Problem 5 help please. I only got 2 points out of 6. What did I do wrong?
d. How many intermediates are formed in the above reaction? 1, 2, 3, or 4? O e. True or false? Enantiomers could be formed based on the information provided. Problem 5. Draw the two chair conformations of cis-1,2-dimethylcyclohexane as Newman projections looking down the C1-C2 and Cs-C4 bonds. Clearly label which is the most and which is the least stable conformation. If they are of equal stability, you must clearly state so. pts 52CH CH3 Ct3 mst t oste stable Problem 6. Draw the two chair conformations of trans-1-(tert-butyl)-3-methylcyclohexane (i.e trans-1-(1.1-dimethylethyl)-3-methylcyclohexane), and identify each substituent as either axia or equatorial. Clearly label which is the most and which is the least stable conformation. If the are of equal stability, you must clearly state so. 6 pts
