The following questions relate to the resolution of (±)-a-phenylethylamine lab. Using the structures below, designate each chiral carbon in the salts as R or S. Are the salts enantiomers or diastereomers? Complete the reaction below assuming only the levorotatory salt is precipitated and isolated. Draw this final product in a correct 3-D orientation. NH2 ÇOOH NH3 COO NH3 COO H3C- H- OH H- CH3 H- NaOH H- OH но- H- но H- Но COOH COOH COOH racemic amine (+) tartaric acid salt salt

The following questions relate to the resolution of (±)-a-phenylethylamine lab. Using the structures below, designate each chiral carbon in the salts as R or S. Are the salts enantiomers or diastereomers? Complete the reaction below assuming only the levorotatory salt is precipitated and isolated. Draw this final product in a correct 3-D orientation. NH2 ÇOOH NH3 COO NH3 COO H3C- H- OH H- CH3 H- NaOH H- OH но- H- но H- Но COOH COOH COOH racemic amine (+) tartaric acid salt salt

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter24: Catalytic Carbon-carbon Bond Formation

Section: Chapter Questions

Problem 24.30P

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