Should be on the Test Flashcards
when not at equilibrium
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
where does reduction occur?
cathode
predicting change in entropy
- molecular complexity (Ar < CO < CO2)
- chemical rxns (A -> 2B = +S [more moles of products])
state function
entropy is a state function (doesn’t care about the path; only the initial and final state)
entropy with constant T
∆S = q(rev)/T
third law of thermodynamics
entropy of a perfectly organized crystal at absolute zero is zero [no disorder]
value of Q at STP
Q = 1
what value of K means for spontaneity
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]
IMF and vapor pressure
IMF determine vapor pressure [stronger IMF = lower vapor pressure]
why do stronger IMF mean lower vapor pressure
more heat must be introduced to break forces of the liquid to go to gas phase
raoult’s law
Pa = XaPa*
Pa* = vp of pure solvent
attracted to water
hydrophilic
repelled by water
hydrophobic
molality
n/kg [m]
solubility of a gas (henry’s law)
s = k(H)P
gases become less soluble at high temps.
IΔE box method
used for:
equilibrium
finding pH
solubility product/precipitation rxns
polyprotic acid
H2SO3 + H2O ⇄ H3O+ HSO3- [K1]
HSO3- + H2O ⇄ OH- SO3 (2-) [K]
K(1)»_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)
amphoteric acids
species that is both an acid or a base
HSO3- + H2O ⇄ H3O+ SO3-
HSO3- + H2O ⇄ OH- H2SO3
salts + properties
can be acidic or basic
NaF + H2O ⇄ Na+ + F- + H2O
F- + H2O ⇄ OH- + HF
NaF is a base, and conjugate is HF
acid strength (family trends)
HF (weak
HCl (stronger)
HBr (stronger)
HI (strongest) [more shielding]
acid strength (oxyacid groups)
HClO < HClO2 < HClO3 < HClO4
the oxygen atoms pull e-density away from the OH group. more oxygens = more easy the H+ comes off
common-ion effect
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
solubility product
AgCl ⇄ Ag+ + Cl-
Ksp = [Ag+][Cl-]
if small: not very soluble
precipitation reactions
precipitation reactions
[Ag+][Cl-] < Ksp
(Q < K) rxn shifts right (no precipitate)
[Ag+][Cl-] = Ksp
(Q = K) solution is saturated
[Ag+][Cl-] > Ksp
(Q > K) rxn shifts left (precipitate forms)
where does oxidation occur?
anode
volt
Joule / coulomb (J/c)
coulomb
measure of charge
e- = 1.6x10^-18 c
e°cell values
+ means spontaneous (galvanic)
— means nonspontaneous (electrolytic)
what happens when you change conc. (rate law)
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
arrhenius equation in y=mx+b
lnk = (-Ea/R)*(1/T)+lnA
y = m x + b