Should be on the Test Flashcards

1
Q

when not at equilibrium

A

Q = [Prod]/[Reac]

(can use Q for ANY concentrations)
[tells us which direction a rxn will shift to achieve equilibrium]
Q < means move right
Q > means move left

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2
Q

where does reduction occur?

A

cathode

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3
Q

predicting change in entropy

A
  1. molecular complexity (Ar < CO < CO2)
  2. chemical rxns (A -> 2B = +S [more moles of products])
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4
Q

state function

A

entropy is a state function (doesn’t care about the path; only the initial and final state)

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5
Q

entropy with constant T

A

∆S = q(rev)/T

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6
Q

third law of thermodynamics

A

entropy of a perfectly organized crystal at absolute zero is zero [no disorder]

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7
Q

value of Q at STP

A

Q = 1

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8
Q

what value of K means for spontaneity

A

K < 1 (lnK is —; ∆G° is +) [spontaneous in reverse]
K > 1 (lnK is +; ∆G° is —) [spontaneous in forward]
K = 1 (lnK is 0; ∆G° is 0) [doesn’t favor either direction]

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9
Q

IMF and vapor pressure

A

IMF determine vapor pressure [stronger IMF = lower vapor pressure]

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10
Q

why do stronger IMF mean lower vapor pressure

A

more heat must be introduced to break forces of the liquid to go to gas phase

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11
Q

raoult’s law

A

Pa = XaPa*

Pa* = vp of pure solvent

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12
Q

attracted to water

A

hydrophilic

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13
Q

repelled by water

A

hydrophobic

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14
Q

molality

A

n/kg [m]

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15
Q

solubility of a gas (henry’s law)

A

s = k(H)P

gases become less soluble at high temps.

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16
Q

IΔE box method

A

used for:

equilibrium

finding pH

solubility product/precipitation rxns

17
Q

polyprotic acid

A

H2SO3 + H2O ⇄ H3O+ HSO3- [K1]
HSO3- + H2O ⇄ OH- SO3 (2-) [K]

K(1)&raquo_space; K(2) ALWAYS because it takes much more energy to remove H+ from a negative molecule vs a neutral molecule
(can ignore the weaker acid when calculating pH)

18
Q

amphoteric acids

A

species that is both an acid or a base

HSO3- + H2O ⇄ H3O+ SO3-
HSO3- + H2O ⇄ OH- H2SO3

19
Q

salts + properties

A

can be acidic or basic

NaF + H2O ⇄ Na+ + F- + H2O
F- + H2O ⇄ OH- + HF

NaF is a base, and conjugate is HF

20
Q

acid strength (family trends)

A

HF (weak
HCl (stronger)
HBr (stronger)
HI (strongest) [more shielding]

21
Q

acid strength (oxyacid groups)

A

HClO < HClO2 < HClO3 < HClO4

the oxygen atoms pull e-density away from the OH group. more oxygens = more easy the H+ comes off

22
Q

common-ion effect

A

the presence of both acid and conjugate base means the base does NOT neutralize the base. because it is at equilibrium, if one side changes, the rxn will shift the rxn back

23
Q

solubility product

A

AgCl ⇄ Ag+ + Cl-

Ksp = [Ag+][Cl-]

if small: not very soluble

24
Q

precipitation reactions

A

precipitation reactions

25
Q

[Ag+][Cl-] < Ksp

A

(Q < K) rxn shifts right (no precipitate)

26
Q

[Ag+][Cl-] = Ksp

A

(Q = K) solution is saturated

27
Q

[Ag+][Cl-] > Ksp

A

(Q > K) rxn shifts left (precipitate forms)

28
Q

where does oxidation occur?

A

anode

29
Q

volt

A

Joule / coulomb (J/c)

30
Q

coulomb

A

measure of charge

e- = 1.6x10^-18 c

31
Q

e°cell values

A

+ means spontaneous (galvanic)

— means nonspontaneous (electrolytic)

32
Q

what happens when you change conc. (rate law)

A

r = k[A]^2 [B]^1

if A doubles: [2]^2 = x4

if A triples: [3]^2 = x9

if B halves: [2]^1 = x1

if B thirds: [3]^1 = x1

33
Q

arrhenius equation in y=mx+b

A

lnk = (-Ea/R)*(1/T)+lnA

y = m x + b