EBK A SMALL SCALE APPROACH TO ORGANIC L
4th Edition
ISBN: 9781305446021
Author: Lampman
Publisher: CENGAGE LEARNING - CONSIGNMENT
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 47, Problem 5Q
Interpretation Introduction
Interpretation:
The preparation of procaine and procaine monohydrochloride by using the p-aminobenzoic acid should be shown and then the amino group that will be protonated first should be determined.
Concept Introduction:
Procaine is aesthetic drug which contains amino ester group, and it is used to reduce intramuscular injection pain of penicillin.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
What initiates a dehydration process between two amino acids, provided their carboxyl groups are exactly aligned with the amine groups of the other?
Refer to the structure of procaine in the table in the essay “Local Anesthetics.” Using p-aminobenzoic acid, give equations showing how procaine and procaine monohydrochloride could be prepared. Which of the two possible amino functional groups in procaine will be protonated first? Defend your choice. (Hint: Consider resonance.)
at a pH value of 2, the amino and carboxyl groups in an amino acid will exist as
Chapter 47 Solutions
EBK A SMALL SCALE APPROACH TO ORGANIC L
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Clorofibrate is hydrolyzed in the body to yield a related compound that is more effective in its action. Write the equation for the hydrolysis of clorofibrate. Identify the kind of acid derivative. What is meant by hydrolysis?arrow_forwardExamine the structure of the following amino acid and answer the questions below: Name the amino acid. Does it exhibit optical activity? Why? Describe the acid-base properties of amino acids. What is zwitterion?arrow_forward(a) Draw the Lewis structure for the amino acid phenylalanine, showing the amino group and the carboxylic group in their un-ionized forms. (b) Draw the Lewis structure for the zwitterionic form of phenylalanine. (c) Which of these structures will be the predominant form at physiological pH?arrow_forward
- Write the name of linkage joining two amino acids.arrow_forwardQ1. The pKa values of Glutamic acid are 2.2, 4.3 and 9.7. H2N но. HO (a) Calculate the pH of a glutamic acid solution in which the a-amine group is 80% deprotonated? (show your calculation!) (b) Draw the ionic forms of glutamic acid that exist at the calculated pH.arrow_forwardExplain the basic principle of the reaction between the amino acid histidine and the ninhydrin reagent.arrow_forward
- Draw the structures of aspirin, caffeine, and acetaminophen. Give the hybridization of each carbon atom and state which is acidic, weakly acidic, and basic. Identify the sites on each compound that make each acidic, weakly acidic, and basic.arrow_forwardComplete the equation to show how pyridine, C5H5N, acts as a Brønsted-Lowry base in water. equation: C5H5N + H2Oarrow_forwardAs the pH changes in an aqueous solution, Glutamic acid can exist in the neutral (zwitterionic) form and three different charged forms (with charge -2, -1 and +1). Draw these four forms of the molecule.arrow_forward
- What are the uses and properties of Astatine and Tennessine?arrow_forwardAll amino acids share a common structure, a central (alpha) carbon with four groups attached. Which of these is NOT one of the four groups attached to the alpha- carbon? O an R group an ammonium group (-NH3+) O a carboxylate group (-COO) a hydronium grouparrow_forwardThe property of water solutions to conduct electric current is possible for all of the 20 standard amino acids. True or False?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Biomolecules - Protein - Amino acids; Author: Tutorials Point (India) Ltd.;https://www.youtube.com/watch?v=ySNVPDHJ0ek;License: Standard YouTube License, CC-BY