What are the absolute configurations at carbons labelled , , and in the molecule below, respectively?

What is the IUPAC name for the given organic molecule?

How many stereoisomers would be obtained by the hydrogenation of compound C?

How many stereocenters does this steroid derivative have?

How many stereoisomers are possible for the compound 2,3,4-trimethylpentane?

How many stereoisomers exist for the given compound?

If (1S,3S)-1-chloro-3-methylcyclohexane undergoes a substitution reaction when reacted with , what product will predominate?

How many different stereoisomer orientations are possible for the given molecule?

What is the IUPAC name for the molecule shown?

What is the absolute configuration of the compound shown?