Solutions and Mixtures Flashcards

1
Q

Gibbs Phase Rule? And what do each of the terms represent?

A

F=C-P+2
F: Degrees of freedom - for a point F=0, for a line F=1 and for an area, F=2. IN TEMP PRESSURE GRAPHS.
C: No. chemical components (for a pure system this is 1).
P: No. phases (3 for a point, 2 for a line, 1 for an area)

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2
Q

What do you know about the chemical potential of two phases of a pure system?

A

for a pure system of phases (l) and (ll),

πœ‡(𝐼) = πœ‡(𝐼𝐼)

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3
Q

As the chemical potential of two phases in a pure system is equal, how can you adapt the change in enthalpy?

A

Ξ”β„Ž = 𝑇Δs

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4
Q

How can you get enthalpy change from a pressure temperature phase diagram?

A

Clapeyron equation.

𝑑𝑃/𝑑𝑇=Δ𝑠/Δ𝑣=Ξ”β„Ž/TΞ”v

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5
Q

How can you get enthalpy change from the liquid/gas or solid/gas phase boundaries?

A

Clausius-Clapeyron equation

𝑑𝑃/𝑑𝑇=PΔ𝑠/𝑅𝑇=π‘ƒΞ”β„Ž/𝑅𝑇^2

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6
Q

The linearized Clausius-Clapeyron plot makes a straight line to use. What are the axis?

A

y axis: lnP

x axis: 1/T

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7
Q

The linearized Clausius-Clapeyron plot makes a straight line to use. What is the equation for its gradient?

A

𝑑 ln 𝑃/𝑑(1/𝑇)= βˆ’Ξ”β„Ž/R

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8
Q

The linearized Clausius-Clapeyron plot makes a straight line to use. What phase boundary does the equation only work for?

A

anything that is a phase boundary with gas. Can be the liquid/gas or the solid/gas.

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9
Q

What is headspace measurment?

A

measure vapour pressure

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10
Q

In a mixture, what is the equation for a(i), the activity?

What are each of the terms?

A

π‘Žπ‘– =𝑃(𝑖)/𝑃(π‘–π‘œ)
(make sure you know correct way it should look, formatting here is wrong)
a: activity - a measure of affinities of solute and solvent to the solution compared to their pure systems.
p(i) : Partial vapour pressures of the solution.
p(io) : Vapour pressures of the pure system

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11
Q

Ideal gas law?

A
pV=nRT
p- Pa
V- m3
n- mols
R-JK-1mol-1
T- K
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12
Q

Activity Coefficient?

A

𝛾(𝑖) =π‘Ž(𝑖)/π‘₯(i)

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13
Q

If 𝛾𝑖 > 1, what does this show?

How will it look on a pressure/composition graph?

A

weaker affinity for solution.
+ve deviation from ideality.
on a graph will have a sad face upwards curve from the ideal line (a straight line)

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14
Q

If 𝛾𝑖 < 1, what does this show?

How will it look on a pressure/composition graph?

A

stronger affinity for solution.
-ve deviation from ideality.
on a graph will have a smiley face downwards curve from the ideal line (a straight line)

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15
Q

If 𝛾𝑖 = 1, what does this show?

How will it look on a pressure/composition graph?

A

ideal solution

straight lines

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16
Q

What is a perfect solution?

A

one that is ideal over an entire concentration

17
Q

For an ideal solution, what does the activity equal? (when the solute is in approximately same concentration as solvent)

A

π‘Ž = π‘₯ (the mol fraction) as 𝛾 accounts for deviations from ideality.

18
Q

What does a linear composition/pressure plot show?

A

ideal solution

19
Q

When the solute is dilute, what can be approximated about the solvent?
Raoults law

A

When the solute conc is v small, both solvent and solute start to behave ideally as molecular interactions become negligible. Vapour pressure of the solvent P is proportional to the mol. fraction of the solvent x.
Therefore:
a β‰… x (x is mol fraction solubility)

20
Q

When the solute is very dilute, what can be approximated about the solute?
Henrys law

A

P = kx
k= henrys law constant (sometimes has a subscript H)
strictly applicable for dilute solutes.

21
Q

The equation for boiling point elevation by dilute solutes?

A

Δ𝑇(𝑏) = 𝐾(𝑏)π‘š(2)
π‘š2: solute molality
𝐾𝑏: ebullioscopic constant (of the solvent)

22
Q

The equation for freezing point depression by dilute solutes?

A

βˆ’π›₯𝑇(𝑓) = 𝐾(𝑓) π‘š(2)
π‘š2: solute molality
𝐾𝑏: cryoscopic constant

23
Q

What is molality?

A

mole of solute in a kg of solvent

24
Q

What is molarity?

A

mole of solute in a litre of solution

25
Q

What is the equation for osmotic pressure?

A
𝛱 = 𝑅𝑇𝑐(2)
where c(2) is molarity