Solutions Flashcards

1
Q

homogeneous mixtures composed of two or more substances that combine to form a single phase, usually the liquid phase; consists of a solvent and a solute

A

solutions

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2
Q

is dissolved in a solvent

A

solute

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3
Q

the component of the solution that remains the same after mixing

A

solvent

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4
Q

process of solvent particles surrounding solute particles via electrostatic interactions

A

solvation/dissolution

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5
Q

process of solvation/dissolution of an aqueous solution (solvent is water)

A

hydration

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6
Q

the maximum amount of solute that can be dissolved in a given solvent at a given temperature; often expressed as molar ____ (the molarity of the solute at saturation)

A

solubility

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7
Q

refers to a molecule in which a cation (metallic ions) is bonded to at least one electron pair donor (various neutral compounds and anions, referred to as ligands)

A

complex ions (coordination compounds)

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8
Q

bonds between a Lewis acid and base that hold complex ions together

A

coordinate covalent bonds

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9
Q

denotes the amount of solute dissolved in a solvent

A

concentration

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10
Q

method of expressing concentration:

used for aqueous solutions and solid-in-solid solutions

A

percent composition by mass

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11
Q

percent composition by mass

A

(mass of solute / mass of solution) x 100%

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12
Q

method of expressing concentration:

used for calculating vapor pressure depression and partial pressures of gases in a system

A

mole fraction (šœ’)

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13
Q

mole fraction (šœ’)

A

šœ’(A) = moles of A / total moles of all species

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14
Q

method of expressing concentration:
the most common unit for concentration and is used for rate laws, the law of mass action, osmotic pressure, pH and pOH, and the Nernst equation

A

molarity (M)

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15
Q

molarity (M)

A

M = moles of solute / liters of solution

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16
Q

method of expressing concentration:

used for boiling point elevation and freezing point depression

A

molality (m)

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17
Q

molality (m)

A

m = moles of solute / kilograms of solvent

18
Q

method of expressing concentration:

the molarity of the species of interest and is used for acid-base and oxidation-reduction reactions

A

normality (N)

19
Q

normality (N)

A

N = number of equivalents / liters of solution

20
Q

dilution equation

A

M(1) V(1) = M(2) V(2)

21
Q

defined as equilibrium in the process of creating a solution, where the solute concentration is at its maximum value for the given temperature and pressure

A

saturation point

22
Q

the equilibrium constant for a dissociation reaction

A

solubility product constant (K(sp))

23
Q

solubility product constant (K(sp))

A

K(sp) = [A^n+]^m * [B^m-]^n

e.g. K(sp) = [Ag+] [Cl-]

24
Q

a calculated value that relates where the system is with respect to the equilibrium position (K(sp))

A

ion product (IP)

25
ion product (IP)
IP = [A^n+]^m * [B^m-]^n e.g. IP = [Ag+] [Cl-]
26
comparison determines the level of saturation and behavior of the solution
comparison of K(sp) and IP
27
comparison of K(sp) and IP: | indicates the solution is unsaturated, and if more solute is added, it will dissolve
IP < K(sp)
28
comparison of K(sp) and IP: | indicates the solution is saturated (at equilibrium), and there will be no change in concentrations
IP = K(sp)
29
comparison of K(sp) and IP: | indicates the solution is supersaturated, and a precipitate will form
IP > K(sp)
30
the equilibrium constant for complex formation; value is usually much greater than K(sp)
formation/stability constant (K(f))
31
decreases the solubility of a compound in a solution that already contains one of the ions in the compound; the presence of that ion in solution shifts the dissolution reaction to the left, decreasing its dissociation
common ion effect
32
physical properties of solutions that depend on the concentration of dissolved particles but not on their chemical identity
colligative properties
33
accounts for vapor pressure depression caused by solutes in solution
Raoult's law
34
Raoult's law
P(A) = šœ’(A) P°(A) where: P(A) = vapor pressure of solvent A when solutes are present šœ’(A) = mole fraction of solvent A in the solution P°(A) = vapor pressure of solvent A in its pure state
35
decreases the evaporation rate of a solvent without affecting its condensation rate, thus decreasing its vapor pressure
presence of other solutes
36
shifts in the phase equilibria dependent on the molality (m) of the solution
freezing point depression and boiling point elevation
37
freezing point depression
ΔT(f) = i K(f) m ``` where: ΔT(f) = freezing point depression i = van't Hoff factor K(f) = proportionality constant characteristic of particular solvent m = molality of solution ```
38
boiling point elevation
ΔT(b) = i K(b) m ``` where: ΔT(b) = boiling point elevation i = van't Hoff factor K(b) = proportionality constant characteristic of particular solvent m = molality of solution ```
39
corresponds to the number of particles into which a compound dissociates in solution e.g. for NaCl i = 2 (1 for Na and 1 for Cl)
van't Hoff factor
40
refers to the "sucking" pressure generated by solutions in which water is drawn into a solution
osmotic pressure (Ļ€)
41
osmotic pressure (Ļ€)
π = iMRT where: π = osmotic pressure