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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

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

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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
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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