Principles of General, Organic, Biological Chemistry
2nd Edition
ISBN: 9780073511191
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
expand_more
expand_more
format_list_bulleted
Question
Chapter 13, Problem 13.79AP
a.
Interpretation Introduction
Interpretation:
Product that forms has to be drawn when
Concept Introduction:
Amide also undergo hydrolysis as like esters. They are much less reactive than the esters. When amide is treated with water in presence of acid as a catalyst, the product formed is
b.
Interpretation Introduction
Interpretation:
Product that forms has to be drawn when
Concept Introduction:
Refer part “a.”.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
V. Classify each amine as 1', 2 or 3'. Give the IUPAC name for each amine.
CH3
a. CH3CHCH,CH2NHCH3
b.
CH3-C-CH,NH2
ČH3
ČH3
Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. What functional group
Erythronolide B does contain?
a.
b.
H₂CH₂C
C.
H₂C
1
H₂C
2
3
4
O
Amide
d. Amine
OH
Erythronolide B
Ketone
Aldehyde
a
CH₂
b
C
d
CH₂
OH
JCH₂
'OH
OH
Which of the following contains an amide?
HO
A.
N.
B.
НО.
ОН
с.
-OH
H₂N
D.
Chapter 13 Solutions
Principles of General, Organic, Biological Chemistry
Ch. 13.1 - Draw out each compound to clearly show what groups...Ch. 13.1 - Prob. 13.2PCh. 13.2 - Prob. 13.3PCh. 13.2 - Give the structure corresponding to each IUPAC...Ch. 13.2 - Prob. 13.5PCh. 13.2 - Give the structure corresponding to each name. a....Ch. 13.3 - Which compound in each pair has the higher boiling...Ch. 13.3 - Rank the following compounds in order of...Ch. 13.4 - Which compounds are -hydroxy acids? tartaric acid...Ch. 13.4 - Prob. 13.10P
Ch. 13.5 - Prob. 13.11PCh. 13.5 - Prob. 13.12PCh. 13.5 - Prob. 13.13PCh. 13.6 - Prob. 13.14PCh. 13.6 - Prob. 13.15PCh. 13.6 - Prob. 13.16PCh. 13.6 - Prob. 13.17PCh. 13.6 - Prob. 13.18PCh. 13.6 - Prob. 13.19PCh. 13.7 - Prob. 13.20PCh. 13.7 - Prob. 13.21PCh. 13.7 - Prob. 13.22PCh. 13.7 - Prob. 13.23PCh. 13.7 - Prob. 13.24PCh. 13.8 - Prob. 13.25PCh. 13.8 - Prob. 13.26PCh. 13.8 - Prob. 13.27PCh. 13.8 - Draw the product formed when each ammonium salt is...Ch. 13.8 - Prob. 13.29PCh. 13.9 - Prob. 13.30PCh. 13.9 - Prob. 13.31PCh. 13.9 - Prob. 13.32PCh. 13.9 - Why is the boiling point of CH3CONH2(221C) higher...Ch. 13.9 - Prob. 13.34PCh. 13.9 - Prob. 13.35PCh. 13.10 - Prob. 13.36PCh. 13 - Prob. 13.37UKCCh. 13 - Prob. 13.38UKCCh. 13 - Prob. 13.39UKCCh. 13 - Prob. 13.40UKCCh. 13 - Prob. 13.41UKCCh. 13 - Prob. 13.42UKCCh. 13 - Prob. 13.43UKCCh. 13 - Prob. 13.44UKCCh. 13 - Prob. 13.45UKCCh. 13 - Prob. 13.46UKCCh. 13 - Prob. 13.47UKCCh. 13 - Prob. 13.48UKCCh. 13 - Prob. 13.49UKCCh. 13 - Prob. 13.50UKCCh. 