b. Write the structure showing lone pairs of electrons and draw all possible resonance structuresforUse curved arrows to track the movement of electron pairs converting oneresonance contributor to the other.:c. Write the structure showing lone pairs of electrons for the molecule below and draw all. Use curved arrows to track thepossible resonance structures for anionic speciesmovement of a pair of electrons. 5. a. Write the structure showing lone pairs of electrons and draw all possible resonance structuresfor para-acetyl phenolate anionof electron pairs converting one resonance contributor to the other (it should be five resonancestructures including the initial).O.Use curved arrows to track the movement

Resonance structures are those which contains the delocalized charges over same molecular entity.

Answered: D. a. Write the structure showing lone…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter5: Resonance

Section: Chapter Questions

Problem 4CTQ

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13. Aniline and nitrobenzene are two substituted benzene compounds that contain nitrogen atoms. A) Use resonance structures to identify all carbon atoms that are electron rich on aniline. Mark the appropriate carbons in the figure below with a d-. NH₂ nitrobenzene aniline Note: this is benzene B) Use resonance structures to identify all carbon atoms that are electron deficient on nitrobenzene. Mark the appropriate carbons in the figure below with a dª.
x-xo B Draw molecule A. On that drawing include the lone pairs and the curved arrows that would produce resonance structure B.
Rank the following active methylene compounds in order of decreasing acid strength. H₂C O CEN H3C. O most acidic least acidic Answer Bank CH3 H3C NO₂ H3C O₂N NO₂ CH3
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Be sure to answer all parts. The pk of three different C-H bonds is given below. For each compound, draw the conjugate base, including all possible resonance structures for compound C. Use skeletal structures when drawing all conjugate bases. compound A H H H pK₂ = 50 Conjugate base of compound A: Conjugate base of compound B: Conjugate base of compound C: edit structure ... compound B resonance structure (negative charge on C) H H edit structure ... (one Lewis structure) edit structure ... (one resonance structure) X H pka = 43 compound C edit structure ... H H pK₂ = 19.2 resonance structure (negative charge on O) H
Question d, e and f
Question Consider molecules A–D. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case?
A. Draw the major resonance structure, then draw curved arrows to show how this can be converted to the Lewis structure given. B. Thionitromethane is redrawn for you. Draw curved arrows to show how this can be converted to the resonance structure you drew in part A.
a. Which of the following has a greater electronegativity? (circle one) Carbon / Cesium b. Explain why you chose your answer in Za.
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