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In chemistry, racemization is a conversion, by heat or by chemical reaction, of an optically active compound into a racemic (optically inactive) form. This creates a 1:1 molar ratio of enantiomers and is referred to as a racemic mixture (i.e. contain equal amount of (+) and (−) forms). Plus and minus forms are called dextrorotation and levorotation. The…
Biological significance, Formation of racemic mixtures & Stereochemistry
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enantiomers racemic enantiomer racemate forms form equal chiral also pure mixture one reactions produce chemical reaction different may pharmaceutical properties
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Racemization | is a | conversion | 0.90 | text |
| Racemization | related to Formation of racemic mixtures | For | 0.60 | section |
| Racemization | related to Formation of racemic mixtures | NaOH | 0.60 | section |
| Racemization | related to Formation of racemic mixtures | HCl | 0.60 | section |
| Racemization | related to Formation of racemic mixtures | The | 0.60 | section |
| Racemization | related to Formation of racemic mixtures | An | 0.60 | section |
| Racemization | related to Stereochemistry | Chiral | 0.60 | section |
| Racemization | related to Stereochemistry | The | 0.60 | section |
| Racemization | related to Stereochemistry | D-glyceraldehyde | 0.60 | section |
| Racemization | related to Stereochemistry | L-glyceraldehyde | 0.60 | section |
| Racemization | related to Stereochemistry | Also | 0.60 | section |
| Racemization | related to Stereochemistry | Cahn | 0.60 | section |
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