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amines amino acids and proteins
amides
chirality
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Form of stereoisomerism -
molecules
with same
structural
formula but different
spatial
arrangements
of atoms/groups
Occurs when organic molecules have a
chiral centre
-
C atom
with
4
different
atoms/groups atoms attached
Isomers are NON-SUPERIMPOSABLE (can't be placed on
top
of each other)
mirror
images of each other
optical isomers are also referred to as
enantiomers
For each
chiral
centre there are
2
possible isomers
Total number of
isomers
= 2 to the power of the number of
chiral
centres
e.g. 1 chiral centre =
2
isomers (2 to the power of 1)
2 chiral centres =
4
isomers (2 squared)
5 chiral centre =
32
isomers (2 to the power of 5)
a type of stereoisomerism is
optical
isomerism
optical isomers are found in molecules that contain a
chiral
centre