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1. Draw the structure of (S) 5-phenoxy-2-cyclohexenone. 2. Give the IUPAC name of this compound: CH3OCH2CH2 но- CHLOH Br 3. Draw the most stable chair conformation of (trans)1-isopropyl-2-methylcyclohexane. 4. CH, CH, State whether these two are: a) the same molecule b) different compounds that are not isomers c) constitutional isomers d) diastereomers e) enantiomers H Br Br H H 000 CH, F H F CH 5. el a) How many stereocenters does this compound have? HO CH b) How many stereoisomers are possible for this compound? 6. Write "most" under the member of each trio which is most stable. Write "least under the member of each trio which is least stable. a) b) 7. Draw a Fischer projection of (R) 3-bromo-2-methylpentane 8 Which of these two would you expect to be more soluble in water? Why? 2-butanone cyclohexanone Which of these two would you expect to have the higher boiling point? Why? 2-pentanone 1-pentanol Write "most" under the compound which will react with Bry/FeBrz most easily. Write "least" under the compound which will be least reactive toward Bry/FeBrz. -OH 0 0