Jump to content

Topicity

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Leyo (talk | contribs) at 16:22, 27 September 2007 (de:). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

In chemistry, topicity is the stereochemical relationship of substituents relative to the structure to which they are attached. Depending on the relationship, such groups can be homotopic, enantiotopic, or diastereotopic.

Homotopic

Homotopic groups in a chemical compound are equivalent groups. Two groups A and B are homotopic if the molecule remains the same (including stereochemically) when the groups are interchanged with the remaining parts of the molecule fixed. Homotopic atoms have the same chemical shift in an NMR spectrum.

Enantiotopic

The stereochemical term enantiotopic refers to the relationship between two groups attached to the same atom which, if replaced, would generate compounds that are enantiomers.

For example, the two hydrogen atoms attached to the second carbon in butane are enantiotopic. Replacement of one hydrogen atom (colored blue) with a bromine atom will produce (R)-2-bromobutane. Replacement of the other hydrogen atom (colored red) with a bromine atom will produce the enantiomer (S)-2-bromobutane.

Butane (R)-2-bromobutane (S)-2-bromobutane

Diastereotopic

The stereochemical term diastereotopic refers to the relationship between two groups attached to the same atom which, if replaced, would generate compounds that are diastereomers.

For example, the two hydrogen atoms attached to the third carbon in (S)-2-bromobutane are diastereotopic. Replacement of one hydrogen atom (colored blue) with a bromine atom will produce (2S,3R)-2,3-dibromobutane. Replacement of the other hydrogen atom (colored red) with a bromine atom will produce the diastereomer (2S,3S)-2,3-dibromobutane.

(S)-2-bromobutane (2S,3R)-2,3-dibromobutane (2S,3S)-2,3-dibromobutane

See also