Stereochemistry 1200-1STERW6
The course covers the following subjects: molecular geometry and chemical bonding; inter- and intramolecular nonbonding interactions; basic principles of stereoelectronic effects; structure of molecules (constitution, configuration, conformation); stereoisomerism - nature of enantiomers and diastereomers; basic concepts of symmetry operations and point groups; macroscopic consequences of the symmetry and dissymmetry of molecules; relative and absolute configuration; conformational analysis; computer-assisted energy estimation and ab initio calculations; stereochemistry of alkanes; conformation of acyclic molecules; conformation of cyclic molecules; prostereoisomerism, prochirality, heterotopic ligands and faces. Stereogenic centres other than carbon atom. Chirality in molecules without the presence of chiral centre - chiral axis and chiral plane. Chirality in macromolecules. Chiroptical properties and chiroptical methods
Type of course
Prerequisites (description)
Learning outcomes
Good knowledge on modern static stereochemistry.
Assessment criteria
Final egzam in written or oral form.
Practical placement
Not applicable.
Bibliography
1. E. L. Eliel, S.H. Wilen, "Stereochemistry of Organic Compounds", John Wiley & Sons, New York, 1994.
2. M. J. T. Robinson, "Organic Stereochemistry", Oxford Univ. Press, Oxford, 2000
Additional information
Additional information (registration calendar, class conductors, localization and schedules of classes), might be available in the USOSweb system: