Chemistry 3 Flashcards

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1
Q

oxidation state

A
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
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2
Q

electrical potential (E°)

A

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)

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3
Q

cell potential

A

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

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4
Q

galvanic cell / voltaic cell

A
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

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5
Q

electrolytic cell

A
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

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6
Q

concentration cell

A

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

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7
Q

Nernst equation

A

E = E° - (0.06/n)*log[lower]/[higher]

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8
Q

free energy and chemical energy

A

∆G° = -nFE°

n = number of moles of e- transferred in balanced redox reaction
F = Faraday's constant
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9
Q

Faraday’s constant

A

9.6 x 10^4 C/mol

charge on one mole of electrons

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10
Q

ideal gas law

A

PV = nRT

R = 0.0821 (Latm)/(molK) or 8.314 J/(mol*K)

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11
Q

ideal gas assumptions

A

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

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12
Q

STP

A
standard temperature and pressure
P = 1 atm
V = 22.4 L
n = 1 mole
T = 273 K (0 °C)
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13
Q

standard conditions

A
P = 1 atm
concentration  = 1 M
T = 298 K (25 °C)
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14
Q

absolute zero

A

a theoretical temperature where all molecular motions cease

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15
Q

combined gas law

A

P1V1 / T1 = P2V2 / T2

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16
Q

real gases

A

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

17
Q

Van der Waals euation

A

increased intermolecular attractions → decrease pressure in real gases

increased molecular volume → increased volume in real gases

18
Q

effusion / diffusion

A

E1 / E2 = √MW2 / √MW1

19
Q

vapor pressure

A

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

20
Q

Raoult’s law

A

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)

21
Q

Henry’s law

A

the solubility of a gas in a liquid is directly proportional to the partial pressure of that gas over that liquid

22
Q

gas solubility

A

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

23
Q

boiling point elevation

A

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
24
Q

freezing point depression

A

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
25
Q

osmotic pressure

A
π = iMRT
i = # of ions formed per molecule
M = molarity
R = gas constant
T = temperature in K
26
Q

molarity

A

moles solute / L solution

27
Q

molality

A

moles solute / kg solvent

*** doesn’t change with temperature

28
Q

ppm

A

(mass solute / total mass solution) (10^6)

*** just a measure of mass percent

ppm = mg/kg = mg/L

29
Q

normality

A

of moles of equivalents / L solution

30
Q

Ksp

A

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

31
Q

ion product / solubility product

A

same relationship to Ksp as Q does to Keq

32
Q

soluble compounds

A

nitrate (NO3 -), ammonium (NH4 +), all alkali metals

33
Q

insoluble compounds

A

*** unless paired with one of the always soluble compounds

carbonate (CO3 -2), phosphate (PO4 -3), sliver (Ag), mercury (Hg), lead (Pb)