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Enantiotopic groups are identical and indistinguishable except in chiral environments. For instance, the CH 2 hydrogens in ethanol (CH 3 CH 2 OH) are normally enantiotopic, but can be made different (diastereotopic) if combined with a chiral center, for instance by conversion to an ester of a chiral carboxylic acid such as lactic acid, or if coordinated to a chiral metal center, or if ...
One example is [Ru(NH 3) 5 (SMeEt)] 2+. The complex cis-VOCl 2 (SMeEt) 2 exists as meso- and a pair of enantiomers. [7] In complexes of thioethers of the type S(CH 2 R) 2 (R ≠ H), the methylene protons are diastereotopic. Examination of the NMR spectra of such complexes reveal that they undergo inversion at sulfur, without dissociation of the ...
Symmetrical norbornanes and similarly rigid compounds (e.g. 7-oxabicyclo[2.2.1]heptane) also show complex signals for the ethylene fragments, made more complicated by additional splitting by the bridgehead protons. Reich gives several additional examples of magnetic inequivalence in acyclic and cyclic systems containing H 2 C-CH 2 fragments. [3]
These are biblical figures unambiguously identified in contemporary sources according to scholarly consensus.Biblical figures that are identified in artifacts of questionable authenticity, for example the Jehoash Inscription and the bullae of Baruch ben Neriah, or who are mentioned in ancient but non-contemporary documents, such as David and Balaam, [n 1] are excluded from this list.
For example, Cp′Fe(PPh 3)(CO)I has four different signals in the 1 H NMR spectrum for the ring hydrogens and five different signals in the 13 C NMR spectrum for the ring carbons. There is therefore no symmetry within the ring even accounting for rotation around the ring–metal axis, but instead there is a diastereotopic relationship as a ...
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