a) I-L-P-F
Interpretation:
The structure of the PTH derivative product that is obtained by Edman degradation of the peptide I-L-P-F is to be given.
Concept introduction:
Edmund degradation involves treatment of a peptide with phenyl isothiocyanate, followed by reaction with trifluoroacetic acid when an anilinothiazolinone (ATZ) is produced. This ATZ rearranges in the presence of acids to yield N-phenylthiohydantoin.
To give:
The structure of the PTH derivative product that is obtained by Edman degradation of the peptide I-L-P-F.
b) D-T-S-G-A
Interpretation:
The structure of the PTH derivative product that is obtained by Edman degradation of the peptide D-T-S-G-A is to be given.
Concept introduction:
Edmund degradation involves treatment of a peptide with phenyl isothiocyanate, followed by reaction with trifluoroacetic acid when an anilinothiazolinone (ATZ) is produced. This ATZ rearranges in the presence of acids to yield N-phenylthiohydantoin.
To give:
The structure of the PTH derivative product that is obtained by Edman degradation of the peptide D-T-S-G-A.
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Chapter 26 Solutions
ORGANIC CHEMISTRY-EBOOK>I<
- Na :S f. F NO2arrow_forwardQ1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. + CI OH woཡི།༠w Br H مه D CI ပ။ Br H, Br Br H₂N OMe R IN Ill N S H CI Br CI CI D OH H 1/111arrow_forwardDraw the two products of the reaction. H₂C. CH₂ H :0: CH3 CH₂ +1arrow_forward
- 93 = Volume 93 = 5.32× 10 3 -23 ст a √ 1073 5.32× 10 3 cm³arrow_forwardASP.....arrow_forwardQuestion 7 (10 points) Identify the carboxylic acid present in each of the following items and draw their structures: Food Vinegar Oranges Yogurt Sour Milk Pickles Acid Structure Paragraph ✓ BI UAE 0118 + v Task: 1. Identify the carboxylic acid 2. Provide Name 3. Draw structure 4. Take a picture of your table and insert Add a File Record Audio Record Video 11.arrow_forward
- Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 IZ IN Molecule 4 Molecule 5 ZI none of the above ☐ Molecule 3 Х IN www Molecule 6 NH Garrow_forwardHighlight each chiral center in the following molecule. If there are none, then check the box under the drawing area. There are no chiral centers. Cl Cl Highlightarrow_forwardA student proposes the following two-step synthesis of an ether from an alcohol A: 1. strong base A 2. R Is the student's proposed synthesis likely to work? If you said the proposed synthesis would work, enter the chemical formula or common abbreviation for an appropriate strong base to use in Step 1: If you said the synthesis would work, draw the structure of an alcohol A, and the structure of the additional reagent R needed in Step 2, in the drawing area below. If there's more than one reasonable choice for a good reaction yield, you can draw any of them. ☐ Click and drag to start drawing a structure. Yes No ロ→ロ 0|0 G Х D : ☐ பarrow_forward
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