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Learn about the concept of chirality and how it relates to nonsuperimposable objects and isomers. Discover how to identify molecules with stereo carbons, specify stereo centers using the R/S system, and assign R or S configurations based on priority.
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Know what is meant by chiral and how it relates to nonsuperimposable objects and isomers • Objects that are not superposable on their mirror images are chiral (from the Greek: cheir, hand). • They show handedness. • The most common cause of chirality in organic molecules is the presence of a carbon with four different groups bonded to it. • A carbon with four different groups bonded to it is called a stereocenter.
How to identify molecules with stereo carbons • *Straight Chain alkanes • *Cycloalkanes
Because stereoisomers are different compounds, each must have a different name. • Here are the stereoisomersof the over-the-counter drug ibuprofen. • The R,S system is a way to distinguish between sterioisomers without having to draw them and point to one or the other.
How to specify stereo centers: the R & S system • The first step in assigning an R or S configuration to a stereocenter is to arrange the groups on the stereocenter in order of priority. • Priority is based on atomic number. • The higher the atomic number, the higher the priority. • Use the next table as a guide
To assign an R or S configuration: 1. Assign a priority from 1 (highest) to 4 (lowest) to each group bonded to the stereocenter. 2. Orient the molecule in space so that the group of lowest priority (4) is directed away from you; the three groups of higher priority (1-3) then project toward you. 3. Read the three groups projecting toward you in order from highest (1) to lowest (3) priority. 4. If reading the groups 1-2-3 is clockwise, the configuration is R; if reading them is counterclockwise, the configuration is S.