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Optical isomerism naming enantiomers

In optical isomerism it becomes essential to give name to the enantiomers, because the formulas can not be employed in oral speech. Therefore, the following systems were evolved. [Pg.129]

Tetrahedral complexes du not exhibit geometrical isomerism. However, they are potentially chiral just as is tetrahedral carbon. The simple form of optical isomerism exhibited by most organic enantiomers, namely four different substituents, is rarely observed because substituents in tetrahedral complexes are usually too labile10 for the complex to be resolved, i.e., they racemize rapidly. However, an interesting series of cyclopentadienyliron phosphine carbonyl compounds (see Chapter 15 for further... [Pg.781]


See other pages where Optical isomerism naming enantiomers is mentioned: [Pg.200]    [Pg.995]    [Pg.1030]    [Pg.72]    [Pg.101]    [Pg.276]    [Pg.180]    [Pg.280]    [Pg.342]    [Pg.8]   


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