Chapter 23 - Redox and Electrode Potentials Flashcards

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1
Q

Define redox

A

A reaction where both reduction and oxidation takes place.

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2
Q

What is the manganate half reaction?

A

MnO4-(aq) + 8H+(aq) + 5e- —> Mn2(aq) + 4H2O(l)

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3
Q

What is the procedure for a Manganate(VII) titration?

A
  1. Add a standard solution of KMnO4 to the burette and measure initial reading.
  2. Using a pipette, add a measured volume of the other solution to a conical flask.
  3. Add an excess of dilute sulphuric acid to the flask to provide H+ ions to reduce MnO4- ions. No indicator is needed as reaction is self-indicating.
  4. During titration, the manganate(VII) is decolourised as it lands in the conical flask until the end point - where it will turn pink. Record new reading on burette.
  5. Repeat titration until concordant results obtained.
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4
Q

How is the meniscus read differently when measuring out KMnO4 in manganate(VII) titrations?

A

Read from the top of the meniscus because potassium permanganate has a deep purple colour so it is hard to see from bottom of meniscus.

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5
Q

Which 2 reducing agents can be analysed using manganate(VII) titrations?

A

Iron (II) ions, Fe2+(aq)

Ethanedioic acid, (COOH)2(aq)

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6
Q

What is the iodine/thiosulfate reaction?

A

2S2O3-(aq) + I2(aq) —> 2I-(aq) + S4O62-(aq)

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7
Q

What is the oxidation reaction in an iodine/thiosulfate reaction?

A

2S2O3-(aq) —> S4O62- + 2e-

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8
Q

What is the reduction reaction in an iodine/thiosulfate reaction?

A

I2(aq) + 2e- —> 2I-(aq)

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9
Q

What can iodine/thiosulfate titrations be used to determine?

A

The ClO- content in household bleach
The Cu2+ content in copper(II) compounds
The Cu content in copper alloys

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10
Q

What is the procedure for an iodine/thiosulfate titration?

A
  1. Add a standard solution of sodium thiosulfate, Na2S2O3, to the burette
  2. Using a pipette, add solution with oxidising agent to conical flask.
  3. Add an excess of potassium iodide. Oxidising agent reacts with iodide ions to produce iodine, which turns the solution yellow-brown
  4. Titrate the solution with sodium thiosulfate. During titration, iodine is reduced back to I- ions so brown colour fades and end point is hard to judge.
  5. Add starch indicator, which turns solution blue-black. End point is when blue-black colour disappears, as all iodine has been reduced to I- ions.
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11
Q

Why is starch indicator added towards the end of the iodine-thiosulfate titration?

A

Because if added too early, the starch-iodine complex may precipitate out of the solution, preventing some of the iodine reacting with the thiosulfate.

Close to the end-point, the iodine concentration is low enough for the complex not to precipitate out.

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12
Q

What is a voltaic cell?

A

A type of electrochemical cell which converts chemical energy into electrical energy.

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13
Q

What property does a voltmeter have in a cell?

A

High resistance

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14
Q

Which way does the current flow in the cell?

A

From negative electrode to positive electrode

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15
Q

How do ions flow between cells?

A

Salt bridge

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16
Q

What is the salt bridge generally made of?

A

Potassium nitrate

Ammonium nitrate

17
Q

What is the electrode made of in a standard hydrogen cell?

A

Platinum

18
Q

When 2 half cells are connected, what is oxidised and what is reduced?

A

More reactive metal is oxidised

Less reactive metal is reduced

19
Q

Define standard electrode potential (E°)

A

The e.m.f. of a half cell compared with a standard hydrogen half cell. Measured at 298K with solution concentrations of 1 mol dm-3 and a gas pressure of 100kPa

20
Q

What is the electrode potential of a hydrogen half-cell?

A

0.00V

21
Q

How do you calculate electrode potential of a cell?

A

E° of the more positive terminal - E° of the more negative terminal.

22
Q

How do we know if a cell is feasable?

A

If the electrode potential of the cell is positive, the reaction is fesable

23
Q

Which electrode goes on the right when asked about a labelled diagram?

A

The half-cell with the more +ve E° (electrode potential)
The metal ions that are more easily reduced

24
Q

Which electrode goes on the left when asked about a labelled diagram?

A

The half-cell with the more -ve E°


The metal ions that are more easily oxidised

25
Q

What does the more positive E° value mean for the position of the equilibrium?

A

Equilibrium lies further to the RIGHT than the other half-cell
So the metal ions are more easily REDUCED than the other half-cell
So the metal is an OXIDISING agent

26
Q

What does the more negative E° value mean for the position of the equilibrium?

A

Equilibrium lies further to the LEFT than the other half-cell
So the metal ions are more easily OXIDISED than the other half-cell.
So the metal is an REDUCING agent

27
Q

State 2 reasons why the actual cell potential may be different from the value calculated.

A

Non- standard conditions


High activation energy, so very slow rate of reaction

28
Q

What’s in a Metal/Metal ion half cell?

A
Metal rod (e.g. Cu)
Dipped into aqueous solution of metal ion (e.g. Cu2+)
29
Q

What’s in a, ion/ion half-cell?

A

Contains ions of the same element in different oxidation states (e.g Fe3+ and Fe2+)
Pt electrode

30
Q

State the key difference between a primary cell and a secondary cell.

A

A primary cell is only used once and is non-rechargeable

A secondary cell is rechargeable

31
Q

State the key characteristics of a fuel cell.

A

A fuel cell uses the energy from the reaction of a fuel with oxygen to create a voltage.


A fuel cell can be run continuously provided that the fuel and oxygen are continually being supplied to the cell.