electrochemistry Flashcards

1
Q

electrochemistry real world applications

A

photosynthesis, conversion of food to energy, combustion, batteries and fuel cells, corrosion and prevention

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2
Q

What is being reduced and oxidized? 2Fe 3+ + HCO2H + 2H2O –> 2Fe2+ + CO2 + 2H30+

A
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3
Q

rules for balancing redox rxns

A
  1. separate into 2 half rxns
  2. balance all elements except O and H
  3. Balance O with H2O
  4. balance H with H+
  5. Balance charge with e-
  6. Find multiplier that allows e- to cancel
  7. combine/add half rxn together
  8. check to be sure balaced- this is for acidic conditions
  9. for basic conditions, add OH- to both sides to eliminate H+, cancel residual water, check again
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4
Q

practice C2O4 2- + MnO4- <–> CO2 + Mn2+

A
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5
Q

galvanic electrochem cell beaker sketch: Fe (s) –> Fe2+ + 2e- , Cu2+ + 2e- –> Cu (s)

A
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6
Q

Standard Hydrogen Electrode (SHE) 2H+ 9aq) + 2e- –. H2(g) purpose

A

a standard to compare the reaction potential of all other substances

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7
Q

cell potentials

A

electrochemical cells generate electricity (e- flow) by physically separating two half rxns, each half cell contributes to overall cell potential (voltage cell can produce)

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8
Q

E° cell equation

A

E°cell= E°oxidation + E°reduction OR E°cell= E°cathode- E°anode

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9
Q

Standard reduction potentials

A

always given in reduction format, use to find oxidation potential by multiplying by (-) flipping rxn

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10
Q

manipulating E° potentials

A
  • flip sign when E°red becomes E°ox
  • if multip;y rxn by constant DO NOT multiply E°red- intensive property
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11
Q

galvanic cell overview

A

-balanced redox rxn for an electrochemical cell
- designate cathode and anode
-SRP to determine the direction of e- flow, calculate E° cell for system
for galvanic cell E°cell should be (+) and spontaneous
- consider phases for all species involved, may need chemically inert conductor Pt or graphite as electrode for non-solid species like H2 (g) specify in diagram

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12
Q

1 coulomb (C)

A

Measure of charge on 6.2x10^18 e-

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13
Q

charge on 1 e-

A

1.6x10^-19 C

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14
Q

1 Faraday (F)

A

charge on 1 mol e- = 96,485 C/mol e-

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15
Q

1 Volt (V) = 1 Joule per Coulomb = 1 J/C

A
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16
Q

Half-reactions are defined by changes in free energy associated with transferring e-

A

since half rxn potential is determined by free energy change from electron transfer, we can find the free energy delta G carried by 1 Coulomb charge – this is SRP for half rxn

17
Q

relationship between E and delta G

A

E has opposite sign as delta G

18
Q

if energy is released (delta G> 0) then

A

electrons will be carried through cell, positive E potential

19
Q

role of Q

A

accounting for concentrations and pressures that are not standard state

20
Q

Q, K, and delta G at at equilibrium

A

Q=K, Delta G= 0

21
Q

when not at EQ, cell potential shifts

A

left or right, depending on cell potential

22
Q

nernst equation

A

Delta G°= -nFE° – see eq sheet for more examples of derivatives

23
Q

spontaneous forward direction

A

delta G° <0, E° cell>0, K >1

24
Q

spontaneous in the reverse direction

A

delta G° >0, E° cell<0, K <1

25
Q

no net rxn: system at eq

A

delta G° 0, E° cell 0, K 1

26
Q

what will happen to cell with identical electrodes and different ion concentrations, how will sys shift to reach eq

27
Q

primary batteries

A

high power, long-lasting, inexpensive, NON-rechargeable (single use) ex: dry cell battery

28
Q

secondary batteries

A

rechargeable for many cycles, ex: lead acid battery, lithium-ion battery

29
Q

fuel cells

A

“clean” run on hydrogen-containing fuel, longer lifetime than traditional batteries, ex: Proton Exchange Membrane

30
Q

corrosion

A

spontaneous, undesirable redox chemistry

31
Q

corrosion prevention

A
  1. protective later (paint)
  2. mix in corrosion-resistant metals (alloy to protect vulnerable material with corrosion-resistant species)
  3. Physically connect the sacrificial anode (donate e- to the system first, protecting another metal from unwanted oxidation (more negative SRP, ex: zinc, mg)
32
Q

electrolysis definition

A

Reverse of galvanic cell: input a voltage to run the electrochemical rxn in non-spontaneous rxn

33
Q

electrolysis applications

A
  • can be used to selectively “plate out” metals that are dissolved in solution
  • industrial processes such as aluminum and copper refinement
34
Q

faraday’s law of electrolysis

35
Q

Electrolysis practice problem

A

check discussion worksheet

36
Q

sketch galvanic cell

A

galvanic cell characteristics:
- spontaneous
- chemical energy turns into electrical energy
- wide range anode/cathode combinations possible
- cell potential determined from E red of half cells
often two diff half rxns

37
Q

sketch concentration cell

A

concentration cell characteristics:
- type of galvanic call
- same half rxn in cathode and anode e
- different concentrations drive cell towards equilibrium (equal concentration)

38
Q

sketch electrolytic cell

A

Electrolytic cell characteristics:
- non-spontaneous
- electrical energy turns into chemical energy
- powered with current
- metal ions from solution (or other products) form at electrode
-some similarities to cathode of galvanic cell
- E red determines which product forms if multiple possible