Concept explainers
(a)
Interpretation:
The structure for
Concept introduction:
In the case of molecules containing a
If the root is a chain, numbering begins from that end of the chain which encounters the
If the root is a ring, then the double or triple bonded carbon atoms are designated as C1 and C2. This must be done such that the locator numbers for the substituents, are minimized. The lower of the two locator numbers for the
(b)
Interpretation:
The structure for
Concept introduction:
In the case of molecules containing a
If the root is a chain, numbering begins from that end of the chain which encounters the
If the root is a ring, then the double or triple bonded carbon atoms are designated as C1 and C2. This must be done such that the locator numbers for the substituents are minimized. The lower of the two locator numbers for the
(c)
Interpretation:
The structure for
Concept introduction:
In the case of molecules containing a
If the root is a chain, numbering begins from that end of the chain which encounters the
If the root is a ring, then the double or triple bonded carbon atoms are designated as C1 and C2. This must be done such that the locator numbers for the substituents are minimized. The lower of the two locator numbers for the
(d)
Interpretation:
The structure for
Concept introduction:
In the case of molecules containing a
If the root is a chain, numbering begins from that end of the chain which encounters the
If the root is a ring, then the double or triple bonded carbon atoms are designated as C1 and C2. This must be done such that the locator numbers for the substituents are minimized. The lower of the two locator numbers for the
(e)
Interpretation:
The structure for cycloheptene is to be drawn.
Concept introduction:
In the case of molecules containing a
If the root is a chain, numbering begins from that end of the chain which encounters the
If the root is a ring, then the double or triple bonded carbon atoms are designated as C1 and C2. This must be done such that the locator numbers for the substituents are minimized. The lower of the two locator numbers for the
Want to see the full answer?
Check out a sample textbook solutionChapter B Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- Draw the structures of the following compounds. (a) 1-isobutyl-4-isopropylcyclohexane; (b) tert-butylcyclopentane;(c) 3,3-diisopropyloctanearrow_forwardGiven each of the IUPAC names provided, draw the corresponding structure. (a) 1-cyclopentylhexane;(b) cyclohexylcyclohexane; (c) 1,2-dicyclopropylnonanearrow_forwardDraw the structures for each of the following molecules. (a) 2-fluorotoluene; (b) 4-ethoxytoluene; (c) 2-ethoxyanisole;(d) 1,3-diphenylheptane; (e) 4,4-diphenyl-1-octene; (f) benzylbenzenearrow_forward
- Draw structures for the following haloalkanes. (a) 2,2-dichloro-3-cyclopropylbutane; (b) 1-bromo-1-chloro-1-iodobutane;(c) 2-bromo-1,1-diiodohexane; (d) 3-chloro-1,1,2,2-tetrafluoropentanearrow_forwardDraw the organic product formed when the following com-pounds undergo a substitution reaction: (a) acetic acid and methylamine; (b) butanoic acid and 2-propanol; (c) formic acidand 2-methyl-1-propanol.arrow_forward1. Draw the organic product formed when the following compounds undergo a substitution reaction ... : (a) acetic acid and methylamine; (b) butanoic acid and 2-propanol; (c) formic acid and 2-methyl- 1-propanol 2. Draw the organic product formed when the following compounds undergo a substitution reaction: (a) acetic acid and 1- hexanol; (b) propanoic acid and dimethylamine; (c) ethanoic acid and diethylamine.arrow_forward
- Given each of the IUPAC names provided, draw the corresponding structure. (a) 2-methylhexane; (b) 3-methylhexane;(c) 2,3-dimethylbutane; (d) 2,2,3-trimethylbutanearrow_forwardDraw the structures for (a) 2-methyl-1,3,5-hexatriene and (b) 1,6-dimethoxyhexa-1,5-diene.arrow_forwardDraw the structures for these molecules. (a) 2-chloropropene; (b) 3-methylbut-1-ene; (c) 2,3-dimethyl-2-butene;(d) 2-ethoxy-3,3-dimethylcyclohexene; (e) 3,4,5-trimethoxycycloheptene; (f) 3-bromo-2-methyl-4-nitrocyclopentene;(g) 3,3-dibromo-4-methylcyclopentene; (h) 4-methyl-2-pentynearrow_forward
- Draw the organic product formed when the following compounds undergo a substitution reaction: (a) acetic acid and methylamine; (b) butanoic acid and 2-propanol; (c) formic acid and 2-methyl-1-propanol.arrow_forwarddraw the skeletal (line-bond) structure of (S)-2-bromo-4-ethylhexane. please be sure to read molecule correctly, I saw someone ask this same question but the homework helper but Methylhexane instead of ethylhexane.arrow_forwardDraw the structure that corresponds to each of the following names. (a) 4-methyl-1-neopentylcyclohexane;(b) isobutylcyclobutane; (c) 5-sec-butylnonanearrow_forward
- 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