everything I tried to have memorized by the ap chemistry exam.
Percent Error =
(|calculated answer - correct answer|/correct answer) x 100
Ammonium:
NH4^+
Bromate:
BrO3^-
Perchlorate:
ClO4^-
Chlorate:
ClO3^-
Chlorite:
ClO2^-
Hypochlorite:
ClO^-
Cyanide:
CN^-
Carbonate:
CO3^2-
Chromate:
CrO4^2-
Sulfate:
SO4^2-
Oxalate:
C2O4^2-
Acetate:
C2H3O2^-
Hydroxide:
OH^-
Iodate:
IO3^-
Periodate:
IO4^-
Nitrate:
NO3^-
Nitrite:
NO2^-
Permanganate:
MnO4^-
Peroxide:
O2^2-
Dichromate:
Cr2O7^2-
Sulfite:
SO3^2-
Phosphate:
PO4^3-
First Important Solubility Rule:
Compounds containing Na^+, K^+, or NH4^+ ions are ALWAYS soluble in water.
Second Important Solubility Rule:
Compounds containing NO3^- ions are always soluble in water.
Potential Difference, or Voltage, of a Galvanic Cell (must be +): Ecell =
Ecathode - Eanode
Reduction:
takes place at the cathode
is gaining e-
Oxidation:
takes place at the anode
is losing e-
A metallic cathode will:
always increase in mass.
Electrons move through the wire from:
anode (decreases in mass) to cathode (increases in mass).
Salt Bridge:
anions will flow to the anode
cations will flow to the cathode
Change in Enthalpy (heat):
ΔH
Change in Entropy (disorder):
ΔS
Difference in Gibbs Free Energy (ΔG) =
ΔH - T(ΔS)
-RTln(K)
Thermodynamically favored at all temperatures when:
ΔH is negative and ΔS is positive.
Never thermodynamically favored at any condition when:
ΔH is positive and ΔS is negative.
Thermodynamically favored at higher temperatures when:
ΔH and ΔS are both positive.
Thermodynamically favored at lower temperatures when:
ΔH and ΔS are both negative.
Zeroth Order:
[A]t - [A]0 = kt
First Order:
ln[A]t - ln[A]0 = kt
Second Order:
1/[A]t - 1/[A]0 = kt
First Order Half-Life:
t1/2 = 0.693/k
Coulomb’s Law:
F = k(q1q2/d²)
F:
Attractive force between the two charged particles.
d²:
Distance between the two charged particles.
q1q2:
Magnitude of charge of each of the two charged particles.
As the magnitude of the charge of the particles goes up:
so does the attractive force between the particles.
As the distance between two charged particles goes down:
their attractive force goes up.
Formal Charge =
# valence e- an atoms has - (# unshared e- + # individual e- bonds assigned to that atom)
Steric Number =
# atoms that central atom is touching - # unshared e- pairs on that central atom
Steric Number
2
3
4
Hybridization
sp
sp²
spÂł
Boyle’s Law (inverse relationship):
P1V1 = P2V2
Charles’ Law (direct relationship):
V1/T1 = V2/T2
Gay-Lussac’s Law (direct relationship):
P1/T1 = P2/T2
The Dilution Equation:
M1V1 = M2V2
Percent Yield =
(Actual Yield/Theoretical Yield) x 100
ΔH =
ÎŁHbonds broken - ÎŁHbonds formed
Percent Dissociation of a Weak Acid =
([H3O^+]equilibrium/[HA]initial) x 100
Percent Dissociation of a Weak Base =
([OH^-]equilibrium/[B]initial) x 100
The Titration Equation:
MAVA = MBVB
Average Atomic Mass:
(mass of isotope)(% abundance)
Overall = avg.1 + avg.2 + …
Atomic radius is greatest at:
the bottom left of the periodic table.
Cations tend to be:
smaller than anions.
First ionization energy is greatest at:
the top right of the periodic table.
Complete combustion means products are:
CO2 and H2O.
rate =
k[A]^m[B]^n
Elements in natural state will have an enthalpy of:
zero.
Kc =
[products]^m/[reactants]^n
Kp =
Pproducts^m/Preactants^n
If K<1:
more reactants; products favored.
If Q>K:
more products; reactants favored; pressure of products will decrease.
The Six Strong Acids:
HCl, HBr, HI, HNO3, H2SO4, HClO4
The Eight Strong Bases:
LiOH, NaOH, KOH, RbOH, CsOH, Ca(OH)2, Sr(OH)2, Ba(OH)2
multiply concentration by 2 for Group 2 hydroxides
At the half-equivalence point:
pH = pKa
[HA] = [A^-]
At the equivalence point:
the acid is all gone.
Materials at higher temperatures or with more molecules have:
more entropy than those with lower/less.
Universal Gas Constant (R) =
0.0821 (L x atm/ mol x K)
Ideal Gas Costant (R) =
8.314 J/mol x K