Short Questions Flashcards

1
Q

Define Compression Factor.

A

Z = PVₘ / RT
where
Z is the compression factor
P is pressure
Vₘ is molar volume
R is universal gas constant
T is temperature

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2
Q

Define Critical Temperature.

A

The temperature at the critical point, above which the substance cannot be liquified by pressure alone. The substance exists in equilibrium between two phases.

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3
Q

Define enthalpy.

A

Enthalpy is the total energy of a system.

It is the sum of the internal energy and the product of the pressure and volume of a system.
H = U + PV

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4
Q

Define expansion work for a gas.

A
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5
Q

Define free maximum work function (Helmholtz free energy).

A
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6
Q

Define Gibbs Free energy.

A
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7
Q

Define heat capacity.

A

Heat capacity is the amount of energy needed to increase the temperature of a system by 1K.

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8
Q

Define molar heat capacity.

A

Molar heat capacity is the amount of energy needed to change the temperature of 1 mole by 1K.

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9
Q

Define partial pressure.

A

The partial pressure of a gas in a mixture is the pressure which it would exert if it occupied the whole volume of the mixture on its own, at the same temperature.

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10
Q

Define pH.

A

pH = -log[H⁺]

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11
Q

Define the standard enthalpy of formation of a substance.

A

Standard enthalpy of formation is the change in enthalpy when 1 mole of a compound is made up from its elements.

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12
Q

Define thermodynamic system.

A
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13
Q

Explain how “a” and “b” in the van der Waals equation of state (pV = [RT/(V-nb)] - an²/V²) account for the inter-particle interactions in real gases.

A

“a” is a constant that explains the attraction between the molecules in the gas.
“b” is the volume occupied by Nₐ number of molecules

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14
Q

Explain how enthalpy corresponds to the heat transferred between the system and the surroundings at constant pressure.

A
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15
Q

Explain how heat capacity at constant volume differs from heat capacity at constant pressure for an ideal gas.

A

At constant volume, a system is constrained to the same volume, and/so all the energy added to the system is used to increase the temperature.

At constant pressure, the system is allowed to expand to maintain constant pressure, so some of the energy added may be used for expansion work, meaning more energy will be needed to increase the temperature.

As a result, the heat capacity at constant volume is smaller than the heat capacity at constant pressure because all the energy added is used for increasing the temperature, rather than expansion work.

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16
Q

Explain how the absorption of gases on solids depends on temperature.

A

As temperature increases, adsorption decreases.

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17
Q

Explain how the First Law of Thermodynamics operates in closed systems.

A

Closed systems allow only heat and work to be exchanged between the system and its surroundings.

18
Q

Explain how the First Law of Thermodynamics operates in isolated systems.

A

Isolated systems do not allow any energy exchange between the system and its surroundings, and as a result the energy remains constant.

19
Q

Explain how the First Law of Thermodynamics operates in open systems.

A

Open systems allow matter, heat and work to be exchanged between the system and its surroundings.

20
Q

Explain the reasons behind deviations from ideality for a gas.

A

The volume of molecules, although small, is not completely negligible.

Molecules have both repulsive and attractive forces operating between them.

21
Q

Explain the terms in the equation
η = (T₂-T₁)/T₂.

A

η is the Efficiency of the system
T₂ is the
T₁ is the

22
Q

Explain three main types of thermodynamic systems.

A

Open systems allow matter, heat and work to be exchanged between the system and its surroundings.

Closed systems allow only heat and work to be exchanged between the system and its surroundings.

Isolated systems do not allow any energy exchange between the system and its surroundings, and as a result the energy remains constant.

23
Q

Explain why the standard enthalpies of formation of oxygen (O₂) and ozone (O₃) are different.

A
24
Q

Give 4 examples of state functions.

A
25
Q

Give an example of an irreversible process.

A
26
Q

Give an example of electrolysis.

A
27
Q

Give two examples of a thermodynamics function that is not a state function.

A

Work and heat

28
Q

How can compression factor be used to describe the deviation of ideality?

A

If Z > 1, is a positive deviation from ideality, and the gas is harder to compress than an ideal gas.

If Z < 1, is a negative deviation from ideality, and the gas is easier to compress than an ideal gas.

29
Q

Name the constant, R in the ideal gas equation of state PV=nRT.

A

Universal Gas constant

30
Q

State Dalton’s Law of Partial Pressures.

A
31
Q

State Faraday’s Laws.

A
32
Q

State Gay-Lussac’s Law.

A
33
Q

State Kohlrausch’s Law of Independent Migration of Ions.

A
34
Q

State the First Law of Thermodynamics.

A

The total energy of a system and its surroundings must remain constant, but energy can change from one form to another.

35
Q

State the Second Law of Thermodynamics for an isolated system.

A
36
Q

State the Second Law of Thermodynamics.

A
37
Q

State the Zeroth Law of Thermodynamics.

A

If system A is in thermal equilibrium with system B, and system B is in thermal equilibirum with system C, then system A is in thermal equilibrium with system C.

38
Q

What is the change of Gibbs Free Energy for a spontaneous process taking place at constant temperature and pressure?

A
39
Q

What is the condition for thermodynamic equilibrium under constant temperature and pressure?

A
40
Q

What is the difference between metallic and ionic conductors/ electrolytes?

A