Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
13th Edition
ISBN: 9780134421353
Author: Karen C. Timberlake
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 14.6, Problem 14.45PP
Draw the condensed structural or line-angle formulas for the products from the hydrolysis of each of the following amides with HC1:
a.
b.
c.
d.
e.N-ethypentanamide
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Draw condensed and skeletal structures for each of the following amines:a. 2-methyl-N-propyl-1-propanamine b. N-ethylethanamine c. 5-methyl-1-hexanamine d. methyldipropylamine e. N,N-dimethyl-3-pentanamine f. cyclohexylethylmethylamine
Draw the structural formula for each of the following amines:
a.
diisopropylamine
b. p-ethylaniline
c. 2-methylcyclopentanamine
d. N-methyl-3-ethylaniline
What acyl chloride and amine are required to synthesize the following amides?a. N-ethylbutanamide b. N,N-dimethylbenzamide
Chapter 14 Solutions
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Ch. 14.1 - What carboxylic acid is responsible for the pain...Ch. 14.1 - What carboxylic acid is found in vinegar?Ch. 14.1 - Prob. 14.3PPCh. 14.1 - Prob. 14.4PPCh. 14.1 - Draw the condensed structural formulas for a and b...Ch. 14.1 - Draw the condensed structural formulas for a and b...Ch. 14.2 - Identify the compound in each group that is most...Ch. 14.2 - Prob. 14.8PPCh. 14.2 - Prob. 14.9PPCh. 14.2 - Prob. 14.10PP
Ch. 14.2 - Prob. 14.11PPCh. 14.2 - Prob. 14.12PPCh. 14.2 - Prob. 14.13PPCh. 14.2 - Prob. 14.14PPCh. 14.3 - Prob. 14.15PPCh. 14.3 - Prob. 14.16PPCh. 14.3 - Prob. 14.17PPCh. 14.3 - Prob. 14.18PPCh. 14.3 - Prob. 14.19PPCh. 14.3 - Prob. 14.20PPCh. 14.3 - Prob. 14.21PPCh. 14.3 - Prob. 14.22PPCh. 14.3 - Prob. 14.23PPCh. 14.3 - Prob. 14.24PPCh. 14.4 - What are the products of the acid hydrolysis of an...Ch. 14.4 - Prob. 14.26PPCh. 14.4 - Prob. 14.27PPCh. 14.4 - Prob. 14.28PPCh. 14.5 - Prob. 14.29PPCh. 14.5 - Prob. 14.30PPCh. 14.5 - Prob. 14.31PPCh. 14.5 - Prob. 14.32PPCh. 14.5 - Prob. 14.33PPCh. 14.5 - Prob. 14.34PPCh. 14.5 - Prob. 14.35PPCh. 14.5 - Prob. 14.36PPCh. 14.5 - Prob. 14.37PPCh. 14.5 - Prob. 14.38PPCh. 14.6 - Prob. 14.39PPCh. 14.6 - Prob. 14.40PPCh. 14.6 - Prob. 14.41PPCh. 14.6 - Prob. 14.42PPCh. 14.6 - Prob. 14.43PPCh. 14.6 - Prob. 14.44PPCh. 14.6 - Draw the condensed structural or line-angle...Ch. 14.6 - Draw the condensed structural or line-angle...Ch. 14.6 - a. Identify the functional groups in dicyclanil....Ch. 14.6 - a. Identify the functional groups in enrofloxacin....Ch. 14 - Prob. 14.49UTCCh. 14 - Prob. 14.50UTCCh. 14 - The ester methyl butanoate has the odor and flavor...Ch. 14 - Prob. 14.52UTCCh. 14 - Phenylephrine is the active ingredient in some...Ch. 14 - Melatonin is a naturally occurring compound in...Ch. 14 - Prob. 14.55UTCCh. 14 - Prob. 14.56UTCCh. 14 - Prob. 14.57APPCh. 14 - 14.58 Write the IUPAC and common names, if any,...Ch. 14 - Prob. 14.59APPCh. 14 - Prob. 14.60APPCh. 14 - Draw the condensed structural or line-angle...Ch. 14 - Prob. 14.62APPCh. 14 - Prob. 14.63APPCh. 14 - 14.64 Draw the condensed structural or line-angle...Ch. 14 - Prob. 14.65APPCh. 14 - 14.66 Write the common name and classify each of...Ch. 14 - Prob. 14.67APPCh. 14 - Draw the condensed structural or line-angle...Ch. 14 - Prob. 14.69APPCh. 14 - Prob. 14.70APPCh. 14 - Write the IUPAC name for each of the following:...Ch. 14 - Prob. 14.72APPCh. 14 - Prob. 14.73APPCh. 14 - Prob. 14.74APPCh. 14 - Prob. 14.75APPCh. 14 - Toradol is used in dentistry to relieve pain....Ch. 14 - Prob. 14.77CPCh. 14 - Draw the line-angle formula and write the IUPAC...Ch. 14 - Prob. 14.79CPCh. 14 - Prob. 14.80CPCh. 14 - Prob. 14.81CPCh. 14 - Prob. 14.82CP
