Unit 13 - An introduction to basic organic chemistry Flashcards
Describe structural formula
Shows how many, and the symbols of, atoms bonded to each carbon atom in an organic molecule (e.g. CH₃CH=CHCH₂CH(OH)CH₃)
Describe displayed formula
A 2D represenation of an organic molecule showing all its atoms and bonds
Define homologous series
A group of organic compounds having the same functional group where each successive member differs by CH₂
Define functional group
An atom or group of atoms in an organic molecule which determines its chemical properties
Define aliphatic compounds
Straight chain or branched chain organic compounds and also cycle organic compounds (alicylcic) that do not contain Benzene (aromatic)
Describe a sigma bond (s)
A single covalent bond formed by the ‘end on’ overlap of atomic orbitals
Describe a pi bond (p)
A covalent bond formed by the ‘sideways’ overalp of p and p or p and d atomic orbitals
Define a structural isomer
Compounds with the same molecular formula but different structural formula
Define a stereoisomer
Compounds with the same structural formula but a different arrangement of atoms in space
Define an optical isomer (enantiomer)
Compounds with mirror images that cannot be superimposed
Describe a chiral centre
A carbon atom with four different atoms or groups of atoms attached
Define homolytic fission
The breaking of a covalent bond where electrons are shared equally with atoms in the bond
Define heterolytic fission
The breaking of a covalent bond where both electrons move onto one of the atoms in the bond
Define a carbocation
An alkyl group with a single positve charge on one of its carbon atoms (e.g. CH₃+)
Describe inductive effect
The uneven sharing of electrons along a covalent bond. Electron donating species (e.g. alkyl groups) have a positive inductive effect. Electron withdrawing species (e.g. oxygen) have a negative inductive effect