what’s the general method for a titration
where is the substance placed where we don’t know the concentration
in the conical flask .
measured using a volumetric pipette
Other substance is placed in the burette
why is a conical flask used instead of a beaker
it’s easier to swirl the mixture in a conical flask without spilling the contents
what’s the method for using the pipette
what’s the method for using the burette
what happens if the jet space in the burette is not filled properly before the titration
it will lead to errors if it then fills in the titration , leading to a larger tire reading
why would we add distilled water to the conical flask during a titration to wash the sides of the flask
so all the acid on the side is washed into the reaction mixture to react with the alkali
- it does not affect the titration reading as water does not react with the reagents or change number of moles of acid added
what are some safety precautions of titrations
acids and alkalis are corrosive
wear eye protection and gloves
what’s the equation for manganate redox titrations
MnO4-(aq) + 8H+ (aq) + 5Fe2+ (aq) => Mn2+(aq) + 4H2O(l) + 5Fe3+(aq)
what’s the colour change in the manganate redox titrations
colourless to pink
what’s the method to find out how much iron is in the iron tablets
what acid would you use for manganate titrations
only use dilute sulphuric acid
what would be produced instead of Mn2+ if insufficient volumes of sulphuric acid is added and what’s the equation
MnO2
MnO4- (aq) + 4H+ (aq) + 3e- => MnO2(s) + 2H2O
why can’t weak acids be used in manganate titrations
it cannot supply the large amount of hydrogen ions needed (8H+)
why can’t a concentrated strong acid such as HCl be used in a manganate titration
The Cl- ions would be oxidised to Cl2 by MnO4- because the Emf value for MnO4-/Mn2+ is bigger than the EMF of Cl2/Cl-
This would lead to a greater volume of manganate being used and poisoned Cl2 being produced
why can’t nitric acid be used in a manganate titration
It’s an oxidising agent .
It oxidises Fe2+ to Fe3+ as EMF for NO3- is bigger than Fe2+ / Fe3+
This would lead to a smaller volume of manganate being used
EQ : give two reasons why it’s essential to avoid this reaction ( MnO4- to MnO2) in a titration between potassium manganate and iron ions . (2)
large titre than expected
cant see end point due to brown colour
EQ : Stare the colour change that occurs at the end point of the titration of MnO4- and why (2)
Colourless
just after end point MnO4- is in excess of
why might adding too much indicator be a problem and how can we fix it
It may react and effect the endpoint reading
- use a smaller volume (2-6 drops)
Why is using a measuring cylinder not good for measuring acid in a titration and what can we use instead
it has a large uncertainty
Use a volumetric pipette
Why is rinsing a burette with deionised water before adding alkali not a good idea and explain improvements
why shouldn’t you wait until solution “just” changes colour in a titration and what can you do to improve it
acid may not have fully reacted with the alkali
- add alkali solution until permanent colour change is seen
give a reason for the colour change of manganate redox reaction
Caused by excess MnO4-