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Hydroxide
OH-
Nitrate
NO3-
Carbonate
CO32-
Sulfate
SO42-
Phosphate
PO43-
Ammonium
NH4+
Methane
CH4
Ammonia
NH3
Hydrogen Peroxide
H2O2
accuracy
closeness of data value to literature value
precision
consistency of all data values
log 2
0.3
log 3
0.48
1 Liter = ? mL and ? cm3
1000 mL and 1000 cm3
t (K) =
t (C) + 273.15 (K)
Pressure: 1 atm = ? torr / mmHg, ? kPa, and ? bar
760 torr / mmHg, 101.3 kPa, and 1.013 bar
Boiling Point of water
100 C
Freezing Point of water
0 C
Amount of substance
mole (mol)
thermodynamic temperature
kelvin (K)
mass
kilogram (kg)
length
meter (m)
time
second (s)
giga-
G = 109
mega
M = 106
kilo
k = 103
hecto
h = 102
deca
da = 101
deci
d = 10-1
centi
c = 10-2
milli
m = 10-3
micro
u = 10-6
nano
n = 10-9
Have No Fear Of Ice Cold Beer
Diatomic gases: H2, N2, F2, O2, I2, Cl2, Br2
Metal Properties: (6)
Malleable and lustrous
Form basic oxides
High melting and boiling points
Lose electrons to form cations
Good conductors of electricity
Solid at room temperature (exception: mercury)
Non-metal Properties: (6)
Brittle and dull
Form acidic oxides
Low melting and boiling points
Gain electrons to form anions
Poor conductors of electricity and heat
Gas or solid at room temperature (exception: bromine)
Atomic radius
½ the bond length between identical atoms;
increases to the left and down the periodic table
Effective Nuclear Charge
Zeff = Z (proton #) - S (# of shielding electrons)
= the amount of positive charge experience by an electron;
increasing to the right and down the periodic table
isoelectronic series
atoms/ions with the same number of electrons but different proton numbers; anions have larger atomic radius, cations have smaller atomic radius
ionization energy/potential
the energy needed to remove an electron from a gaseous, neutral atom… = change in enthalpy (delta H)
increases to the right and up (1st ionization energy)
2nd ionization energy: after 1st electron is removed, the 2nd ionization is harder and higher energy; easier for 1st group and smaller elements than group 2, but still a high energy;
alkaline earth metals have a higher than usual 1st ionization energy because of p orbital valence electrons;
group 15 higher energy than group 16 because of half filled orbitals
group 2 have higher energy than group 13 because of group 2 filled orbital
electron affinity
the amount of energy released/required when an electron is added to a gas-phase atom
increase to the right and up; becomes more negative
noble gases have low affinity (they have all of their valence electrons);
if an element can perfectly half fill their orbital with the electron, it will have a higher affinity than an adjacent element with an already half-filled orbital (group 4 > group 5)
electronegativity
the ability of an atom to attract electrons to itself in a covalent bond
increase to the right and up
noble gases are negligible
Soluble Salts (5)
group 1 metal cations
NO3-
ClO4-
C2H3O2-
NH4+
Insoluble Salts (7)
Ag+
Pb2+
Hg2+
OH-
S2-
CO32-
PO43-
Strong Acids: (7) + acronym
HI Hi
HCl Class (is)
HBr Boring.
HNO3 No (it isn’t)
HClO3 Class (is) Over
HClO4 Class (is) Over
H2SO4 So (what)
Strong Bases (4)
Group 1 Metal Hydroxides
Ba(OH)2
Sr(OH)2
Ca(OH)2
Weak Acids: (3)
HF
HCN
CH3COOH
Weak Base: (2)
NH3
CH3NH2
Colligative properties
depend upon the concentration of solute molecules or ions, but not the identity of the solute
ex: salt makes water harder to freeze
Non-colligative properties
depend on the identity of the dissolved species and the solvent
ex: surface tension varies between substances, color depends on substances
Surface Tension
property of a liquid that allows it to resist an external force, due to cohesion
non-colligative
Viscosity
measure of a liquids resistance to flow
non-colligative
Solubility
ability of a solute to for a solution with a solvent
non-colligative
Color and density
do not depend on the number of particles
non-colligative
Boiling Point
when the vapor pressure = atmospheric pressure; liquid is converted into gas
colligative
BP at sea level
100 C
BP above sea level
decreases; as elevation increases the atmospheric pressure decreases and this BP is easier to reach
BP below sea level
increases; as elevation decreases the atmospheric pressure increases because the air is denser
Vapor-Pressure Depression
vapor pressure without solute is higher than VP with a non-volatile solute; adding solute increases boiling point by lowering VP and requiring higher temp to reach atmospheric pressure; Raoult’s Law
colligative
Raoult’s Law (Vapor Pressure)
VP of solution = mole fraction of solvent x VP of solvent
colligative
Boiling Point Elevation
BP of a liquid will be higher when a non-volatile solute is added; large van’t Hoff factor increases BP
Change in BP = solvent’s BP-elevation constant x i x molal
colligative
Freezing-Point Depression
a drop in the minimum temp at which a substance freezes when a non-volatile solute is added; solution has a lower FP due to the solute
ex: alcohol lowers the FP of water
Change in FP = (-) solvent’s FP-depression constant x i x molal
colligative
Osmotic Pressure
the pressure required to stop osmosis
Osmotic Pressure (atm) = i x M x universal gas constant x temp (K)
colligative
van’t Hoff Factor
“i”
the number of particles a solute breaks down into
ex: MgCl2 … i = 3 because of Mg2+, Cl-, and Cl-
Normality
N= number of equivalents x M
Combined Gas Law
(P1V1)/(n1T1) = (P2V2)/(n2T2)
Boyle’s Law
P1 V1 = P2 V2
Charles’s Law
V1/T1 = V2/T2
Avogado’s Law
V1/n1 = V2/n2 where n is the number of moles
Gay-Lussac’s Law
P1/T1 = P2/T2
Dalton’s Law of Partial Pressure
total pressure of the mixture is equal to the sum of the partial pressures of individual gases
Ptotal= P1 + P2 + …
P1 = X1 x Ptotal where X1 is the mole fraction of gas 1
Gas density
Density = m / v
Density = (P x M) / (R x T)
Effusion
A confined gas escaping through a small hole, which gas effused faster are ones with lower molecular weight
Graham’s Law of Effusion
r1/r2 = √(M2/M1) where r is the effusion rate and M is the molar mass
inversely proportional
Ideal Gas Law
PV = nRT
STP
Standard Temp and Pressure: 273K, 1 atm, 1 mol = 22.4 L
1st Order Half-life
t1/2= 0.693/k
Properties of Work (2)
ΔE = q + w (change in internal energy = heat + work)
w = -P x ΔV (work = -Pressure x change in volume)
Arrhenius Acid
produces H+ ions
Arrhenius Base
produces OH- ions
Bronsted-Lowry Acid
a proton (H+) donor
Bronsted-Lowry Base
a proton (H+) acceptor
Lewis Acid
accepts a pair of electrons
Lewis Base
donates a pair of electrons
Henderson-Hasselbach Equation:
pH=
pH = pKa + Log ([A-]/[HA])
determine the ratio of acid to conjugate base in a buffer solution
Heat absorbed/released:
q= mass x C x delta T
q= mass X delta H
*In calorimetry: q= C x delta T
Common Oxidizing agents: (4)
O2
O3
H2SO4
halogens
Common Reducing Agents: (4)
H2
Fe
Zn
Alkali metals (Group 1)
Bohr’s Principle
model of the atom describes electrons orbiting around the nucleus in a circular path
Pauli Exclusion Principle
no two electrons in an atom can have the exact same four quantum numbers
Heisenberg Uncertainty Principle
it is impossible to know both the location and momentum of an electron at the same time
Hund’s Rule
every orbital in a subshell must be occupied with an electron first before the electrons begin occupying in pairs
Aufbau Principle
electrons fill orbitals in the order of increasing energy levels
VSEPR: 2 bonding 0 lone
Linear: 180 deg
ex: CO2

VSEPR: 3 bonding 0 lone
Trigonal Planar: 120 deg
ex: BF3

VSEPR: 2 bonding 1 lone
Bent/V-shaped: <120 deg
ex: SO2

VSEPR: 4 bonding 0 lone
Tetrahedral: 109.5 deg
ex: CH4

VSEPR: 3 bonding 1 lone
Trigonal Pyramidal: 107.5 deg
ex: NH3

VSEPR: 2 bonding 2 lone
Bent/V-shaped: 104.5 deg
ex: H2O

VSEPR: 5 bonding 0 lone
Trigonal bipyramidal: 90 and 120 deg
ex: PCl5
