ORG CHEM CONNECT CARD
6th Edition
ISBN: 9781264860746
Author: SMITH
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Question
Chapter 27, Problem 58P
Interpretation Introduction
Interpretation: The sequence of an octapeptide that contains amino acids is to be deduced by using the experimental data.
Concept introduction: Peptide linkage is formed between the amino group of one amino acid and the carboxyl group of other amino acid with the loss of water molecule. Amino acids are naturally occurring compounds in which the amino group is present on the alpha carbon of carboxyl group. The name of amino acids is represented by the one-letter and three-letter abbreviations. Edman degradation is used to identify the N-terminal amino acids.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
1. Determine the relationship between the following molecules as identical, diastereomers, or enantiomers (6
points, 2 points each).
OH
OH
OH
A-A
OH
HOT
HO-
ACHN
and
HO-
ACHN
OH
HO
HO
°
OH
and
OH
OH
SH
and
...SH
20,0
Complete the electron pushing mechanism to
y drawing the necomery unicaciones and carved on for
Step 1: Add curved arms for the tint step, traiment with NalilĻ. The Nation
458
Step 2: Added for the second step, inalment with), how the "counterion
bar
Step 3: Daw the products of the last simplom organic and one incoganic spacient, including all nonbonding
please provide the structure for this problem, thank you!
Chapter 27 Solutions
ORG CHEM CONNECT CARD
Ch. 27.1 - Prob. 1PCh. 27.1 - Problem 29.2
What form exists at the isoelectric...Ch. 27.1 - Problem 29.3
Explain why the of the group of an...Ch. 27.1 - Prob. 4PCh. 27.2 - Problem 29.5
What -halo carbonyl compound is...Ch. 27.2 - Problem 29.6
The enolate derived from diethyl...Ch. 27.2 - Problem 29.7
What amino acid is formed when is...Ch. 27.2 - Problem 29.8
What aldehyde is needed to synthesize...Ch. 27.2 - Problem 29.9
Draw the products of each...Ch. 27.3 - Prob. 10P
Ch. 27.3 - Prob. 11PCh. 27.3 - Prob. 12PCh. 27.4 - Problem 29.13
What alkene is needed to synthesize...Ch. 27.5 - Problem 29.14
Draw the structure of each peptide....Ch. 27.5 - Problem 29.15
Name each peptide using both the...Ch. 27 - Draw the product formed when the following amino...Ch. 27 - With reference to the following peptide: a...Ch. 27 - Prob. 31PCh. 27 - Histidine is classified as a basic amino acid...Ch. 27 - Tryptophan is not classified as a basic amino acid...Ch. 27 - What is the structure of each amino acid at its...Ch. 27 - What is the predominant form of each of the...Ch. 27 - 29.37 What is the predominant form of each of the...Ch. 27 - a. Draw the structure of the tripeptide A–A–A, and...Ch. 27 - 29.39 Draw the organic products formed in each...Ch. 27 - 29.40 What alkyl halide is needed to synthesize...Ch. 27 - Prob. 50PCh. 27 - Draw the structure for each peptide: (a) Phe–Ala;...Ch. 27 - 29.52 For the tetrapeptide Asp–Arg–Val–Tyr:
a....Ch. 27 - Prob. 53PCh. 27 - Prob. 54PCh. 27 - 29.55 Draw the amino acids and peptide fragments...Ch. 27 - Prob. 56PCh. 27 - Prob. 57PCh. 27 - Prob. 58PCh. 27 - 29.59 An octapeptide contains the following amino...Ch. 27 - 29.60 Draw the organic products formed in each...Ch. 27 - 29.65 Draw the mechanism for the reaction that...Ch. 27 - 29.66 Which of the following amino acids are...Ch. 27 - 29.67 After the peptide chain of collagen has been...Ch. 27 - Prob. 68PCh. 27 - Prob. 69PCh. 27 - 29.70 The anti-obesity drug orlistat works by...Ch. 27 - Prob. 71P
Knowledge Booster
Similar questions
- Draw the Fischer projection from the skeletal structure shown below. HO OH OH OH OH H Q Drawing Atoms, Bonds and Rings Charges I ☐ T HO H H OH HO I CH2OH H OH Drag H OH -CH2OH CHO -COOH Undo Reset Remove Donearrow_forwardplease provide the structure for this problem, thank youarrow_forwardpresented by Morallen Lig Intermine the hand product for the given mution by adding atoms, bonds, nonhonding diarion panda скуль Step 3: Comp the draw the product Step 2: Agama workup Compithe 429 ملولةarrow_forward
- Reaction A 0,0arrow_forwardpresented by Morillon Leaning Predict the organic product for the min кусур HSC Adithane carved arnown to come than that to the condon slchroruis in acid in in aquishri with ноюarrow_forward6.15PM Sun Mar 30 K Draw the major product of this reaction. Include any relevant stereochemistry. Ignore inorganic byproducts. Problem 1 of O H [PhзPCH2CH3]*C|¯ NaH Drawing > Q Atoms, Bonds and Draw or tap a nearrow_forward
- 8:17 PM Sun Mar 30 Draw the major product of this reaction. Ignore inorganic byproducts. HSCH2CH2CH2SH, BF3 Probler Drawing Ato Bonds Clarrow_forwardpresented by Mr L How the coprion. (Il Done in no wraction, dew the starting redential) доarrow_forward8:16 PM Sun Mar 30 K Draw the major product of this reaction. Ignore inorganic byproducts. Proble 1. CH3MgBr 2. H3O+ F Drawingarrow_forward
- о но оarrow_forwardName the major organic product of the following action of 4-chloro-4-methyl-1-pentanol in neutral pollution 10+ Now the product. The product has a molecular formula f b. In a singly hain, the starting, material again converts into a secule with the molecular kormula CIO. but with comply Draw the major organic structure inhalationarrow_forwardMacmillan Learning Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C,H,NH*)(CICTO3), commonly known as PCC. Draw the proposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by PCC when carried out in an anhydrous solvent such as CH₂C₁₂. PCC Intermediate OH CH2Cl2 Draw the intermediate. Select Draw Templates More с H Cr о Product Draw the product. Erase Select Draw Templates More H о Erasearrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning