Thermodynamics Flashcards

(47 cards)

1
Q

IDEAL GASES

A

PV = nRT

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2
Q

Gas constant (R)

A

8.3145 LkPa/Kmol

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3
Q

What does a high temp correlate to for pressure?

A

A higher temperature would increase the kinetic energy of the atoms.

Therefore the atoms would move faster and collide more (INCREASING PRESSURE)

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4
Q

What does a low temperature correlate to for pressure?

A

A low temperature would mean that the atoms have a low kinetic energy and therefore MOVE SLOWER.

Less Collisions = Lower pressure

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5
Q

1 ATM

A

101325 Pa
or
101.325 kPa

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6
Q

STP

A

Standard Temperature & Pressure.
* 0°C or 273 k
* 1 ATM

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7
Q

ΔU

A
  • ΔU = q + w
  • ΔU = q +pΔV
  • ΔU = C x ΔT
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8
Q

How would ΔU be demonstrated if the surroundings gain 10.80kJ ?

A

ΔU = - 10.8 kJ

negative value

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9
Q

How would ΔU be demonstrated if the system gains 10.80kJ ?

A

ΔU = 10.8kJ

positive value

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10
Q

First law of thermodynamics

A

ΔU = Q - W

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11
Q

Precision

A

The consistency of results with each other

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12
Q

Accuracy

A

The consistency of results with the true value

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13
Q

In regard to entropy, how does it determine the direction of a reaction?

A

A reaction will always proceed in the direction of increasing disorder .

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14
Q

TRUE OR FALSE

A reaction proceeds in the direction of increased orderliness

A

FALSE

A reaction always proceeds in the direction of increased disorder.

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15
Q

Define…

Entropy

A

The degree of measure of disorder in a system.

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16
Q

TRUE OR FALSE

Generally, in high temperatures there is a higher level of disorder

A

TRUE

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17
Q

Second law of thermodynamics

A

The change in entropy of a system must be greater than 0 for a spontaneous change to occur.

  • ΔS_tot = ΔS_sys + ΔS_sur < 0: non-spontaneous
  • ΔS_tot = ΔS_sys + ΔS_sur > 0 : spontaneous
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18
Q

TRUE OR FALSE

During a spontaneous change in an isolated system, the entropy decreases.

A

FALSE

For isolated systems, the entropy always increases during a spontaneous change. ΔS_tot > 0

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19
Q

Change in entropy [ΔS]

A
  • ΔS = q_rev / T
  • ΔS = ΔH / T
20
Q

TRUE OR FALSE

There is NO DISORDER at 0 kelvin

21
Q

Third law of thermodynamics

A

There is no entropy at absolute zero.

22
Q

Formula

Gibbs free energy

A
  • G = H - TS
  • ΔG = ΔH - TΔS
23
Q

Criterion of spontaneity

A

ΔS
* ΔS > 0 : Spontaneous
* ΔS < 0 Non-spontaneous

ΔG
* ΔG < 0 : Spontaneous
* ΔG > 0 : Non-spontaneous

24
Q

Coupled reactions

A

Reactions that are energetically unfavourable can be ‘coupled’ with favourable reactions.

This can be achieved when the overall change in standard gibbs free energy is negative (therefore spontaneous/favourable)

25
Δr_G°
Δr_G° = -RT lnK | R (universal constant) = 8.31 J/Kmol
26
# TRUE OR FALSE At equilibrium ΔrG = 0
**TRUE**
27
Δr_G
Δr_G = Δr_G° + RT lnK
28
Equilibrium constant [K]
**K** = ( **C** *^c* ) ( **D** *^d* )/ (**A** *^a*) ( **B** *^b*)
29
Molar gibbs energy
Gm = G/n * n = number of moles * G = Gibbs free energy
30
# Formulas... Enthalpy
* H = U + PV * H =
31
Triple point
The point in which the substance exists in all three phases at the same time in equilibrium.
32
Critical point
The **temperature** and **pressure** point on a phase diagram where the LIQUID and GASEOUS phases of a substance merge together into one substance called the **supercritical fluid**
33
Gibbs phase rule
The number of intensive variables that must be defined to determine the state of a system. **F = C - P + 2**
34
Intensive variable
A variable that is **NOT** dependent on the quantity of the system (**e.g.** water) | E.g. : **Pressure**, **Density**, **Temperature**
35
Extensive variable
A variable that is dependent on the quantity of the system | E.g. : **Volume**, **Mass**, **number of moles**
36
# TRUE OR FALSE Determining a state requires all the variables of a system
**TRUE**
37
Gibbs phase rule formula
**F = C - P +2** * F = # of intensive variables * C = # of components * P = # of phases
38
Clausius-Clapeyron equation
Δln p / ΔT = Δ_evap_ H / RT^2
39
chemical potential
μ_A = μ°_A + RT lnX_A
40
How can you determine the gibbs free energy of a reaction?
G = (n_A)(μ_A ) + (n_B)(μ_B)
41
# TRUE OR FALSE Raising the temperature on an exothermic reaction will shift the equilibrium to the right
**FALSE** There will be more heat on the product side so the equilibrium will counter by shifting to the **reactants / left**
42
Van't Hoffs equation | Normal
ln(K2/K1) = ΔH/R (T2-T1/T2T1)
43
Van't Hoff equation | In respect to ΔH
ΔH = R ln(K2/K1) (t2t1/t2-t1)
44
Clausius-clapeyron equation
Ln(P2/P1)= ΔH/R (T2-T1/ T2T1) * P = vapor pressure
45
# TRUE OR FALSE Increasing the temp for an Endothermic reaction shifts to the right
**TRUE**
46
# TRUE OR FALSE The reaction shifting to the reactants means the reactants decrease
**FALSE** The reactants will increase if the reaction shifts towards them.
47
Le chatelier’s principle
**Endothermic reaction** * Increase temp = more products * Decrease temp = more reactants **Exothermic reaction** * Increase temp = more reactants * Decrease temp = more products