Chapter 20 - Electrochemistry Flashcards

1
Q

Balancing Redox Reactions (Acidic)

A
  1. Divide equation into half reactions
  2. Balance Half reactions (Add H2O to balance Os and add H+ to balance Hs.
  3. Multiply each side by an integer to make sure electrons are equal
  4. Combine half reactions to form final redox reaction and cancel species
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2
Q

Balancing Redox Reactions (Basic)

A

1.Divide equation into half reactions
2. Balance Half reactions (Add H2O to balance Os and add H+ to balance Hs.
3. For every H+, add an OH- to each side of the equation. For every H+ and OH- pair, simplify it to H2O
4. Multiply each side by an integer to make sure electrons are equal
5. Combine half reactions to form final redox reaction and cancel species

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3
Q

Voltaic Cell

A

a device where the flow of electrons goes through an external circuit instead of directly between reactants in the same reaction vessel

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4
Q

Anode

A

(-), the electrode at which oxidation occurs

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5
Q

Cathode

A

(+), the electrode at which reduction occurs

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6
Q

Electron direction

A

Electrons always flow from Anode (where oxidation occurs) to Cathode (where reduction occurs) in spontaneous reactions

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7
Q

Salt Bridge

A

allows for ion migration between two substances to maintain neutrality of charge

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8
Q

Volt is equal to…

A

J/C
(Joules/coulombs)

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9
Q

Electron value

A

1.6 x 10^-16 C
1 mol = 96485 C

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10
Q

Cell potential

A

Written as Ecell, measures the potential difference between the two electrodes of a voltaic cell. It is measured in volts. This value should always be positive.

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11
Q

Standard Cell Potential

A

Written as E°cell, this measures the potential difference between the two electrodes of a voltaic cell in standard conditions (1atm, 0° C, 1 M).
The standard Cell Potential is the same as the Standard Reduction potentials, meaning that it can be used to find the values of the standard reduction potentials of the half reactions that make up the whole reaction, using the equation
E°cell = E°red.(cathode) - E°red.(anode)

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12
Q

Electrical Potential

A

Measures the potential energy per electrical charge. Changing the mole value of the equation does not change the potential energy value, as the ratio would remain the same.
Ex:
Zn + 2e- -> Zn E°red = -0.76 V
10Zn + 20e- -> 10Zn E°red = -0.76 V

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13
Q

Half Reaction Tables

A

Tables list half reaction with an assigned E°red value.
The higher the value, the half-reaction will have a higher tendency to become reduced but lower tendency to become oxidized.
Alternatively, the lower the value, the half-reaction will have a lower tendency to become reduced but a higher tendency to become oxidized.

Knowing this, we can also apply our knowledge of oxidizing and reducing agents to this. Those who get reduced are considered oxidizing agents while those who get oxidized are considered reducing agents. Looking at the table, since half-reactions with a high E°red value will be easiest to reduce but most difficult to oxidize, thus meaning that they are potent oxidizing agents. Alternatively, half-reactions with a low E°red value will be hardest to reduce but easiest to oxidize, thus meaning that they are potent reducing agents.
Keep in mind that the oxidizing agents will be on the reactants side of the equation (the one with the electrons) while the reducing agents will be on the products side of the equation.

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14
Q

Oxidizing Agents

A

Halogens (F, Cl, Br, I, At, Ts)
Oxygen (O2)
Oxyanions (anions containing oxygen that follows the format of AxOyZ-)
These species will have positive values of E°red and thus easily undergo reduction

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15
Q

Reducing Agents

A

H2
Alkali metals (Li, Na, K, Rb, Cs, Fr)
Alkaline-Earth Metals (Be, Mg, Ca, Sr, Ba, Ra)
These species have negative values of E°red and thus can easily undergo oxidation

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16
Q

Spontaneity of a reaction

A

E° = E°red(red. process) - E°red(ox. process)
Equation is generalized to determine spontaneity. A negative value means that is it non spontaneous while a positive value indicates the the reaction is spontaneous.

17
Q

Free energy and spontaneity

A

∆G = -nFE
n = number of moles of electrons transferred
F = 96485 J/V-mol
units is in J/mol
Occurs at constant temperature and pressure

18
Q

Standard State of Free Energy

A

∆G° = -nFE°

19
Q

A

E° = ∆G/-nF = -RTlnK/-nF = RT/nF (lnK)

20
Q

Nernst Equation

A

E = E° - RT/nF (lnQ) = E° - 2.303RT/nF (logQ)

When T = 298:
E = E° - 0.0592V/n (logQ)
units in volts

21
Q

Concentration cells

A

Same as voltaic cells except it only uses one type of substance. The current is driven by a difference in concentration between the two cells. The concentration cell will attempt to reach an equilibrium of concentrations by transferring electrons from the higher concentration the the cell with lower concentration.

22
Q

Electrolysis

A

Nonspontaneous reactions that are driven by an external power source to occur. They take place in electrolytic cells.

23
Q

Coulombs

A

1C = A x S
A = Amperes (charge of current)
S = seconds
This equation is used to find the number of coulombs passing through a cell during a given time frame.

24
Q

Electroplating

A

Always occurs at the cathode where metal is placed upon it. By using the equation It = nF, we can find the amount of charge passing through the cell.
I = current in amperes or coulombs/sec
t = seconds
n = moles of electrons
F = 96485 C/mol-e