The reaction of (R)-1-bromobutane with Lil in DMF yields:(S)-1-lodobutane(S)-2-lodobutane(R)-1-lodobutane2-buteneChoose the best reagent(s) for carrying out the conversion of the reaction belowCH,CH-снсH,cоон сн,сон + носсн,соонNABH, ethanolB) KMNO, Hy,0(1) BH, (2) H,0"0, Zn/H,0Arrange the following compounds in decreasing order of reactivity towards Nal in acetone:L. Methyt bromideI. Isopropyl bromideI. Ethyl bromideIV. t-butyl bromideA V, I, I, IB), II, II, IVIV, II, II, ILIL, II, IVA hydrocarbon (Y) partially hydrogenates with the Lindlar's catalyst to form an alkene. When (Y) undergoes axidative cleavage withozone, it yields a singe carboxylic acid product. The hydrocarbon (M is:2-hexen-1-ol2-hexyne2-butynecyclohexane

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ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

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Question

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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