Redox and electrode potentials Flashcards

(53 cards)

1
Q

What is the definition of an oxidising agent?

A

An oxidising agent is a species that accepts electrons and is reduced and also oxidises the other species.

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2
Q

What is the definition of a reducing agent?

A

A reducing agent is a species that loses electrons and is oxidised and also reduces the other species.

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3
Q

What is the definition of a titration?

A

The concentration of a solution is determined by titrating with a solution of known concentration.

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4
Q

What is a redox titration?

A

In a redox titration, an oxidising agent is titrated against a reducing agent therefore electrons are transferred from one species to another.

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5
Q

What are the names of the 2 common redox titrations on the syllabus?

A

Manganate (VII) titrations

and

Iodine -thiosulfate titrations.

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6
Q

What acid is used for the potassium manganate (VII) titration and why?

Explain why the 4 other acids are not used for this titration.

A

dilute H2SO4 because it does not oxidse under these conditions and does not react with the manganate (VII) ions

HCl can be oxidised to chlorine by the manganate (VII) ions

Nitric acid is an oxidising agent and may oxidise the substance being analysed

Ethanoic acid is a weak acid and the conc of H+ ions is insufficient

Concentration sulfuric acid may oxidise the substance being analysed.

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7
Q

In a potassium manganate (VII) titration, what is the oxidising agent and what is the reducing agent?

A

The oxidising agent is manganate (VII) - reduced to Mn2+

The reducing agent is iron, oxidised to Fe3+.

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8
Q

In a potassium manganate (VII) titration, why is the iron dissolved to form Iron(II) sulfate?

Why is it dissolved in excess dilute H2SO4?

A

The dilute H2SO4 is used to provide acidic conditions which is essential for the reaction. This reaction needs H+ ions otherwise MnO4- wont be reduced properly to Mn2+.

Dilute H2SO4 is in excess because if there isnt enough acid, MnO4- forms MnO2 instead which is a brown solid therefore gives inaccurate results. Therefore its in excess to make sure all MnO4- reacts correctly by keeping conditions consistently acidic throughout the titration.

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9
Q

What is the equation for the potassium manganate titration?

A

MnO4−​ + 8H+ +5Fe2+ -> Mn2+ + 5Fe3+ + 4H2​O

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10
Q

In the potassium manganate (VII) titration, which solution is in the burette and which is in the flask?

A

The potassium manganate is in the burette and the Iron(II)sulfate is in the flask.

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11
Q

What is the colour change and indicator used for the potassium manganate (VII) titration?

A

The manganate (VII) ion (MnO4-) is deep purple and acts as its own indicator. (Self indicating )

Each drop of MnO4- added is immediately reduced by Fe2+ and becomes Mn2+ (pale pink - but the solution looks colourless because Mn2+ is so faint. When all the Fe2+ is used up, the next drop of MnO4- cant react therefore it stays as MnO4- (purple) but its very dilute so appears pale pink.

So the colour change is colourless -> pale pink because you never had a flask that is fully purple at the start. it begins as colourless because the purple is added drop by drop and disappears until the end point (pale pink)

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12
Q

What is the equation for the Iodine-thiosulfate titrations?

A

2SO2O3 2-(aq) + I2(aq) -> 2I-(aq) + S4O6 2-(aq)

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13
Q

What is the colour change of the Iodine-thiosulfate titration?

A

The light brown/yello colour of the iodine turns paler as it is converted to colourless iodide ions. When the solution is a straw colour, starch is added to clarify the end point and turns the solution blue/black until all the iodine reacts, at which point the colour disappears.

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14
Q

For the Iodine-thiosulfate titration, which solution is in the burette and which is in the flask?

A

The sodium thiosulfate (NaS2O3) is in the burette

The Iodine (I2) is in the conical flask with the starch indicator (added near the end point)

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15
Q

For the iodine thiosulfate titration, which solution is the oxidisng agent and which is the reducing agent.

A

Iodine gains electrons -> I= therefore is reduced so is the oxidising agent

Sodium thiosulfate loses electrons so is the reducing agent

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16
Q

In the manganate (VII) titration and the iodine-thiosulfate titration, what are the spectator ions?

A

For the manganate (VII) titration, potassium manganate (VII) and Iron(II)sulfate are used therefore the spectator ions are K+ and SO4 2- because they do not change oxidation states so are ignored

For the iodine-thiosulfate titration, sodium thiosulfate gives Na+ and the iodine solution is often prepared with KI, giving K+ therefore the spectator ions are Na+ and K+ (if potassium iodide is used to dissolve iodine.

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17
Q

What is the definition of a spectator ion?

A

A spectator ion is an ion that is present in a reaction mixture but does not take part in the reaction and remains unchanged.

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18
Q

What is the equation for percentage purity of a titration?

A

percentage purity = mass of sample / mass of impure sample x 100

this equation is measuring the purity of the solution in the flask. The burette solution (known concentration) is the pure substance and the impure substance is the substance being analysed in the flask (of unknown concentration)

You titrate to find the moles then convert the moles into the mass.

