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The document discusses optical isomerism, which involves the spatial arrangements of groups around a chiral atom that can rotate plane-polarized light. It distinguishes between dextrorotatory (denoted by (+)) and laevorotatory (denoted by (-)) substances, highlighting that a mixture of equal amounts of both isomers is optically inactive. Examples provided include 2-chlorobutane and lactic acid, emphasizing the equal magnitude but opposite signs of their optical rotations.
- Author
- kadammabhii
- Language
- EN