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1. Draw the best chair conformation of trans 1-sec-butyl-2-methylcyclohexane. 1. Draw the best chair conformation of trans 1-sec-butyl-2-methylcyclohexane. 2. Consider this compound: a) How many chiral carbons does this compound have? b) What is the maximum number of stereoisomers that could exist for this compound? Show how you arrived at your answer. 3. Assign priorities to the groups on this chiral carbon. Label it as R or S. 4. Draw a Fischer projection of: (R) 2-chloro-1-fluoropropane 5. Are these two compounds: a) the same b) enantiomers OR c) diastereomers? Explain how you arrived at your