chapter 13 (exam 2) Flashcards

(57 cards)

1
Q

solution

A

-homogeneous mixture made of 2 or more different chemical substances in the SAME phase
-made of solvent and solute

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2
Q

solvent

A

the substance in the solution that in the LARGEST amount
-longer name, larger amount

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3
Q

if it solution is (aq)

A

the solvent is water

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4
Q

solute

A

the substance in the SMALLER amount
-smaller name, smaller amount

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5
Q

if one of the substances is a liquid and all the others are solids or gases…

A

the liquid would be the solvent, not matter how much of it there is

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6
Q

solution formation is a result from IMFs of the solute and solvent which shows

A

-miscible, “like dissolves like”
-polar with polar and non polar with non polar

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7
Q

nature usually has spontaneous mixing, but uniform mixing is

A

more energetically favorable

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8
Q

dilute solution

A

contains SMALL quantities of solute relative to the amount of solvent

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9
Q

concentrated solution

A

contains LARGE quantities of solute relative to the amount of solvent

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10
Q

molarity equation

A

M= moles solute/solution volume (L)

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11
Q

molality equation

A

m= moles solute/ mass of solvent (kg)

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12
Q

mass percent

A

%m/m= (mass solute)/ (total mass solution) x100%

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13
Q

parts per million

A

ppm= mass solute (g)/ mass solution (g) x10^6

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14
Q

volume percent

A

%v/v= (vol solute/ vol solution) x100%

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15
Q

mole fraction

A

Xa= moles of component A/ total moles in solution

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16
Q

mass solution =

A

mass solute + mass solvent

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17
Q

solubility

A

the amount of a substance that will dissolve in a given amount of a solvent

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18
Q

solubility of a substance depends on

A

-entropy (tendency to spontaneous mixing)
- types of IMFs

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19
Q

a solution will form solvent-solute interactions that are

A

comparable or stronger than the solvent-solvent or solute-solute interactions

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20
Q

when the solvent-solute interactions are weaker than the sum of the solute-solute and solvent-solvent interactions…

A

the solution can only form if the energy difference is small enough to be overcome by and increase in entropy

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21
Q

if solvent-solute > solvent-solvent and solute solute

A

solution forms

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22
Q

if solvent-solute < solvent-solvent and solute solute

A

solution may or may not form depending on the disparity

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23
Q

if solvent-solute = solvent-solvent and solute solute

A

solution will form

24
Q

formation of a solution step 1

A

1) solute separated into its constituent parts
- the ΔH solute > 0

25
formation of a solution step 2
2) solvent particles are separated from each other to make room for solute particles - the ΔH solvent > 0
26
formation of a solution step 3
3) the solute particles and solvent particles are mixed together - the ΔH mix < 0
27
ΔH solution
ΔH solute(+) + Δ H solvent(+) + ΔH mixing(-)
28
if ΔH solution is < 0
exothermic -releases heat
29
if ΔH solution > 0
endothermic -absorbs heat
30
in some cases, solution formation with small positive or negative enthalpy of solution the
entropic contributions dominate and the solution forms easily -the ΔG < 0
31
in some cases, the enthalpy of solution is expected to be large positive or negative the
the entropic contribution is too small to overcome the enthalpy so the solution will not form -the ΔG > 0
32
enthalpy of solvation
energy difference btw a free ion and the solvated ion
33
enthalpy of hydration
when solvent is water -the heat released when 1 mole of gas ions dissolves in water
34
the enthalpy of hydration is _____ for ionic compounds
always large and exothermic
35
ΔH hydration=
ΔH solvent + ΔH mixing
36
as the attraction btw solvent particles and the ion increases
the enthalpy of hydration becomes more exothermic
37
larger ion charge and small ionic radius leads to a
stronger attraction -more exothermic enthalpy of hydration
38
ΔH solution =
ΔH hydration - ΔH lattice energy
39
when the absolute value of ΔH solute < ΔH hydration --->
ΔH solution <0 -increase in temp so container feels hot
40
when the absolute value of ΔH solute > ΔH hydration --->
ΔH solution >0 - decrease in temp so container feels cold
41
when the absolute value of ΔH solute = ΔH hydration --->
ΔH solution = 0 -no noticeable change
42
stage one of solution equilibrium
-solution process starts by solute particles surrounded by the solvent particles -solute particles decrease over time
43
solution equilibrium stage 2
-at some point, there's high enough concentration of solute particles in solution and they will precipitate when they bump into each other
44
solution equilibrium stage 3
-the rate of dissolution (dissolving) = rate of recrystallization (precipitation) -solution is at dynamic equilibrium
45
saturated
solution has the solute and the solvent in dynamic equilibrium
46
saturated solution
-solution containing the max amount of dissolved solute at equilibrium
47
if you add more solute to a saturated solution
it will not dissolve -the solution concentration won't change at that temp
48
supersaturated
solution has more solute than saturated is said to be -must be heated, dissolved, then cooled down
49
unsaturated
solution has less solute than saturation is said to be
50
supersaturated solutions are ___ and excess solute normally___
-unstable -precipitated out of solution
51
when a solution is saturated
-its at dynamic equilibrium -net rate of dissolution of solute is zero -net rate of precipitation of solute is zero
52
as temperature increases (sol)
solubility usually increases -depends on the enthalpy of solution
53
if ΔH solution < 0 (exothermic) has its temp decreased
the solubility increases
54
if ΔH solution > 0 (endothermic) has its temp increased
the solubility increases
55
solubility of gases in liquids decreases with increasing
temperature
56
henry's law
as the pressure of a gas increases, the solubility of the gas increases
57
S/ Cg=
kH Pgas