HC=CH Reagents available a. HCI e. На, Рd i. H2 / Lindlar's catalyst b. HBr f. OsO4 then NaHSO3 j. Na / NH3 с. Вг2 g. O3 then (CH3)2S k. (sia)2 BH then H2O2, NaOH d. Cl2 h. 2 equivalents of NaNH2 1. 1 equivalent of NaNH2 The above synthesis scheme was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this scheme, identify the reagents necessary to accomplish the following steps in the production of (3R,4S)-3,4-dibromohexane from acetylene: Step 4: Step 1: Step 3 :
HC=CH Reagents available a. HCI e. На, Рd i. H2 / Lindlar's catalyst b. HBr f. OsO4 then NaHSO3 j. Na / NH3 с. Вг2 g. O3 then (CH3)2S k. (sia)2 BH then H2O2, NaOH d. Cl2 h. 2 equivalents of NaNH2 1. 1 equivalent of NaNH2 The above synthesis scheme was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this scheme, identify the reagents necessary to accomplish the following steps in the production of (3R,4S)-3,4-dibromohexane from acetylene: Step 4: Step 1: Step 3 :
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter22: Organic And Biological Molecules
Section: Chapter Questions
Problem 176MP
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