ORGANIC CHEMISTRY I

Introduction to Organic Chemistry and Hydrocarbons

By the end of the lesson, the learner should be able to:
Define organic chemistry and hydrocarbons
Explain why carbon forms many compounds
Classify hydrocarbons into alkanes, alkenes, and alkynes
Identify the bonding in carbon compounds

Teacher exposition: Definition of organic chemistry. Discussion: Unique properties of carbon - tetravalency, catenation, multiple bonding. Q/A: Examples of hydrocarbons in daily life. Introduction to three main groups of hydrocarbons.

Carbon models, Hydrocarbon structure charts, Molecular model kits

KLB Secondary Chemistry Form 3, Pages 86-87

ORGANIC CHEMISTRY I

Sources of Alkanes - Natural Gas, Biogas, and Crude Oil

By the end of the lesson, the learner should be able to:
Identify natural sources of alkanes
Describe composition of natural gas and biogas
Explain crude oil as major source of alkanes
Describe biogas digester and its operation

Discussion: Natural gas composition (80% methane). Explanation: Biogas formation from organic waste decomposition. Teacher demonstration: Biogas digester model/diagram. Q/A: Environmental benefits of biogas production.

Biogas digester model/diagram, Natural gas composition charts, Organic waste samples

KLB Secondary Chemistry Form 3, Pages 86-87

ORGANIC CHEMISTRY I

Fractional Distillation of Crude Oil
Cracking of Alkanes - Thermal and Catalytic Methods

By the end of the lesson, the learner should be able to:
Explain fractional distillation process
Perform fractional distillation of crude oil
Identify different fractions and their uses
Relate boiling points to molecular size
Define cracking of alkanes
Distinguish between thermal and catalytic cracking
Write equations for cracking reactions
Explain industrial importance of cracking

Experiment: Fractional distillation of crude oil using improvised column. Collect fractions at different temperatures (120°C intervals up to 350°C). Test fractions for appearance, flammability, and viscosity. Record observations and relate to molecular size.
Teacher exposition: Definition and purpose of cracking. Discussion: Thermal vs catalytic cracking conditions. Worked examples: Cracking equations producing smaller alkanes, alkenes, and hydrogen. Q/A: Industrial applications and hydrogen production.

Crude oil sample, Boiling tubes, High-temperature thermometer, Sand/porcelain chips, Bunsen burner, Test tubes
Cracking process diagrams, Chemical equation charts, Catalyst samples for demonstration

KLB Secondary Chemistry Form 3, Pages 87-89
KLB Secondary Chemistry Form 3, Pages 89-90

ORGANIC CHEMISTRY I

Alkane Series and Homologous Series Concept

By the end of the lesson, the learner should be able to:
Define homologous series using alkanes
Write molecular formulas for first 10 alkanes
Identify characteristics of homologous series
Apply general formula CₙH₂ₙ₊₂ for alkanes

Teacher exposition: Homologous series definition and characteristics. Table completion: Names, molecular formulas, and structures of first 10 alkanes. Discussion: General formula application. Pattern recognition: Gradual change in physical properties.

Alkane series chart, Molecular formula worksheets, Periodic table

KLB Secondary Chemistry Form 3, Pages 90-92

ORGANIC CHEMISTRY I

Nomenclature of Alkanes - Straight Chain and Branched

By the end of the lesson, the learner should be able to:
Name straight-chain alkanes using IUPAC rules
Identify parent chains in branched alkanes
Name branched alkanes with substituent groups
Apply systematic naming rules correctly

Teacher demonstration: Step-by-step naming of branched alkanes. Rules application: Longest chain identification, numbering from nearest branch, substituent naming. Practice exercises: Various branched alkane structures. Group work: Name complex branched alkanes.

Structural formula charts, IUPAC naming rules poster, Molecular model kits

KLB Secondary Chemistry Form 3, Pages 90-92

ORGANIC CHEMISTRY I

Nomenclature of Alkanes - Straight Chain and Branched

By the end of the lesson, the learner should be able to:
Name straight-chain alkanes using IUPAC rules
Identify parent chains in branched alkanes
Name branched alkanes with substituent groups
Apply systematic naming rules correctly

Teacher demonstration: Step-by-step naming of branched alkanes. Rules application: Longest chain identification, numbering from nearest branch, substituent naming. Practice exercises: Various branched alkane structures. Group work: Name complex branched alkanes.

Structural formula charts, IUPAC naming rules poster, Molecular model kits

KLB Secondary Chemistry Form 3, Pages 90-92

ORGANIC CHEMISTRY I

Isomerism in Alkanes - Structural Isomers
Laboratory Preparation of Methane

By the end of the lesson, the learner should be able to:
Define isomerism in alkanes
Draw structural isomers of butane and pentane
Distinguish between chain and positional isomerism
Predict number of isomers for given alkanes
Describe laboratory preparation of methane
Perform methane preparation experiment safely
Test physical and chemical properties of methane
Write equation for methane preparation

Teacher exposition: Isomerism definition and types. Practical exercise: Draw all isomers of butane and pentane. Discussion: Physical property differences between isomers. Model building: Use molecular models to show isomeric structures.
Experiment: Heat mixture of sodium ethanoate and soda lime. Collect methane gas over water. Tests: Color, smell, combustion, reaction with bromine in dark. Record observations in table format. Safety precautions during gas collection.

Molecular model kits, Isomerism charts, Structural formula worksheets
Sodium ethanoate, Soda lime, Round-bottomed flask, Gas collection apparatus, Bromine water, Wooden splints

KLB Secondary Chemistry Form 3, Pages 92-94
KLB Secondary Chemistry Form 3, Pages 94-96

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethane

By the end of the lesson, the learner should be able to:
Prepare ethane using sodium propanoate and soda lime
Compare preparation methods of methane and ethane
Test properties of ethane gas
Write general equation for alkane preparation

Experiment: Prepare ethane from sodium propanoate and soda lime. Compare with methane preparation method. Carry out similar tests as for methane. Discussion: General pattern for alkane preparation from sodium alkanoates.

Sodium propanoate, Soda lime, Gas collection apparatus, Testing materials

KLB Secondary Chemistry Form 3, Pages 94-96

ORGANIC CHEMISTRY I

Physical Properties of Alkanes

By the end of the lesson, the learner should be able to:
Describe physical properties of alkanes
Explain trends in melting and boiling points
Relate molecular size to physical properties
Compare solubility in different solvents

Data analysis: Study table of physical properties of first 10 alkanes. Graph plotting: Boiling points vs number of carbon atoms. Discussion: Intermolecular forces and property trends. Q/A: Solubility patterns in polar and non-polar solvents.

Physical properties data tables, Graph paper, Calculators, Solubility demonstration materials

KLB Secondary Chemistry Form 3, Pages 96-97

ORGANIC CHEMISTRY I

Chemical Properties of Alkanes - Combustion and Substitution

By the end of the lesson, the learner should be able to:
Write equations for complete and incomplete combustion
Explain substitution reactions with halogens
Describe conditions for halogenation reactions
Name halogenated alkane products

Worked examples: Combustion equations for various alkanes. Teacher demonstration: Methane + bromine in sunlight (or simulation). Discussion: Free radical mechanism in substitution. Practice: Write equations for chlorination of methane.

Molecular models, Halogenation reaction charts, Chemical equation worksheets

KLB Secondary Chemistry Form 3, Pages 97-98

ORGANIC CHEMISTRY I

Uses of Alkanes in Industry and Daily Life
Introduction to Alkenes and Functional Groups

By the end of the lesson, the learner should be able to:
List major uses of different alkanes
Explain industrial applications of alkanes
Describe environmental considerations
Evaluate economic importance of alkanes
Define alkenes and unsaturation
Identify the C=C functional group
Write general formula for alkenes (CₙH₂ₙ)
Compare alkenes with alkanes

Discussion: Uses of gaseous alkanes as fuels. Teacher exposition: Industrial applications - carbon black, methanol production, hydrogen source. Q/A: Environmental impact and cleaner fuel initiatives. Assignment: Research local uses of alkane products.
Teacher exposition: Alkenes definition and unsaturation concept. Introduction: C=C double bond as functional group. Table study: First 6 members of alkene series. Comparison: Alkenes vs alkanes - formulas and structures.

Industrial application charts, Product samples, Environmental impact materials
Alkene series charts, Molecular models showing double bonds, Functional group posters

KLB Secondary Chemistry Form 3, Pages 98-100
KLB Secondary Chemistry Form 3, Pages 100-101

ORGANIC CHEMISTRY I

Nomenclature of Alkenes

By the end of the lesson, the learner should be able to:
Apply IUPAC rules for naming alkenes
Number carbon chains to give lowest numbers to double bonds
Name branched alkenes with substituents
Distinguish position isomers of alkenes

Teacher demonstration: Step-by-step naming of alkenes. Rules application: Longest chain with double bond, numbering from end nearest double bond. Practice exercises: Name various alkene structures. Group work: Complex branched alkenes with substituents.

IUPAC naming charts for alkenes, Structural formula worksheets, Molecular model kits

KLB Secondary Chemistry Form 3, Pages 101-102

ORGANIC CHEMISTRY I

Isomerism in Alkenes - Branching and Positional

By the end of the lesson, the learner should be able to:
Draw structural isomers of alkenes
Distinguish between branching and positional isomerism
Identify geometric isomers in alkenes
Predict isomer numbers for given molecular formulas

Practical exercise: Draw all isomers of butene and pentene. Teacher exposition: Branching vs positional isomerism in alkenes. Model building: Use molecular models for isomer visualization. Discussion: Geometric isomerism introduction (basic level).

Molecular model kits, Isomerism worksheets, Geometric isomer models

KLB Secondary Chemistry Form 3, Pages 102

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethene

By the end of the lesson, the learner should be able to:
Prepare ethene by dehydration of ethanol
Describe role of concentrated sulfuric acid
Set up apparatus safely for ethene preparation
Test physical and chemical properties of ethene

Experiment: Dehydration of ethanol using concentrated H₂SO₄ at 170°C. Use sand bath for controlled heating. Pass gas through NaOH to remove impurities. Tests: Bromine water, acidified KMnO₄, combustion. Safety precautions with concentrated acid.

Ethanol, Concentrated H₂SO₄, Round-bottomed flask, Sand bath, Gas collection apparatus, Testing solutions

KLB Secondary Chemistry Form 3, Pages 102-104

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethene
Alternative Preparation of Ethene and Physical Properties

By the end of the lesson, the learner should be able to:
Prepare ethene by dehydration of ethanol
Describe role of concentrated sulfuric acid
Set up apparatus safely for ethene preparation
Test physical and chemical properties of ethene
Describe catalytic dehydration using aluminum oxide
Compare different preparation methods
List physical properties of ethene
Explain trends in alkene physical properties

Experiment: Dehydration of ethanol using concentrated H₂SO₄ at 170°C. Use sand bath for controlled heating. Pass gas through NaOH to remove impurities. Tests: Bromine water, acidified KMnO₄, combustion. Safety precautions with concentrated acid.
Demonstration: Alternative method using Al₂O₃ catalyst. Comparison: Acid vs catalytic dehydration methods. Data analysis: Physical properties of alkenes table. Discussion: Property trends with increasing molecular size.

Ethanol, Concentrated H₂SO₄, Round-bottomed flask, Sand bath, Gas collection apparatus, Testing solutions
Aluminum oxide catalyst, Glass wool, Alternative apparatus setup, Physical properties charts

KLB Secondary Chemistry Form 3, Pages 102-104

ORGANIC CHEMISTRY I

Chemical Properties of Alkenes - Addition Reactions

By the end of the lesson, the learner should be able to:
Explain addition reactions due to C=C double bond
Write equations for halogenation of alkenes
Describe hydrogenation and hydrohalogenation
Explain addition mechanism

Teacher exposition: Addition reactions definition and mechanism. Worked examples: Ethene + Cl₂, Br₂, HBr, H₂. Discussion: Markovnikov's rule for unsymmetrical addition. Practice: Various addition reaction equations.

Addition reaction charts, Mechanism diagrams, Chemical equation worksheets

KLB Secondary Chemistry Form 3, Pages 105-107

ORGANIC CHEMISTRY I

Oxidation Reactions of Alkenes and Polymerization

By the end of the lesson, the learner should be able to:
Describe oxidation by KMnO₄ and K₂Cr₂O₇
Explain polymerization of ethene
Define monomers and polymers
Write equations for polymer formation

Demonstration: Decolorization of KMnO₄ by alkenes. Teacher exposition: Polymerization process and polymer formation. Examples: Ethene → polyethene formation. Discussion: Industrial importance of polymerization. Practice: Write polymerization equations.

Oxidizing agents for demonstration, Polymer samples, Polymerization charts, Monomer-polymer models

KLB Secondary Chemistry Form 3, Pages 107-108

ORGANIC CHEMISTRY I

Tests for Alkenes and Uses

By the end of the lesson, the learner should be able to:
Perform chemical tests to identify alkenes
Use bromine water and KMnO₄ as test reagents
List industrial and domestic uses of alkenes
Explain importance in plastic manufacture

Practical session: Test known alkenes with bromine water and acidified KMnO₄. Observe rapid decolorization compared to alkanes. Discussion: Uses in plastics, ethanol production, fruit ripening, detergents. Assignment: Research alkene applications.

Test alkenes, Bromine water, Acidified KMnO₄, Plastic samples, Uses reference charts

KLB Secondary Chemistry Form 3, Pages 108-109

ORGANIC CHEMISTRY I

Introduction to Alkynes and Triple Bond
Nomenclature and Isomerism in Alkynes

By the end of the lesson, the learner should be able to:
Define alkynes and triple bond structure
Write general formula for alkynes (CₙH₂ₙ₋₂)
Identify first members of alkyne series
Compare degree of unsaturation in hydrocarbons
Apply IUPAC naming rules for alkynes
Name branched alkynes with substituents
Draw structural isomers of alkynes
Identify branching and positional isomerism

Teacher exposition: Alkynes definition and C≡C triple bond. Table study: First 6 members of alkyne series with structures. Discussion: Degrees of unsaturation - alkanes vs alkenes vs alkynes. Model demonstration: Triple bond representation.
Teacher demonstration: Systematic naming of alkynes using -yne suffix. Practice exercises: Name various alkyne structures. Drawing exercise: Isomers of pentyne and hexyne. Group work: Complex branched alkynes with multiple substituents.

Alkyne series charts, Triple bond molecular models, Unsaturation comparison charts
IUPAC naming rules for alkynes, Structural formula worksheets, Molecular model kits

KLB Secondary Chemistry Form 3, Pages 109-110
KLB Secondary Chemistry Form 3, Pages 110-111

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethyne

By the end of the lesson, the learner should be able to:
Prepare ethyne from calcium carbide and water
Set up gas collection apparatus safely
Test physical and chemical properties of ethyne
Write equation for ethyne preparation

Experiment: Calcium carbide + water reaction. Use sand layer for heat absorption. Collect ethyne over water. Tests: Color, smell, combustion, bromine water, acidified KMnO₄. Safety: Dry apparatus, controlled water addition.

Calcium carbide, Sand, Flat-bottomed flask, Dropping funnel, Gas collection apparatus, Testing solutions

KLB Secondary Chemistry Form 3, Pages 111-112

ORGANIC CHEMISTRY I

Physical and Chemical Properties of Alkynes

By the end of the lesson, the learner should be able to:
Describe physical properties of alkynes
Compare alkyne properties with alkenes and alkanes
Write combustion equations for alkynes
Explain addition reactions of alkynes

Data analysis: Physical properties of alkynes table. Comparison: Alkynes vs alkenes vs alkanes properties. Worked examples: Combustion reactions of ethyne. Teacher exposition: Two-step addition reactions due to triple bond.

