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Reagents 2 equivalents of NaNH2 H2, Lindlar's catalyst Na / NH3 a. HBr m. HBr, H2O2, hv c. H2O, H2SO4 b. n. o. d. Br2 р. H2SO4, HgSO4 (sia)2BH then H2O2, NaOH 1 equivalent of NaNH2 е. Clz f. H2, Pd g. Br2, H20 h. Cl2, H20 OsO4 then NaHSO3 j. q. CI r. S. NBS, hv t. Br2, hv i. Cl2, hv u. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH Og then (CH3)2S V. HCI I. Previous Next

Reagents 2 equivalents of NaNH2 H2, Lindlar's catalyst Na / NH3 a. HBr m. HBr, H2O2, hv c. H2O, H2SO4 b. n. o. d. Br2 р. H2SO4, HgSO4 (sia)2BH then H2O2, NaOH 1 equivalent of NaNH2 е. Clz f. H2, Pd g. Br2, H20 h. Cl2, H20 OsO4 then NaHSO3 j. q. CI r. S. NBS, hv t. Br2, hv i. Cl2, hv u. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH Og then (CH3)2S V. HCI I. Previous Next

Chemistry
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
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Reagents a. HBr m. 2 equivalents of NaNH2 b. HBr, H2O2, hv c. H20, H2SO4 d. Br2 H2, Lindlar's catalyst Na / NH3 H2SO4, H9SO4 (sia)2BH then H2O2, NaOH n. O. 5 р. е. Cl q. 1 equivalent of NANH2 H2, Pd g. Br2, H2O h. Cl2, H2O OsO4 then NaHSO3 j. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH Og then (CH3)2S f. r. S. NBS, hv Br2, hv Cl2, hv t. i. u. V. HCI I. 2 Previous Next
Transcribed Image Text:Reagents a. HBr m. 2 equivalents of NaNH2 b. HBr, H2O2, hv c. H20, H2SO4 d. Br2 H2, Lindlar's catalyst Na / NH3 H2SO4, H9SO4 (sia)2BH then H2O2, NaOH n. O. 5 р. е. Cl q. 1 equivalent of NANH2 H2, Pd g. Br2, H2O h. Cl2, H2O OsO4 then NaHSO3 j. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH Og then (CH3)2S f. r. S. NBS, hv Br2, hv Cl2, hv t. i. u. V. HCI I. 2 Previous Next
i. Öz then (CH3)2S 3 Using the Organic Chemistry Roadmaps in the appendix of your textbook as a guide, identify the reagents necessary to accomplish the following steps in the above synthesis of 3- hexanone from acetylene: Step 3: Step 5: Step 7:
Transcribed Image Text:i. Öz then (CH3)2S 3 Using the Organic Chemistry Roadmaps in the appendix of your textbook as a guide, identify the reagents necessary to accomplish the following steps in the above synthesis of 3- hexanone from acetylene: Step 3: Step 5: Step 7:
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