Concept explainers
(a)
Interpretation:
The structure of fluorobenzene is to be drawn.
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents.
(b)
Interpretation:
The structure of
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents.
(c)
Interpretation:
The structure of
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents.
(d)
Interpretation:
The structure of
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents.
(e)
Interpretation:
The structure of
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents.
(f)
Interpretation:
The structure of
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents.
Want to see the full answer?
Check out a sample textbook solutionChapter B Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- Given each of the IUPAC names provided, draw the corresponding structure. (a) 1-(1,1-dimethylethyl)-2,4-diethylcyclohexane; (b) 1,4-dibutyl-2-(1-methylpropyl)cyclooctane; (c) 1,1-dicyclopropyl-3-(1,1-dimethylethyl)cycloheptanearrow_forwardDraw 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 structures of the following compounds. (a) 1-isobutyl-4-isopropylcyclohexane; (b) tert-butylcyclopentane;(c) 3,3-diisopropyloctanearrow_forward
- Draw the structure of each of the following molecules (a) 2,2-dimethylcyclopentane-1-carboxylic acid;(b) (R)-3-chloropentanoic acid; (c) (2R,3S)-2,3-dinitrobutanedioic acidarrow_forwardGiven each of the IUPAC names provided, draw the corresponding structure. (a) 1-ethoxy-3-methoxyhexane;(b) 1,5-dipropoxypentane; (c) 4-butoxy-1,2-dimethoxyheptanearrow_forwardDraw the structures of: (a) 1-ethenyl-3-nitrobenzene; (b) (1-methylpentyl)benzene; (c) 2-methyl-1,3,5-trinitrobenzene.arrow_forward
- Draw the structures for (a) hex-2-ene; (b) hex-3-ene; (c) hept-1-ene; (d) oct-2-yne; (e) cycloheptene.arrow_forwardDraw the structure of each of the following molecules. (a) pentanoyl chloride; (b) 4-(2-methylpropyl)heptanedioyl chloride; (c) (S)-5-phenyloctanoyl chloridearrow_forwardDraw the structure of each of the following molecules. (a) pentanoyl chloride; (b) 4-(2-methylpropyl)heptanedioyl chloride;(c) (S)-5-phenyloctanoyl chloridearrow_forward
- (a) Draw and name all five isomers of formula C3H5F.(b) Draw all 12 acyclic (no rings) isomers of formula C4H7Br. Include stereoisomers.arrow_forward9. Which of the following compounds, is the most acidic: (a) 2-methylhex-3-yne, (b) 2,5-dimethylhex-3-yne or (c) 2,2,5-trimethylhex-3-yne?arrow_forwardDraw the structures of all monobromo derivatives of 2-methylpentane, C6H13Br, which have the bromine on a primary carbon.arrow_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