(1) (2) (3) OH (4) 2-ethoxy-1-butanol. (racemic) OH Suggest reagents and experimental conditions for each step in this synthesis. From the choices provided, suggest appropriate reagents for each step. More than one reagent may be necessary. Use the minimum number of steps possible. Enter your answer as a letter, or a series of letters, in the order necessary to bring about the steps shown. Reagents: OH Br (a) (CH3)3 COK, THF (d) H₂SO4, H₂O (b) OsO4, H₂O2 (c) ethylene oxide OH (e) m-chloroperoxybenzoic acid (mCPBA) (f) pyridinium chlorochromate (PCC) (9) H₂SO4 (anhydrous) (h) NaOH (1) PBr3 (j) Na, NH3 (1) (k) NBS, heat (N-bromosuccinimide) Previous Next
(1) (2) (3) OH (4) 2-ethoxy-1-butanol. (racemic) OH Suggest reagents and experimental conditions for each step in this synthesis. From the choices provided, suggest appropriate reagents for each step. More than one reagent may be necessary. Use the minimum number of steps possible. Enter your answer as a letter, or a series of letters, in the order necessary to bring about the steps shown. Reagents: OH Br (a) (CH3)3 COK, THF (d) H₂SO4, H₂O (b) OsO4, H₂O2 (c) ethylene oxide OH (e) m-chloroperoxybenzoic acid (mCPBA) (f) pyridinium chlorochromate (PCC) (9) H₂SO4 (anhydrous) (h) NaOH (1) PBr3 (j) Na, NH3 (1) (k) NBS, heat (N-bromosuccinimide) Previous Next
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter9: Nucleophilic Substitution And Β-elimination
Section: Chapter Questions
Problem 9.46P: When cis-4-chlorocyclohexanol is treated with sodium hydroxide in ethanol, it gives mainly the...
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