Organic Chemistry I - AQA Chemistry A-level

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61 Terms

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Chain isomers

Isomers resulting from branching in the carbon chain

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Displayed formula

Structural isomer showing all bonds between atoms

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Empirical formula

Smallest whole number ratio of atoms in a compound

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E-Z isomerism

Stereoisomerism due to restricted rotation around a double bond

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Free-radical

Molecule with an unpaired valence electron

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Functional group

Atoms responsible for characteristic reactions in a compound

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Functional group isomers

Isomers with different functional groups

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General formula

Empirical formula representing an entire class of compounds

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Homologous series

Compounds with the same functional group and properties

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Molecular formula

Total number of atoms of each element in a compound

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Position isomer

Isomers with the same carbon backbone but different group positions

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Skeletal formula

Diagram showing bonds between atoms with assumed hydrogens

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Stereoisomerism

Isomerism when double bonded carbons have different groups

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Structural formula

Formula showing atom arrangement but not all bonds

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Structural isomerism

Compounds with the same molecular but different structural formula

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Catalytic converter

Device reducing emissions in a car using a catalyst

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Catalytic cracking

Cracking at high temperature with a zeolite catalyst

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Combustion of alkanes

Process releasing energy by oxidising carbon and hydrogen

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Cracking

Process breaking C-C bonds in alkanes to produce shorter chains

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Crude oil

Finite resource from ancient biomass, mainly hydrocarbons

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Fractional distillation

Separating substances by boiling points, e.g., crude oil fractions

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Hydrocarbons

Compounds of carbon and hydrogen only

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Saturated

Organic compounds with single C-C bonds

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Thermal cracking

High temp cracking producing alkenes

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Chlorofluorocarbons

CFCs containing carbon, chlorine, and fluorine

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Electrophile

Electron acceptor in organic reactions

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Elimination

Reaction forming a C=C bond by losing atoms

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Free radicals

Species with unpaired electrons

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Free radical substitution

UV light reaction forming halogenoalkanes

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Nucleophile

Donates electron pair to form covalent bond

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Nucleophilic substitution

Electron pair donor replacing a species

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Ozone

Forms naturally, absorbs UV radiation

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Ozone depletion

Chlorine catalyses ozone decomposition

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Polar bond

Unequally distributed electron covalent bond

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Addition polymer

Polymer from addition polymerisation of C=C monomers

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Addition polymerisation

Formation of addition polymers from short chain monomers

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Alkenes

Unsaturated hydrocarbons with C=C bond

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Carbocation

Carbon atom with a positive charge

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Major/minor products

Products from electrophilic addition based on stability

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Monomer

Short chain molecule forming a polymer

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Plasticiser

Chemical added to polymers for flexibility

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Polymer

Long-chain molecules from small monomers

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Repeat unit

Part of a polymer forming the complete polymer chain

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Unsaturated

Organic compounds with at least one C=C bond

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Alcohols

Contain -OH functional group; e.g., methanol, ethanol

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Biofuel

Fuel derived from living matter, e.g., ethanol

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Carbon-neutral fuel

Fuel with no net increase in atmospheric CO2

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Distillation

Separating liquids by boiling point differences

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Fermentation of glucose

Industrial process producing ethanol from glucose

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Hydration of alkenes

Process to produce alcohols from alkenes

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Oxidation of alcohols

Alcohols react with acidified potassium dichromate

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Aldehyde

Molecule with C=O group forming silver mirror with Tollens’ reagent

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Alkene

Molecule with C=C group decolourising bromine water

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Carboxylic Acid

Molecule with COOH group reacting with sodium carbonate

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Functional Group

Atoms responsible for characteristic compound reactions

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Infrared Spectroscopy

Technique to identify bonds and functional groups in molecules

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Mass Spectrometry

Identifies compounds and determines molecular mass

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Molecular Formula

Total atoms of each element in a compound

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Relative atomic mass

Average mass of an element's atom compared to carbon-12

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Relative molecular mass

Average mass of one molecule compared to carbon-12

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Wavenumber

Represents energy and frequency of absorbed IR radiation