and Gibb’s free energy under standard conditions (298K, 25°C, 1 atm, 1 M)

∆H, ∆S, ∆G are not under standard conditions

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15
Q

What is vaporization? How does it affect temperature? Is the process endothermic or exothermic and why?

A

Vaporization is when high kinetic energy molecules move from the liquid to gas phase. As more molecules move to the gas phase, the temperature of the liquid decreases. This process is endothermic because the liquid needs energy input from the surroundings (such as the sun) to turn into gas.

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16
Q

How is boiling different than vaporization?

A

Boiling is a specific type of vaporization that occurs only under certain conditions. Boiling only occurs above the BP of a liquid.

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17
Q

Define boiling point in terms of vapor pressure.

A

The boiling point of a liquid is when the vapor pressure above the liquid equals the ambient pressure (external pressure)

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18
Q

How does temperature affect vapor pressure?

A

Vapor pressure INCREASES as temperature INCREASES because more molecules have sufficient kinetic energy to escape to the gas phase.

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19
Q

What is condensation? What conditions facilitate condensation?

A

Condensation is when gas molecules move into the liquid phase. The process is facilitated by lower temperature or higher pressure.

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20
Q

Describe what happens to the molecules in a solid and their energy as temperature increases.

A

As temperature increases, molecules have greater freedom of movement and energy disperses (increase in number of microstates). If there is enough energy then atoms or molecules will escape into the liquid phase.

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21
Q

What is sublimation? Example?

A

Solid to gas

Example: Dry ice (solid CO2)

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22
Q

What is deposition?

A

Gas to solid

23
Q

Draw a phase diagram and label the following: solid, liquid, gas, sublimation, deposition, melting, freezing, condensation, vaporization, triple point, critical point, equilibrium

A

Pg 212 or google pic

24
Q

What is the triple point of a phase diagram?

A

This is the temperature and pressure at which the three phases exist in equilibrium.

25
Q

What is the critical point of a phase diagram?

A

The temperature and pressure ABOVE WHICH there is not distinction between the phases.

26
Q

What is a supercritical fluid? (think density!)

A

Fluid at the critical point. As a liquid is heated in a close system, the density of the liquid decreases and the vapor pressure increases. The critical point is the temperature and pressure at which the density of the liquid and vapor pressure are equal so there is no distinction between the phases.

27
Q

What is the heat of vaporization at the critical point?

A

Zero

28
Q

Define heat (Q).

A

The TRANSFER of energy from one substance to another as a result of their DIFFERENCES IN TEMPERATURE

29
Q

Why is heat a process function?

A

We can quantify how much heat is transferred from one substance to another as a result of their difference in temperature.

30
Q

What is the unit of heat?

A

joule (J) or calorie (cal)

31
Q

What is the conversion between joules and cals?

A

1 cal = 4.184 J

32
Q

What is calorimetry?

A

The process of measuring transferred heat.

33
Q

What is the difference between a coffee-cup calorimeter and a bomb calorimeter?

A

Coffee-cup is a constant pressure calorimeter.

Bomb calorimeter is constant volume.

34
Q

What is the equation for heat transfer given a specific heat?

A

q = mc∆T

35
Q

Define specific heat. What is the specific heat of H2O(l)?

A

The amount of energy needed to raise the temperature of one gram of a substance by 1 degree Celsius (or 1 Kelvin).

c H20(l) = 1 cal/gK

36
Q

What is enthalpy name at the solid-liquid boundary?

A

Heat of fusion

37
Q

Is enthalpy positive or negative going from the solid to liquid phase?

A

Enthalpy is positive because energy is absorbed

38
Q

What is enthalpy name at the liquid-gas boundary?

A

Heat of vaporization

39
Q

What is the formula used to calculate q during phase changes? How does temperature affect phase changes?

A

q = mL
m is mass and L is latent heat (heat of fusion or evap)

Temperature does NOT change during phase changes. This is why q=mc∆T is not used.

40
Q

Define enthalpy.

A

Heat change at constant PRESSURE

41
Q

Is bond breakage endothermic or exothermic? What about bond formation?

A

Bond breakage is endothermic (need energy input to break bond).

Bond formation is exothermic (energy is released when bond is formed).

42
Q

What are the units of enthalpy?

A

kJ/mol

43
Q

What is entropy?

A

Measure of dispersion of energy at a specific temperature

44
Q

What is the equation for calculating entropy? What are the units?

A

∆S = Q/T
Q is heat gained or lost in a reversible process
T is temperature

Units = J/mol K

45
Q

What is kept constant when calculating Gibb’s Free Energy?

A

Temperature and pressure are constant

46
Q

What does it mean when ∆G = 0?

A

The system is at equilibrium

∆H = T∆S

47
Q

If ∆H is + and ∆S is + what is the spontaneity of the reaction?

A

Spontaneous at high T

∆G = ∆H - T∆S

48
Q

If ∆H is + and ∆S is - what is the spontaneity of the reaction?

A

Non spontaneous at all T

∆G = ∆H - T∆S

49
Q

If ∆H is - and ∆S is + what is the spontaneity of the reaction?

A

Spontaneous at all T

∆G = ∆H - T∆S

50
Q

If ∆H is - and ∆S is - what is the spontaneity of the reaction?

A

Spontaneous at low T

∆G = ∆H - T∆S

51
Q

What equations relate G and Keq? G and react quotient Q?

A

∆G = -RT ln (Keq)

∆G = RT ln (Q/Keq) NOTICE THE LACK OF NEG SIGN

52
Q

What is the ln of a number less than one?

A

Negative

53
Q

What is the ln of a number greater than one?

A

Positive