Physical properties charts, Comparison tables, Combustion equation examples

KLB Secondary Chemistry Form 3, Pages 112-113

ORGANIC CHEMISTRY I

Addition Reactions of Alkynes and Chemical Tests

By the end of the lesson, the learner should be able to:
Write equations for halogenation of alkynes
Describe hydrogenation and hydrohalogenation
Compare reaction rates: alkynes vs alkenes
Perform chemical tests for alkynes

Worked examples: Two-step addition reactions of ethyne with Br₂, Cl₂, H₂. Discussion: Faster reaction rates in alkynes compared to alkenes. Practical session: Test alkynes with oxidizing agents. Comparison: Rate of decolorization vs alkenes.

Addition reaction charts, Chemical equation worksheets, Test solutions, Stopwatch for rate comparison

KLB Secondary Chemistry Form 3, Pages 113-115

ORGANIC CHEMISTRY I
CHLORINE AND ITS COMPOUNDS

Uses of Alkynes and Industrial Applications
Introduction and Preparation of Chlorine

By the end of the lesson, the learner should be able to:
List industrial uses of alkynes
Explain oxy-acetylene welding applications
Describe use in synthetic fiber production
Evaluate importance as chemical starting materials
Define chlorine and state its position in the periodic table. Describe the occurrence of chlorine in nature. Describe laboratory preparation of chlorine gas. Write balanced equations for chlorine preparation.

Discussion: Industrial applications of alkynes in adhesives, plastics, synthetic fibers. Teacher demonstration: Oxy-acetylene flame principles (or video). Q/A: Starting materials for chemical synthesis. Assignment: Research local industrial uses.
Q/A: Review Group VII elements and electron configuration of chlorine ( 8.7). Discussion: Occurrence as sodium chloride in sea water and rock salt. Practical work: Experiment 6.1 - Preparation using MnO2 + concentrated HCl. Setup apparatus as in Figure 6. Safety precautions for handling chlorine gas.

Industrial application charts, Welding equipment demonstration/video, Synthetic fiber samples
Manganese(IV) oxide, Concentrated HCl, Gas collection apparatus, Water, Concentrated H2SO4, Blue litmus paper, Gas jars

KLB Secondary Chemistry Form 3, Pages 115-116
KLB Secondary Chemistry Form 4, Pages 195-196

CHLORINE AND ITS COMPOUNDS

Physical Properties of Chlorine
Chemical Properties of Chlorine - Reaction with Water

By the end of the lesson, the learner should be able to:
Investigate the physical properties of chlorine gas. Explain the method of collection used for chlorine. Test the solubility of chlorine in water. State the density and color of chlorine gas.

Practical work: Experiment 6.2 - Testing chlorine gas preserved from previous experiment. Recording observations in Table 6. Testing: Color, smell (caution - no direct smelling), density, solubility in water. Demonstration: Inverting gas jar in water trough. Discussion: Why collected by downward delivery.

Preserved chlorine gas, Water trough, Gas jars, Observation tables, Safety equipment
Chlorine gas, Distilled water, Blue and red litmus papers, Colored flower petals, Gas jars, Boiling tubes

KLB Secondary Chemistry Form 4, Pages 196-197

CHLORINE AND ITS COMPOUNDS

Chemical Properties of Chlorine - Reaction with Metals
Chemical Properties of Chlorine - Reaction with Non-metals

By the end of the lesson, the learner should be able to:
Investigate reactions of chlorine with metals. Write balanced equations for metal-chlorine reactions. Explain the formation of metal chlorides. Demonstrate exothermic nature of these reactions.

Practical work: Experiment 6.4 - Reactions with burning magnesium, hot iron wire, dry chlorine over hot iron coil (Figure 6.2). Recording observations in Table 6. Observations: White fumes (MgCl2), glowing iron wire, black crystals (FeCl3). Discussion: Formation of higher oxidation state chlorides. Safety: Proper ventilation and eye protection.

