Concept explainers
(a)
Interpretation:
The structure of pentylbenzene should be drawn.
Concept Introduction:
When the mixture of hydrocarbons from natural resources such as coal or petroleum are separated, certain compounds are emerged with pleasant odors and are thus known as
Hydrocarbons with sigma bonds and delocalization of pi electrons between carbon atoms, thus forms a circle is said to be aromatic hydrocarbons.
Aromatic compounds are named as a benzene derivative.
Rules of drawing structures of aromatic compounds are:
- First identify the substituents which are linked with benzene ring.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs) of benzene ring.
(b)
Interpretation:
The structure of o-dichlorobenzene should be drawn.
Concept Introduction:
When the mixture of hydrocarbons from natural resources such as coal or petroleum are separated, certain compounds are emerged with pleasant odors and are thus known as aromatic hydrocarbons.
Hydrocarbons with sigma bonds and delocalization of pi electrons between carbon atoms, thus forms a circle is said to be aromatic hydrocarbons.
Aromatic compounds are named as a benzene derivative.
Rules of drawing structures of aromatic compounds are:
- First identify the substituents which are linked with benzene ring.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs) of benzene ring.
(c)
Interpretation:
The structure of m-bromoaniline should be drawn.
Concept Introduction:
When the mixture of hydrocarbons from natural resources such as coal or petroleum are separated, certain compounds are emerged with pleasant odors and are thus known as aromatic hydrocarbons.
Hydrocarbons with sigma bonds and delocalization of pi electrons between carbon atoms, thus forms a circle is said to be aromatic hydrocarbons.
Aromatic compounds are named as a benzene derivative.
Rules of drawing structures of aromatic compounds are:
- First identify the substituents which are linked with benzene ring.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs) of benzene ring.
(d)
Interpretation:
The structure of 4-chloro-1,2-diethylbenzene should be drawn.
Concept Introduction:
When the mixture of hydrocarbons from natural resources such as coal or petroleum are separated, certain compounds are emerged with pleasant odors and are thus known as aromatic hydrocarbons.
Hydrocarbons with sigma bonds and delocalization of pi electrons between carbon atoms, thus forms a circle is said to be aromatic hydrocarbons.
Aromatic compounds are named as a benzene derivative.
Rules of drawing structures of aromatic compounds are:
- First identify the substituents which are linked with benzene ring.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs) of benzene ring.

Want to see the full answer?
Check out a sample textbook solution
Chapter 13 Solutions
GENERAL,ORGANIC, & BIOLOGICAL CHEM-ACCES
- Can you please explain this problem to me? I'm very confused about it. Please provide a detailed, step-by-step explanation for me! (ME EX1) Prblm 22arrow_forwardCan you please explain this problems to me? I'm very confused about it. Please provide a detailed, step-by-step explanation for me! (ME EX1) Prblm 30arrow_forwardThis organic molecule is dissolved in a basic aqueous solution: O ? olo RET A short time later sensitive infrared spectroscopy reveals the presence of a new C-OH stretch absorption. That is, there Ar must now be a new molecule present with at least one C - OH bond. In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule. $ Add/Remove steparrow_forward
- So the thing is im trying to memorize VESPR Shapes in order to be able to solve problems like so, and I need help with making circles like the second image that's in blue or using an x and y axis plane in order to memorize these and be able to solve those type of problems. Especially like the ones given in the top / first image. (180 , 120 , 109.5) Can you help me with this.arrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward2. (15 points) Draw an appropriate mechanism for the following reaction. H N. H* + H₂Oarrow_forward
- Draw a tripeptide of your choosing at pH 7. Have the N-terminus on the left and the C-terminus on the right. Then: Draw a triangle around the α-carbons. Draw a box around the R-groups. Circle the atoms capable of hydrogen bonding. Highlight the atoms involved in the formation of the peptide bonds. What type of structure have you drawn? (primary, secondary, tertiary or quaternary protein structure). make sure its a tripeptidearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- Don't used Ai solution and don't used hand raitingarrow_forward> Organic Functional Groups Naming and drawing alkyl halides structure CI Br CI CI Explanation Check 2 name 1-chloro-2,4,9-trimethylnonane CI 2-iodo-2,3-dimethylbutane FEB 19 € E M tv MacBook Airarrow_forwardCan you please explain to me this problem im very confused and lost. Help me step by step and in detail im soo lost.arrow_forward
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning




