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 (𝜒)

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13
Q

mole fraction (𝜒)

A

𝜒(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
Q

ion product (IP)

A

IP = [A^n+]^m * [B^m-]^n

e.g. IP = [Ag+] [Cl-]

26
Q

comparison determines the level of saturation and behavior of the solution

A

comparison of K(sp) and IP

27
Q

comparison of K(sp) and IP:

indicates the solution is unsaturated, and if more solute is added, it will dissolve

A

IP < K(sp)

28
Q

comparison of K(sp) and IP:

indicates the solution is saturated (at equilibrium), and there will be no change in concentrations

A

IP = K(sp)

29
Q

comparison of K(sp) and IP:

indicates the solution is supersaturated, and a precipitate will form

A

IP > K(sp)

30
Q

the equilibrium constant for complex formation; value is usually much greater than K(sp)

A

formation/stability constant (K(f))

31
Q

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

A

common ion effect

32
Q

physical properties of solutions that depend on the concentration of dissolved particles but not on their chemical identity

A

colligative properties

33
Q

accounts for vapor pressure depression caused by solutes in solution

A

Raoult’s law

34
Q

Raoult’s law

A

P(A) = 𝜒(A) P°(A)

where:
P(A) = vapor pressure of solvent A when solutes are present
𝜒(A) = mole fraction of solvent A in the solution
P°(A) = vapor pressure of solvent A in its pure state

35
Q

decreases the evaporation rate of a solvent without affecting its condensation rate, thus decreasing its vapor pressure

A

presence of other solutes

36
Q

shifts in the phase equilibria dependent on the molality (m) of the solution

A

freezing point depression and boiling point elevation

37
Q

freezing point depression

A

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
Q

boiling point elevation

A

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
Q

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)

A

van’t Hoff factor

40
Q

refers to the “sucking” pressure generated by solutions in which water is drawn into a solution

A

osmotic pressure (π)

41
Q

osmotic pressure (π)

A

π = iMRT

where:
π = osmotic pressure