
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Question
Chapter 4.2, Problem 2ATS
Interpretation Introduction
Interpretation:
From the given compounds, the compounds that have same parent have to be identified.
Concept Introduction:
Nomenclature of organic chemicals:
The naming of the organic compounds is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving names, thus
- The largest number of Carbon present in the chain is called as a parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
To identify: the same parent having two compounds.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
+
Reset
Provide the correct IUPAC name for the compound shown here.
4-methylhept-2-ene
(Z)- (E)-
1-6-5-2-3-4-
cyclo iso tert- sec- di tri
hept hex oct meth eth pent
ane yne ene yl
+
Provide the correct IUPAC name for the compound shown here.
Reset
H3C
H
H
C
CH3
CH-CH3
1-3-methylpent ene
trans- cis-
5-6-3-1-2-4-
tert- tri sec- di cyclo iso
but pent hex meth prop eth
yl ane ene yne
☑
drawing, no ai
Chapter 4 Solutions
Organic Chemistry, Binder Ready Version
Ch. 4.2 - Prob. 1LTSCh. 4.2 - Prob. 1PTSCh. 4.2 - Prob. 2ATSCh. 4.2 - Prob. 3ATSCh. 4.2 - Prob. 4ATSCh. 4.2 - Prob. 2LTSCh. 4.2 - Prob. 5PTSCh. 4.2 - Prob. 6ATSCh. 4.2 - Prob. 3LTSCh. 4.2 - Prob. 7PTS
Ch. 4.2 - Prob. 8ATSCh. 4.2 - Prob. 9ATSCh. 4.2 - Prob. 4LTSCh. 4.2 - Prob. 10PTSCh. 4.2 - Prob. 11ATSCh. 4.2 - Prob. 5LTSCh. 4.2 - Prob. 12PTSCh. 4.2 - Prob. 13ATSCh. 4.3 - Prob. 6LTSCh. 4.3 - Prob. 14PTSCh. 4.3 - Prob. 15ATSCh. 4.6 - Prob. 7LTSCh. 4.6 - Prob. 16PTSCh. 4.6 - Prob. 17ATSCh. 4.6 - Prob. 18ATSCh. 4.7 - Prob. 19CCCh. 4.8 - Prob. 8LTSCh. 4.8 - Prob. 20PTSCh. 4.8 - Prob. 21ATSCh. 4.11 - Prob. 9LTSCh. 4.11 - Prob. 22PTSCh. 4.11 - Prob. 23ATSCh. 4.11 - Prob. 10LTSCh. 4.11 - Prob. 24PTSCh. 4.11 - Prob. 25PTSCh. 4.11 - Prob. 26PTSCh. 4.11 - Prob. 27ATSCh. 4.12 - Prob. 11LTSCh. 4.12 - Prob. 28PTSCh. 4.12 - Prob. 29ATSCh. 4.12 - Prob. 30CCCh. 4.12 - Prob. 12LTSCh. 4.12 - Prob. 31PTSCh. 4.12 - Prob. 32ATSCh. 4.12 - Prob. 13LTSCh. 4.12 - Prob. 33PTSCh. 4.12 - Prob. 34ATSCh. 4.12 - Prob. 35ATSCh. 4.14 - Prob. 36CCCh. 4.14 - Prob. 37CCCh. 4.14 - Prob. 38CCCh. 4 - Prob. 39PPCh. 4 - Prob. 40PPCh. 4 - Prob. 41PPCh. 4 - Prob. 42PPCh. 4 - Prob. 43PPCh. 4 - Prob. 44PPCh. 4 - Prob. 45PPCh. 4 - Prob. 46PPCh. 4 - Prob. 47PPCh. 4 - Prob. 48PPCh. 4 - Prob. 49PPCh. 4 - Prob. 50PPCh. 4 - Prob. 51PPCh. 4 - Prob. 52PPCh. 4 - Prob. 53PPCh. 4 - Prob. 54PPCh. 4 - Prob. 55PPCh. 4 - Prob. 56PPCh. 4 - Prob. 57PPCh. 4 - Prob. 58PPCh. 4 - Prob. 59PPCh. 4 - Prob. 60PPCh. 4 - Prob. 61PPCh. 4 - Prob. 62PPCh. 4 - Prob. 63PPCh. 4 - Prob. 64IPCh. 4 - Prob. 65IPCh. 4 - Prob. 67IPCh. 4 - Prob. 68IPCh. 4 - Prob. 69IP
Knowledge Booster
Similar questions
- drawing, no aiarrow_forwardDraw the major organic product when each of the bellow reagents is added to 3,3-dimethylbutere. ✓ 3rd attempt Part 1 (0.3 point) H.C CH CH + 1. BHG THF 210 NaOH NJ 10000 Part 2 (0.3 point) HC- CH HC 2741 OH a Search 1. He|DA HO 2. NIBH さ 士 Ju See Periodic Table See Hint j = uz C H F F boxarrow_forwardSynthesis of 2-metilbenzimidazol from 1,2-diaminobenceno y propanona.arrow_forward
- Predict the product of the following reaction. 1st attempt HI 1 product 50300 Jul See Periodic Table See Hint P Br 石尚 Iarrow_forwardIndicate the substitutes in one place, if they are a diazonio room.arrow_forwardIndicate the product formed in each reaction. If the product exhibits tautomerism, draw the tautomeric structure. a) о + CH3-NH-NH2 CO2C2H5 b) + CoH5-NH-NH2 OC2H5arrow_forward
- Indicate the formula of the compound, that is the result of the N- alquilación (nucleofílic substitution), in which an additional lateral chain was formed (NH-CH2-COOMe). F3C. CF3 NH NH2 Br о OMe K2CO3, DABCO, DMFarrow_forwardSynthesis of 1-metilbenzotriazole from 1,2-diaminobenceno.arrow_forwardSynthesis of 1-metilbenzotriazole.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