Chapter 12: Q35d E (page 385)
At what approximate positions might the following compounds show
IR absorptions?
Short Answer
(d) It shows one distinguishing absorption due to ester at 1735
Chapter 12: Q35d E (page 385)
At what approximate positions might the following compounds show
IR absorptions?
(d) It shows one distinguishing absorption due to ester at 1735
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Get started for freeWhich of the following bases could be used to deprotonate 1-butyne?
(a) KOH
What functional groups might the following molecules contain?
(a) A compound with a strong absorption at 1710 cm-1
(b) A compound with a strong absorption at 1540 cm-1
(c) A compound with strong absorptions at 1720 cm-1 and 2500 to 3100cm-1
Amino acids can be prepared by reaction of alkyl halides with diethyl acetamidomalonate, followed by heating the initial alkylation product with aqueous HCl. Show how you would prepare alanine, , one of the twenty amino acids found in proteins, and propose a mechanism for acid-catalyzed conversion of the initial alkylation product to the amino acid.
Question: How might you use IR spectroscopy to distinguish between the following pairs of isomers?
Predict the product(s) and provide the mechanism for each reaction below. What does each mechanism have in common?
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