7. Draw all reasonable resonance forms for the following compounds and answer part e.Draw your answers beneath the given resonance forms, which you do not need to redraw.Draw appropriate arrows between the resonance forms.You do not need to show 'curly arrows' to interconvert resonance forms, but you are welcome to do so if youfind it useful.•Point values reflect relative difficulty, not the number of resonance forms to be drawn.a.[2 pts]b.Cl[2 pts][3 pts]d.14[2 pts]

All resonance forms are drawn in these images with proper use of arrows.

Answered: 7. Draw all reasonable resonance forms…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter5: Resonance

Section: Chapter Questions

Problem 28CTQ

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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
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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.
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Ranking resonance structures Rank the resonance structures in each row of the table from major to minor. For example, in the first row, select (major) for the major resonance contributor. If two or more structures in the same row contribute equally, rank them equally by selecting the same number. X. :ö: :ö: ータ H. Rank) (Rank) H. H. H. H. H. (Rank) (Rank) (Rank) (Rank) 74°F DELL F4 F5 F6 F7 F8 F9 F10 F11 F12 PrtScr $
Answers for sub items D and E.
structure. For any correct answers, select the "No problems" box. Items (5 images) (Drag and drop into the appropriate area below) For each answer above that was identified as incorrect, select a reason why the curved arrow(s) did not generate a valid resonance ONH2 NH2 H,C CH2 H.C HC CH2 Incorroct Aspect
Compare columns I and II, and write A if the value in column l is greater than in l B if the value in column 1l is greater than in ! cif both values are equal D if the value in column 1 cannot be compared with that in II Number of Resonance Structures Column II Column I
Question 2 please
Each of the following proposed resonance moves has a flaw. For ones that are completely incorrect, explain why. For ones that can be easily corrected, make that correction.
Consider the image of BH, with the formal changed placed on the boron. H -B-H Identify where is the actual charge is located. Drag the appropriate label to each position. Answer Bank H. 8+ 8- H- B H H.

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