During kinetic resolution, the reaction of a racemic mixture of an N-acetylated amino acid with a chiral amine results in the separation of the two enantiomers of the acetylated amino acids. What is the product of the initial step of this reaction as shown below? NH₂ OH NH salts (Racemic mixture) A) They form amides. B) They form diastereomers. C) They form salts. D) They form meso compounds.

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During kinetic resolution, the reaction of a racemic mixture of an N-acetylated amino acid with a chiral amine results in the
separation of the two enantiomers of the acetylated amino acids. What is the product of the initial step of this reaction as
shown below?
NH₂
OH
NH
salts
(Racemic mixture)
A) They form amides.
B) They form diastereomers.
C) They form salts.
D) They form meso compounds.
E) They form enantiomers
Transcribed Image Text:During kinetic resolution, the reaction of a racemic mixture of an N-acetylated amino acid with a chiral amine results in the separation of the two enantiomers of the acetylated amino acids. What is the product of the initial step of this reaction as shown below? NH₂ OH NH salts (Racemic mixture) A) They form amides. B) They form diastereomers. C) They form salts. D) They form meso compounds. E) They form enantiomers
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