Results 1–6 of 6 for enantiomer
Enantiomers are a chiral molecule and its non-superposable mirror image. The two forms rotate the plane of polarised light by equal amounts in the opposite directions. Also called optical isomers.
Diastereoisomers (diastereomers) are stereoisomers of a compound having two or more chiral centers that are not a mirror image of another stereoisomer of the same compound. For example, in the structure below, 1 and 2 are enantiomers and so are 3 and 4; 1 and 3 are diastereoisomers, as are 2 and 4. Unlike enantiomers, diastereoisomers need not have closely similar physical and chemical properties
Racemic mixture is a mixture of dextrorotatory and levorotatory optically active isomers in equal amounts. Because the two enantiomers rotate plane-polarised light in opposite directions, a racemic mixture does not rotate plane-polarised light. These mixtures are prefixed by ± or dl-.
Racemisation is a conversion, by heat or by chemical reaction, of an optically active compound into an optically inactive form which half of the optically active substance becomes its miror image (enantiomer).
Resolution is a process by which a racemic mixture is separated into its two pure enantiomers.
Stereoisomers are compounds that have identical chemical constitution, but differ as regards the arrangement of the atoms or groups in space. Stereoisomers fall into two broad classes: optical isomers (enantiomers) and geometric isomers (cis-trans).
Generalic, Eni. "Enantiomer." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
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