Chemistry Unit One
Chemistry Unit One
Apparatus
Reagents
Aluminium sulphate, calcium nitrate, copper (II) sulphate, iron (II) sulphate, iron (III) chloride,
lead nitrate, zinc nitrate, aqueous sodium hydroxide and distilled water.
Procedure
1. Using a clean spatula, scoop about a quarter spatulaful of aluminium sulphate and put it into a
test tube.
2. Add about 10 cm3 of distilled water into the contents of the test tube. Shake until all the solid
dissolves. Label this solution as Al3+.
3. Take about 1 cm3 of the solution and put into a test tube. Add two drops of aqueous sodium
hydroxide to the contents of the test tube and then record your observations.
4. Add more drops of sodium hydroxide solution until in excess. Record your observations.
5. Repeat the procedure above for the rest of the salts, each in turn and complete the table below.
Table 1.1: Test results for presence of cations using NaOH(aq) Cation A few drops of
aqueous NaOH, Excess of aqueous NaOH, Al3+ Ca2+ Cu2+ Fe2+ Fe3+ Pb2+ Zn2+
Great, you're setting up an experiment to test for cations using aqueous sodium hydroxide. Based
on your procedure, here’s how the reactions typically occur for each cation:
Aqueous ammonia is commonly used in qualitative analysis to test for metal cations. When
added in small amounts, it can form precipitates, and in excess, it may dissolve some precipitates
due to complex ion formation.
Explanation:
1. Complex Formation: Copper (II) and zinc (II) ions dissolve in excess ammonia because
they form soluble complex ions.
2. No Precipitate for Calcium: Calcium does not react significantly with aqueous
ammonia.
3. Precipitates Form Due to Hydroxide Formation: Some metal cations react with
hydroxide ions in ammonia to form insoluble hydroxides, resulting in precipitates.
Question
1. Identify cations that formed colored precipitates with a few drops of aqueous NaOH and
aqueous ammonia.
2. Identify the cations that dissolved in excess of NaOH. Why do you think they dissolved?
3. Identify the cations that dissolved in excess of aqueous ammonia. Why do you think they
dissolved?
4. Did you use dilute or concentrated solutions of NaOH and ammonia? Give reasons for the use
of this level of concentration.
1. Cations that formed colored precipitates with a few drops of NaOH and aqueous
ammonia:
o Cu²⁺ (Copper (II)): Forms a blue precipitate of Cu (OH)₂.
o Fe²⁺ (Iron (II)): Forms a green precipitate of Fe(OH)₂, which turns brown due to
oxidation.
o Fe³⁺ (Iron(III)): Forms a reddish-brown precipitate of Fe(OH)₃.
2. Cations that dissolved in excess NaOH:
o Al³⁺, Pb²⁺, and Zn²⁺ form hydroxide precipitates that dissolve in excess NaOH,
forming soluble complex ions such as:
Al(OH)₄⁻ (tetrahydroxoaluminate ion)
Pb(OH)₄²⁻ (tetrahydroxoplumbate ion)
Zn(OH)₄²⁻ (tetrahydroxozincate ion)
o These cations dissolve because they can form complex ions in alkaline conditions.
3. Cations that dissolved in excess aqueous ammonia:
o Cu²⁺ and Zn²⁺ dissolve in excess ammonia due to complex formation:
Cu²⁺ forms a deep blue solution of [Cu(NH3)4]2+[Cu(NH₃)₄]^{2+}
(tetraamminecopper(II) complex).
Zn²⁺ forms a colorless solution of [Zn(NH3)4]2+[Zn(NH₃)₄]^{2+}
(tetraamminezinc(II) complex).
o They dissolve because ammonia acts as a ligand, forming soluble coordination
complexes.
4. Dilute or concentrated solutions of NaOH and ammonia:
o Dilute solutions are typically used to ensure controlled precipitation and prevent
rapid complex formation.
o Excess of either reagent is added gradually to test solubility behavior. Using
concentrated solutions could lead to unwanted side reactions or excessive ion
complexation.
5. What do you think will happen when you use cold or warm solutions of NaOH and
ammonia? Explain your answer.
o Warm solutions of NaOH and ammonia typically increase the reaction rate.
Some precipitates may form faster, and dissolution might occur more readily in
excess reagent.
o Cold solutions slow down reaction kinetics. Precipitates may form more slowly,
and some reactions may be incomplete. For example, the complexation reactions
of Cu²⁺ with ammonia might take longer or be less pronounced.
Heat can also affect solubility: Some hydroxides, like Ca(OH)₂, dissolve slightly better
in warm water, while others remain mostly insoluble.
These principles help in identifying cations based on their unique precipitation and solubility
behaviors. Would you like more detailed explanations on any of these processes?
