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In chemistry, stereoselectivity is the property of a chemical reaction in which a single reactant forms an unequal mixture of stereoisomers during a non-stereospecific creation of a new stereocenter or during a non-stereospecific transformation of a pre-existing one. The selectivity arises from differences in steric and electronic effects in the…
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one reaction chiral formed stereochemistry products two center possible another relative enantiomer example optically single mixture pre-existing selectivity degree stereoisomer
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Stereoselectivity | is a | property of a chemical reaction in which a single reactant forms an unequal mixture of stereoisomers during a non-stereospecific creation of a new stereocenter or during a non-s… | 0.90 | text |
| Stereoselectivity | is a | dehydrohalogenation of 2-iodobutane which yields 60 | 0.90 | text |
| Stereoselectivity | related to Examples | An | 0.60 | section |
| Stereoselectivity | related to Examples | Since | 0.60 | section |
| Stereoselectivity | related to Examples | Cram's | 0.60 | section |
| Stereoselectivity | related to Examples | The | 0.60 | section |
| Stereoselectivity | related to Examples | In | 0.60 | section |
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