Content Frame
[Skip Breadcrumb Navigation]

Molecule Gallery

Index of Bruice Model Files : Chapter 6

Model
Comment
EthanolConstitutional isomers.
MethoxymethaneConstitutional isomers.
cis-1,4-DimethylcyclohexaneStereoisomers: cyclic compounds.
trans-1,4-DimethylcyclohexaneStereoisomers: cyclic compounds.
(E)-2-PenteneStereoisomers: alkenes.
(Z)-2-PenteneStereoisomers: alkenes.
TetracyclineStructure for problem 5.
(R)-4-OctanolStereoisomers: chiral object.
(S)-4-OctanolStereoisomers: chiral object.
(R)-2-BromobutaneStereoisomerism: enantiomers.
(S)-2-BromobutaneStereoisomerism: enantiomers.
(S)-2-ButanolNaming enantiomers. I.
(R)-3-ChlorohexaneNaming enantiomers. II. An exercise.
(R)-SeudenolA natural racemic mixture.
(S)-SeudenolA natural racemic mixture.
(R)-2-BromobutaneStereoisomerism: enantiomers.
(S)-2-BromobutaneStereoisomerism: enantiomers.
(R)-(+)-GlyceraldehydeAbsolute configurations.
2-Hydroxypropanoic acid, Lactic acidNaming enantiomers. III. Lactic acid.
(S)-NaproxenAbsolute configuration and specific rotation.
CholesterolMultiple asymmetric centers.
(2S,3S)-2,3-DibromobutaneEnantiomers.
(2R,3R)-2,3-DibromobutaneEnantiomers.
(2R,3S)-2,3-DibromobutaneMeso stereoisomer.
2,3-ButanediolChiral or achiral?
(2R,3R)-3-Chloro-2-butanolTwo asymmetric carbon atoms. I. Threo enantiomers.
(2R,3S)-3-Chloro-2-butanolTwo asymmetric carbon atoms. II. Erythro enantiomers.
(2S,3R)-3-Chloro-2-butanolTwo asymmetric carbon atoms. III. Diastereoisomers.
(2S,3S)-3-Chloro-2-butanolTwo asymmetric carbon atoms. III. Diastereoisomers.
(2R,3R)-(+)-Tartaric acidR,S nomenclature for more than one center.
ChloramphenicolR,S nomenclature for more than one center. Problem 46.
EphedrineR,S nomenclature for more than one center. Problem 47.
(S)-3-MethylhexeneThe arbitrariness of the R,S designations.
(R)-3-MethylhexaneThe arbitrariness of the R,S designations.
(R)-CarvoneBiological discrimination of enantiomers.
(S)-CarvoneBiological discrimination of enantiomers.
(S)-ThalidomideProblems with some racemic drugs.
2-Butyl cationLack of selectivity in alkene hydrobromination.
1-Isopropyl-2-methylcyclopenteneStereochemical consequence of alkene hydrogenation.
cis-1-Isopropyl-2-methylcyclopentaneStereochemical consequence of alkene hydrogenation.
trans-2-Pentene bromonium ionStereochemical consequence of alkene bromination.
(2R,3S)-2,3-DibromopentaneStereochemical consequence of alkene bromination.
cis-2-Butene bromonium ionStereochemical consequence of alkene bromination.
2,3-DibromobutaneStereochemical consequence of alkene bromination.





Copyright © 1995 - 2021 Pearson Education . All rights reserved. Pearson Prentice Hall is an imprint of Pearson .
Legal Notice | Privacy Policy | Permissions

[Return to the Top of this Page]