Optical isomerism is a form of isomerism (specifically stereoisomerism) whereby the different 2 isomers are the same in every way except being non-superimposable mirror images of each other. Optical isomers are known as chiral molecules Optical isomers are often called stereoisomers (in fact, stereoisomers constitute a more general group, since stereoisomerism needn't necessarily imply optical activity). Two types of molecules which differ only in their relative stereochemistry are said to be enantiomers of each other. A mixture of equal amounts of both enantiomers is said to be a racemic mixture. This form of isomerism can arise when an atom (usually carbon) is surrounded by four different functional groups. Swapping two of the groups round can arise in two different molecules - mirror images of each other. A rule for determining which isomeric form (usually called D-... and L-.. an amino acid is, is called the CORN rule. The groups: COOH, R, NH2 and H (where R is an unnamed carbon chain) -- - - are arranged round the chiral center C-atom. If the above groups are arranged clockwise round the atom then it is the L-form. Anticlockwise means the D-form. Properties of optical isomers They are identical with respect to ordinary chemical reactions, but differences arise when they are in the presence of other chiral molecules. For example Spearmint chewing gum and Caraway seeds respectively contain L-carvone and D-carvone - enantiomers of carvone. These smell differently to most people because our taste receptors also contain chiral molecules which behave differently in the presence of different enantiomers. D-form Amino acids tend to taste sweet whereas L-forms are usually tasteless. This is again due to our chiral taste molecules. The smells of oranges and lemons are examples of the D and L enantiomers. Penicillin works by stereoisomeric means. The antibiotic only works on peptide links of D-alanine which occur in the cell walls of bacteria - but not in humans. The antibiotic can only kill the bacteria and not us because we don't have these D-amino acids. The anti-nausea drug Thalidomide was widely prescribed to pregnant women until it was linked to birth defects. It was later discovered that one enantiomer was responsible for the teratogenic effects. (*)The term non-superimposable distinguishes mirror images which are superimposable, such as the mirror image of the letter "A", on the original, from those that aren't. The classic example of this are human hands--the left hand is a non-superimposable mirror image of the right hand: No matter how the two hands are oriented relative to one another, one cannot line up all the major features of one hand with the other, whereas such an operation is trivial for a non-chiral mirror image (e.g., our letter "A"). (**)The convention of designating one enantiomer of some compounds as D-, and the other as L-, leads to considerable confusion. This designation does not indicate which enantiomer is dextrorotatory and which is levorotatory. Rather, it says that the compound's stereochemistry is related to that of the dextrorotatory or levorotatory enantiomer of glyceraldehyde. Nine of the nineteen L-amino acids commonly found in proteins are dextrorotatory (at a wavelenght of 589 nm), and D-fructose is also referred to as levulose because it is levorotatory. The designations (+) and (-), however, indicate optical isomers that rotate plane polarized light to the right and left, repectively. A new approach, the Cahn Ingold Prelog priority rules, uses the R-... or S-... to name the chiral molecules based on the atomic numers of the atoms or groups of atoms, the ligands, that are attached to the chiral center. The ligands are given a priority (the higher the atomic number the higher the priority) and if the priorities increase in a clockwise direction, they are said to be R-.... Otherwise, if they are prioritized in a counterclockwise direction they are said to be S-.... The R-... / S-... scheme is not mappable to any of the previously mentioned notations; they are based on the direction of rotation of polarized light and the R-... / S-... scheme is based on atomic number. One cannot predict the other. Photons in polarized light all oscillate in a geometric plane as opposed to the random oscillations they present normally. That plane is bisected by an axis determined by the photon's direction of travel. In otherwords: optically active isomers rotate the plane that the photons oscillate in. The polarized light is actually rotated in a racemic mixture as well but it is rotated to the left or right each time it passes through the one of the two optically active isomers, that are actually enantiomers of each other, and yielding a net rotation of zero degrees. Since it is rotated a small amount each time it interacts with or passes through the atoms and particles that make up an optically active molecule. This assumes that it will pass through an equal number of dextro and levo molecules. The rules of entropy should assure such a system. And give us equations to calculate the rotation of the polarized light based upon the concentrations of all of the optically active isomers in the solution, and the amount of solution that the polarized light passes through. Somebody want to play "fill in the data?" Stereoisomers Stereoisomers have the same atoms and groups but different positions in space. There are two types of stereoisomers, geometrical isomers and optical isomers. Chiral isomers These have a requirement that they must possess a tetrahedral carbon atom to which four different atoms or groups are attached. These isomeric structures form two non-superimposable mirror images. This is called chirality or handedness, and is also known as optical isomerism. * a chiral centre R-isomer S-isomer chiral isomers form non-superimposable mirror images Properties of optical isomers Optical isomers rotate the plane of polarised light. The extent of the rotation is proportional to the concentration of the solution. i.e. One isomer might rotate plane of polarised light 10° to the left (laevorotatory) and the other might rotate plane of polarised light10° to the right (dextrorotatory). For most biochemical molecules the isomers are distinguished as the D- or L- structures, e.g. D-glucose is the optical isomer of L-glucose. Only one chiral isomer is generally found in Biochemistry, thus the amino acids that form the structure of proteins are L-amino acids, and the sugars found in our diet are D-sugars. Optical isomerism From Wikipedia, the free encyclopedia. optical isomers: isomers that are mirror images of each other and that are optically active. Optical isomers are compounds that by the nature of their "handed" or chiral structure have the ability to rotate polarized light from a standard reference plane. Structurally, optical isomers differ in the placement of atoms about a chiral center. The easiest way to identify a chiral center is to remember that a chiral center has no axis of symmetry. To satisfy this, a chiral carbon must have four different groups attached to it. Chiral carbons can be separated into two absolute configurations, R and S. In order to decide the absolute configuration, the groups attached to the chiral carbon should be numbered from 1-4, giving #1 to the group of highest priority , #2 to the second highest, #3 to the third highest and #4 to the fourth. Priority is given to groups that are or contain atoms of higher atomic number, and then to the larger of the hydrocarbon chains. After the priority is assigned, the molecule must be drawn to depict the group of the least priority, #4, pointing into the plane of the page. If the priority can be counted clockwise the molecule has the R configuration. If the priority can be counted counterclockwise, it has the S configuration. polarimeter An instrument for measuring the state of polarization of a beam of light or other form of electromagnetic radiation.