Reagentsa.HBrm.2 equivalents of NaNH2b. HBr, H2O2, hvc. H20, H2SO4d. Br2H2, Lindlar's catalystNa / NH3H2SO4, H9SO4(sia)2BH then H2O2, NaOHn.O.5р.е. Clq.1 equivalent of NANH2H2, Pdg. Br2, H2Oh. Cl2, H2OOsO4 then NaHSO3j. Hg(OAc)2, H2O then NABH4k. BH3 then H2O2, NaOHOg then (CH3)2Sf.r.S.NBS, hvBr2, hvCl2, hvt.i.u.V.HCII.2PreviousNext i. Öz then (CH3)2S3Using 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:

We have to identify the reagents nessato accomplish the following given reaction as follows in step…

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

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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