
Concept explainers
(a)
Interpretation:
The structure of the compound m-ethylphenol has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(b)
Interpretation:
The structure of the compound p-nitrobenzenesulfonic acid has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(c)
Interpretation:
The structure of the compound (E)-2-phenyl-2-pentene has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(d)
Interpretation:
The structure of the compound o-bromoaniline has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(e)
Interpretation:
The structure of the compound 4-bromo-1-chloro-2-methylbenzene has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(f)
Interpretation:
The structure of the compound m-chlorostyrene has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(g)
Interpretation:
The structure of the compound o-nitroanisole has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(h)
Interpretation:
The structure of the compound 2,4-dichloromethylbenzene has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.
(i)
Interpretation:
The structure of the compound m-chlorobenzoic acid has to be drawn.
Concept Introduction:
Criteria for substitution in benzene ring:
- The groups present on first and second position on benzene ring are said to be at ortho position.
- The groups present on first and third position on benzene ring are said to be at meta position.
- The groups present on first and fourth position on benzene ring are said to be at pera position.

Want to see the full answer?
Check out a sample textbook solution
Chapter 18 Solutions
ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL
- if the answer is no reaction than state that and please hand draw!arrow_forward"I have written solutions in text form, but I need experts to rewrite them in handwriting from A to Z, exactly as I have written, without any changes."arrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- Please correct answer and don't used hand raitingarrow_forwardreciprocal lattices rotates along with the real space lattices of the crystal. true or false?arrow_forwardDeducing the reactants of a Diels-Alder reaction vn the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ O If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Click and drag to start drawing a structure. Product can't be made in one step. Explanation Checkarrow_forward
- Predict the major products of the following organic reaction: Δ ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. Larrow_forward> Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ • If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. If your answer is no, check the box under the drawing area instead. Explanation Check Click and drag to start drawing a structure. Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accesarrow_forwardPredict the major products of the following organic reaction: O O + A ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. eserved. Terms of Use | Privacy Center >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





