1. Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a Wittig reagent. 2,3-diphenyl-2-butene 2. Predict the products of the following reactions. CH; O CO3 CH;CH,CHCH,CHCH;CH 0-H H30* CH3 CH3 CrO3 CH;CH,CHCH,CHCH,CCH,CH; H. 1 2 CH; CH3 CH0-H 3. A useful and general method for the synthesis of alcohols is the addition of Grignard reagents to carbonyl compounds. Show what Grignard reagent and what carbonyl compound you would start with to prepare the alcohol below. List all possibilities. 2 -DirsY from Grignard 4 Carbor 2-methyl-butanol Directly

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1. Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a Wittig reagent.
2,3-diphenyl-2-butene
2. Predict the products of the following reactions.
CH; 0
base
C03
CH3CH,CHCH,CHCH,CH
0-H
CH3
CH3 O
CrO3
CH3CH,CHCH,CHCH,CCH,CH;
H;O*
CH3
15678 9
CH3 CH2 0-H
3. A useful and general method for the synthesis of alcohols is the addition of Grignard reagents to carbonyl
compounds. Show what Grignard reagent and what carbonyl compound you would start with to prepare the
alcohol below. List all possibilities. 7
2-methyl--butanol
2-METHYL-2-BUTANGe
- Grignard CarbonyYI
- DirectlY from
olt
Transcribed Image Text:1. Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a Wittig reagent. 2,3-diphenyl-2-butene 2. Predict the products of the following reactions. CH; 0 base C03 CH3CH,CHCH,CHCH,CH 0-H CH3 CH3 O CrO3 CH3CH,CHCH,CHCH,CCH,CH; H;O* CH3 15678 9 CH3 CH2 0-H 3. A useful and general method for the synthesis of alcohols is the addition of Grignard reagents to carbonyl compounds. Show what Grignard reagent and what carbonyl compound you would start with to prepare the alcohol below. List all possibilities. 7 2-methyl--butanol 2-METHYL-2-BUTANGe - Grignard CarbonyYI - DirectlY from olt
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