Organic Chemistry Teaching Tools consists of ten lovely topic sets and here we show what's inside each set.
Buy any combination of sets and you'll find they fit together perfectly. You can sort them, rename them, even reclassify them to suit your exam. Whatever the order, you'll enjoy great lessons with a great set of tools.
The Organic Chemistry series topic sets:
- set 1 - alcohols and phenol
- set 2 - alkanes and fuels
- set 3 - alkenes and bonding
- set 4 - amides amines amino acids and nitriles
- set 5 - instrumental methods and synthesis pathways
- set 6 - benzene and methylbenzene
- set 7 - carbonyl compounds carboxylic acids and carbohydrates
- set 8 - haloalkanes and acid chlorides
- set 9 - nomenclature and isomerism
- set 10 - polymers proteins DNA and protein synthesis
1. alcohols and phenol 
alcohols - homologous series - structure
alcohols - classification
alcohols - breaking the RO-H bond - reaction with sodium
alcohols - halogenation with hydrochloric acid and ZnCl2 catalyst
alcohols - breaking the R-OH bond - with phosphorus and iodine
alcohols - breaking the R-OH bond - with hydrogen halide
alcohols - elimination of water - mechanism
alcohols - oxidation - structure
alcohols - triiodomethane reaction
alcohols - breaking the RO-H bond - esterification
alcohols - breaking the RO-H bond - with acyl chlorides
alcohols - breaking the R-OH bond with PCl5
alcohols - elimination of water using concentrated acid
alcohols - breaking the R-OH bond - elimination of water using heat
arenes - phenol – acidity
arenes - phenol - reactions of - OH; sodium and sodium hydroxide
arenes - phenol - reactions of - OH; esterification
arenes - phenol - test using iron(III) chloride
arenes - phenol - reaction of the ring - nitration
arenes - phenol - reaction of the ring - bromination
alkanes and fuels
2. alkanes and fuels
hydrocarbons - introduction
boiling points - intermolecular forces
alkanes - structure - homologous series
cycloalkanes - structure
bonding - hybridisation - bonding in methane
alkanes - IUPAC nomenclature
alkanes - combustion
alkanes – free radical substitution - chlorination
alkanes – free radical substitution
alkanes – reactions - chlorination of methane
alkanes – free radical substitution - chain reaction
alkanes – free radical substitution - chlorination - summary
alkanes – free radical substitution - bromination - exercise
fuels - formation of oil
fuels - fractional distillation
alkanes - fuels - catalytic converter
alkanes – fuels - supply and demand
carbon compounds - reforming alkanes for fuel
alkanes - fuels - acid rain
alkanes - fuels - isomerisation of alkanes for fuel
alkanes – fuels - cracking alkanes for fuel
carbon compounds - thermal cracking of alkanes
alkanes - fuels - octane rating
alkanes - fuels - air pollution
3. alkenes and bonding
alkenes - structure - homologous series
carbon compounds - alkenes – boiling points
alkenes - IUPAC nomenclature
alkenes - IUPAC nomenclature - exercise - cis and trans
alkenes - addition of bromine
alkenes - addition of bromine - mechanism
alkenes - addition of hydrogen
alkenes - addition of hydrogen halide
alkenes - addition of hydrogen halide-mechanism
alkenes - addition of hydrogen halide - Markovnikov's rule
alkenes – addition of water
alkenes - addition with concentrated H2SO4 - mechanism
alkenes - oxidation
bonding - hybridisation - bonding in methane
bonding - hybridisation - bonding in ethyne
bonding - hybridisation - bonding in ethene
set 4 - amides amines amino acids and nitriles
amides - nomenclature
amides - form amines with bromine
amides - hydrolysis
amides - physical properties
amides - reduction
amines – structure
amines – classification
amines – boiling temperature
boiling points – exercise
amines – solubility
amines – complex ions
amines – making amines – reduction of nitriles
amines – making amines – reduction of nitro compounds
amines – acting as bases
amines – with nitric(III) acid
amines – coupling reaction
amines – compared with ammonia
amines – making amines – ammonia and halogenoalkanes
amines – form amides with acyl chlorides
amino acids – optical activity
amino acids – acids and bases
amino acids – form a peptide
amino acids – structure
amino acids – hydrogen bonding
amino acids – hydrolysis of a peptide
nitriles – structure
nitriles – physical properties
nitriles – reduction
nitriles – hydrolysis
nitriles – making nitriles - exercises
set 5 - instrumental methods and synthesis pathways
analysis and detection - mass spectrometry - fragments
analysis and detection - mass spectrometer
analysis and detection – mass spectrometry - exercise
analysis and detection - infrared spectroscopy
analysis and detection – low resolution NMR