1. What are anions? Anions are negatively charged ions that form when atoms gain
electrons. They are commonly found in ionic compounds and solutions.
oChloride (Cl⁻)
oSulfate (SO₄²⁻)
oNitrate (NO₃⁻)
oCarbonate (CO₃²⁻)
oPhosphate (PO₄³⁻)
2. What is a precipitation reaction? How is it used to identify salts?
A precipitation reaction occurs when two soluble compounds in solution react to form an
insoluble solid, called a precipitate. These reactions help identify specific salts based on
solubility rules. For example:
o Testing for sulfate ions (SO₄²⁻): Adding barium chloride (BaCl₂) solution to a
sample with sulfate results in a white precipitate of BaSO₄, confirming the
presence of sulfate ions.
o Testing for chloride ions (Cl⁻): Adding silver nitrate (AgNO₃) solution leads
to a white precipitate of AgCl, indicating chloride.
o Testing for carbonate ions (CO₃²⁻): Adding dilute hydrochloric acid (HCl)
causes effervescence due to CO₂ gas release, confirming the presence of
carbonates.
These tests are key in qualitative analysis, helping chemists identify unknown substances based
on predictable reaction patterns.
Investigating solubility of salts in water
Apparatus
Reagents
Sodium carbonate, lead carbonate, lead sulphate, lead nitrate, barium sulphate, barium chloride
and lead (II) chloride.
Procedure
1. Scoop a spatula endful amount of sodium carbonate and put it into a test tube. 2. Add water to
the salt, stir and make observations. 3. Repeat the procedure for the rest of the salts.
You’re setting up an experiment to investigate the solubility of different salts in water. Here’s
what you can expect:
Expected Results
Some salts are soluble in water, while others are insoluble due to their ionic lattice structure and
water interactions. Based on solubility rules:
Soluble Salts
o Sodium carbonate (Na₂CO₃) – Readily dissolves in water.
o Lead nitrate (Pb(NO₃)₂) – Soluble in water.
o Barium chloride (BaCl₂) – Dissolves easily in water.
Insoluble Salts
o Lead carbonate (PbCO₃) – Forms a precipitate, indicating low solubility.
o Lead(II) chloride (PbCl₂) – Slightly soluble in cold water, more soluble in warm
water.
o Lead sulphate (PbSO₄) – Virtually insoluble in water.
o Barium sulphate (BaSO₄) – Highly insoluble in water.
Explanation of Results
Soluble salts dissolve because their ions interact strongly with water molecules,
breaking apart into solution.
Insoluble salts remain as precipitates because their ionic bonds are too strong for water
molecules to disrupt.
Lead(II) chloride has increased solubility in warm water due to greater kinetic energy
allowing more dissociation.
To test for presence of anions in compounds
Apparatus
Reagents
Distilled water, solids of: sodium carbonate, sodium chloride, potassium iodide, sodium nitrate
and sodium sulphate; calcium hydroxide solution, solids of: sodium sulphite, lead (II) nitrate, 2M
nitric acid, aluminium foil, silver nitrate, barium nitrate and acidified potassium dichromate.
Procedure
Below is a summary of the expected observations when testing for various anions using different
reagents:
In qualitative analysis, gases are identified through simple chemical tests based on their
characteristic reactions with different reagents. Below is a structured table summarizing the
expected observations for common gases.
Explanation:
Each gas exhibits unique properties that lead to the observed chemical reactions:
Ammonia (NH₃)
o Basic in nature, turning red litmus paper blue due to the presence of hydroxide
ions in solution.
o Has a pungent odor and is highly soluble in water.
Carbon Dioxide (CO₂)
o Weakly acidic, reacts with lime water to form an insoluble calcium carbonate
precipitate, causing the milky appearance.
o Slightly soluble in water, forming carbonic acid.
Chlorine (Cl₂)
o Strong oxidizing agent, capable of bleaching litmus papers due to its ability to
react with water to form hydrochloric acid and hypochlorous acid.
o Toxic and has a distinct pungent odor.
Hydrogen (H₂)
o Highly flammable; reacts explosively with oxygen, producing water vapor and
releasing energy in the form of a ‘pop’ sound.
o Colorless and odorless.
Oxygen (O₂)
o Supports combustion, reigniting a glowing splint due to its role in oxidation
reactions.
o Essential for respiration and many chemical reactions.
Sulphur Dioxide (SO₂)
o Acts as a reducing agent, turning acidified potassium dichromate from orange
to green by reducing chromium(VI) to chromium(III).
o Has a sharp, irritating smell and is moderately soluble in water.
This forms an insoluble calcium carbonate precipitate, turning lime water milky.