paper 3 Flashcards
why is an electric heater used over a bunsen sometimes
volatile reactants that are flammable are not open to a naked flame
describe the process of recrystalisation
- dissolve sample in a minimum volume of hot solvent
- this will remove impurities
- allow to cool to recrystalise
- then remove the solvent by filtering under reduced pressure in a buchner flask.
wash with cold water and dry
when heating in a crucible what is the bad thing about using large amounts of calcium sulphate
decomposition will be incomplete
why should super small amounts of solid not be used when heating in a crucible
because the percentage uncertainties will be huge
what si the point of the lid when heating in a crucible
it prevents loss of solid product - but notably should be loose fitting to allow gas to escape
say the crucible when heating a solid product is wet what is the problem with this
water would be lost in the heating process as well as mass - the change in mass would be too great
what are potential errors in using a gas syringe
*gas escapes before bung inserted
*syringe sticks
* some gases like carbon dioxide or sulphur
dioxide are soluble in water so the true amount of
gas is not measured.
how do you make a solution
- Weigh the sample bottle containing the required mass of
solid on a 2 dp balance - Transfer to beaker and reweigh sample bottle
- Record the difference in mass
- Add 100cm3 of distilled water to the beaker. Use a glass rod to help stir
-* Pour solution into a 250cm3 graduated flask via a funnel. * Rinse beaker and funnel and add washings from the
beaker and glass rod to the volumetric flask. * make up to the mark with distilled water using a dropping
pipette for last few drops. * Invert flask several times to ensure uniform solution.
describe the method for carrying out a titration
*rinse equipment (burette with acid, pipette with alkali, conical flask
with distilled water) *pipette 25 cm3 of alkali into conical flask
*touch surface of alkali with pipette ( to ensure correct amount is
added) *adds 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 (alkali) to colourless (acid): end point pink
colour just disappears] [use if NaOH is used] *methyl orange [yellow (alkali) to red (acid): end point orange]
[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 dropwise at
end point *note burette reading before and after addition of acid
*repeats titration until at least 2 concordant results are obtained- two
readings within 0.1 of each other
what is a good compound to neutralise acid
calcium carbonate
in calorimetry why is it bad if the reaction is slow
If the reaction is slow then the exact temperature rise can be
difficult to obtain as cooling occurs simultaneously with the
reaction
what errors can occur in calorimetry
- heat transfer from surroundings (usually loss)
- approximation in specific heat capacity of solution. The method assumes all
solutions have the heat capacity of water. - neglecting the specific heat capacity of the calorimeter- we ignore any heat
absorbed by the apparatus. * reaction or dissolving may be incomplete or slow. * Density of solution is taken to be the same as water
what can be done to improve the readings taken in calorimetry
take readings at regular intervals
what can be done to increase the accuracy of temperature taken in calorimtry
- heat transfer from surroundings (usually loss)
- approximation in specific heat capacity of solution. The method assumes all
solutions have the heat capacity of water. - neglecting the specific heat capacity of the calorimeter- we ignore any heat
absorbed by the apparatus. * reaction or dissolving may be incomplete or slow. * Density of solution is taken to be the sa
why in rate equation reactions can large excess be used
In reactions where there are several reactants, if the
concentration of one of the reactant is kept in a large
excess then that reactant will appear not to affect rate
and will be pseudo-zero order . This is because its
concentration stays virtually constant and does not
affect rate