Concept explainers
a)
Interpretation:
- The resonance contributors for the given compound has to be drawn.
Concept Introduction:
Resonance Contributor: The appropriate structure with the localized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.
Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.
Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.
b)
Interpretation:
- The resonance contributors for the given compound has to be drawn.
Concept Introduction:
Resonance Contributor: The appropriate structure with the localized electrons is called a resonance contributor, a resonance structure, or a contributing resonance structure.
Delocalized electrons: The sharing of electrons between two or more atoms known as delocalization of electrons. In order to have delocalized electrons, the system must be planar and have alternative double bonds and single bonds.
Resonance hybrid: The actual structure with delocalized electrons is called a resonance hybrid.
Want to see the full answer?
Check out a sample textbook solutionChapter 8 Solutions
Organic Chemistry
- kindly match the correct product (answer)arrow_forwardFor each molecule below, draw the conjugate acid or conjugate base or both if the molecule hasboth a conjugate acid and a conjugate base (e.g., water).arrow_forwardConsider the following bases: a. For each base above, circle the atom/atoms with the highest PE (will release the most P.E.when a lone pair on this atom combines with an H+ ) b. Rank the bases 1 (highest P.E./strongest base) to 7 (lowest PE/weakest base), and explainyour reasoning.arrow_forward
- Summarize the relationship between pKa and acid strength by completing the following sentences: a. The higher the pKa of an acid, the stronger or weaker the acid. b. The lower the pKa of an acid, the stronger or weaker the acid.arrow_forward2. Use curved arrows to show electron movement in the reactant side and draw the product/s of the Lewis acid-base (nucleophile-electrophile) reaction. Label the nucleophile and the electrophile. Draw in all lone pairs and charges where appropriate. Iarrow_forwardClassify each reaction as either a proton transfer reaction, or a reaction of a nucleophile with an electrophile. Use curved arrows to show how the electron pairs move.arrow_forward
- Draw all contributing resonance structures for the molecule shown below. Circle themajor resonance contributor.arrow_forwardfor each pair of compounds, circle the the most acidic proton in each molecule, and then indicate which is the stronger acid of the twoarrow_forwardDraw all possible resonance contributors.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning