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1. (Review) What are the absolute configurations of these two molecules? 4. What sequence would best...

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1. (Review) What are the absolute configurations of these two molecules? 4. What sequence would best accomplish this transfor
1. (Review) What are the absolute configurations of these two molecules? 4. What sequence would best accomplish this transformation? снион Low- CHICH .COH CHE (a) I(S) and II(S) (b) I(R) and II(S) (a) [1] SOCI, [2] (CH3)2NH (b) [1] NH3, [2] excess CHI (c) NaBH, [2] (CH3)2NH (d) LiN(CH)2 (c) I(S) and II(R) (d) I(R) and II(R) 2. (Review) What is the IUPAC name for the following compound? 5. (Review) Reduction of an alkyne to an E alkene can be accomplished with which set of reagents? (a) Na, NH (b) Ha, with a poisoned Pd catalyst (c) NaBHe in methanol (d) NaH followed by an acid quench (a) 7,7-diethyl-2,4,5-trimethylnonane (b) 7-ethyl-2,4,5-trimethyloctane (c) 6-ethyl-2,4,5-trimethyloctane 6. What is the product of the following reaction? (d) 3,3-diethyl-5,6,8-trimethylnonane O CEN 1. CH. MgBr 2. Ho (quench) 3. Nitriles can be hydrolyzed in the presence of acid to give what functional group as the final product? (a) aldehydes (b) carboxylic acids (c) amides (d) imines

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What sequence would best accomplish this transformation? 1. (Review) What are the absolute configurations of 4. these two mol

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