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Preparation of salts. Learn how to decide which method to use and how o carry out that method according to the mark scheme.
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WHAT METHOD
Insoluble salt → precipitation
Soluble Na⁺ / K⁺ / NH₄⁺ salt → titration
Other soluble salts → acid + excess metal or insoluble base
Describe how to carry out an acid–alkali titration
M1 rinse burette with acid and fill it,
M2 use a pipette to measure a fixed volume of alkali into a conical flask,
M3 add a few drops of suitable indicator,
M4 slowly add acid from the burette while swirling,
M5 stop when indicator changes colour and record the final reading
Describe how to prepare a soluble salt from an acid and an insoluble base
M1 warm the dilute acid,
M2 add excess insoluble base until no more reacts,
M3 filter to remove unreacted solid,
M4 heat filtrate to evaporate water,
M5 allow solution to cool and crystallise
Describe how to prepare a soluble salt from an acid and a metal
M1 add excess metal to dilute acid,
M2 wait until fizzing stops,
M3 filter to remove excess metal,
M4 evaporate solution,
M5 leave to crystallise
Describe how to prepare an insoluble salt using precipitation
M1 mix two soluble salt solutions,
M2 an insoluble precipitate forms,
M3 filter to collect the precipitate,
M4 wash with distilled water,
M5 dry the solid
Explain why excess insoluble base is added when making a soluble salt
M1 ensures all the acid reacts,
M2 excess solid can be removed by filtration
Explain why titration must be used to make sodium, potassium or ammonium salts
M1 their salts are all soluble,
M2 excess reactant cannot be filtered off
Describe how to make sodium chloride crystals using titration
M1 titrate hydrochloric acid with sodium hydroxide using an indicator,
M2 repeat without indicator using same volumes,
M3 evaporate solution to form crystals
Describe how to obtain pure dry crystals from a solution
M1 heat solution to evaporate some water,
M2 leave to cool,
M3 crystals form,
M4 filter and dry crystals
Explain why an indicator is needed in a titration
M1 shows when neutralisation has occurred,
M2 indicated by a colour change
Explain why phenolphthalein is suitable for titration
M1 colourless in acid and pink in alkali, M2 sharp colour change at the end point
Describe how to improve accuracy in a titration
M1 repeat titration several times,
M2 use concordant results,
M3 read burette at eye level
Explain what is meant by the end point in a titration
M1 the point where the indicator changes colour,
M2 shows neutralisation is complete
Explain why the indicator is not added when making the salt solution
M1 indicator would contaminate the salt,
M2 affects purity
Describe how to test for sulfate ions
M1 add dilute hydrochloric acid,
M2 add barium chloride solution,
M3 white precipitate forms
Describe how to test for chloride ions
M1 add dilute nitric acid,
M2 add silver nitrate solution,
M3 white precipitate forms
Explain why distilled water is used when washing a precipitate
M1 removes soluble impurities,
M2 does not add new ions
Describe how to prepare copper sulfate crystals in the laboratory
M1 warm sulfuric acid,
M2 add excess copper oxide,
M3 filter off excess solid,
M4 evaporate filtrate,
M5 leave to crystallise
Explain why copper oxide is suitable for making copper sulfate
M1 it is insoluble,
M2 excess can be filtered off
Describe how to know when no more base should be added
M1 base remains unreacted,
M2 no further reaction occurs
Explain why crystals are dried after filtration
M1 to remove water,
M2 obtain a dry solid
Describe how to prepare lead(II) iodide
M1 mix lead nitrate and potassium iodide solutions,
M2 yellow precipitate forms,
M3 filter and wash precipitate
Explain why lead(II) iodide is insoluble
M1 insoluble salt formed from two soluble salts,
M2 precipitates out of solution
Describe what concordant titres mean
M1 results close together,
M2 within 0.1 cm³
Explain why swirling the flask during titration is important
M1 ensures complete mixing,
M2 prevents localised reaction
Explain why burette readings are taken at eye level
M1 reduces parallax error,
M2 improves accuracy