Concept explainers
Interpretation: The location of counter ion
Concept introduction: Lewis structure is a representation of molecules in which dots are shown to represent unshared electrons and lines are shown to represent bonds. These lines and dots represent distribution of electrons in the molecule.
When one single structure is unable to describe all the properties of a single-molecule, a phenomenon called resonance comes into play. This arises when two or more than two Lewis structures are possible for one molecule. All such structures are called resonating structures and have same placement of atoms in them but these have different locations of bond pairs and lone pairs. The resonating structures are inter-convertible with each other. The resultant of all the resonating or contributing structures is called the resonance hybrid.

Want to see the full answer?
Check out a sample textbook solution
Chapter 5 Solutions
Custom eBook for Organic Chemistry
- Provide the reagents for the following reactions.arrow_forwardIf I have 1-bromopropene, to obtain compound Z, I have to add two compounds A1 and A2. Indicate which compounds are needed. P(C6H5)3arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. O CH3CH2NH2, TSOH Select to Draw >arrow_forward
- Indicate the products obtained by reacting fluorobenzene with a sulfonitric mixture.arrow_forwardIf I have 1-bromopropene, to obtain compound A, I have to add NaOH and another compound. Indicate which compound that would be. C6H5 CH3arrow_forwardIf I have 1-bromopropene and I want to obtain (1,1-dipropoxyethyl)benzene, indicate the compound that I should add in addition to NaOH.arrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts. Ο HSCH2CH2CH2SH, BF3 Select to Draw I Submitarrow_forwardFeedback (7/10) Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. Incorrect, 3 attempts remaining Ο (CH3CH2)2NH, TSOH Select to Draw V N. 87% Retryarrow_forwardIf I want to obtain (1,1-dipropoxyethyl)benzene from 1-bromopropene, indicate the product that I have to add in addition to NaOH.arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
- Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage LearningPrinciples of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning




