ORGANIC CHEMISTRY II

Introduction to Alkanols and Nomenclature
Isomerism in Alkanols
Laboratory Preparation of Ethanol
Industrial Preparation and Physical Properties

By the end of the lesson, the learner should be able to:
Define alkanols and identify functional group
- Apply nomenclature rules for alkanols
- Draw structural formulae of simple alkanols
- Compare alkanols with corresponding alkanes
Explain positional and chain isomerism
- Draw isomers of given alkanols
- Name different isomeric forms
- Classify isomers as primary, secondary, or tertiary

Q/A: Review alkanes, alkenes from Form 3
- Study functional group -OH concept
- Practice naming alkanols using IUPAC rules
- Complete Table 6.2 - alkanol structures
Study positional isomerism examples (propan-1-ol vs propan-2-ol)
- Practice drawing chain isomers
- Exercises on isomer identification and naming
- Discussion on structural differences

Molecular models, Table 6.1 and 6.2, alkanol structure charts, student books
Isomer structure charts, molecular models, practice worksheets, student books
Sugar, yeast, warm water, conical flask, delivery tube, lime water, thermometer
Table 6.3, industrial process diagrams, ethene structure models, property comparison charts

KLB Secondary Chemistry Form 4, Pages 167-170
KLB Secondary Chemistry Form 4, Pages 170-171

ORGANIC CHEMISTRY II

Chemical Properties of Alkanols I
Chemical Properties of Alkanols II
Uses of Alkanols and Health Effects

By the end of the lesson, the learner should be able to:
Test reactions of ethanol with various reagents
- Write equations for ethanol reactions
- Identify products formed
- Explain reaction mechanisms

Experiment 6.2: Test ethanol with burning, universal indicator, sodium metal, acids
- Record observations in Table 6.4
- Write balanced equations
- Discuss reaction types

Ethanol, sodium metal, universal indicator, concentrated H₂SO₄, ethanoic acid, test tubes
Acidified potassium chromate/manganate, ethanoic acid, concentrated H₂SO₄, heating apparatus
Charts showing alkanol uses, health impact data, methylated spirit samples, discussion materials

KLB Secondary Chemistry Form 4, Pages 173-175

ORGANIC CHEMISTRY II

Introduction to Alkanoic Acids
Laboratory Preparation of Ethanoic Acid

By the end of the lesson, the learner should be able to:
Define alkanoic acids and functional group
- Apply nomenclature rules
- Draw structural formulae
- Compare with alkanols

Study carboxyl group (-COOH) structure
- Practice naming using IUPAC rules
- Complete Table 6.5 and 6.6
- Compare functional groups of alkanols and acids

Alkanoic acid structure charts, Table 6.5 and 6.6, molecular models, student books
Ethanol, KMnO₄, concentrated H₂SO₄, distillation apparatus, thermometer, round-bottom flask

KLB Secondary Chemistry Form 4, Pages 177-179

ORGANIC CHEMISTRY II

Physical and Chemical Properties of Alkanoic Acids

By the end of the lesson, the learner should be able to:
Investigate chemical reactions of ethanoic acid
- Test with various reagents
- Write chemical equations
- Analyze acid strength

Experiment following Table 6.8: Test ethanoic acid with indicators, metals, carbonates, bases
- Record observations
- Write equations
- Discuss weak acid behavior

2M ethanoic acid, universal indicator, Mg strip, Na₂CO₃, NaOH, phenolphthalein, test tubes

KLB Secondary Chemistry Form 4, Pages 180-182

ORGANIC CHEMISTRY II

Esterification and Uses of Alkanoic Acids
Introduction to Detergents and Soap Preparation
Mode of Action of Soap and Hard Water Effects

By the end of the lesson, the learner should be able to:
Explain ester formation process
- Write esterification equations
- State uses of alkanoic acids
- Prepare simple esters
Explain soap molecule structure
- Describe cleaning mechanism
- Investigate hard water effects
- Compare soap performance in different waters

Complete esterification experiments
- Study concentrated H₂SO₄ as catalyst
- Write general esterification equation
- Discuss applications in food, drugs, synthetic fibres
Study hydrophobic and hydrophilic ends
- Demonstrate micelle formation
- Test soap in distilled vs hard water
- Observe scum formation
- Write precipitation equations

Ethanoic acid, ethanol, concentrated H₂SO₄, test tubes, heating apparatus, cold water
Castor oil, 4M NaOH, NaCl, evaporating dish, water bath, stirring rod, filter paper
Soap samples, distilled water, hard water (CaCl₂/MgSO₄ solutions), test tubes, demonstration materials

KLB Secondary Chemistry Form 4, Pages 182-183
KLB Secondary Chemistry Form 4, Pages 186-188

ORGANIC CHEMISTRY II

Soapless Detergents and Environmental Effects
Introduction to Polymers and Addition Polymerization

By the end of the lesson, the learner should be able to:
Explain soapless detergent preparation
- Compare advantages/disadvantages
- Discuss environmental impact
- Analyze pollution effects

Study alkylbenzene sulphonate preparation
- Compare Table 6.9 - soap vs soapless
- Discussion on eutrophication and biodegradability
- Environmental awareness

Flow charts of detergent manufacture, Table 6.9, environmental impact data, sample detergents
Polymer samples, monomer structure charts, molecular models, calculators, polymer formation diagrams

KLB Secondary Chemistry Form 4, Pages 188-191

ORGANIC CHEMISTRY II

Addition Polymers - Types and Properties

By the end of the lesson, the learner should be able to:
Identify different addition polymers
- Draw structures from monomers
- Name common polymers
- Relate structure to properties

Study polystyrene, PTFE, perspex formation
- Practice identifying monomers from polymer structures
- Work through polymer calculation examples
- Properties analysis

Various polymer samples, structure identification exercises, calculation worksheets, Table 6.10

KLB Secondary Chemistry Form 4, Pages 195-197

ORGANIC CHEMISTRY II
ORGANIC CHEMISTRY I

Condensation Polymerization and Natural Polymers
Introduction to Organic Chemistry and Hydrocarbons

By the end of the lesson, the learner should be able to:
Explain condensation polymerization
- Compare with addition polymerization
- Study natural polymers
- Analyze nylon formation

Study nylon 6,6 formation from diamine and dioic acid
- Natural polymers: starch, protein, rubber
- Vulcanization process
- Compare synthetic vs natural

Nylon samples, rubber samples, condensation reaction diagrams, natural polymer examples
Carbon models, Hydrocarbon structure charts, Molecular model kits

KLB Secondary Chemistry Form 4, Pages 197-200

ORGANIC CHEMISTRY I

Sources of Alkanes - Natural Gas, Biogas, and Crude Oil
Fractional Distillation of 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
Explain fractional distillation process
Perform fractional distillation of crude oil
Identify different fractions and their uses
Relate boiling points to molecular size

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.
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.

Biogas digester model/diagram, Natural gas composition charts, Organic waste samples
Crude oil sample, Boiling tubes, High-temperature thermometer, Sand/porcelain chips, Bunsen burner, Test tubes

KLB Secondary Chemistry Form 3, Pages 86-87
KLB Secondary Chemistry Form 3, Pages 87-89

ORGANIC CHEMISTRY I

Cracking of Alkanes - Thermal and Catalytic Methods
Alkane Series and Homologous Series Concept

By the end of the lesson, the learner should be able to:
Define cracking of alkanes
Distinguish between thermal and catalytic cracking
Write equations for cracking reactions
Explain industrial importance of cracking

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.

Cracking process diagrams, Chemical equation charts, Catalyst samples for demonstration
Alkane series chart, Molecular formula worksheets, Periodic table

KLB Secondary Chemistry Form 3, Pages 89-90

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

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.

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

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethane
Physical Properties of Alkanes
Chemical Properties of Alkanes - Combustion and Substitution

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
Describe physical properties of alkanes
Explain trends in melting and boiling points
Relate molecular size to physical properties
Compare solubility in different solvents

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.
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.

Sodium propanoate, Soda lime, Gas collection apparatus, Testing materials
Physical properties data tables, Graph paper, Calculators, Solubility demonstration materials
Molecular models, Halogenation reaction charts, Chemical equation worksheets

KLB Secondary Chemistry Form 3, Pages 94-96
KLB Secondary Chemistry Form 3, Pages 96-97

ORGANIC CHEMISTRY I

Uses of Alkanes in Industry and Daily Life

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

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.

Industrial application charts, Product samples, Environmental impact materials

KLB Secondary Chemistry Form 3, Pages 98-100

ORGANIC CHEMISTRY I

Introduction to Alkenes and Functional Groups

By the end of the lesson, the learner should be able to:
Define alkenes and unsaturation
Identify the C=C functional group
Write general formula for alkenes (CₙH₂ₙ)
Compare alkenes with alkanes

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.

Alkene series charts, Molecular models showing double bonds, Functional group posters

KLB Secondary Chemistry Form 3, Pages 100-101

ORGANIC CHEMISTRY I

Nomenclature of Alkenes
Isomerism in Alkenes - Branching and Positional

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
Molecular model kits, Isomerism worksheets, Geometric isomer models

KLB Secondary Chemistry Form 3, Pages 101-102

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethene
Alternative Preparation of Ethene and Physical Properties
Chemical Properties of Alkenes - Addition Reactions

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
Addition reaction charts, Mechanism diagrams, Chemical equation worksheets

KLB Secondary Chemistry Form 3, Pages 102-104

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
Introduction to Alkynes and Triple Bond

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
Alkyne series charts, Triple bond molecular models, Unsaturation comparison charts

KLB Secondary Chemistry Form 3, Pages 108-109

ORGANIC CHEMISTRY I

Nomenclature and Isomerism in Alkynes

By the end of the lesson, the learner should be able to:
Apply IUPAC naming rules for alkynes
Name branched alkynes with substituents
Draw structural isomers of alkynes
Identify branching and positional isomerism

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.

IUPAC naming rules for alkynes, Structural formula worksheets, Molecular model kits

KLB Secondary Chemistry Form 3, Pages 110-111

ORGANIC CHEMISTRY I

Laboratory Preparation of Ethyne
Physical and Chemical Properties of Alkynes
Addition Reactions of Alkynes and Chemical Tests
Uses of Alkynes and Industrial Applications

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
Describe physical properties of alkynes
Compare alkyne properties with alkenes and alkanes
Write combustion equations for alkynes
Explain addition reactions of alkynes

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.
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.

Calcium carbide, Sand, Flat-bottomed flask, Dropping funnel, Gas collection apparatus, Testing solutions
Physical properties charts, Comparison tables, Combustion equation examples
Addition reaction charts, Chemical equation worksheets, Test solutions, Stopwatch for rate comparison
Industrial application charts, Welding equipment demonstration/video, Synthetic fiber samples

KLB Secondary Chemistry Form 3, Pages 111-112
KLB Secondary Chemistry Form 3, Pages 112-113