Titration Flashcards
what’s the general method for a titration
- rinse equipment
- pipette 25cm3 of alkali into conical flask
- touch surface of alkali with pipette
- add acid solution from burette
- make sure the jet space in the burette is filled with acid
- add a few drops of indicator and refer to colour change at end point
- phenolphthalein ( pink to colourless ) ( use if NaOH is used)
- methyl orange ( yellow to red) ( use if HCl is used)
- use a white tile underneath the flask to help observe the colour change
- add acid to alkali whilst swirling the mixture and add acid drop wise at end point
- note burette reading before and after addition of acid
- repeat titration until at least 2 concordant results are obtained - two results within 0.1 of each other
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
- rinse pipette with substance to go in it
- pipette 25cm3 of solution A into conical flask
- bottom of meniscus should sit on this line
- touch surface of solution with pipette
what’s the method for using the burette
- should be rinsed out with substance that will be put in it
- if not rinsed the acid or alkali added may be diluted by residual water or may react with substances left from a previous titration .
- this would lead to the conc of the substance being lowered and a larger titre
- don’t leave funnel in burette because small drops or liquid may fall from funnel during titration leading to a false burette reading ( smaller titre volume )
- make sure jet space in burette is filled with solution and air bubbles are removed
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
purple to colourless
what’s the method to find out how much iron is in the iron tablets
- weigh accurately two iron tablets
- grind up the tablets with a little 1moldm-3 sulphuric acid , using pestle and mortar.
- through a funnel , transfer the resulting paste into a 100cm3 volumetric flask .Use a further small volumes of 1moldm-3 sulphuric acid to rinse the ground up tablets into the flask
- then add sufficient 1moldm-3 sulphuric acid to make up the solution to exactly 100cm3 . stopper the flask and shake it to make sure all the contents are thoroughly mixed . They will not all be in solution although Fe2+ ions which were present in the tablets will be dissolved .
- Titrate 10cm3 portions of the solution with the 0.0050moldm-3 potassium manganate . end point is marked by the first permanent purple colour
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