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Date: 17-9-2020
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Date: 25-3-2016
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Date: 8-1-2020
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The "right hand" and "left hand" nomenclature is used to name the enantiomers of a chiral compound. The stereocenters are labeled as R or S.
Consider the first picture: a curved arrow is drawn from the highest priority (1) substituent to the lowest priority (4) substituent. If the arrow points in a counterclockwise direction (left when leaving the 12 o' clock position), the configuration at stereocenter is considered S ("Sinister" → Latin= "left"). If, however, the arrow points clockwise,(Right when leaving the 12 o' clock position) then the stereocenter is labeled R ("Rectus" → Latin= "right"). The R or S is then added as a prefix, in parenthesis, to the name of the enantiomer of interest.
Example
(R)-2-Bromobutane
(S)-2,3- Dihydroxypropanal
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