Ch. 9: Solutions Flashcards

1
Q

Define solvation.

A

The electrostatic interaction between solute and solvent molecules. It involved the breaking of interactions between solvent molecules and between solute interactions and forming new intermolecular interactions between the solute and solvent.

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2
Q

Is solvation endothermic or exothermic when new interactions are stronger than the original ones?

A

Exothermic. This process is favored at low temperatures.

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3
Q

Is solvation endothermic or exothermic when new interactions are weaker than the original ones?

A

Endothermic. This process is favored at high temperatures.

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4
Q

What is an ideal solution?

A

When the overall strength of the new interaction is approximately equal to the strength of the original interactions. Thus, the overall enthalpy is zero.

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5
Q

How does entropy change upon dissolution?

A

Increases

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6
Q

Define solubility.

A

The maximum amount of a substance that can be dissolved in a particular solvent at a given temperature. When the maximum amount is added, the dissolved solute is in equilibrium.

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7
Q

Are group 1 metals and nitrate salts soluble or insoluble?

A

They are soluble!

Nitrate = NO3 -

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8
Q

What is the difference between molarity, molality, and normality?

A
molarity = moles of solute / L of solution
molality = moles of solute / kg solvent
normality = molarity x n = equivalents / L of solution
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9
Q

What equation is used to calculate the concentration of a solution after dilution?

A

M₁V₁=M₂V₂

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10
Q

Define the saturation point of a solution.

A

The saturation point is equilibrium. This is when the solute concentration is at its maximum value.

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11
Q

How does Ksp change for gas and non-gas solutes?

A

Non-gas: An increase in temperature will increase Ksp

Gas: An increase in temperature will decrease Ksp because more particles will escape to the gas phase.

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12
Q

What is the ion product of a salt?

A

Analogous to Q, it is the concentrations of the ionic constituents at that given moment in time.

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13
Q

What does it mean when IP < Ksp?

A

The solution is unsaturated and the solute will continue to dissolve

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14
Q

What does it mean when IP > Ksp?

A

The solution is saturated and precipitation will occur

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15
Q

What does it mean when IP = Ksp?

A

The solution is saturated and thus at equilibrium. The rate of the forward and reverse reactions are equal.

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16
Q

Why do ion complexes have a high Ksp?

A

The complexes have multiple polar bonds that allow for dipole-dipole interactions to occur, which stabilizes the dissolution of the complex ion.

17
Q

What is the common ion effect?

A

Reduced molar solubility of a salt when it is dissolved in a solution that already contains one of its constituent ions as compared to its solubility in a pure solvent.

18
Q

How is the common ion effect explained by Le Chatelier’s principle?

A

When a solution already contains one of the ions from the products side of the reaction, the system will shift toward the left side, reforming the solid salt. This results in reduced molar solubility and less solid is dissolved in the solution.

19
Q

How does the common ion effect change Ksp?

A

It doesn’t! Ksp stays the same because Ksp is an inherent property that doesn’t take into account other ions in a solution. The common ion effect changes IP not Ksp.

20
Q

What are colligative properties? Examples?

A

Physical properties of solutions that depend on the concentration of dissolved particles but not on the chemical identity of the solution.

Ex. vapor pressure depression, BP elevation, FP depression, and osmotic pressure

21
Q

What is Raoult’s Law? What does it account for?

A

It accounts for vapor pressure depression. As solute is added to a solvent, the vapor pressure of the SOLVENT decreases proportionately. The solute molecules added block the evaporation of solvent molecules but not their condensation.

22
Q

What is Raoult’s Law equation?

A

Pₐ = XₐPₐ°

Pₐ is vapor pressure of solvent a when solutes are present
Xₐ is the mole fraction of solvent A in the solution
Pₐ° is the vapor pressure of solvent A in its pure state

23
Q

How are BP elevation and VP depression related?

A

As VP decreases, more energy is needed to evaporate the solute in order for the vapor pressure to equal ambient pressure. Therefore BP rises.

24
Q

What is the change in BP elevation equation?

A

ΔTb = i(Kb)m

ΔTb is the increase in BP
i is the van’t Hoff factor
(Kb) = constant
m = molality of the solution (mol/kg solvent)

25
Q

What is the density of water?

A

1 kg/ L = 1 g/mL = 1000 kg/m3

26
Q

What’s the logic behind freezing point depression?

A

The solutes in the solvent prevent lattice formation due to blocking the interaction between solvent molecules. Energy needs to be removed so that the solvent molecules move slower and are able to find each other to form a lattice. Removing energy decreases the temperature, therefore the freezing point decreases.

27
Q

Define osmotic pressure.

A

It is a “sucking” pressure generated by solutions in which water is drawn into a solution.

28
Q

What is the osmotic pressure equation?

A

π = iMRT

i = van't Hoff factor
M = molarity
R = ideal gas constant
T = temperature