CCEA A-Level Life and Health Sciences 0008
Experimental Techniques
Human Body Systems
Physical Chemistry in Industrial Processes
Brain ScienceDouble Award
Material ScienceDouble Award
Medicine, Drugs and Clinical TrialsDouble Award
Scientific Method, Investigation, Analysis and Evaluation
Organic Chemistry
Medical PhysicsA2 option
Sound and LightA2 option
Genetics, Stem Cell Research and CloningA2 option
MicrobiologyDouble Award
Oral Health and DentistryDouble Award
Histology and PathologyDouble Award
Analytical Chemistry TechniquesDouble Award
Enabling TechnologyDouble Award
Organic Chemistry
- 10 subtopics
- 30 things to know
- A2 2
What Organic Chemistry covers
Organic Chemistry is examined in Unit A2 2, Organic Chemistry — examined, a core unit. It covers organic formulae, homologous series and functional groups, IUPAC naming and types of organic reaction, structural isomerism and E/Z isomerism, alkanes from crude oil, combustion and halogenation, vehicle pollutants, catalytic converters and biofuels, alkenes, pi bonds and electrophilic addition, classifying alcohols, making ethanol and its effects as a drug, oxidation of alcohols, IR spectroscopy and mass spectrometry, addition polymers, plastic waste and nylon and Preparing and purifying aspirin.
Where it is assessed
A2 2
Organic Chemistry — a written examination, compulsory.
Check the CCEA specification ↗The 10 subtopics
Each one has its own page.
- Organic formulae, homologous series and functional groupsHydrocarbons, empirical and molecular formulae with worked calculations, structural, skeletal and general formulae, homologous series and functional groups.Open →
- IUPAC naming and types of organic reactionIUPAC stems, suffixes and numbering rules with worked names, and addition, elimination, substitution, oxidation, reduction, hydrolysis and polymerisation reactions.Open →
- Structural isomerism and E/Z isomerismChain, position and functional group isomers of alkanes, alcohols and carbonyl compounds, stereoisomers, the conditions for E/Z isomerism, and cis and trans names.Open →
- Alkanes from crude oil, combustion and halogenationAlkanes and their formula, fractional distillation of crude oil, cracking and reforming with equations, complete and incomplete combustion, and the free-radical chlorination of methane.Open →
- Vehicle pollutants, catalytic converters and biofuelsCarbon monoxide, oxides of nitrogen, sulfur dioxide, particulates and unburned hydrocarbons, oil spills, catalytic converters and their limits, and biodiesel and bioethanol against fossil fuels.Open →
- Alkenes, pi bonds and electrophilic additionAlkenes and the bromine water test, naming alkenes, sigma and pi bonds, hydrogenation and margarine, trans fats, electrophilic addition of hydrogen bromide and bromine, and hydration.Open →
- Classifying alcohols, making ethanol and its effects as a drugPrimary, secondary and tertiary alcohols, making alcohols from halogenoalkanes, hydration of ethene and fermentation compared, and ethanol's effects and harms as a recreational drug.Open →
- Oxidation of alcohols, IR spectroscopy and mass spectrometryDehydration of alcohols, oxidation with acidified dichromate to aldehydes, acids and ketones, Benedict's and Fehling's tests, infrared absorptions and the fingerprint region, and mass spectra.Open →
- Addition polymers, plastic waste and nylonAddition polymerisation of ethene and propene, monomers from repeat units, polythene waste, incineration and gas cleaning, recycling and cracking, biodegradable polymers, and nylon-6,6.Open →
- Preparing and purifying aspirinSynthesising aspirin from salicylic acid, filtering and recrystallising the crude product, the iron(III) chloride test, theoretical and percentage yield, melting point purity checks and improving the method.Open →
What you need to know
Answer each one before you reveal it.
A compound contains 40.0% carbon, 6.7% hydrogen and 53.3% oxygen by mass, and its relative molecular mass is 180. What is its molecular formula?
How is crude oil separated by fractional distillation?
Describe the free-radical mechanism for the chlorination of methane.
How does a catalytic converter reduce the harm caused by vehicle emissions?
Compare biofuels with fossil fuels as sources of energy for transport.
Describe the electrophilic addition mechanism for the reaction of ethene with hydrogen bromide.
What are the IUPAC stems for carbon chains of one to six atoms?
What are structural isomers?
What is the general formula of the alcohols?
Write an equation for the dehydration of ethanol by concentrated phosphoric acid.
Why must a monomer contain a C=C double bond to form an addition polymer?
How is aspirin made in the laboratory?
How do suffixes show the functional group in an IUPAC name?
