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1st OS rule
groups 1 and 2 have charge of group number. No exceptions.
2nd OS rule
H is +1 except H2= 0 and metal hydrides (NaH/CaH, os H = -1)
3rd OS rule
O is -2 except O2, O3 = 0 and peroxides (H2O2, O os = -1 and OF2, os = +2)
4th OS rule
F is -1 except F2 = 0
5th OS rule
Halides (Cl, Br, I) = -1 except when bonded to O or F (HClO4, Cl os = +7)
Good salt bridge ions
Na+, K+, Cl-, NO2-
what makes a good salt bridge ion
Soluble, not reactive with the electrodes or species in solution
good inert electrodes
P+, C (graphite)
Cell diagram notation
anode 1st then cathode, || = salt bridge, | = phase change, comma would separate different species in same phase, use electrode if no solids (must start and end with a solid), read left to right reactant to product, no spectator ions.
standard reduction potentials table
higher = more “positive”, strong oxidants (oxidizing agent) (take e-), is reduced
lower = more “negative”, strong reductants (reducing agent) (donate e-), is oxidized
E°cell > 0
spontaneous
E°cell < 0
not spontaneous
E°cell = 0
at equilibrium
E° indicates?
standard state (1M), P = 1 atm, at 25° C
-ΔG
spontaneous
+ΔG
not spontaneous
ΔG = 0
at equilibrium
primary batteries
Not rechargeable, high power, longer lasting, inexpensive
primary battery example
Dry cell, named Leclanche for its inventor
secondary batteries
rechargeable for many cycles (run cell in reverse by electrolysis to recharge)
secondary battery example
Lead-acid battery, lithium ion battery
fuel cells
must provide fuel in continuous supply (can use different fuels: H2 is the lightest)
corrosion process
spontaneous (fast or slow), undesirable redox chemistry
corrosion example
(anode) Fe(s) → Fe2+(aq) + 2e- (cathode) O2(s) + 4H+(aq) + 4e- → 2H2O(l)
1st corrosion prevention
create protective layer (paint or already oxidized material; statue of liberty)
2nd corrosion prevention
mix in some corrosion resistant metals
3rd corrosion prevention
physically connect a sacrificial anode to the system (sacrificial = will donate its own e- first, protecting another metal)
pH = ?
-log[H+]
[H+] =
10-pH
ne = ?
total moles of e- used
I = ?
current, usually amps (c/s)
F (in faraday’s law)
96485 c/mol
galvanic cell
spontaneous, chemical energy turns into electrical energy, wide range of anode/cathode combos possible, cell potential determined from Ered of half cells, often 2 different half rxns. Flows: anode e-→e- cathode. anode: [M+] increases (solid decreases). cathode: [M+] decreases (solid increases).
Concentration cell
type of galvanic cell, same half rxns in cathode and anode, different concentrations drive the cell toward equilibrium (equal concentrations). (anode) xM[M+] <<yM[M+] (cathode)
Electrolytic cell
non spontaneous, electrical energy turns into chemical energy, powered with current, metal ions from solution (or other products) form at the electrode, some similarities to the cathode of a galvanic cell, Ered determines which product forms if multiple possible. Flows: cathode e- ← e- anode
anions(-) go to the
anode
cations(+) go to the
cathode
in the external circuit e- migrate
from the anode to the cathode
oxidized is
anode
reduced
cathode