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4) The enantiomer of L-tartaric acid is D-tartaric acid. Draw the structure of D-tartaric acid, and label each chiral carbon as R or S.

4) The enantiomer of L-tartaric acid is D-tartaric acid. Draw the structure of D-tartaric acid, and label each chiral carbon as R or S.

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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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H₂N 3) Why does the (RR)-1,2-diaminocyclohexane form a solid complex with L-tartaric acid while the (SS)-1,2-diaminocyclohexane does not? (Hint: redraw the reaction scheme from the bottom of page 1 of this lab and use this in your explanation). 4) The enantiomer of L-tartaric acid is D-tartaric acid. Draw the structure of D-tartaric acid, and label each chiral carbon as R or S. 5) Which enantiomer of trans-1,2-diaminocylohexane would you expect that the D-tartaric acid would form a solid complex with? Explain. NH₂ H₂N NH₂ HO H HO₂C OH CO₂H How O₂C H₂N OH CO₂ NHS + HO O₂C H₂N H OH CO₂ NH3 (aq)
Transcribed Image Text:H₂N 3) Why does the (RR)-1,2-diaminocyclohexane form a solid complex with L-tartaric acid while the (SS)-1,2-diaminocyclohexane does not? (Hint: redraw the reaction scheme from the bottom of page 1 of this lab and use this in your explanation). 4) The enantiomer of L-tartaric acid is D-tartaric acid. Draw the structure of D-tartaric acid, and label each chiral carbon as R or S. 5) Which enantiomer of trans-1,2-diaminocylohexane would you expect that the D-tartaric acid would form a solid complex with? Explain. NH₂ H₂N NH₂ HO H HO₂C OH CO₂H How O₂C H₂N OH CO₂ NHS + HO O₂C H₂N H OH CO₂ NH3 (aq)
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