6) To synthesize 3-octyne, you could use bromination and elimination from an intermediate 6) created using which of the following sequences of reactions? 1) propyne, NaNH, 2) 1-bromopentane 3) aqueous H₂SO4, cat. HgSO4 A) I B) II C) III D) IV E) V IV II 1) 1-butyne, NaNH, 2) 1-bromobutane 3) H₂, Lindlar's cat. 1) 1-butyne, NaNH2 2) 1-bromobutane 3) Na, NH3(1) V 1) propyne, NaNH, 2) 1-bromopentane 3) H₂, Ni₂B (P-2) 1) 1-butyne, NaNH, 2) 1-bromobutane 3) H₂, Pd/C

6) To synthesize 3-octyne, you could use bromination and elimination from an intermediate 6) created using which of the following sequences of reactions? 1) propyne, NaNH, 2) 1-bromopentane 3) aqueous H₂SO4, cat. HgSO4 A) I B) II C) III D) IV E) V IV II 1) 1-butyne, NaNH, 2) 1-bromobutane 3) H₂, Lindlar's cat. 1) 1-butyne, NaNH2 2) 1-bromobutane 3) Na, NH3(1) V 1) propyne, NaNH, 2) 1-bromopentane 3) H₂, Ni₂B (P-2) 1) 1-butyne, NaNH, 2) 1-bromobutane 3) H₂, Pd/C

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 71AP: A problem often encountered in the oxidation of primary alcohols to acids is that esters are...

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