Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Question
Chapter 18.5, Problem 7P
Interpretation Introduction
Interpretation:
Side chain of amino acid that can form an imine with the substrate has to be identified.
Concept introduction:
Amino acids are the molecules which containing an
Amino acids are the basic structural building units of protein and other
An imine is a compound having
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Which of the attached amines can be used to resolve a racemic mixture of amino acids?
In a typical amino acid zwitterion, the carboxylate end is
O neutral
O attached to an amine
O positively charged
soluble in a nonpolar solvent
O negatively charged
« Previous
Which of the following amino acid side chains can form an imine with a substrate?
Chapter 18 Solutions
Essential Organic Chemistry (3rd Edition)
Ch. 18.1 - Prob. 1PCh. 18.2 - If H218O were used to hydrolyze lysozyme, which...Ch. 18.3 - Which of the following amino acid side chains can...Ch. 18.3 - Arginine and lysine side chains fit into trypsins...Ch. 18.4 - Which of the following amino acid side chains can...Ch. 18.4 - Prob. 6PCh. 18.5 - Prob. 7PCh. 18.5 - Draw the mechanism for the hydroxide-ion-catalyzed...Ch. 18.5 - What advantage does the enzyme gain by forming an...Ch. 18.7 - Prob. 10P
Ch. 18.7 - Prob. 11PCh. 18.8 - How many conjugated double bonds are there in a....Ch. 18.8 - Instead of adding to the 4a-position and...Ch. 18.8 - In succinate dehydrogenase, FAD is covalently...Ch. 18.8 - Prob. 15PCh. 18.9 - Acetolactate synthase is another TPP-requiring...Ch. 18.9 - Acetolactate synthase can also transfer the acyl...Ch. 18.9 - Prob. 18PCh. 18.9 - Prob. 19PCh. 18.10 - Prob. 21PCh. 18.11 - Prob. 23PCh. 18.11 - Which compound is more easily decarboxylated?Ch. 18.11 - Explain why the ability of PLP to catalyze an...Ch. 18.11 - Explain why the ability of PLP to catalyze an...Ch. 18.12 - What groups are interchanged in the following...Ch. 18.13 - Why is the coenzyme called tetrahydrofolate?Ch. 18.13 - What amino acid is formed by the following...Ch. 18.13 - How do the structures of tetrahydrofolate and...Ch. 18.13 - What is the source of the methyl group in...Ch. 18 - Prob. 32PCh. 18 - Prob. 33PCh. 18 - From what vitamins are the following coenzymes...Ch. 18 - Prob. 35PCh. 18 - For each of the following reaction, name both the...Ch. 18 - Explain why serine proteases do not catalyze...Ch. 18 - Prob. 38PCh. 18 - For each of the following enzyme catalyzed...Ch. 18 - Trisephosphate isomerase (TIM) catalyzes the...Ch. 18 - Prob. 41PCh. 18 - What acyl groups have we seen transferred by...Ch. 18 - When UMP is dissolved in T2O, exchange of T for H...Ch. 18 - Prob. 44PCh. 18 - When transaminated, the three branched-chain amino...Ch. 18 - Aldolase shows no activity if it is incubated with...
Knowledge Booster
Similar questions
- DRAW THE CHEMICAL STRUCTURE OF THE FOLLOWING:1) Methyl 5-methyl-6-oxohexanoate2) 5-Amino-3-methylpentan-2-ol3) Isopropyl 3-hydroxypropanoate4) 3-Oxocyclohexanecarbaldehyde5) 5-Methyl-6-oxohexanamide6) p-Chloromethylbenzene7) 2,5,5-Trimethyl-4-oxohept-2-enoic acidarrow_forwardThe hydrolysis of an ester can be sped up by both acidic and basic conditions. Aminolysis of an ester can be sped up by acidic conditions, but not by basic conditions. Explain why.arrow_forwardWhich of the following substituent is an ortho/para-directing deactivator? a amino group b halogen group c phenyl group d carboxyl grouparrow_forward
- Ethyleneimine reacts with cysteine side chains in proteins to form S - aminoethyl derivatives. The peptide bonds on the carboxyl side of these modified cysteine residues are susceptible to hydrolysis by trypsin . Why?arrow_forward9. How do you know if a malenimide based reagent will conjugate to nitrogen or sulphur in an amino acid? но protein -protein SH NH2arrow_forwardNet charge and isoelectric point of an amino acid with an ionizable side group.Consider the net charge and isoelectric point of an amino acid with ionizable side (R-) group.(a) Identify the acidic amino acid(s) capable of having a negatively charged carboxyl side group.(b) Identify the basic amino acid(s) capable of having a positively charged amino side group.(c) For an amino acid with a side (R-) chain that can ionize to a negative charge, derive a general expression in terms of measured pH and known pKa values of α-carboxyla-amino (pKca), α-amino(pKaa),and side group (pKRa), respectively, for the net charge of an amino acid Consider the net charge and isoelectric point of an amino acid with ionizable side (R-) group.(d) For an amino acid with a side (R-) chain that can ionize to a positive charge, derive a general expression in terms of measured pH and known pKa values ofα-carboxyl (pKca), α-amino (pKaa), and side group (pKRa), respectively, for the net charge of the amino acid.(e)…arrow_forward
- Based on the image attached, it shows methyl salicylate reacts with Ethanamine, and Ether act as a solvent to form N-ethylbenzamide as a product. Explains the mechanism reaction of conversion ester to an amide.arrow_forwardDraw the struetre of the following three isomeic amides with chemical feruula CHNO. Amide #1: (E)-N,N-dimethyl-2-butenamide Amide #2: (7)-N-methyl-3-pentenamide Amide #3: (7)-3-hexenamide C'onsider Z sterenchemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers asing the drop-down memu in the hottom right comer. Sepamte structares with - signs from the drop-down mena. O00. IF ChemDoodle ChemDoodie ChemDoodle just the first one is what I could really use help on Amide #1: (E)-N,N-dimethyl-2-butenamidearrow_forwardDraw the structure for each of the following peptides in their fully protonated forms. Indicate which protons are dissociable in the structure. a) Gly-Lys-Arg-Phe b) Y-D-S-C-Qarrow_forward
- Which of the following substituent is an ortho/para-directing activator and an ortho/para-directing deactivator? a amino group b halogen group c nitro group d carboxyl grouparrow_forwardThe aminolysis of acetic anhydride will produce aniline and ammonia as major products. True or Falsearrow_forwardCompounds with polyfunctional groups must follow priority rule. Which of the following compound is correctly named. Justify your claim and construct its correct structure. А: 3-amino-7-carboxy-4-oxoheptanamide 3-amino-7-carbanoyl-4-oxoheptanoic acid 3-amino-4-ox0-7-carbanoylheptanoic acid 3-amino-4-oxo-7-carboxyheptanamide В: С: D:arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning