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Chapter 5 STEREOCHEMISTRY Stereochemistry
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CHIRALITY AND ENATIOMERS 1.Chiral Object – an object that IS NOT superimposable with its mirror image. 2.Achiral Object – an object that IS superimposable (i.e. identical) with its mirror image. 3.Enantiomers – stereoisomers, which are non- superimposable mirror images. Stereochemistry
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CHIRAL CARBON ATOMS ** mirror Stereochemistry 1.Chiral Carbon Atoms (also known as asymmetric carbon atoms) – carbon atoms bonded to FOUR DIFFERENT groups. Chiral atoms are generally called chiral centers. 2.Some rules: A.If a molecule has NO chiral center, it is usually, but not necessarily achiral. B.If a molecule has just ONE chiral center, it is definitely chiral. C.If a molecule has MORE THAN ONE chiral center, it may or may not be chiral.
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THE MIRROR IMAGES OF CARBON CENTERS WITH THREE DIFFERENT SUBSTITUENTS ARE SUPERIMPOSABLE IDENTICAL WITH THE ORIGINAL 120 o mirror Stereochemistry
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THE MIRROR IMAGES OF CARBON CENTERS WITH FOUR DIFFERENT SUBSTITUENTS (CHIRAL CARBON ATOMS) ARE NOT SUPERIMPOSABLE NOT IDENTICAL WITH THE ORIGINAL 120 o mirror *** Stereochemistry
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CARBON CENTERS WITH FOUR DIFFERENT SUBSTITTUENTS (CHIRAL CARBON ATOMS) DO NOT HAVE INTERNAL MIRROR PLANES OF SYMMETRY Stereochemistry
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CHIRAL COMPOUNDS ALSO DO NOT HAVE INTERNAL MIRROR PLANES OF SYMMETRY MIRROR IMAGE IDENTICAL WITH ORIGINAL MIRROR IMAGE IS NOT IDENTICAL WITH ORIGINAL Stereochemistry
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THE CAHN – INGOLD – PRELOG CONVENTION 1.Assign a “priority” and a number to each group, bonded to the chiral carbon atom. Highest priority group gets number 1, second in priority – number 2, third in priority – number 3, lowest in priority – number 4. a.First compare the atoms immediately bonded to the chiral center. The atom with highest atomic weight is highest in priority and therefore # 1, the atom with lowest atomic weight is #4. b.If two or more atoms of the immediate environment are identical, compare the next set of atoms along the chains, applying the criterion from (a). REMEMBER: One higher-priority atom is more important than any number of lower-priority atoms. Stereochemistry
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THE CAHN – INGOLD – PRELOG CONVENTION c.Treat double- and triple-bonded atoms as an equivalent number of single-bonded atoms, i.e. imagine that the - bonds are broken and the atoms at both ends of the bond are duplicated (if it is a double bond) or triplicated (if it is a triple bond). Stereochemistry
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THE CAHN – INGOLD – PRELOG CONVENTION R S 2. Orient the molecule in a fashion such that the lowest in priority group (number 4) is in back and view the molecule along the bond from the chiral center to group #4. Draw a curved arrow, starting from #1, through #2, to #3. If the arrow points in a clockwise direction – R-enantiomer, if the arrow points in a counter-clockwise direction – S-enantiomer. Stereochemistry
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THALIDOMIDE: DISASTROUS BIOLOGICAL ACTIVITY OF THE “WRONG” ENANTIOMER Stereochemistry
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