A formula which shows the simplest whole number ratio of atoms of each element in a compound
Molecular formula
A formula which shows the actual number of atoms of each element in a molecule
Molar gas volume
The volume of one mole of gas under specified conditions of temperature and pressure e.g, 24 dm³ at 20 °C (293K) and one atmosphere pressure
Percentage yield
actual yield / theoretical yield x 100
Atom economy
mass of desired product / total mass of products x 100
Homologous series
Compounds which have the same general formula, similar chemical properties, show a gradation in physical properties and successive members differ by a CH2 unit
Functional group
Reactive group within a compound
Structural isomers
Molecules which have the same molecular formula but a different structural formula
Geometric isomers
Molecules with the same structural formula, but different arrangement of atoms due to the presence of one or more C=C bond
Saturated hydrocarbon
Contains no C=C bond
Hydrocarbon
Contains hydrogen and carbon only
Substitution
Replacing one atom or group with a different atom or group
Homolytic fission
Bond breaking in which one of the shared electrons goes to each atom
Heterolytic fission
Bond breaking in which both electrons in the shared pair go to a single atom
Radical
A particle with an unpaired electron
Unsaturated hydrocarbon
Contains at least one C=C
Sigma bond
A covalent bond formed by the linear overlap of atomic orbitals
Pi bond
A covalent bond formed by the sideways overlap of p orbitals
Bond length
The distance between the nuclei of two covalently bonded atoms
Hydrogenation
Addition of a hydrogen molecule across a C=C
Electrophile
An ion or molecule that attacks regions of high electron density
Primary carbocation
A carbocation which has one carbon atom directly bonded to the positively charged carbon
Secondary carbocation
A carbocation which has two carbon atoms directly bonded to the positively charged carbon
Tertiary carbocation
A carbocation which has three carbon atoms directly bonded to the positively charged carbon
Polymerisation
Joining together of many small molecules (monomers) to form a large molecule
Monomers
Many small molecules which join together to form a polymer
Polymer
A large molecule formed when monomers join together
Primary halogenoalkane
A halogenoalkane which has one carbon atom directly bonded to the carbon atom that is honded to the halogen. (Exceptions are halomethanes.)
Secondary halogenoalkane
A halogenoalkane which has two carbon atoms directly bonded to the carbon atom that is bonded to the halogen
Tertiary halogenoalkane
A halogenoalkane which has three carbon atoms directly bonded to the carbon atom that is bonded to the halogen
Reflux
Repeated boiling and condensing of a (reaction) mixture
Hydrolysis
Breaking up molecules by reaction with water
Nucleophile
An ion or molecule, with a lone pair of electrons, that attacks regions of low electron density
Elimination
A reaction in which a small molecule is removed from a larger molecule
Miscibility
Liquids which mix in all proportions i.e. form a single layer
Primary alcohol
An alcohol which has one carbon atom directly bonded to the carbon atom that is bonded to the -OH group. (Exception is methanol)
Secondary alcohol
An alcohol which has two carbon atoms directly bonded to the carbon atom that is bonded to the -OH group
Tertiary alcohol
An alcohol which has three carbons atoms directly bonded to the carbon atom that is bonded to the -OH group
Ground state (infrared spectroscopy)
A molecular vibration which is in the lowest possible energy state
Wavenumber
The reciprocal of the wavelength and it is measured in cm³