6. Using the Amidomalonate synthesis (as shown below), what alkyl bromide would you use to prepare the α-amino acid Leucine? [The product would be a mixture of R and S enantiomers]. Draw your answer inside the box for reactant 2 (consult Table 1 for the structure of Leucine). CO₂CH2CH3 H CO₂CH₂CH₂ 1. OCH2CH3 2. HN. CH3 ° 3. H3O/Heat Θ Leucine
6. Using the Amidomalonate synthesis (as shown below), what alkyl bromide would you use to prepare the α-amino acid Leucine? [The product would be a mixture of R and S enantiomers]. Draw your answer inside the box for reactant 2 (consult Table 1 for the structure of Leucine). CO₂CH2CH3 H CO₂CH₂CH₂ 1. OCH2CH3 2. HN. CH3 ° 3. H3O/Heat Θ Leucine
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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![6. Using the Amidomalonate synthesis (as shown below), what alkyl bromide would you use to prepare
the α-amino acid Leucine? [The product would be a mixture of R and S enantiomers]. Draw your answer
inside the box for reactant 2 (consult Table 1 for the structure of Leucine).
CO₂CH2CH3
H
CO₂CH₂CH₂ 1. OCH2CH3
2.
HN.
CH3
°
3. H3O/Heat
Θ
Leucine](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F6e68433c-fe04-4cba-83a5-718f8ed7a40c%2F17329145-b287-4ad7-88a5-a607372fae96%2Fz9mwj3k_processed.jpeg&w=3840&q=75)
Transcribed Image Text:6. Using the Amidomalonate synthesis (as shown below), what alkyl bromide would you use to prepare
the α-amino acid Leucine? [The product would be a mixture of R and S enantiomers]. Draw your answer
inside the box for reactant 2 (consult Table 1 for the structure of Leucine).
CO₂CH2CH3
H
CO₂CH₂CH₂ 1. OCH2CH3
2.
HN.
CH3
°
3. H3O/Heat
Θ
Leucine
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