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Principles in
STEREOCHEMISTRY
Prof.Dr  Adel Selem
By: Mahmoud Galal Zidan
Lecture 1
Historical Background
•
•
Acidimetric carbon atom which
attached with four different
function• 2-butanol
• 2 Cl – Butane
• Lactic acid (2-Hydroxypropionic acid )
Isomerism 2n where n is the no of athemetric Carbon
Carbon not athemetric because of C=O
Pair of enantiomers
• Are two optically active isomers each one is the mirror image of
the other
• They have identical properties
• One of them rotate the light to the right an another rotate the
light to the left
Racemic Mixture
• When two enantiomers are mixed together a rotation caused
by a molecule of one isomer is exactly canceled by an equal
and opposite rotation caused by a molecule of its enantiomer
• Or it’s the mixture of equal amount of optical inactive .
Compound containing one
asymmetric carbon atom
• Glyceraldehyde C3H6O3 ( CnH2nOn )
Compound containing two
dissimilar asymmetric carbon
atom• aldoTetriose
OH In right  D
OH In left  L
Diastereomers
(1,4) . (2,3) one of the is not mirror image to other but they are
non super possible – they have different physical properties .
• 2,3 dichloropentane
• Amino Acid ( alanine )
Compound containing two similar
asymmetric carbon atom
• 2,3 dichloropentane
• Aldopentose
Lecture 2
Absolute Configuration
• Chloro Bromo Iodo Methane
• Mesoform : is the isomers containing plane of symmetry
Plane of symmetry
• Glyceraldehyde
• Aldo Tetrose
• Tartaric acid
• Aldopentose
Racemic Mixture
• Formation of ( Cyano hydrides )
• Formation of ( α – halo acid )
• Malonic Ester
• Ethyl acetate

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