CHEMISTRY
13th Edition
ISBN: 9781292228860
Author: Timberlake
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 14.5, Problem 14.31PP
Interpretation Introduction
To determine:
- The condensed structural or line structural for ethylamine.
- The condensed structural or line structural for N-methylaniline.
- The condensed structural or line structural for butyl propylamine.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
b.
H3C
CH3
1.
2. H3O+
H3C
MgBr
H3C
Predict the major products of this reaction:
excess
H+
NaOH
?
A
Note that the first reactant is used in excess, that is, there is much more of the first reactant than the second.
If there won't be any products, just check the box under the drawing area instead.
Explanation
Check
Click and drag to start drawing a
structure.
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Priv
1. For each of the reaction "railroads" below, you are either asked to give the structure(s) of the starting
material(s) or product(s), or provide reagents/conditions to accomplish the transformation, as
indicated by the boxes.
a.
NaOMe
H+
.CO,H
HO₂C
MeOH (excess)
MeOH
H3C
Br
يع
CH3
1. LiAlH4
2. H3O+
3. PBг3
H3C
1. Et-Li
2. H3O+
-CO₂Me
-CO₂Me
OH
CH3
CH3
ল
CH3
Chapter 14 Solutions
CHEMISTRY
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
- Predict the intermediate 1 and final product 2 of this organic reaction: NaOMe ག1, ད།་, - + H You can draw 1 and 2 in any arrangement you like. 2 work up Note: if either 1 or 2 consists of a pair of enantiomers, just draw one structure using line bonds instead of 3D (dash and wedge) bonds at the chiral center. Explanation Check Click and drag to start drawing a structure. Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Parrow_forwardWhat is the total energy cost associated with the compound below adopting the shown conformation? CH3 HH DH CH3arrow_forwardΗΝ, Draw Final Product C cyclohexanone pH 4-5 Edit Enamine H3O+ CH3CH2Br THF, reflux H Edit Iminium Ionarrow_forward
- How many hydrogen atoms are connected to the indicated carbon atom?arrow_forwardIdentify the compound with the longest carbon - nitrogen bond. O CH3CH2CH=NH O CH3CH2NH2 CH3CH2C=N CH3CH=NCH 3 The length of all the carbon-nitrogen bonds are the samearrow_forwardIdentify any polar covalent bonds in epichlorohydrin with S+ and 8- symbols in the appropriate locations. Choose the correct answer below. Η H's+ 6Η Η Η Η Η Ηδ Η Ο Ο HH +Η Η +Η Η Η -8+ CIarrow_forward
- H H:O::::H H H HH H::O:D:D:H HH HH H:O:D:D:H .. HH H:O:D:D:H H H Select the correct Lewis dot structure for the following compound: CH3CH2OHarrow_forwardRank the following compounds in order of decreasing boiling point. ннннн -С-С-Н . н-с- ННННН H ΗΤΗ НННН TTTĪ н-с-с-с-с-о-н НННН НН C' Н н-с-с-с-с-н НН || Ш НННН H-C-C-C-C-N-H ННННН IVarrow_forwardRank the following compounds in order of decreasing dipole moment. |>||>||| ||>|||>| |>|||>|| |||>||>| O ||>>||| H F H F H c=c || H c=c F F IIIarrow_forward
- choose the description that best describes the geometry for the following charged species ch3-arrow_forwardWhy isn't the ketone in this compound converted to an acetal or hemiacetal by the alcohol and acid?arrow_forwardWhat is the approximate bond angle around the nitrogen atom? HNH H Harrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles 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 Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary 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