235[Review Topics]ReagentsHBra.b.C. H₂O, H₂SO4d.Br₂Cl₂H₂, PdBr₂, H₂OCl₂, H₂OOsO4 then NaHSO3e.f.g.h.i.j.k.I.[References]HBr, H₂O2, hvHg(OAc)2, H₂O then NaBH4BH3 then H₂O2, NaOHO3 then (CH3)2Sm.n.O.p.q.r.S.t.u.V.2 equivalents of NaNH₂H₂, Lindlar's catalystNa/NH3H₂SO4, HgSO4(sia)2BH then H₂O₂, NaOH1 equivalent of NaNH2NBS, hvBr₂, hvCl₂, hvHCIIdentify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene:Step 4: vStep 5: FStep 7:PreviousNextSave and Exit

Given that : We have to identify the reagents for the above given steps in the synthesis of…

3 CI [Review Topics] Reagents HBr HBr, H₂O₂, hv a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. [References] k. 1. Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH 03 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia) BH then H₂O₂, NaOH 1 equivalent of NaNH₂ NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: V Step 5: F Step 7: Previous Next> Save and Exit

3 CI [Review Topics] Reagents HBr HBr, H₂O₂, hv a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. [References] k. 1. Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH 03 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia) BH then H₂O₂, NaOH 1 equivalent of NaNH₂ NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: V Step 5: F Step 7: Previous Next> Save and Exit

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter4: Polar Bonds, Polar Reactions

Section: Chapter Questions

Problem 8CTQ

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