Mar 12, 2007 · Two molecules that are non-superimposable, non-mirror images are called diastereomers. The left pair are the (2R,3R) and the (2R,3S) compounds. The right pair are …

We can draw 3-dimensional structures for these molecules based on the tetrahedral structure of their C atoms and we know that they have many different conformations due to rotation about …

The (2R,3R) and (2S,3S) stereoisomers are enantiomers (different mirror images). There are two pairs of diastereomers: (2R,3R) and (2R,3S); (2S,3S) and (2R,3S).

compounds with more than 2 stereocenters have more than 2 stereoisomers e.g., 2-bromo-3-chlorobutane (2R,3R) and (2S,3S) are enantiomers (2R,3S) and (2S,3R) are enantiomers in …

compounds with more than 2 stereocenters have more than 2 stereoisomers e.g., 2-bromo-3-chlorobutane (2R,3R) and (2S,3S) are enantiomers (2R,3S) and (2S,3R) are enantiomers in …

Aldrich-237639; (2R,3R)- (-)-2,3-Butanediol 0.97; CAS Number: 24347-58-8; Linear Formula: CH3CH (OH)CH (OH)CH3; find related products, papers, technical documents, MSDS & more …

There is, first of all , a pair of enantiomeers: these are the (2R,3R) and (2S,3S) isomers. Note that the mirror image of 2R,3R is 2S,3S ( i.e., the mirror image inverts the configuration at each …

make a general comparison of the physical properties of the enantiomers, meso form and racemic mixture of a compound such as tartaric acid. Make certain that you can define, and use in …

Sep 10, 2020 · When my textbook is discussing stereoisomers with more than one chiral centers, it's using notation like (2 S,3 S) being an enantiomer with (2 R,3 R) and so forth.

Any other pair, such as 2R,3R and 2S,3R, are diastereomers of each other, since they are stereoisomers that are not enantiomers (not mirror images of each other).