A?chiral?centre?in a molecule is a carbon atom that has four different atoms or group of atoms attached
This gives rise to two optical isomers which are also called?enantiomers
The enantiomers are?mirror images?of each other and cannot be superimposed
The presence of the chiral centre in the molecule allows two enantiomers to exist which are stereoisomers as the molecules have the same atoms bonded to each other, but they are differently arranged in space
When the molecule contains more than one chiral centre (asymmetric carbon) more than two optical isomers will be formed
If there are two chiral centres, each chiral centre will rotate the plane of polarised light clockwise and anticlockwise
There are?four?possible optical isomers
Each chiral centre gives rise to two optical isomers; therefore, the molecule has a total of four optical isomers
Chiral centres in cyclic molecules
To determine the chiral centre in a cyclic molecule, the carbon bonded to four different atoms or groups of atoms should be found
Eg. 1,2-aminocyclohexanol has two chiral centres so it can form four optical isomers
To decide where the chiral centres are in a cyclic molecule, the carbon atoms bonded to four different atoms or atom groups should be found
Exam Tip
Use a?molecular modelling kit?and make the models of enantiomers to help you understand that the two molecules are non-superimposable and therefore non-identical.
Identifying Chirality & Geometrical Isomerism
Identify chirality
Identifying?chiral?centres?in cyclic and non-cyclic compounds is very straightforward as it is the carbon with four different atoms or atom groups in a molecule
This gives rise to?two?optical isomers
When more than two chiral centres are present, more than two optical isomers exist
A molecule with?three?chiral centres will have?six?optical isomers
A molecule containing chiral centres is called a?chiral molecule
Identifying geometrical isomers
Molecules with restricted rotation about the C-C bond can have geometrical isomers
This includes unsaturated and cyclic compounds
Eg. alkenes and cyclopentane
When the groups are positioned on the same side of the C-C double bond, the compound is a?cis?isomer
When the groups are positioned on opposite sides of the C-C double bond the compound is a?trans?isomer