ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<
3rd Edition
ISBN: 9781119781448
Author: Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 19.2, Problem 4ATS
(a)
Interpretation Introduction
Interpretation: The structure for the given IUPAC name has to be identified.
Concept Introduction:
Guidelines in drawing the structure from the given IUPAC name:
- The parent chain has to be identified by the root word.
Illustration:
Root word | Parent chain identification |
ane | |
ene | |
yne |
- The substituents on the parent chain have to be identified by the primary suffix name. The substituent name always follows with a number which indicates at which carbon atom the substituent is attached on the parent chain.
Illustration:
Primary suffix | Substituent identification |
methyl | |
ethyl | |
isopropyl |
- The
functional groups have to be identified by the secondary suffix name. The functional group name always follows with a number which indicates at which carbon atom the functional group is attached on the parent chain.
Illustration:
Functional group | Functional group identification |
ol | Alcohol |
al | |
one |
- Finally the structure can be drawn based on these identifications.
(b)
Interpretation Introduction
Interpretation: The structure for the given IUPAC name has to be identified.
Concept Introduction:
Guidelines in drawing the structure from the given IUPAC name:
- The parent chain has to be identified by the root word.
Illustration:
Root word | Parent chain identification |
ane | Alkane |
ene | Alkene |
yne | Alkyne |
- The substituents on the parent chain have to be identified by the primary suffix name. The substituent name always follows with a number which indicates at which carbon atom the substituent is attached on the parent chain.
Illustration:
Primary suffix | Substituent identification |
methyl | |
ethyl | |
isopropyl |
- The functional groups have to be identified by the secondary suffix name. The functional group name always follows with a number which indicates at which carbon atom the functional group is attached on the parent chain.
Illustration:
Functional group | Functional group identification |
ol | Alcohol |
al | Aldehyde |
one | Ketone |
- Finally the structure can be drawn based on these identifications.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
If I have 1-bromopropene and I want to obtain (1,1-dipropoxyethyl)benzene, indicate the compound that I should add in addition to NaOH.
Draw the major product of this reaction. Ignore inorganic byproducts.
Ο
HSCH2CH2CH2SH, BF3
Select to Draw
I
Submit
Feedback (7/10)
Draw the major product of this reaction. Ignore inorganic byproducts.
Assume that the water side product is continuously removed to drive the reaction toward products.
Incorrect, 3 attempts remaining
Ο
(CH3CH2)2NH, TSOH
Select to Draw
V
N.
87%
Retry
Chapter 19 Solutions
ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<
Ch. 19.2 - Prob. 1LTSCh. 19.2 - Prob. 1PTSCh. 19.2 - Prob. 2PTSCh. 19.2 - APPLY the skill
Compounds with two ketone groups...Ch. 19.2 - Prob. 4ATSCh. 19.3 - Prob. 5CCCh. 19.4 - Prob. 6CCCh. 19.5 - Prob. 7CCCh. 19.5 - Prob. 2LTSCh. 19.5 - Prob. 8PTS
