# Nomenclature of optical isomers

The nomenclature of optical isomers: The d/l system was developed by Fischer and Rosanoff around 1900. Totally arbitrarily, (+) glyceraldehyde was defined as being D because the OH group attached to the C2 is on the right-hand side of the molecule. While (–) glyceraldehyde was defined as L because the OH group is on the left-hand side.

(1) The d/l system (named after the Latin dexter and laevus, right, and left) names the molecules by relating them to the molecule glyceraldehyde. This system of nomenclature represents an older system for distinguishing enantiomers of amino acids and carbohydrates. This arbitrary type of configuration (d/l system) is known as “Relative Configuration.”

(a) To name complex amino acids and carbohydrates in Fischer projection, take the carbonyl group (aldehyde, ketone or carboxylic acid) on the top and CH2OH on the bottom.

(b) The D descriptor is used when the –OH or –NH2 on the 2nd carbon (from bottom) points to the right and L is used when the –OH or –NH2 points to the left. Thus, from the stereochemistry of only one stereocenter (i.e. 2nd carbon from the bottom) the stereochemistry of all other stereocenters in the molecule is defined.

(c) The d/l nomenclature does not indicate which enantiomer is dextrorotatory and which is levorotatory. It just says that the compound’s stereochemistry is related to that of the dextro – or Levo – enantiomer of glyceraldehyde. For example, d-fructose is levorotatory. Hence, it is stated that all-natural amino acids are L while natural carbohydrates are D. Thus, (+) glucose has the D-configuration, and (+) ribose has the L-configuration.

## The Cahn Ingold Prelog (CIP) Sequence Rule

An absolute configuration refers to the spatial arrangement of the atoms of the chiral molecules and its stereochemical description using terms (R) or (S). Cahn, Ingold, and Prelog introduce Sequence Rules to assign an order of priority to the atoms or the groups directly attached to a stereocenter. The absolute configuration of a given stereocenter is defined as either (R) or (S) by applying these rules.

Rule 1: Atom of higher atomic number is given priority over those of lower atomic number e.g.,
I > Br > Cl > F >O > N > C > H.
Rule 2: Isotope of higher atomic weight takes precedence. e.g., 3H (tritium) > 2H (deuterium) > 1H (hydrogen)
Rule 3: When two or more atoms directly attached to a stereocenter are the same, the order of priority depends on the next atom along the chain. e.g.,
–CO2CH3 > –CO2H > CONH2 > COCH3 > CHO > CH2OH

Rule 4: If an atom is double bonded to another atom, treat it as if it were singly bonded to two of those atoms. If an atom is triply bonded to another atom, treat it as if it were singly bonded to three of these atoms. Convert the unsaturated group directly attached to the stereocenter into the saturated group to decide the order of priority e.g.,

Assign the numbers to the functional groups in the order of priority using the above sequence rules. Draw a generic tetrahedral center and position the molecule so that the atom/group with the lowest priority projects the most into space. The (R) – configuration is assigned to a clockwise decreasing order, while the (S) – configuration is given to an anti-clockwise decreasing order.

Rule 5: A longer group may not necessarily have a higher priority over another smaller group. e.g. –CH2Cl has a higher priority than –CH2CH2CH2CH3.
Rule 6: If the lowest priority group is in the front of the plane of the molecule then the assignment is reversed. i.e., clockwise is S and anticlockwise is R.

Rule 7: If there are multiple chiral carbons in a molecule, the configuration of the entire molecule can be defined by using a number that specifies the location of the stereocenter preceding configuration e.g., (1R, 4S). e.g.,

Also read: Elements of symmetry