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HC=CH Reagents a. HCI b. HBr 2 equivalents of NANH2 H2, Lindlar's catalyst Na / NH3 p. H2SO4, HgSO4 q. (sia)½BH then H2O2, NaOH 1 equivalent of NaNH2 m. n. c. H20, H2SO4 d. Br2 Cl2 f. H2, Pd g. Br2, H20 h. Cl2, H20 i. 0. е. r. OsO4 then NaHSO3 Hg(OAc)2, H2O then NaBH4 k. BH3 then H2O2, NaOH I. Oz then (CH3)½S j. above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. s synthesis starting with acetylene, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compo

HC=CH Reagents a. HCI b. HBr 2 equivalents of NANH2 H2, Lindlar's catalyst Na / NH3 p. H2SO4, HgSO4 q. (sia)½BH then H2O2, NaOH 1 equivalent of NaNH2 m. n. c. H20, H2SO4 d. Br2 Cl2 f. H2, Pd g. Br2, H20 h. Cl2, H20 i. 0. е. r. OsO4 then NaHSO3 Hg(OAc)2, H2O then NaBH4 k. BH3 then H2O2, NaOH I. Oz then (CH3)½S j. above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. s synthesis starting with acetylene, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compo

Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter6: Alkanes & Alkenes
Section: Chapter Questions
Problem 19CTQ
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compound b in HC=CH Reagents а. НС m. 2 equivalents of NANH2 b. HBr H2, Lindlar's catalyst Na / NH3 p. H2SO4, HgSO4 q. (sia)2BH then H2O2, NaOH n. c. H20, H2SO4 d. Br2 0. е. Clp H2, Pd g. Br2, H20 h. Cl2, H2O i. f. r. 1 equivalent of NaNH2 OsO4 then NaHSO3 j. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH I. O3 then (CH3)2S The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis starting with acetylene, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound i.
Transcribed Image Text:compound b in HC=CH Reagents а. НС m. 2 equivalents of NANH2 b. HBr H2, Lindlar's catalyst Na / NH3 p. H2SO4, HgSO4 q. (sia)2BH then H2O2, NaOH n. c. H20, H2SO4 d. Br2 0. е. Clp H2, Pd g. Br2, H20 h. Cl2, H2O i. f. r. 1 equivalent of NaNH2 OsO4 then NaHSO3 j. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH I. O3 then (CH3)2S The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis starting with acetylene, reagents from the table are used to carry out the indicated steps (shown in blue). In the box below, draw the structure of compound i.
compound j i compound i compound h compound g compound f 1 compound e compound d 1. HC=CH compound a compound c HC=CH compound b
Transcribed Image Text:compound j i compound i compound h compound g compound f 1 compound e compound d 1. HC=CH compound a compound c HC=CH compound b
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