Magnesium ribbon, Iron wire, Chlorine gas, Deflagrating spoon, Combustion tube, Anhydrous CaCl2, Gas jars
Red phosphorus, Hydrogen gas, Chlorine gas, Deflagrating spoon, Gas jars, Bunsen burner, Safety equipment

KLB Secondary Chemistry Form 4, Pages 199-201

CHLORINE AND ITS COMPOUNDS

Oxidising Properties of Chlorine
Reaction of Chlorine with Alkali Solutions

By the end of the lesson, the learner should be able to:
Investigate chlorine as an oxidizing agent. Test reactions with reducing agents. Write ionic equations for redox reactions. Identify color changes in oxidation reactions.

Practical work: Experiment 6.6 - Bubbling chlorine through sodium sulphite solution, testing with barium nitrate and lead nitrate. Reactions with hydrogen sulphide and ammonia. Recording observations in Table 6. Color changes and precipitate formation. Writing ionic equations: SO3²⁻ + Cl2 + H2O → SO4²⁻ + 2Cl⁻ + 2H⁺.

Sodium sulphite solution, Barium nitrate, Lead nitrate, Hydrogen sulphide gas, Aqueous ammonia, Chlorine gas, Test tubes
Sodium hydroxide solutions (dilute cold, concentrated hot), Chlorine gas, Beakers, Bunsen burner, Thermometer

KLB Secondary Chemistry Form 4, Pages 201-202

CHLORINE AND ITS COMPOUNDS

Oxidising Properties - Displacement Reactions
Test for Chloride Ions
Uses of Chlorine and its Compounds

By the end of the lesson, the learner should be able to:
Investigate displacement reactions of chlorine with halides. Test reactions with bromides and iodides. Write ionic equations for displacement reactions. Explain the order of reactivity of halogens.
List the industrial uses of chlorine. Explain the use of chlorine in water treatment. Describe manufacture of chlorine compounds. Relate properties to uses of chlorine.

Practical work: Experiment 6.8 - Bubbling chlorine through potassium bromide and potassium iodide solutions. Observations: Colorless to orange (Br2), colorless to brown (I2). Writing ionic equations: Cl2 + 2Br⁻ → 2Cl⁻ + Br2, Cl2 + 2I⁻ → 2Cl⁻ + I Discussion: Displacement as evidence of relative reactivity.
Discussion: Industrial applications - HCl manufacture, bleaching agents for cotton and paper industries, water treatment and sewage plants. Study Figure 6.3(a) - bleaching chemicals. Applications: Chloroform (anaesthetic), solvents (trichloroethane), CFCs, PVC plastics, pesticides (DDT), germicides and fungicides. Q/A: Relating chemical properties to practical applications.

Potassium bromide solution, Potassium iodide solution, Chlorine gas, Test tubes, Observation charts
Sodium chloride, Concentrated H2SO4, Lead(II) nitrate solution, Aqueous ammonia, Glass rod, Test tubes, Bunsen burner
Charts showing industrial uses, Samples of bleaching agents, PVC materials, Photographs of water treatment plants, Industrial application diagrams

KLB Secondary Chemistry Form 4, Pages 203-204
KLB Secondary Chemistry Form 4, Pages 205-207

CHLORINE AND ITS COMPOUNDS

Uses of Chlorine and its Compounds

By the end of the lesson, the learner should be able to:
List the industrial uses of chlorine. Explain the use of chlorine in water treatment. Describe manufacture of chlorine compounds. Relate properties to uses of chlorine.

Discussion: Industrial applications - HCl manufacture, bleaching agents for cotton and paper industries, water treatment and sewage plants. Study Figure 6.3(a) - bleaching chemicals. Applications: Chloroform (anaesthetic), solvents (trichloroethane), CFCs, PVC plastics, pesticides (DDT), germicides and fungicides. Q/A: Relating chemical properties to practical applications.

Charts showing industrial uses, Samples of bleaching agents, PVC materials, Photographs of water treatment plants, Industrial application diagrams

KLB Secondary Chemistry Form 4, Pages 205-207

CHLORINE AND ITS COMPOUNDS

Hydrogen Chloride - Laboratory Preparation

By the end of the lesson, the learner should be able to:
Describe laboratory preparation of hydrogen chloride gas. Set up apparatus for HCl preparation. Investigate physical properties of HCl gas. Explain the method of collection used.