13 - Prob. 13.51APCh. 13 - Prob. 13.52APCh. 13 - Prob. 13.53APCh. 13 - Draw the structure of a compound of molecular...Ch. 13 - Prob. 13.55APCh. 13 - Prob. 13.56APCh. 13 - Give an acceptable name for each compound.Ch. 13 - Prob. 13.58APCh. 13 - Prob. 13.59APCh. 13 - Prob. 13.60APCh. 13 - Prob. 13.61APCh. 13 - Prob. 13.62APCh. 13 - Prob. 13.63APCh. 13 - Give an acceptable name for each amine or amide....Ch. 13 - Draw the structure corresponding to each name. a....Ch. 13 - Draw the structure corresponding to each name. a....Ch. 13 - Prob. 13.67APCh. 13 - Draw the structure of each amine or ammonium salt....Ch. 13 - Prob. 13.69APCh. 13 - Which compound in each pair is more water soluble?...Ch. 13 - Prob. 13.71APCh. 13 - Prob. 13.72APCh. 13 - Prob. 13.73APCh. 13 - Prob. 13.74APCh. 13 - Prob. 13.75APCh. 13 - Prob. 13.76APCh. 13 - Prob. 13.77APCh. 13 - Prob. 13.78APCh. 13 - Prob. 13.79APCh. 13 - Prob. 13.80APCh. 13 - Prob. 13.81APCh. 13 - Prob. 13.82APCh. 13 - Prob. 13.83APCh. 13 - Prob. 13.84APCh. 13 - Prob. 13.85APCh. 13 - Prob. 13.86APCh. 13 - Prob. 13.87APCh. 13 - Draw the products of each acid-base reaction.Ch. 13 - Prob. 13.89APCh. 13 - Prob. 13.90APCh. 13 - Prob. 13.91APCh. 13 - Prob. 13.92APCh. 13 - Ritalin is the trade name for methylphenidate, a...Ch. 13 - Prob. 13.94APCh. 13 - Prob. 13.95CPCh. 13 - Prob. 13.96CPCh. 13 - Prob. 13.97CPCh. 13 - Prob. 13.98BTCCh. 13 - Prob. 13.99BTCCh. 13 - Prob. 13.100BTC
Knowledge Booster
Similar questions
- List the products of each amine reaction. H b. CH;-N-CH-CH, + HCN CH3arrow_forwardArrange the following amines in increasing boiling point. O₂N. NH₂ NH₂ NH₂ A a. Carrow_forwardQuinapril (trade name Accupril) is a drug used to treat hypertension and congestive heart failure.a.Identify the functional groups in quinapril. b.Classify any alcohol, amide, or amine as 1°, 2°, or 3°. c. At which sites can quinapril hydrogen bond to water? d.At which sites can quinapril hydrogen bond to acetone [(CH3)2CO]? e. Label the most acidic hydrogen atom. f.Which site is most basic?arrow_forwardWhich of the following is an amine? Select one: a. HCONH2 b. CH3COCH3 c. CH3F d. CH3NH2arrow_forwardWhich compound can react with ammonia to produce an amide? A) CHCH-CH-ОН B) C) D) CH,CH,CH,CH,-Ĉ-OHarrow_forwardVI. What ammonium salt is formed when each amine is treated with HCI? Draw the structure of the resulting salt. a. -NH2 b. -CH,NHCH3arrow_forwardWhat are the products of the reaction between acetyl chloride and diethylamine? HCl and N,N-diethylacetamide Оа. o b. HCl and diethylamine chloride ос. HCl and N-ethylacetamide d. Diethylacetamide and acidarrow_forwardClassify each amine in the following compounds as 1°, 2°, or 3°. NH2 a. H,N b. CH,CH20. N-CH, spermine (isolated from semen) meperidine (a narcotic) Trade name: Demerolarrow_forward17-50 Draw the structure of the amine salt produced when each of the following amines reacts with HCl. a. CH3-CH,-CH2-NH2 b. CH3-NH-CH3 CH3 c. CH,-CH-CH;-NH, d.[NH-CH;-Ch -NH-CH-CHarrow_forwardWhat ammonium salt is formed when each amine is treated with HCl? Draw the structure of the resulting salt.arrow_forwardWhich of the following is an amide? Select one: a. CH3NH2 b. CH3OH c. HCONH2 d. CH2Oarrow_forward2. Draw the product when each of the amines acts as a base when combined with water. Name the ion that forms. a) CH-CHL- Nith + Hy0 b) CHy-NH-CH CHy + HgOarrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios
Recommended textbooks for you
- 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
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY