[References compound a compound b NaN compound c r. Reagents a. HX m. Na/NH b. HBr, H2O2, hv n. H,SO, HgSO C. H2O, H2SO4 0. (sia), BH then H2O2, NaOH d. X P. 1 equivalent of NaNH2 e. Hz, Pd 9. NBS, hv f. X2, H2O X.hu 9. Oso, then NaHSO, (CH), COK h. Hg(OAC), H20 then NaBH4 t PBT 1. BH, then H20, NaOH u. SOCH j. Othen (CH3)2S V. HYPO k. 2 equivalents of NaNH2 W. H Cro 1. Hz. Lindiar's catalyst X PCC y 104 S. This synthesis was designed using the Organic Chemistry Road Map found in the appendix of your textbook. In this synthesis, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound a . Use the wedge/hash bond tools to indicate stereochemistry where it exists. . If the reaction produces a racemic mixture, draw both stereoisomers. If both (?) and (Z) forms of the alkene can be produced in the reaction, draw both isomers. Separate structures with + signs from the drop-down menu. er 10 [Retorences! This synthesis was designed using the Organic Chemistry Road Map found in the appendix of your textbook. In this synthesis, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound a . Use the wedge/hash bond tools to indicate stereochemistry where it exists. If the reaction produces a racemic mixture, draw both stereoisomers. If both (E) and (Z) forms of the alkene can be produced in the reaction, draw both isomers. Separate structures with + signs from the drop-down menu. . In the table of reagents, X can refer to either Bror CI. . 00 ChemDoodle 1