Practical work: Experiment 6.10 - Preparation using rock salt (NaCl) + concentrated H2SO Setup apparatus as in Figure 6.3(b). Testing physical properties and recording in Table 6.6. Tests: Solubility (fountain experiment), reaction with ammonia, effect on litmus. Collection by downward delivery due to density. Writing equation: NaCl + H2SO4 → NaHSO4 + HCl.

Rock salt (NaCl), Concentrated H2SO4, Gas collection apparatus, Ammonia solution, Litmus papers, Water trough, Gas jars

KLB Secondary Chemistry Form 4, Pages 207-208

CHLORINE AND ITS COMPOUNDS

Chemical Properties of Hydrogen Chloride

By the end of the lesson, the learner should be able to:
Prepare aqueous hydrogen chloride (hydrochloric acid). Investigate acid properties of HCl solution. Test reactions with metals, bases, and carbonates. Compare HCl in water vs organic solvents.

Practical work: Experiment 6.11 - Preparation of aqueous HCl using apparatus in Figure 6. Testing with metals (Zn, Fe, Mg, Cu), NaOH, carbonates, lead nitrate. Recording observations in Table 6.7. Testing HCl in methylbenzene - no acid properties. Discussion: Ionization in water vs molecular existence in organic solvents. Writing equations for acid reactions.

Distilled water, Filter funnel, Metals (Zn, Fe, Mg, Cu), NaOH solution, Carbonates, Lead nitrate, Methylbenzene, Indicators

KLB Secondary Chemistry Form 4, Pages 208-211

CHLORINE AND ITS COMPOUNDS

Large-scale Manufacture of Hydrochloric Acid
Uses of Hydrochloric Acid

By the end of the lesson, the learner should be able to:
Describe industrial production of hydrochloric acid. Identify raw materials and conditions used. Explain the controlled combustion process. Draw flow diagrams of the industrial process.
List the industrial uses of hydrochloric acid. Explain applications in metal treatment. Describe use in water treatment and manufacturing. Relate acid properties to industrial applications.

Study of Figure 6.4 - Large-scale manufacture setup. Discussion: Raw materials (H2 from electrolysis/cracking, Cl2 from electrolysis). Controlled combustion: H2 + Cl2 → 2HCl in jet burner. Dissolving HCl gas in water over glass beads. Safety: Explosive nature of H2/Cl2 mixture, use of excess chlorine. Industrial considerations: 35% concentration, transport in rubber-lined steel tanks.
Discussion: Applications - rust removal and descaling, galvanizing preparation, electroplating preparation, water treatment (chlorination), sewage treatment. Manufacturing uses: dyes, drugs, photographic materials (AgCl), pH control in industries. Q/A: How acid properties make HCl suitable for these uses. Case studies: Metal cleaning processes, water purification systems.

Flow diagrams, Industrial photographs, Glass beads samples, Charts showing electrolysis processes, Safety equipment models
Samples of rusted and cleaned metals, Photographic materials, pH control charts, Industrial application videos, Water treatment diagrams

KLB Secondary Chemistry Form 4, Pages 211-212
KLB Secondary Chemistry Form 4, Pages 212-213

CHLORINE AND ITS COMPOUNDS

Environmental Pollution by Chlorine Compounds and Summary

By the end of the lesson, the learner should be able to:
Explain environmental effects of chlorine compounds. Describe the impact of CFCs on ozone layer. Discuss pollution by chlorine-containing pesticides. Summarize key concepts of chlorine chemistry.

Discussion: Environmental impacts - chlorine gas forming acid rain, CFCs (life span CCl3F = 75 years, CCl2F2 = 110 years) breaking down ozone layer. DDT as persistent pesticide, PVC as non-biodegradable plastic. NEMA role in environmental protection, Stockholm Convention on DDT. Control measures and alternatives. Revision: Key reactions, properties, uses, and environmental considerations. Summary of halogen chemistry concepts.

Environmental pollution charts, Ozone layer diagrams, DDT restriction documents, PVC waste samples, NEMA guidelines, Summary charts of reactions

KLB Secondary Chemistry Form 4, Pages 213-215