How are the compounds in each pair related to each other? Are they identical, enantiomers, diastereomers, constitutional isomers, or not isomers of each other?

draw the enantiomers and diastereomers of the following compound.

HN- H3C HN -NH "CH3 OH H. CH3 H,C. Br H3C CH3 CH3 HO. Br HO,

6) Which of the following terms best describes the pair of compounds shown: enantiomers, diastereomers, or the same compound? CH3 H- CO₂H NH₂ CO₂OH H+N³H CH3

What is the relationship between the following two structures? O diastereomers O enantiomers same O conformers F F F 27 OCH3 H3CO F F 1

Draw Fischer projection and determine the configuration

Which of the following pairs of stereoisomers are related as enantiomers? a) A & B; C&D b) A& C; B&D c) A&D; B&C d) C&D; B&C

Are these structures the same compound, enantiomers, diastereomers, or meso?

The structures of 4 isomers of ketopentose are shown. 1) which of the structures are diastereomers of structure A? C, B, or D 2) which of the structures are enantiomers of structure C? B, A, or D 3) which of the structures are stereoisomers of strcuture A?C, D, or B

Olfactory receptors in our noses, used for the detection of odors, are chiral. Therefore, in some cases, we can tell the difference between enantiomers by their odor. Carvone is one such compound that we can distinguish between the R and S enantiomer by their odor. br 1. Identify the chiral center in carvone and draw the R and S enantiomers in the indicated boxes.