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
- 10. Under certain conditions interacts with sodium nitrite: A. Resorcinol B. Nicotinic acid C. Butadion D. Morphine hydrochloride E. Benzoic acidarrow_forwardThe hydrolysis of an amide in acidic conditions forms A. a carboxylate salt and an alcohol B. a carboxylate salt and an amine C. an alcohol and an amine salt (an ammonium ion) D. a carboxylic acid and an amine salt (an ammonium ion)arrow_forwardIn general, amines are nucleophilic due to: Select one: a. Existence of negative charge in amine group b. Amines are more electronegative than other functional groups C. Lone pairs in the amine group available for donation d. None of the abovearrow_forward
- Acidic forms of barbituric acid derivatives exist in the form: A. Lactone form B. Lactam form C. Lactimal formarrow_forwardThe following are central stimulants: Select one or more: A. Barbiturates. B. Morphine. C. Benzodiazepines. D. Cocaine. E. Amphetamines.arrow_forwardWhat will happen to the body if the Ibuprofen and Aspirin will form an acid anhydrate inside it?arrow_forward
- Draw the structural formulas for the carboxylic acid chloride molecule used to make each of the following amides: C-NH-CH, a. CH, b. CH,CH,CH,-C-NH- CH,CH, CH, O CH, C. CH,CH-C-N-CH, CH,CH, d. CH,CH,-N-C- CH,CH, |arrow_forwardA. Use the structure of aniline provided and draw the complete structural formula for each of the following: N-Methylaniline N,N-Dimethylaniline 3-Octanamine 4-Chloro-5-iodo-1-nonanamine N-Isopropylanilinearrow_forwardBy functional group interconversion, which of the following compounds is not a good starting material for the synthesis of primary amine. A. Alkylhalide B. Alcohol C. Aldehyde D. Acetonitrilearrow_forward
- Pre-Lab Study Questions 1. What is the functional group in amines? In amides? 2. What products are formed when amides are hydrolyzed? 3. Draw the condensed structural formulas for each of the following amines and amides: a. 1-propanamine b. 2-methyl-3-hexamine c. N-methylpentamide d. N,N-dimethylbenzamide 139arrow_forwardWhich of the following is a suitable name for the ester CH3CH2CH2CH2CO2CH2CH2CH2CH3 Select one: a. pentyl butanoate b. nonanoate c. butyl pentanoate d. pentanebutanate Amides have Select one: a. an -OR group bonded to the carbonyl C atom b. an -NH2, -NHR, or NR2 group bonded to the carbonyl C atom c. an -OH group bonded to the carbonyl C atomarrow_forwardDraw structural formulas for the two compounds you could use to prepare the amine shown by reductive amination. aarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher: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,
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
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,
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
General Chemistry | Acids & Bases; Author: Ninja Nerd;https://www.youtube.com/watch?v=AOr_5tbgfQ0;License: Standard YouTube License, CC-BY