Molecule Gallery

Index of Bruice Model Files : Chapter 6

Model	Comment
Ethanol	Constitutional isomers.
Methoxymethane	Constitutional isomers.
cis-1,4-Dimethylcyclohexane	Stereoisomers: cyclic compounds.
trans-1,4-Dimethylcyclohexane	Stereoisomers: cyclic compounds.
(E)-2-Pentene	Stereoisomers: alkenes.
(Z)-2-Pentene	Stereoisomers: alkenes.
Tetracycline	Structure for problem 5.
(R)-4-Octanol	Stereoisomers: chiral object.
(S)-4-Octanol	Stereoisomers: chiral object.
(R)-2-Bromobutane	Stereoisomerism: enantiomers.
(S)-2-Bromobutane	Stereoisomerism: enantiomers.
(S)-2-Butanol	Naming enantiomers. I.
(R)-3-Chlorohexane	Naming enantiomers. II. An exercise.
(R)-Seudenol	A natural racemic mixture.
(S)-Seudenol	A natural racemic mixture.
(R)-2-Bromobutane	Stereoisomerism: enantiomers.
(S)-2-Bromobutane	Stereoisomerism: enantiomers.
(R)-(+)-Glyceraldehyde	Absolute configurations.
2-Hydroxypropanoic acid, Lactic acid	Naming enantiomers. III. Lactic acid.
(S)-Naproxen	Absolute configuration and specific rotation.
Cholesterol	Multiple asymmetric centers.
(2S,3S)-2,3-Dibromobutane	Enantiomers.
(2R,3R)-2,3-Dibromobutane	Enantiomers.
(2R,3S)-2,3-Dibromobutane	Meso stereoisomer.
2,3-Butanediol	Chiral or achiral?
(2R,3R)-3-Chloro-2-butanol	Two asymmetric carbon atoms. I. Threo enantiomers.
(2R,3S)-3-Chloro-2-butanol	Two asymmetric carbon atoms. II. Erythro enantiomers.
(2S,3R)-3-Chloro-2-butanol	Two asymmetric carbon atoms. III. Diastereoisomers.
(2S,3S)-3-Chloro-2-butanol	Two asymmetric carbon atoms. III. Diastereoisomers.
(2R,3R)-(+)-Tartaric acid	R,S nomenclature for more than one center.
Chloramphenicol	R,S nomenclature for more than one center. Problem 46.
Ephedrine	R,S nomenclature for more than one center. Problem 47.
(S)-3-Methylhexene	The arbitrariness of the R,S designations.
(R)-3-Methylhexane	The arbitrariness of the R,S designations.
(R)-Carvone	Biological discrimination of enantiomers.
(S)-Carvone	Biological discrimination of enantiomers.
(S)-Thalidomide	Problems with some racemic drugs.
2-Butyl cation	Lack of selectivity in alkene hydrobromination.
1-Isopropyl-2-methylcyclopentene	Stereochemical consequence of alkene hydrogenation.
cis-1-Isopropyl-2-methylcyclopentane	Stereochemical consequence of alkene hydrogenation.
trans-2-Pentene bromonium ion	Stereochemical consequence of alkene bromination.
(2R,3S)-2,3-Dibromopentane	Stereochemical consequence of alkene bromination.
cis-2-Butene bromonium ion	Stereochemical consequence of alkene bromination.
2,3-Dibromobutane	Stereochemical consequence of alkene bromination.

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