Ch. 19.5 - Prob. 9ATSCh. 19.5 - Prob. 10CCCh. 19.5 - Prob. 11CCCh. 19.5 - Prob. 12CCCh. 19.5 - Prob. 13CCCh. 19.6 - Prob. 3LTSCh. 19.6 - Prob. 14PTSCh. 19.6 - Prob. 15PTSCh. 19.6 - Prob. 16ATSCh. 19.6 - Prob. 17CCCh. 19.6 - Prob. 18CCCh. 19.6 - Prob. 20PTSCh. 19.6 - Prob. 21ATSCh. 19.6 - Prob. 22CCCh. 19.7 - Prob. 5LTSCh. 19.7 - Prob. 23PTSCh. 19.7 - Prob. 24ATSCh. 19.7 - Prob. 25CCCh. 19.8 - Prob. 26CCCh. 19.8 - Prob. 27CCCh. 19.9 - Prob. 28CCCh. 19.9 - Prob. 29CCCh. 19.10 - Prob. 30CCCh. 19.10 - Prob. 31CCCh. 19.10 - Prob. 32CCCh. 19.10 - Prob. 33CCCh. 19.10 - Prob. 6LTSCh. 19.10 - Prob. 34PTSCh. 19.10 - Prob. 35PTSCh. 19.10 - Prob. 36ATSCh. 19.10 - Prob. 37ATSCh. 19.10 - Prob. 38CCCh. 19.11 - Prob. 39CCCh. 19.12 - Prob. 7LTSCh. 19.12 - Prob. 40PTSCh. 19.12 - Prob. 41ATSCh. 19.13 - Prob. 42CCCh. 19 - Prob. 43PPCh. 19 - Prob. 44PPCh. 19 - Prob. 45PPCh. 19 - Prob. 46PPCh. 19 - Prob. 47PPCh. 19 - Prob. 48PPCh. 19 - Prob. 49PPCh. 19 - Prob. 50PPCh. 19 - Prob. 51PPCh. 19 - Prob. 52PPCh. 19 - Prob. 53PPCh. 19 - Prob. 54PPCh. 19 - Prob. 55PPCh. 19 - Prob. 56PPCh. 19 - Prob. 57PPCh. 19 - Prob. 58PPCh. 19 - Prob. 59PPCh. 19 - Prob. 60PPCh. 19 - Predict the major product(s) obtained when each of...Ch. 19 - Prob. 62PPCh. 19 - Prob. 63PPCh. 19 - Prob. 64PPCh. 19 - Prob. 65PPCh. 19 - Prob. 66PPCh. 19 - Prob. 67PPCh. 19 - Prob. 68PPCh. 19 - Prob. 69PPCh. 19 - Prob. 70PPCh. 19 - Prob. 71PPCh. 19 - Prob. 72PPCh. 19 - Prob. 73PPCh. 19 - Prob. 74IPCh. 19 - Prob. 75IPCh. 19 - Prob. 76IPCh. 19 - Prob. 77IPCh. 19 - Prob. 78IPCh. 19 - Prob. 79IPCh. 19 - Prob. 80IPCh. 19 - Prob. 81IPCh. 19 - Prob. 83IPCh. 19 - Prob. 84IPCh. 19 - Prob. 85IPCh. 19 - Prob. 86IPCh. 19 - Prob. 87IPCh. 19 - Prob. 88IPCh. 19 - Prob. 89IPCh. 19 - Prob. 90IPCh. 19 - Prob. 91IPCh. 19 - Prob. 92IPCh. 19 - Prob. 93IPCh. 19 - Prob. 94CPCh. 19 - Prob. 95CPCh. 19 - Treatment of the following ketone with LiAIHa...
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
- If I want to obtain (1,1-dipropoxyethyl)benzene from 1-bromopropene, indicate the product that I have to add in addition to NaOH.arrow_forwardIndicate the products obtained when fluorobenzene reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained when chlorobenzene acid reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forward
- Indicate the products obtained by reacting benzenesulfonic acid with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained by reacting ethylbenzene with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained when tert-butylbenzene reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forward
- Indicate the products obtained when acetophenone reacts with a sulfonitric acid mixture (HNO3 + H2SO4). Indicate the majority if necessary.arrow_forwardIndicate the products obtained from the reaction of N-(4-methylphenyl)acetamide with a sulfonitric acid mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_forwardIndicate the products obtained from the reaction of 4-(trifluoromethyl)benzonitrile with a sulfonitric mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_forward
- Indicate the products obtained in the reaction of p-Toluidine with a sulfonitric acid mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_forwardIndicate the products obtained from the reaction of 4-methylbenzonitrile with a sulfonitric acid mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_forwardIndicate the products obtained from the reaction of 2-nitrophenol with a sulfonitric acid mixture (H2SO4 + HNO3). Indicate the majority if necessary.arrow_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 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