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19
Q

What is a use of the manganate (VII) titration?

A

To find the percentage purity of iron supplements

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20
Q

What is the use of the iodine - thiosulfate titration?

A

The amount of chlorate (I), ClO-, in bleach

The amount of copper (II), CU2+, in copper (II) compounds

The copper content of alloys.

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21
Q

How can the iodine - thiosulfate titration be used to find the water of crystallisation for hydrate ethanediodic acid?

A

You use iodine to find how much pure acid is present, then calcuate the number of water of crystallisation.

This is useful as it tells you the exact composition and purity of a hydrated compound.

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22
Q

What is the definition of a standard electrode potential?

A

The standard electrode potential is the voltage measure when a half-cell is connected to a standard hydrogen electrode under standard conditions.

23
Q

What are the standard conditions for a standard electrode potential?

A

Ion concentration of 1.00 mol dm-3
A temperature of 298 K
A pressure of 100 KPa

24
Q

What 3 factors do the position of equilibrium and an electrode potential depend on?

A

Temperature, pressure of gases and concentration of reagents.

25
Why is a high resistance voltmeter added to the circuit?
So that no current flows, acting like an open circuit, allowing the maximum potential difference is calculated.
26
What is the E.M.F?
The E.M.F is the maximum potential difference (voltage) of a cell when no current flows (in an open circuit)
27
Why is the standard hydrogen cell used to determine the standard electrode potential of other half cells
Because the standard hydrogen electrode is used as a reference electrode as it gives a value of 0.00 V and therefore all other electrode potentials are compared to this standard.
28
What does the standard hydrogen electrode half cell consist of? What is the equation for the standard hydrogen electrode?
It consists of hydrogen gas in equilibrium with H+ ions of concentration 1.00 mol dm-3 (at 100KPa) An inert platinum electrode is in contact with the hydrogen gas and H+ ions. 2H+ (aq) + 2e- ⇌ H2 (g)
29
What are the 3 types of half cells?
Metal / metal ion Non metal / non metal ion Ion / ion (the ions are in different oxidation states)
30
What is the equation for the standard cell potential?
Standard cell potential = standard potential of positive electrode (reduction) - standard potential of negative electrode (oxidation).
31
Where is the redox equilibrium established in a half cell?
On the surface of the platinum catalyst.
32
What makes a reaction in an electrochemical cell feasible?
If the standard cell potential is positive. If its negative it is not feasible
33
What are the limitations of standard electrode potentials to predict reactions?
The feasibility of a reaction can be determined from the electrode potential however it gives no information about the rate of reaction. Another limitation is many redox reactions arent aqueous. Another limitation is the standard electrode potential only applied under standard conditions therefore if conditions change, le chatelier's principle occurs.
34
Are primary and secondary cells non-rechargeable or rechargable?
Primary cells are non-rechargeable (irreversible) Secondary cells are rechargeable.
35
What is the name of the first primary cell invented? What did it consist of?
The Daniell cell which consisted of a simple metal-metal ion system. There was a zinc rod immersed in a solution of zinc sulfate, a copper cylinder filled with copper sulfate solution and a porous pot that separated the copper sulfate from the zinc sulfate. Zinc acted as the negative electrode and the copper as the positive. However, the cell is impractical to use as a portable device because of the hazardous liquids in the cell.
36
What are the most common types of non-rechargeable primary cells?
Zinc - carbon cells has a zinc casting which acts as the negative electrode, a paste of ammonium chloride which acts as an electrolyte as well as the positive electrode, a carbon rod which acts as an electron carrier in the cell. As the cell discharges, the zinc casting eventually wears away and the corrosive contents of the electrolyte paste can lead out - disadvantage relatively cheap.
37
What is a different variation of the zinc - carbon cell?
Use of an alkaline paste in the electrolyte as they have a longer operating life but are more expensive than regular zinc-carbon cells.
38
What is a secondary cell?
A rechargeable cell which included chemical reactions that can be reversed by applying a voltage greater than the cell voltage, causing electrons to push in the opposite direction.
39
What are the common rechargeable (secondary) cells?
Lead - acid batteries NiCad cells Lithium cells.
40
Describe a lead-acid battery What are they used in? What are the strengths and weaknesses of them?
Consist of 6 cells joined together in a series. The cells use lead metal as the negative electrode and lead (IV) oxide as the positive electrode. The electrolyte is sulfuric acid. Used in a commercial car battery. When the car is in motion, the generator provides a push of electrons that reverses the reaction and regenerates lead and lead (IV) oxide. They are designed to produce a high current for a short period of time therefore used in powering a starter motor in car engines. The disadvantage of lead-acid batteries are: they are very heavy contain toxic materials: lead and lead (IV) oxide the sulfuric acid electrolyte is very corrosive.
