I need some help with these two questions: 9. Draw the most stable chair conformer of (1R, 2R)-1-bromo-2-chlorocyclohexane. Draw a Newman projection of this conformer looking down the C1-C2 and C5-C4 bonds. 10. Draw all the possible isomers of 1,3 - dibromocyclohexane (use wedgse and dashes). Identify enantiomers, diastereo
Sometimes, elimination reactions may lead to multiple stereoisomers; that is, they could lead to either the cis or the trans isomer, or in more complicated structures, either the Z or the E isomer. Of course, if there were some inherent stability difference between these isomers, that could be a factor that plays a role in influencing the outcome.