redox and electrochemistry Flashcards

1
Q

rules for redox

A

sum of all ox no in a neutral compound is 0
sum of ox no in an ions is equal to the charge of the ion
th ox no of any uncombined element is 0
the ox no of oxygen is always -2 expect peroxides or when combined with F
the ox no of H is always +1 except hydride when -1
in a compound group 1= ox no of +1
group2=+2
group 3= +3
group 7 can have all different ox no but assume -1 unless asked to find it

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2
Q

what is a redox reaction

A

When both Ox and reduc happen
ox= loss of electron or increase of ox no
reduc= gain of electrons or decrease of ox no
metals tend to be ox and non metals tend to reduc

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3
Q

Oxidising agent

A

is a reagent that oxidises (takes electrons from) another species

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4
Q

reducing agent

A

is a reagent that reduces (adds electrons too) another species

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5
Q

Oxidation

A

is the loss of electrons/increase in oxidation number

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6
Q

reduction

A

reduction is the gain of electrons/ the decrease in oxidation number

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7
Q

electron transfer

A

oxidation is loss
reduction is gain

metals tend to lose- oxidation
non metals tend to gain- reduction

for a reaction to be redox there must be reduction and oxidation so something must lose electrons and something must gain

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8
Q

constructing a redox equation from half equations

A

First × the half equations by a factor so that the number of electrons in both are the same

next add the 2 equations together

then cancel out hydrogen or water

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9
Q

constructing half equations

A

1) balance the elements being oxidised/reduced
2)balance the oxidation numbers:use electrons
3)balance charge using H+ if acid or OH- is alkali
4) add water to balance out H and Os

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10
Q

constructing redox equations from oxidation numbers

A

identify reactants and products

balance only elements which are oxidised or reduced + identify their total ox number change

balance the change
total increase in ox no = total decrease in ox number

check if other elements need balancing

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11
Q

redox titration using acidified manganate

A

acidified K maganate is a strong ox agent

self indicating
manganate ions (Mn04 -) = purple
Mn2+ ions = very pale pink

manganate reduced to Mn2+
purple to pink

typically maganate is in burette and reducing agent is in conical flask

when complete solution in flask goes from og reducing agent colour normally colourless = very pale pink permanently

half equ =

Mn04 - +5e- +8H+ —> Mn2+ + 4H20

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12
Q

redox titration between iodine and thiosulfate

A

thiosulphate ion S2O3 2- reduces I2 to 2I- and forms S4O6 2- tetrathionate ion

2S2O3 2- + I2 —> 2I- + S4O6 2-

brown to colourless

problem- brown colour fades overtime so hard to detect when disappears

solution- add starch indicator to I2, blueblack to straw coloured (in exam say colourless)

sodium thiosulfate is in burette and iodine solution is in flask

this analysis is use to analyse
household bleach
copper compounds
copper alloys

remember between equations don’t change moles in calculations of I2 as all the i2 from 1 is used in the other

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13
Q

what does the electrochemical series show?

A

gives the standard electrode potential values for reduction half equations

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14
Q

relevance of standard electrode potential values

A

give measure of relative ease of reduction or oxidation

compare the reducing/oxidising powers of diff species

more positive greater tendency to gain electrons and be be reduced + oxidising agent (stronger the more positive)

more negative greater tendency to lose electrons and be oxidised + reducing agent (stronger the more negative)

2H+ + 2e- —> H2 = 0.00

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15
Q

which direction of the electrochemical series reactions is reduction and which is oxidation

A

forward is always REDUCTION
equ pos right

Backwards is always OXIDATION
equ pos left

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16
Q

what are standard half cells used for?

A

to measure the standard electrode potential

17
Q

what conditions are required for a standard half cell

A

standard conditions

and must have species from half equ in equilibrium

18
Q

three types of standard half cell

A

Metal ion/ metal half cell-
metal=electrode (where transfer of electrons occurs)
metal ion = in solution + 1moldm-3 (electrolyte)

Metal ion/ Metal ion half cell-
pt or graphite (inert) electrode (used to make electrical contact with sol + transfer of electrons occurs on surface)
both metal ions in solution + 1moldm-3

Non metal/ mom-metal ion-
pt or graphite electrode (“)
non metal ion is in electrolyte solution 1moldom-3
non metal is solid liquid or gas, usually gas + stored in container 1atm
e.g. hydrogen half cell

LEARN DRAWINGS

19
Q

standard electrode potential def
KEY

A

of a half cell is the e.m.f of a half cell compared with a standard hydrogen half cell, under standard conditions

20
Q

how to measure standard electrode potential of a half cell?

A

half cell is connected to a standard H half cell by a salt bridge( filter paper soaked in ionic sol) - allows movement of ions between half cells (completing the circuit)

under standard conditions

electrical current flows through- electrons flow through connecting wires

measured by high resistance voltmeter

21
Q

What to remember when drawing diagram to measure standard electrode potential

A

Salt bridge

standard conditions

wires + voltmeter

which of the 3 types of half cell are present ( H is always non metal with cage for gas)

label what electrode made of + if pos ( larger standard electrode potential value) or neg ( smaller standard electrode potential value)

label movement of ions and electrons

22
Q

equation for standard cell potential

A

cell = reduction - oxidation

RedOx

should always be positive

23
Q

predicting feasibility of redox reaction

A

use standard electrode potential

species undergoing reduction MUST have a more positive standard electrode potential

or it isn’t feasible

24
Q

limitations of predictions using standard cell potentials

A

kinetics-reaction may be too slow as Ea is too high so may not be observed despite being feasible

non standard conc of solutions-
gives value for electrode potential diff to standard electrode potential resulting in cell potential value diff to standard

25
worked example question what would happen to the electrode potential value for this half cell is the conc of Cu2+ increases from 1moldm-3 to 2 Cu2+ + 2e- ---> Cu E=+0.34
equ pos shifts right to minimise increase forward reaction favoured electrons more readily gained electrode potential becomes more pos
26
Modern storage cells don't have to remember
source of electrical energy 2 types: primary- non rechargeable provide energy till all chems reacted so voltage falls and become flat secondary- chems react reaction then reversed by recharging and then used again
27
Fuel cells def KEY
uses energy from the reaction of a fuel with oxygen to create a voltage diff to storage cells as o2 flows in and product flows out as energy generated cont most modern fuel cells = H or H rich fuels
28
2 types of hydrogen fuel cell
alkaline hydrogen fuel cell Acid hydrogen fuel cell
29
Alkaline Hydrogen-oxygen fuel cell reactions
reduction reaction- 1/2O2(g) + H2O(l) + 2e- ---> 2OH-(aq) E=+0.4 oxidation- H2(g) + 2OH-(aq) ----> 2H2O(l) + 2e- E=-0.83 overall- H2(g) + 1/2O2(g) ---> H20(l) standard cell potential = 1.23 electrolyte not used up
30
Acid hydrogen-oxygen fuel cell reactions
oxidation reaction- 1/2O2(g) + 2H2(g) + 2e- ---> 2OH-(aq) E=+1.23 reduction- 2H+(aq) + 2e- ----> 2H2(g) E=0.00 overall- H2(g) + 1/2O2(g) ---> H20(l) standard cell potential = 1.23 electrolyte not used up