Choose the best reagent(s) for carrying out the conversion of the reaction below: CH-CH-CHCH,cоон сн;сон + носсн,соон NABH, ethanol KMno, H,0* (1) BH3, (2) H,O* O, Zn/H;O

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Chapter1: Chemical Foundations
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Choose the best reagent(s) for carrying out the conversion of the reaction below:
CH-CH-CHCH,cоон сн;сон + носсн,соон
NABH, ethanol
KMno, H,0*
(1) BH3, (2) H,O*
0, Zn/H;0
Arrange the following compounds in decreasing order of reactivity towards Nal in acetone:
1. Methyl bromide
II. Isopropyl bromide
II. Ethyl bromide
IV. t-butyl bromide
IV, II, I, I
B 1, I, II, IV
IV, II, II, I
D 1, II, II, IV
A hydrocarbon (Y) partially hydrogenates with the Lindlar's catalyst to form an alkene. When (M) undergoes oxidative cleavage with
ozone, it yields a single carboxylic acid product. The hydrocarbon (Y) is:
2-hexen-1-ol
2-hexyne
2-butyne
cyclohexane
Transcribed Image Text:Choose the best reagent(s) for carrying out the conversion of the reaction below: CH-CH-CHCH,cоон сн;сон + носсн,соон NABH, ethanol KMno, H,0* (1) BH3, (2) H,O* 0, Zn/H;0 Arrange the following compounds in decreasing order of reactivity towards Nal in acetone: 1. Methyl bromide II. Isopropyl bromide II. Ethyl bromide IV. t-butyl bromide IV, II, I, I B 1, I, II, IV IV, II, II, I D 1, II, II, IV A hydrocarbon (Y) partially hydrogenates with the Lindlar's catalyst to form an alkene. When (M) undergoes oxidative cleavage with ozone, it yields a single carboxylic acid product. The hydrocarbon (Y) is: 2-hexen-1-ol 2-hexyne 2-butyne cyclohexane
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