d. НО. e. a. b. CO₂H CH₂ 8. How would you accomplish the following syntheses? 1. Oxalyl chloride (or thionyl chloride) 2. OH ? OH 1. CH3CH₂Li (2 eq) 2. H₂O OH CO₂H OH 9. Using the carboxylic acid below as your only carbon source, how would you make the give amide? HN 10. Propose a reasonable synthetic route to prepare butanal from butanoic acid.

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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d.
НО.
e.
a.
b.
CO₂H
CH₂
1. Oxalyl chloride (or thionyl chloride)
2.
8. How would you accomplish the following syntheses?
OH
?
1. CH3CH₂Li (2 eq)
2. H₂O
OH
OH
CO₂H
OH
9. Using the carboxylic acid below as your only carbon source, how would you make the given
amide?
HN
10. Propose a reasonable synthetic route to prepare butanal from butanoic acid.
Transcribed Image Text:d. НО. e. a. b. CO₂H CH₂ 1. Oxalyl chloride (or thionyl chloride) 2. 8. How would you accomplish the following syntheses? OH ? 1. CH3CH₂Li (2 eq) 2. H₂O OH OH CO₂H OH 9. Using the carboxylic acid below as your only carbon source, how would you make the given amide? HN 10. Propose a reasonable synthetic route to prepare butanal from butanoic acid.
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