Salt Preparation Cheat Sheet by fongrsy

A salt is a compound formed when the hydrogen ion in an acid is replaced by a metallic ion or an ammonium ion. It is an ionic compound with high melting and boiling point. Soluble salts dissolve in water to form oppositely charged ions in aqueous solutions thus it can conduct electr­icity.

Water is present in the crystals of certain salts which gives the salt its crysta­lline proper­ties. The water present is known as water of crysta­lli­zation which is easily removed by heating.

E.g: Copper(II) sulfate crystals (CuSO4.5H2O)

Hydrated Salt (Upon Heating)  Anhydrous Salt + Water

Method:
Acid + Metal (Mg, Al, Zn, Fe)
Acid + Insoluble Base (MgO, ZnO, CuO)
Acid + Insoluble Carbonate (MgCO3, ZnCO3)

The insoluble reactant used is in excess. This is to ensure that all the acid is used up. The excess reactant is filtered from the salt solution at the end of the reaction. The salt solution formed is then heated to evaporate some water away to obtain a saturated solution then cooled to allow crysta­lli­zation to occur to produce the salt crystals.

When is all the acid used up?
1. When there is no more efferv­escence produced (Metal / Carbonate)
2. When there is a residue of reactant left behind (Base)

Only moderately reactive metals can be used.

Steps:
1. Add excess reactant into the acid and stir until the efferv­escence stops.
2. Filter to remove excess reactants. Collect the filtrate (salt solution).
3. Heat filtrate to obtain a concen­trated salt solution.
4. Test for saturation with a glass rod.
5. Leave the solution to cool and crysta­lise.
6. Filter to obtain crystals.
7. Wash with cold distilled water and dry with clean filter paper.

Method:
Acid + Soluble Base / Alkali ( NaOH, KOH, NH3(aq) )

As both the reactants in this method are solutions, titration is used to add the exact volume of one reactant to the other. An indicator is used in the beginning to determine the volume of the reactants required. However, the experiment is repeated without the indicator so as to not contam­inate the salt produced.

1. Fill up a burette with dilute acid. Note the initial burette reading (V1 cm³).
2. Pipette 25.0 cm³ of aqueous alkali solution into a conical flask.
3. Add 1−2 drops of methyl orange indicator to the solution.
4. Add dilute acid slowly from the burette until the solution just turns orange. This is the end-point.
5. Stop adding acid. Record the final burette reading (V2 cm³).

Repeat the experi­ment:
1. Pipette 25.0 cm³ of alkali solution into a beaker. Do not add indicator.
2. Add (V2 – V1) cm³ of dilute acid from the burette.
3. Heat to saturate the solution.
4. Cool and crysta­llise to obtain the salt.
5. Filter and dry.

Method:
Reaction with 2 aqueous solutions.
2 Salt Solutions OR 1 Salt Solution & 1 Dilute Acid

In order to SEPARATE the insoluble salt from its reacting mixture, its starting reactants MUST BE soluble. This is to ensure that the insoluble salt produced can be filtered away from the reaction mixture.

AB (aq) + CD (aq) → AD (s) + BC (aq)
A⁺ (aq) + D^- (aq) → AD (s)

Steps:
1. Add solution AB to solution CD in a beaker. A white precip­itate of AD forms.
2. Filter to obtain the precip­itate.
3. Wash the precip­itate with cold, distilled water to remove impuri­ties.
4. Leave the precip­itate of AD to dry.

E.g Ba(NO3)2 (aq) + Na2SO4 (aq) → BaSO4 (s) + 2NaNO3 (aq)