In stereochemistry, topicity is the stereochemical relationship between substituents and the structure to which they are attached. Depending on the relationship, such groups can be heterotopic, homotopic, enantiotopic, or diastereotopic.
In stereochemistry, topicity is the stereochemical relationship between substituents and the structure to which they are attached. Depending on the relationship, such groups can be heterotopic, 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 achiral when the groups are interchanged with some other atom (such as bromine) while the remaining parts of the molecule stay fixed. Homotopic atoms are always identical, in any environment. Homotopic NMR-active nuclei have the same chemical shift in an NMR spectrum. For example, the four hydrogen atoms of methane (CH4) are homotopic with one another, as are the two hydrogens or the two chlorines in dichloromethane (CH2Cl2).
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).