Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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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:
(1)
(2)
(3)
(4)
(a) CH3O Na+, CH3OH (d) H₂O
(b) OsO4, H₂O2
(c) 1. BH3
2. H₂O2/NaOH
(e) NaOH, H₂O
(f) CH3 CH₂ OH
(9) CH3 CN
(j) Na, NH3 (1)
(h) Naº, THF (k) NBS, light
(1) PBr3
(N-bromosuccinimide)
(l) NaNH,
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Transcribed Image Text: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: (1) (2) (3) (4) (a) CH3O Na+, CH3OH (d) H₂O (b) OsO4, H₂O2 (c) 1. BH3 2. H₂O2/NaOH (e) NaOH, H₂O (f) CH3 CH₂ OH (9) CH3 CN (j) Na, NH3 (1) (h) Naº, THF (k) NBS, light (1) PBr3 (N-bromosuccinimide) (l) NaNH, Previous Next
Using your reaction roadmap as a guide, show how to convert 1-butene into dibutyl ether. You must use 1-butene as the source of all carbon atoms in
the dibutyl ether.
Br
1-butene
OH
O Na+
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Transcribed Image Text:Using your reaction roadmap as a guide, show how to convert 1-butene into dibutyl ether. You must use 1-butene as the source of all carbon atoms in the dibutyl ether. Br 1-butene OH O Na+
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