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Questa Cmap, creata con IHMC CmapTools, contiene informazioni relative a: Stereoisomers, stereoisomers are possible only due to either rigidity elements in the molecule structures, two ring substituents are blocked by the ring in either trans isomer configuration, rigidity elements in the molecule structures are double bonds, exchanging group positions on the same carbon gives no structure change if are symmetric tetrahedral structures, exchanging group positions on the same carbon gives no structure change if are symmetric alkenes, stereoisomers are possible only due to either asymmetry in the molecule structures, ring molecules can bear two ring substituents, double bonds are rigid (not rotable), priority groups on the same side ZUSAMMEN this is because of priorities Left: Winner = ethyl > methyl Right: W = methyl > hydrogen, cis isomer configuration have ring substituents on the same side, Z isomer configuration have priority groups on the same side ZUSAMMEN, rigidity elements in the molecule structures gives rise to Z-E and cis-trans isomery, rigidity elements in the molecule structures are ring molecules, rigid (not rotable) blocked as TRANS = \_ \ shaped main chain, stereoisomers are obtained by exchanging group positions on the same carbon, rigid (not rotable) thus blocking configuration in either E isomer configuration, E isomer configuration have priority groups on opposite sides ENTGEGEN, trans isomer configuration have ring substituents on opposite sides, rigid (not rotable) blocked as CIS =\_/ shaped main chain, asymmetry in the molecule structures as in mirror-like enantiomers