What are the three types of structural isomerism?
What is the general formula of the alkenes?
How are alcohols classified as primary, secondary or tertiary?
Which alkenes form when butan-2-ol is dehydrated?
Write an equation for the formation of poly(ethene) from ethene.
Write the equation for the synthesis of aspirin from salicylic acid.
What is a hydrocarbon?
What rules are followed when numbering a carbon chain in an IUPAC name?
Name the two structural isomers of C₄H₁₀.
What is the general formula of the alkanes?
Which pollutants form when alkane fuels burn in engines?
Why are alkenes described as unsaturated?
Classify butan-1-ol, butan-2-ol and 2-methylpropan-2-ol.
What oxidising agent is used to oxidise alcohols, and what colour change shows that a reaction has occurred?
Write an equation for the formation of poly(propene) from propene.
What type of reaction converts salicylic acid into aspirin?
Take Organic Chemistry further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Empirical formula vs Molecular formula
Empirical formula: the simplest whole-number ratio of atoms of each element in a compound. Molecular formula: the actual numbers of atoms of each element present, a whole-number multiple of the simplest ratio.
Sigma bond vs Pi bond
Sigma bond: a covalent link formed by head-on overlap of orbitals between two nuclei. Pi bond: a covalent link formed by sideways overlap of p orbitals above and below the plane.
Addition polymerisation vs Condensation polymerisation
Addition polymerisation: the joining of unsaturated monomers into a chain with no other product formed. Condensation polymerisation: the joining of monomers with two functional groups each, releasing a small molecule at every link.
Questions from this topic
Each one with the model answer underneath.
- 1
What is a hydrocarbon?
Model answer
A hydrocarbon is a compound made of carbon and hydrogen atoms only. Methane, CH₄, and ethene, C₂H₄, are both hydrocarbons.
- 2
What is the difference between an empirical formula and a molecular formula?
Model answer
An empirical formula gives the simplest whole-number ratio of atoms of each element in a compound. A molecular formula gives the actual number of atoms of each element in one molecule.
- 3
How are the empirical and molecular formulae of a compound related?
Model answer
The molecular formula is a whole-number multiple of the empirical formula. The multiple is the relative molecular mass divided by the empirical formula mass.
- 4
A hydrocarbon contains 85.7% carbon by mass and has a relative molecular mass of 56. What are its empirical and molecular formulae?
Model answer
The empirical formula is CH₂ and the molecular formula is C₄H₈. Hydrogen is 14.3%, and 85.7 ÷ 12 : 14.3 ÷ 1 = 7.14 : 14.3 = 1 : 2. The empirical mass is 14, and 56 ÷ 14 = 4.
- 5
A compound contains 40.0% carbon, 6.7% hydrogen and 53.3% oxygen by mass, and its relative molecular mass is 180. What is its molecular formula?
Model answer
The molecular formula is C₆H₁₂O₆. Carbon gives 40.0 ÷ 12 = 3.33 mol and oxygen 53.3 ÷ 16 = 3.33 mol, against 6.7 mol of hydrogen. The 1 : 2 : 1 ratio gives CH₂O, of mass 30, and 180 ÷ 30 = 6.
- 6
A sample of a hydrocarbon contains 2.4 g of carbon and 0.6 g of hydrogen, and its relative molecular mass is 30. What is its molecular formula?
Model answer
The molecular formula is C₂H₆. Carbon gives 2.4 ÷ 12 = 0.2 mol and hydrogen 0.6 ÷ 1 = 0.6 mol, a 1 : 3 ratio. The empirical formula CH₃ has mass 15, and 30 ÷ 15 = 2.
What is inside Levo
Six ways to work the same material.
Organic Chemistry revision questions
- What does Organic Chemistry cover in CCEA A-Level Life and Health Sciences?
- 10 subtopics: organic formulae, homologous series and functional groups, iupac naming and types of organic reaction, structural isomerism and e/z isomerism, alkanes from crude oil, combustion and halogenation, vehicle pollutants, catalytic converters and biofuels, alkenes, pi bonds and electrophilic addition, classifying alcohols, making ethanol and its effects as a drug, oxidation of alcohols, ir spectroscopy and mass spectrometry, addition polymers, plastic waste and nylon and preparing and purifying aspirin. Each one has its own page with questions and model answers.
- How is Organic Chemistry organised?
- By the CCEA 0008 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in Organic Chemistry, on a schedule.
Attempt a question from memory, write the correct version, then attempt it again. Levo records the jump between your first attempt and your last, and brings each question back on the day you are due to forget it.
Or £46 a year, about £3.83 a month. Cancel anytime.