Chapter 23 - Redox & Electrode Potentials Flashcards

1
Q

How do you make a simple half cell?

A

A metal rod dipped into a solution of its aqueous metal ion

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2
Q

What is an ion half cell and give an example?

A
  • It contains ions of the same element in different oxidation states
  • For example a mixture of aqueous iron(ii) and iron(iii)
  • The redox equilibrium would be Fe3+(aq) + e- -> Fe2+(aq)
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3
Q

What sort of electrode is used in an ion half-cell and why?

A

There is no metal to transport electrons either into or out of the half cell so an inert metal electrode e.g platinum is used

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4
Q

What is the standard electrode potential?

A

The e.m.f of a half-cell compared with a standard hydrogen half-cell measured at 298k, solution concentrations of 1moldm-3 and a gas pressure of 100kPa

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5
Q

What does the standard electrode potential show?

A

The tendency to gain electrons compared with the hydrogen half-cell

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6
Q

Give an example of a salt bridge and explain why this is used?

A

A strip of filter paper soaked in aqueous potassium nitrate

Contains a conc. electrolyte that does not react with either solution

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7
Q

What does a more negative electrode potential value suggest?

A
  • A greater tendency to lose electrons and undergo oxidation
  • Less tendency to gain electrons and undergo reduction
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8
Q

What does a more positive electrode potential value suggest?

A
  • A greater tendency to gain electrons and undergo reduction
  • Less tendency to lose electrons and undergo oxidation
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9
Q

In an ion half cell how can getting 1 moldm-3 solutions be difficult? What is the solution?

A
  • It could be challenging to dissolve enough solute to get this conc.
  • If there are equal ion concentrations it can give you the same electrode potential value
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10
Q

How do you calculate standard cell potential?

A

Electrode potential of positive electrode - Electrode potential of negative electrode

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11
Q

Given the equations:
A: Cr3+(aq) + 3e- -> Cr(s)
B: Cu2+(aq) + 2e- -> Cu(s)
C: Ag+(aq) +e- -> Ag(s)

And their standard electrode potentials A: -0.77 B: +0.34 C: +0.80

Will C react with A and B?

A
  • Redox system C has a more positive electrode potential value
  • C will therefore have a greater tendency to be reduced than A or B
  • Oxidising agent on the left of C (Ag+(aq)) should react with reducing agents on the right of A and B (Cr(s) and Cu(s))
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12
Q

How is reaction rate a limitation of predictions using electrode potential values?

A
  • Some reactions have very large activation energies
  • Electrode potentials may indicate the feasibility of a reaction but they give no indication on the rate of the reaction
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13
Q

How is concentration a limitation of predictions using electrode potential values?

A
  • Many reactions take place using solutions which are not 1moldm-3 and so the value of the electrode potential would be different
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14
Q

Give an example of how concentration could alter electrode potential

A

E.g for Zn2+(aq) + 2e- -> Zn(s)

  • If the conc. of Zn2+(aq) is greater than 1moldm-3, equilibrium will shift to the right, removing electrons and the electrode potential would be less negative
  • If the conc. of Zn2+(aq) is less than 1moldm-3, equilibrium will shift to the left, increasing electrons in system and the electrode potential will be more negative
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15
Q

What is a primary cell?

A
  • Non-rechargeable

- Electrical energy is provided by oxidation and reduction at the electrodes

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16
Q

What is a secondary cell?

A
  • Rechargable

- The cell reaction producing electrical energy can be reversed during recharging

17
Q

What is a fuel cell?

A

It uses the energy from the reaction of a fuel with oxygen to create a voltage and the changes that take place at each electrode

18
Q

Advantages of fuel cell?

A

(1) Fuel cells can operate continuously provided that fuel and oxygen are supplied into the cell
(2) Fuel cells do not have to be recharged

19
Q

Will Cl2 react with Fe2+

A

The Electrode potential value for Cl2/Cl- is more positive than Fe3+/Fe2+ so Cl2 is more readily reduced than Fe3+, therefore Cl2 will react with Fe2+

You want the left hand side of the more positive and the right hand side of the more negative

20
Q

How do you calculate standard cell potential?

A

Electrode potential of cell being reduced - electrode potential of cell being oxidised

21
Q

Half equations for the reaction of Fe2+ with Cr2O72-

A

Cr2O72−(aq) + 14H+(aq) + 6e− → 2Cr3+(aq) + 7H2O(l)

Fe2+(aq) → Fe3+(aq) + e−

22
Q

Ionic equation for reaction of Fe2+ with MnO4-

A

MnO4−(aq) + 5e− + 8H+(aq) → Mn2+(aq) + 4H2O(l)

Fe2+(aq) → Fe3+(aq) + e−

23
Q

How do you balance an equation using oxidation numbers?

A

1) Assign oxidation numbers to identify atoms that change their oxidation number
2) Balance the amount of oxidation and reduction using only species that have elements which have changed oxidation number
3) Balance any remaining atoms

24
Q

How do you check whether an equation is balanced?

A

Ensure both sides of the equation are balanced by charge

25
Q

How do you predict a half equation?

A

1) Assign oxidation numbers
2) Balance the electrons according to oxidation numbers
3) Balance any remaining atoms
- if oxygen has been lost a likely product is H2O
- balance hydrogen produced with H+ on other side of the equation

26
Q

What is added to the Burette and what is added to the comical flask in a manganate titration?

A

Burette - standard solution if potassium manganate (VII)

Conical flask - solution being analysed and an excess of sulfuric acid to provide H+ ions for reduction of MnO4-

27
Q

When is the end point of a manganate titration and what is the colour change?

A
  • The first permanent pink colour

- colourless to light pink

28
Q

How do you analyse the percentage purity of an iron(II) compound?

A

1) calculate the amount of known oxidising agent that reacted
2) Determine the amount of Fe2+ that reacted (in sample)
3) Scale up to find the amount of Fe2+ in the original solution
4) Find the mass of the hydrated iron/Fe
5) Find percentage purity

29
Q

How can you be presented with non-familiar redox titrations?

A

1) Mangante (VII) titrations can be used to analyse reducing agents that reduce MnO4- to Mn2+ e.g fe2+ and ethanedioic acid
2) KMnO4 can be replaced with another oxidising agent e.g acidified dichromate (VI)

30
Q

What is added to the Burette and what is added to the conical flask in an iodine-thiosulfate titration?

A

Burette - Na2S2O3

Conical flask - oxidising agent to be analysed and potassium iodide (liberates iodine)

31
Q

What are the colour changes during iodine-thiosulfate titration?

A

1) When potassium iodide is added to oxidising agent it produces a solution which is a yellow brown colour

2) During titration solution turns from brown to pale straw colour (iodine getting reduced)

3) After starch indicator is added it turns from black to colourless at end point

32
Q

What other oxidising agents can be analysed using iodine?

A

1) Chlorate(I) ions ClO-

2) Copper(II) ions Cu2+