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NaN, compound a compound b + compound c Reagents m. Na / NH, n. H,SO, H9SO. o. (sia),BH then H,O, NaOH 1 equivalent of NaNH, NBS, hv a. HX b. HBr, H,O2, hv C. H,0, H,SO, d. X2 e. H, Pd f. X H,0 g. Oso, then NaHSO, h. Hg(OAc), H,0 then NABH,t L BH, then H,O,, NaOH . O, then (CH,),S k. 2 equivalents of NaNH, L H, Lindiar's catalyst p. X, hv s. (CH,,COK PBr, u. SocI, v. H,PO, w. H;Cro, X. PCC y. 10. his synthesis was designed using the Organic Chemistry Road Map found in the appendix of your textbook. a 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 • 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.

NaN, compound a compound b + compound c Reagents m. Na / NH, n. H,SO, H9SO. o. (sia),BH then H,O, NaOH 1 equivalent of NaNH, NBS, hv a. HX b. HBr, H,O2, hv C. H,0, H,SO, d. X2 e. H, Pd f. X H,0 g. Oso, then NaHSO, h. Hg(OAc), H,0 then NABH,t L BH, then H,O,, NaOH . O, then (CH,),S k. 2 equivalents of NaNH, L H, Lindiar's catalyst p. X, hv s. (CH,,COK PBr, u. SocI, v. H,PO, w. H;Cro, X. PCC y. 10. his synthesis was designed using the Organic Chemistry Road Map found in the appendix of your textbook. a 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 • 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.

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Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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er 10 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 Br or Cl. ...0 ChemDoodle 1126AM
Transcribed Image Text:er 10 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 Br or Cl. ...0 ChemDoodle 1126AM
NaN, compound a - compound b compound c Reagents a. HX b. HBr, H,O2, hv c. H,O, H,SO, d. X2 e. H, Pd f. X2. H,0 g. Oso, then NaHSO, h. Hg(OAc),, H0 then NABH, t. i BH, then H,0,, NaOH i O, then (CH),S k. 2 equivalents of NaNH2 L Ha, Lindiar's catalyst m. Na / NH, n. H,SO, HgSO, o. (sia),BH then H,O, NaOH p. 1 equivalent of NANH, 9. NBS, hv X2, hv (CH)),COK PBr, u. SOC, v. H,PO, w. H,Cro, r. S. х. РСС y. 10. 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) und (Z) forms of the alkene can be produced in the reaction, draw both isomers. Separate structures with + signs from the drop-down menu.
Transcribed Image Text:NaN, compound a - compound b compound c Reagents a. HX b. HBr, H,O2, hv c. H,O, H,SO, d. X2 e. H, Pd f. X2. H,0 g. Oso, then NaHSO, h. Hg(OAc),, H0 then NABH, t. i BH, then H,0,, NaOH i O, then (CH),S k. 2 equivalents of NaNH2 L Ha, Lindiar's catalyst m. Na / NH, n. H,SO, HgSO, o. (sia),BH then H,O, NaOH p. 1 equivalent of NANH, 9. NBS, hv X2, hv (CH)),COK PBr, u. SOC, v. H,PO, w. H,Cro, r. S. х. РСС y. 10. 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) und (Z) forms of the alkene can be produced in the reaction, draw both isomers. Separate structures with + signs from the drop-down menu.
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