thermodynamics 2 Flashcards

(30 cards)

1
Q

Q: Give two examples of energy transformation.

A

A: Potential to kinetic (falling ball), and kinetic to potential (rising lift).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Q: How can a closed system exchange energy with its surroundings?

A

A: Through heat or work.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Q: What kind of work do most chemical reactions perform?

A

A: Most chemical reactions only perform pV (pressure-volume) work, which is usually negligible due to small volume changes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Q: What is enthalpy (H)?

A

A: Enthalpy is the total energy of a system, defined as H = U + pV, where U is internal energy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Q: What is the equation for enthalpy (H)?

A

A: H = U + pV

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Q: What happens to ΔH when a system does no pV work but absorbs 10 kJ of heat?

A

A: ΔU = +10 kJ and ΔH = ΔU = +10 kJ, so enthalpy increases by 10 kJ.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Q: Why are enthalpy changes (ΔH) more useful than absolute values?

A

A: Because changes in enthalpy indicate heat flow, which relates directly to energy changes in a reaction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Q: What does a positive ΔH signify?

A

A: The system absorbs heat (endothermic process).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Q: What does a negative ΔH signify?

A

A: The system releases heat (exothermic process).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Q: Does the sign of ΔH alone determine the favorability of a reaction?

A

A: No, enthalpy alone is not sufficient to determine favorability.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Q: What additional concept is needed to understand reaction favorability?

A

A: Entropy (S), which measures the disorder or number of ways a system can be arranged.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Q: What happens to entropy when gas molecules spread out in a closed system?

A

A: Entropy increases due to increased disorder.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Q: What is the relationship between entropy and the number of arrangements of a system?

A

A: Entropy is proportional to the number of ways the system can be arranged (W).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Q: Is the entropy change (ΔS) positive when a system becomes more disordered?

A

A: Yes, ΔS is positive when disorder increases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Q: What is the total entropy change equation?

A

A: ΔS_total = ΔS_system + ΔS_surroundings

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Q: What is Boltzmann’s interpretation of entropy?

A

A: Entropy is related to the number of microstates (W): S ∝ ln(W)

17
Q

Q: What is the formula relating entropy change to heat and temperature?

A

A: ΔS = ΔQ / T

18
Q

Q: In the ice cube example, why does heat flow from the room to the ice?

A

A: Due to a temperature difference between the surroundings (273.1 K) and the system (273 K).

19
Q

Q: What is the entropy change in the system when heat flows into ice at 273 K?

A

A: ΔS_system = |ΔQ| / 273 K

20
Q

Q: What is the entropy change in the surroundings during the ice cube example?

A

A: ΔS_surroundings = |ΔQ| / 273.1 K

21
Q

Q: Why is the total entropy change positive in the melting ice cube example?

A

A: Because ΔS_system > ΔS_surroundings, meaning the overall ΔS_total is positive.

22
Q

Q: What happens when there is no temperature gradient between system and surroundings?

.

A

A: No further heat flow occurs

23
Q

Q: What is the condition for a process to be thermodynamically favorable?

A

A: ΔS_total > 0

24
Q

Q: How is entropy best visualized?

A

A: As a measure of the level of disorder in a system

25
Q: What is the definition of Gibbs free energy (G)?
A: A thermodynamic function that combines enthalpy and entropy to predict spontaneity: G = H - TS
26
Q: What does ΔG tell us about a process?
A: Whether the process is thermodynamically favorable (but not how fast it occurs).
27
Q: What is the formula for ΔS_surroundings in terms of ΔH_system?
A: ΔS_surroundings = -ΔH_system / T
28
Q: Do we work with absolute values or changes in thermodynamic functions?
A: We work with changes: ΔG, ΔH, and ΔS.
29
Q: What is the universal gas constant (R)?
A: 8.314 J·mol⁻¹·K
30
Q: What is Avogadro’s number (NA)?
A: 6.022 × 10²³ mol⁻¹