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Unformatted text preview: 2. Write structural formulas for all the constitutionally isomeric compounds having the given molecular formula a. C 3 H 7 F Write TWO constitutional isomers of C 2 H 6 such that ONE is ALKENE and ONE is CYCLOALKANE. 3. Write the Newman projections for the most stable conformation of each of the following. Show any lone pairs. a. HO-OH b. H 2 C +-CH 3 4. Encircle the more stable stereoisomer within each pair. a. and 5. a. Write one pair of cis / trans isomers for Dimethylcyclopropane b. For FClC = CHBr 6. Write the products of the following Acid-Base reactions. H 3 N + BF 3 + (CH 3 ) 3 C + CH 3 OH 7. In each of the following acid-base equilibria, label each molecule as Acid (A), Base (B) (on the left) Conjugate Acid (CA) and Conjugate Base (CB) (on the right). Also, place under each question mark an arrow showing the direction of the equilibrium. NH 3 + ? + NH 4 + 36 16 9.3 Number shown under formulae are pK a values needed for determining the direction of equilibrium....
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