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. oll (a) CH3O Na+, CH3OH (d) H₂O (b) OsO4, H₂O2 (c) 1, BH₁ 1-butene. OH O Na 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 ser bring about the steps shown. Reagents: (j) Na, NH3 (1) (9) CH₂ CN (e) NaOH, H₂O (h) Naº, THF (k) NBS, light (N-bromosuccinimide)

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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.
(1)
(3)
(a) CH3O Na+, CH3OH (d) H₂O
(b) OsO4, H₂O2
(c) 1. BH3
g
(2) I
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:
(4) C
Br
2. H₂O2/NaOH
1-butene
(9) CH3 CN
(e) NaOH, H₂O (h)Naº, THF
(f) CH3 CH₂ OH (1) PBr3
OH
O
Na+
(j) Na, NH3 (1)
(k) NBS, light
Submit Answer Retry Entire Group 1 more group attempt remaining
(I) NaNH,
(N-bromosuccinimide)
Transcribed Image Text:TReferences] 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. (1) (3) (a) CH3O Na+, CH3OH (d) H₂O (b) OsO4, H₂O2 (c) 1. BH3 g (2) I 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: (4) C Br 2. H₂O2/NaOH 1-butene (9) CH3 CN (e) NaOH, H₂O (h)Naº, THF (f) CH3 CH₂ OH (1) PBr3 OH O Na+ (j) Na, NH3 (1) (k) NBS, light Submit Answer Retry Entire Group 1 more group attempt remaining (I) NaNH, (N-bromosuccinimide)
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