(a)
Interpretation:
In Bacitracin A, the amino acid residues and the configuration of the same along with non-amino acid residue need to be identified.
Concept introduction:
The amino acid residue is in a given compound is identified by finding the peptide bond. Then assigning the side chain for the corresponding amino acid residue. If the configuration of the amino acid residue is “L-amino acid” means it is naturally occurring and if it is a “D-amino acid” it is enantiomer of “L-amino acid”
To identify: the amino acid residue in Bacitracin A that are naturally occurring.
(b)
Interpretation:
In Bacitracin A, the amino acid residues and the configuration of the same along with non-amino acid residue need to be identified.
Concept introduction:
The amino acid residue is in a given compound is identified by finding the peptide bond. Then assigning the side chain for the corresponding amino acid residue. If the configuration of the amino acid residue is “L-amino acid” means it is naturally occurring and if it is a “D-amino acid” it is enantiomer of “L-amino acid”
To identify: the amino acid residue in Bacitracin A that are D-amino acids.
(c)
Interpretation:
In Bacitracin A, the amino acid residues and the configuration of the same along with non-amino acid residue need to be identified.
Concept introduction:
The amino acid residue is in a given compound is identified by finding the peptide bond. Then assigning the side chain for the corresponding amino acid residue. If the configuration of the amino acid residue is “L-amino acid” means it is naturally occurring and if it is a “D-amino acid” it is enantiomer of “L-amino acid”
To identify: the amino acid residue in Bacitracin A that are not naturally occurring and its enantiomer also.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 25 Solutions
ORGANIC CHEMISTRY-PRINT MULTI TERM
- 2. 200 LOD For an unknown compound with a molecular ion of 101 m/z: a. Use the molecular ion to propose at least two molecular formulas. (show your work) b. What is the DU for each of your possible formulas? (show your work) C. Solve the structure and assign each of the following spectra. 8 6 4 2 (ppm) 150 100 50 ō (ppm) 4000 3000 2000 1500 1000 500 HAVENUMBERI-11arrow_forwardComplete the spectroscopy with structurearrow_forwardComplete the spectroscopy with structurearrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)