Ch.23 redox and electrode potentials
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oxidising agent
takes electrons from species being oxidised
reducing agent
adds electrons to the species being reduced
manganate(VII) redox titration
MnO4- ions are reduced to Mn2+ KMnO4 in burette (deep purple so read from top of meniscus) pipette measured amount of analysed solution into conical flask with an excess of HCl to provide H+ to act as reducing agent no indicator reaction is self indicating end point when first permanent pink colour indicating an excess of MnO4- ions
iron manganate(VII) titration
Fe2+ –> Fe3+
what other oxidising agents can be used instead of MnO4-
acidified potassium dichromate Cr2O72- (orange) —> Cr3+ (green)
iodine/thiosulfate redox titrations
IO3 - + 5I - + 6H + —> 3I2 + 3H2O I2 + 2S2O3 2- —> 2I - + S4O6 2- 2 S2O3 2- is oxidised to S4O6 2- I2 is reduced to 2I- add standard solution of Na2S2O3 to burette pipette analysing solution into conical flask add excess of potassium iodide oxidising agent reacts with iodine ions forming iodine making the solution yellow brown as titration occurs iodine is reduced back to I- colour fades when straw colour add starch indicator solution turns deep blue black colour disappears at end point
what are some alternative oxidising agents for an iodine/thiosulfate titration
chlorate(1) ClO- ir reduced to Cl- copper(11) Cu2+ is reduced to CuI
copper in iodine/thiosulfate titrations
copper salts can be disolved in water to produce Cu2+ Cu can be reacted with an acid to form Cu2+ copper alloys can be dissolved in conc nitric acid then neutralised to form Cu2+ Cu2+ react with I- forming I2 and white CuI precipitate mixture appears brown
voltaic cell
converts chemical energy into electrical energy
half cell
contains chemical species present in redox half equation
metal/metal ion half cell
metal rod dipped into a solution if its aqueous metal ions
ion/ion half cell
ions of the same state but with different oxidation states platinum electrode is used
electrode potentials
when both half cells are metal/metal ion the more reactive metal releases electrons more readily and is oxidised electrode with more reactive metal is oxidised - - electrode electrode with less reactive metal is oxidised - + electrode
standard electrode potential
E* measure of the tendency to be reduced and gain electrons e.m.f of a half cell connected to a standard hydrogen half cell under standard conditions E* of a standard hydrogen half cell is 0V
what are standard conditions
298K 25*C 100 kPa
measuring a standard electrode potential
half cell connected to standard H electrode connected by a wire to allow a controlled flow of e- 2 solutions connected by a salt bridge allowing ions to flow composed of an unreactive electrolyte solution filter paper soaked in KNO3 forward reaction on data tables is always reduction most - E* value at top
the more - the E* value
greater tendency to lose electrons less tendency to gain more reactive a metal is less reactive a non metal is stronger the reducing agent it is
standard cell potential from standard electrode potential
E* cell = E(+) - E(-)
limitations of feasibility predictions using E*
no indication of the rate of the reaction
primary cells
non rechargeable
secondary cells
rechargeable
the more + an E* value is
the stronger an oxidising agent it is greater tendency to gain electrons less tendency to lose electrons less reactive a metal is more reactive a non metal is
how should u make sure the electrochemical series is set up
E* values with most - at top and most + at bottom e- always in the reactants top right will be strongest reducing agent bottom left will be strongest oxidising agent
when is a reaction not feasible reaction
when the E* cell is -