The reaction of (R)-1-bromobutane with Lil in DMF yields:

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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The reaction of (R)-1-bromobutane with Lil in DMF yields:
(S)-1-lodobutane
(S)-2-lodobutane
(R)-1-lodobutane
2-butene
Choose the best reagent(s) for carrying out the conversion of the reaction below
CH,CH-снсH,cоон сн,сон + носсн,соон
NABH, ethanol
B) KMNO, Hy,0
(1) BH, (2) H,0"
0, Zn/H,0
Arrange the following compounds in decreasing order of reactivity towards Nal in acetone:
L. Methyt bromide
I. Isopropyl bromide
I. Ethyl bromide
IV. t-butyl bromide
A V, I, I, I
B), II, II, IV
IV, II, II, I
LIL, II, IV
A hydrocarbon (Y) partially hydrogenates with the Lindlar's catalyst to form an alkene. When (Y) undergoes axidative cleavage with
ozone, it yields a singe carboxylic acid product. The hydrocarbon (M is:
2-hexen-1-ol
2-hexyne
2-butyne
cyclohexane
Transcribed Image Text:The reaction of (R)-1-bromobutane with Lil in DMF yields: (S)-1-lodobutane (S)-2-lodobutane (R)-1-lodobutane 2-butene Choose the best reagent(s) for carrying out the conversion of the reaction below CH,CH-снсH,cоон сн,сон + носсн,соон NABH, ethanol B) KMNO, Hy,0 (1) BH, (2) H,0" 0, Zn/H,0 Arrange the following compounds in decreasing order of reactivity towards Nal in acetone: L. Methyt bromide I. Isopropyl bromide I. Ethyl bromide IV. t-butyl bromide A V, I, I, I B), II, II, IV IV, II, II, I LIL, II, IV A hydrocarbon (Y) partially hydrogenates with the Lindlar's catalyst to form an alkene. When (Y) undergoes axidative cleavage with ozone, it yields a singe carboxylic acid product. The hydrocarbon (M is: 2-hexen-1-ol 2-hexyne 2-butyne cyclohexane
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