Using π electrons and/or lone pairs in the following conjugated system, create a resonance form by moving electrons as far as possible. Be sure to include alllone pairs and charges.Part: 0 / 2Part 1 of 2Add curved arrow notation to show how electrons will move to form a different resonance form.+-NEN:X:0OmFE215U

Resonating structures are given below Explanation:Step 1:Resonance structure are :-

Answered: Using π electrons and/or lone pairs in…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Two major resonance structures are possible for the anion shown. One resonance form is given, but it is incomplete. Complete the given structure by adding nonbonding electrons and formal charges. Draw the remaining structure, including nonbonding electrons and formal charges. Omit curved arrows. Structure A: complete the structure by adding nonbonding electrons and formal charges. H H H I Structure B: draw the remaining resonance structure, including nonbonding electrons and formal charges. H- : z: H H
Add lone pairs to the central atoms as necessary to complete the Lewis structures. Do not worry about the positions of the lone pairs on the central atom. Focus on the number of lone pairs. XEF2 SF, Erase Select Draw Rings More Erase Select Draw Rings More S F Xe Xe F :
In the following compound, identify all carbon atoms that you expect will be different in electron density. Drag the appropriate partial charges to these carbon atoms. S+ ..
3. Draw three resonance structures of the following molecule, using curved arrows to show electron-pair movement: + OCH3 H -H 1
Which of the following species is a valid resonance structure of A? Use curved arrows to show how A is converted to any valid resonance structure. When a compound is not a valid resonance structure of A, explain why not.
5. |Draw any relevant resonance structures for the compounds below. Use arrow pushing to show movement of electrons.
In the following Lewis structure of [(CH3)2OH]+, every atom, bond and lone pair is positioned. To complete the structure, drag the formal charge tags to the appropriate atom(s). Each marker may be used more than once, or not at all. If an atom has a formal charge of zero, do not drag a tag to it. When you drag the marker in, place the little crosshairs in the upper left corner of the marker directly over the atom(s) in question (not above them). H H-C-O-C-H HHH - H I Η Η Η 0 0 + 2+ 2-
Use resonance to support your choice in part (a). First, add curved arrow(s) to show the delocalization of the negative charge using the following pattern: a lone pair next to a pi bond. Modify the second structure given to draw the new resonance structure. Include formal charges in your structure. Use the + and- tools to add/remove charges to an atom, and use the single bond tool to add/remove double bonds. HO: JOH Edit Drawing HO HQ OH
Draw a resonance structure that places a pi bond in a different position. Include all lone pairs in your structure. 0:01 H

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