41
Describe a NiCad cell What are the strengths and weaknesses of this cell?
Nickel-cadmium cells. Used in many standard sizes and voltages so that can replace almost any application of traditional zinc-carbon cells. Although they are more expensive, because they can be recharged hundreds of times, they are more commercially viable. The negative electrode = cadmium The positive electrode = nickel (II) hydroxide-oxide system Cadmium is a toxic metal so the disposal of old NiCad cells is an environmental issue. NiCad cells gradually lose their charge after repeated charge cycles when the cell is not fully discharged. Lithium - ion cells dont have this issue.
42
Describe the lithium ion cell What are these cells used in? What are the strengths and weaknesses of these cells.
Lithium ion cells power phones and laptops. Lithium is used because it has a very low density and relatively high electrode potential. The cell consists of a positive lithium cobalt oxide electrode. a negative carbon electrode a porous polymer membrane electrolyte the polyer electrolyte cant leak since its not a liquid or paste, which presents advantages over other types of cells. The cells consist of a sandwich of different layers of lithium cobalt oxide and carbon. When the cell is charged and discharged, the lithium ions flow between the negative and positive through the solid electrolyte. NiCad cells gradually lose their charge after repeated charge cycles when the cell is not fully discharged. Lithium-ion cells dont have this issue. Some disadvantages: A global shortage of lithium is lieky to make lithium ion cells unsustainable. If the cells arent recycled but thrown away in landfills, then a huge amount of lithium becomes lost to future generations Reports of lithium ion cell fires have raised concerns about their safety. Lithium is a very reactive element in group 1, which is why it has a high electrode potential.
43
What is a fuel cell?
A fuel cell is an electrochemical cell in which fuel donates electrons at one electrode and oxygen gains electrons at the other electrode.
44
How does a fuel cell work?
As the fuel enters the cell it becomes oxidised which sets up a potential difference or voltage within the cell. Different electrolytes and fuels can be used to set up different types of fuel cells.
45
What is the name of the fuel cell on the syllabus?
The hydrogen - oxygen fuel cell
46
What is the hydrogen-oxygen fuel cell?
A fuel cell which combined both elements to release energy and water. The fuel cell consists of a reaction chamber with separate inlets for H2(g) and O2(g), an outlet for the product - water, an electrolyte of aq NaOH and a semi-permable membrane that separates the H2(g) and O2(g)
47
What are the benefits of the hydrogen-oxygen fuel cell?
Water is the only reaction product so the fuel cells have environmental advantages over other types of cells. The reaction is the same as hydrogen combusting in oxygen but since the reaction takes place at room temp without combustion, all the bond energy is converted in electrical energy instead of heat and light. No harmful oxides of nitrogen produced - which normally happens in high temp combustions where air is present Fuel cells have been used on space craft, where the product can be used as drinking water for astronauts.
48
What are the risks and problems of hydrogen - oxygen fuel cells?
Hydrogen is a highly flammable gas and the production and storage of hydrogen carries safety hazards. Very thick walled cylinders and pipes are needed to store hydrogen which has economic impacts. The production of hydrogen is a by-product of the crude oil industry therefore its a non-renewable finite source Until a cheap way is found to make hydrogen, the widespread use in fuel cells is limited Hydrogen has high energy density (the amount of energy contained in 1g of the fuel is high compared to other fuels) but because its a gas, its energy density per unit volume is low which means larger container are needed compared to liquid fuels
49
What is one difference between fuel cells and other cells?
The cell operates continuously as long as there is a supply of hydrogen and oxygen - the energy is not stored in the cell.
50
What is the equation for the zinc-carbon cell?
Zn2+ (aq) + 2e- -> Zn (s) E0 = -0.76V 2NH4+ (aq) + 2e- -> 2NH3 (g) + H2 (g) E0 = +0.74 2NH4+ (aq) + Zn (s) -> 2NH3 (g) + H2(g) + Zn2+ (aq) Eθcell = +1.50V
51
What is the equation for the lead-acid battery?
Pb (s) + SO4 2- (aq) -> PbSO4 (s) + 2e- E0 = -0.36V PbO2 (s) + 4H+ (aq) + SO4 2- (aq) + 2e- -> PbSO4 (s) + 2H2O (l) Eθ = +1.70 V bO2 (s) + 4H+ (aq) + 2SO42- (aq) + Pb (s) -> 2PbSO4 (s) + 2H2O (l) Eθcell = +2.06 V
52
What is the equation for the NiCad cell?
Nickel - cadmium cell Cd (s) + 2OH- (aq) -> Cd(OH)2 (s) + 2e- Eθ = -0.82V NiO(OH) (s) + H2O (l) + e- -> Ni(OH)2 (s) + OH- (aq) Eθ = +0.38V 2NiO(OH) (s) + 2H2O (l) + Cd (s) -> 2Ni(OH)2 (s) + Cd(OH)2 (s) Eθ = +1.2 V
53
What is the equation for the Lithium ion cell?
Li (s) → Li+ (s) + e– Eθ = -3 V Li+ (s) + CoO2 (s) + e– → Li + (CoO2) – (s) Eθ = +1 V Li (s) + CoO2 (s) → Li + (CoO2) – (s) Eθcell = +3.5