analysis and detection – high resolution NMR
analysis and detection – NMR - exercise
reactions - organic synthesis - exercise
reactions - exercise - pathways
set 6 - benzene and methylbenzene
arenes - introduction - benzene
arenes - physical properties - melting and boiling points
arenes - electrophilic aromatic substitution - examples
arenes - electrophilic aromatic substitution - chlorination
arenes - electrophilic aromatic substitution - bromination
arenes - electrophilic aromatic substitution - nitration
arenes - electrophilic aromatic substitution - sulfonation
arenes - electrophilic aromatic substitution - Friedel - Crafts alkylation
arenes - electrophilic aromatic substitution - Friedel - Crafts acylation
arenes - electrophilic aromatic substitution - exercise
arenes - structure of benzene
arenes - methylbenzene compared with benzene
arenes - methylbenzene - activating and deactivating substituents
arenes - methylbenzene - chlorination of side chain
arenes - methylbenzene - oxidation of side chain
set 7 - carbonyl compounds carboxylic acids and carbohydrates
carbonyl compounds - nomenclature
carbonyl compounds - carbon - oxygen double bond
carbonyl compounds - nucleophilic addition
carbonyl compounds - reduction
carbonyl compounds - oxidation
carbonyl compounds - tests - Tollen's reagent
carbonyl compounds - triiodomethane
carbonyl compounds - tests - Fehling's solution
carbonyl compounds - condensation reaction
carboxylic acids – structure
carboxylic acids – making and breaking esters
carboxylic acids – form salts
carboxylic acids – form acyl chloride
carboxylic acids – acid derivatives
carbohydrates - monosaccharides
carbohydrates – alpha and beta glucose
carbohydrates – disaccharides
carbohydrates – polysaccharides
carbohydrates – polysaccharides – hydrolysis
carbohydrates - reducing sugars - Fehling's test
set 8 - haloalkanes and acid chlorides
halogenoalkanes - homologous series - structure
halogenoalkanes- IUPAC nomenclature
halogenoalkanes - classification - exercise
halogenoalkanes – classification
halogenoalkanes - rate of hydrolysis
halogenoalkanes - substitution
halogenoalkanes – elimination or substitution
halogenoalkanes – chlorofluoroalkanes
halogenoalkanes – depletion of the ozone layer
halogenoalkanes - substitution reactions - polarity of C-X
halogenoalkanes - substitution reactions - SN2
halogenoalkanes - substitution reactions - why not SN2
halogenoalkanes - substitution reactions - SN1
substitution reactions: why SN1
halogenoalkanes - substitution reactions - exercise
acid chlorides – structure
acyl chlorides – compared with halogenoalkanes
acid chlorides – with nucleophile
acyl chlorides - with nucleophiles - mechanism
acid derivatives – acid anhydride
set 9 - nomenclature and isomerism
alkanes - IUPAC nomenclature
isomerism - structural isomerism - position isomerism
isomerism - structural isomerism – functional group isomerism
isomerism - stereoisomerism - geometric isomerism - bond rotation
isomerism - stereoisomerism - geometric isomerism
isomerism - stereoisomerism - geometric isomerism - exercises
isomerism - stereoisomerism - optical isomerism - chiral carbon
isomerism - stereoisomerism - optical isomerism - enantiomers
isomerism - stereoisomerism - optical isomerism - optical activity
isomerism -stereoisomerism - optical isomerism - exercises
isomerism - structural isomerism - introduction
isomerism - structural isomerism – chain isomerism
isomerism - structural isomerism - exercise
set 10 - polymers proteins DNA and protein synthesis
polymers – addition and condensation
polymers – condensation polymers
polymers – addition polymers I
polymers – natural polymers – rubber
polymers – addition polymers II
polymers - proteins - wool
polymers - polyalkenes - stereoisomers
polymers - elastomer
polymers - bakelite - nylon - phenol
proteins – primary structure
proteins – secondary structure
proteins – secondary structure - interactions
proteins – secondary structure – interactions
proteins - secondary structure - enzyme inhibitors
proteins – secondary structure – ionic or salt bridges
proteins – secondary structure – exercise
proteins – tertiary structure
proteins – tertiary structure – hydrophobic groups
proteins – quaternary structure – dynamics
proteins – quaternary structure - haemoglobin
proteins – structure – exercise
proteins – enzymes - effect of pH
proteins – enzymes - effect of temperature
proteins – enzymes – effect of concentration
DNA – nucleic acids – model
DNA – base pairs and nucleotides
DNA – nucleic acids – structure
DNA – transcription to mRNA
DNA – translation of mRNA to make protein
help
help – how to use the software
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