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.
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EBK ORGANIC CHEMISTRY
- which one is more acidic ch3oH or ch3Nh2. explain why please.arrow_forwardDraw Resonance Structure of the following cation. Draw curved arrows to indicate the movement of electrhs. A Instructionsarrow_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_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_forwardSee attached file ?arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting structures, draw the curved electron-pushing arrows for a proton transfer reaction and draw the resulting product. Be sure to account for all bond-breaking and bond-making steps. O HH Base .0 H R HH HH •6•H :O: HH Select to Add Arrows Base Select to Draw Productarrow_forward
- Be sure to answer all parts. Draw the products of the following acid-base reaction. CH3 CH3 + H₂SO4 - draw structure ... conjugate acid H O O edit structure ... conjugate basearrow_forwarddraw the step one product and draw curved arrows to show the nucleophilic addition step.arrow_forwardBriefly explain why the I end of the molecule is more electrophilic than the Cl end.arrow_forward
- Rank the following compounds in order of decreasing basicity, putting the most basic compound first. NH₂ A. || > | > ||| > IV B. | > | > ||| > IV C. | > ||| > | > IV D. IV> | > ||| > | NH₂ Br III NH₂ F3C IV NH₂arrow_forwardIdentify the electrophile and the nucleophile in each of the following reaction steps. Then draw curved arrows to illustrate the bond-making and bond-breaking processes.arrow_forward3. Draw all resonance structures for the following radicals.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning