Chemistry 3 Flashcards
oxidation state
any elemental atom: 0 Fl: -1 H w/ a metal: -1 H: +1 O: -2 O in peroxides: -1 Group V: -3 Group VI: -2 Group VII: -1
electrical potential (E°)
tell us the degree to which a species wants e-
positive E° → more likely to be reduced than H ions
negative E° → less likely to be reduced than H ions
E° values assigned are relative reduction potential of that species compared to hydrogen half cell: 2H+ + 2e → H2 (E° = 0 V)
cell potential
half-reactions always come in pairs → one oxidation and one reduction
***don’t use stoichiometry → one mole of x has same reduction potential as two moles of x
galvanic cell / voltaic cell
cathode = + and reduction anode = - and oxidation
cell potential always positive
can be created using any two metals, regardless of reduction potentials → e- will flow from species with lower reduction potential to species with higher reduction potential
electrolytic cell
cathode = - and reduction anode = + and oxidation
*** external voltage applied → species with the lower reduction potential will be reduced
cell potential always negative
sum of externally applied voltage and the negative E° cell must be positive
concentration cell
special type of galvanic cell
same electrodes and solution are used in both beakers
positive cell potential if there is a difference in the molarities of the two solutions
E° cell always = 0
Nernst equation
E = E° - (0.06/n)*log[lower]/[higher]
free energy and chemical energy
∆G° = -nFE°
n = number of moles of e- transferred in balanced redox reaction F = Faraday's constant
Faraday’s constant
9.6 x 10^4 C/mol
charge on one mole of electrons
ideal gas law
PV = nRT
R = 0.0821 (Latm)/(molK) or 8.314 J/(mol*K)
ideal gas assumptions
gas molecules have negligible volume compared to the volume occupied by the gas
all intermolecular forces between gas molecules are negligible
*** gas molecules = no volume and no intermolecular forces
STP
standard temperature and pressure P = 1 atm V = 22.4 L n = 1 mole T = 273 K (0 °C)
standard conditions
P = 1 atm concentration = 1 M T = 298 K (25 °C)
absolute zero
a theoretical temperature where all molecular motions cease
combined gas law
P1V1 / T1 = P2V2 / T2
real gases
greatest deviation between ideal gas behavior and real gas behavior occurs:
1) temperature is extremely low → actual size of molecules becomes comparable to distance in between them → real gas will occupy greater volume than expected by equation
2) pressure is extremely high → intermolecular interaction between gas molecules becomes more prevalent → real gas will produce smaller pressure than expected by equation
PV/nRT > 1 → deviation from ideal gas law due mostly to molecular volume assumption
PV/nRT < 1 → deviation from ideal gas law due mostly to intermolecular forces assumption
Van der Waals euation
increased intermolecular attractions → decrease pressure in real gases
increased molecular volume → increased volume in real gases
effusion / diffusion
E1 / E2 = √MW2 / √MW1
vapor pressure
partial pressure of the gaseous form of a liquid that exists over that liquid when the liquid and gas are in equilibrium
↑ temperature → ↑ vapor pressure
addition of a non-volatile solute → ↓ vapor pressure
addition of volatile solute → depends on vapor pressure of volatile solute
Raoult’s law
vapor pressure w/ a non-volatile solute: Vp = XVp°
X = mole fraction of the pure solvent
Vp° = vapor pressure of the pure solvent
vapor pressure w/ a volatile solute: Vp = Vpsolvent + Vpsolute = (Xsolvent)(Vp°solvent) + (Xsolute)(Vp°solute)
Henry’s law
the solubility of a gas in a liquid is directly proportional to the partial pressure of that gas over that liquid
gas solubility
increased temperature → decreased solubility
increasing vapor pressure of gas X over a liquid increases the solubility of gas X in that liquid
polar and non-polar gases easily form homogenous mixtures
boiling point elevation
boiling point of a liquid is elevated when a non-volatile solute is added
∆T = kb m i kb = constant m = molality i = # ions formed per molecule
freezing point depression
freezing point of a liquid is depressed when a non-volatile solute is added
∆T = kf m i kf = constant m = molality i = # ions formed per molecule
osmotic pressure
π = iMRT i = # of ions formed per molecule M = molarity R = gas constant T = temperature in K
molarity
moles solute / L solution
molality
moles solute / kg solvent
*** doesn’t change with temperature
ppm
(mass solute / total mass solution) (10^6)
*** just a measure of mass percent
ppm = mg/kg = mg/L
normality
of moles of equivalents / L solution
Ksp
leave out pure liquids/solids → Ksp equations only have numerator
temperature is the only thing that changes Ksp
Ksp can only be observed in a saturated solution → saturation is the point at which dissolution reaction has reached equilibrium
ion product / solubility product
same relationship to Ksp as Q does to Keq
soluble compounds
nitrate (NO3 -), ammonium (NH4 +), all alkali metals
insoluble compounds
*** unless paired with one of the always soluble compounds
carbonate (CO3 -2), phosphate (PO4 -3), sliver (Ag), mercury (Hg), lead (Pb)