For each answer above that was identified as incorrect, select a reason why the curved arrow(s) did not generate a valid resonancestructure. For any correct answers, select the “No problems" box.Items (5 images) (Drag and drop into the appropriate area below)ONH2CHH.CH3CCHH,CH,CIncorrect AspectAtom movementOctet exceededNo problemsFormal chargee- movement--------- For each answer above that was identified as incorrect, select a reason why the curved arrow(s) did not generate a valid resonancestructure. For any correct answers, select the "No problems" box.Items (5 images) (Drag and drop into the appropriate area below)H3CCH2H3CH3CCHH3CIncorrect AspectNo problemsFormal chargeAtom movementOctet exceedede- movement

The image has a total of 4 different reactions showing resonance. In resonance structures, only…

For each answer above that was identified as incorrect, select a reason why the curved arrow(s) did not generate a valid resonance structure. For any correct answers, select the "No problems" box. Items (5 images) (Drag and drop into the appropriate area below) NH2 ONH2 CH CH CH, H3C H,C H,C H,C ncorrect Aspect Octet exceeded Formal charge e- movement Atom movement No problems :0=0

For each answer above that was identified as incorrect, select a reason why the curved arrow(s) did not generate a valid resonance structure. For any correct answers, select the "No problems" box. Items (5 images) (Drag and drop into the appropriate area below) NH2 ONH2 CH CH CH, H3C H,C H,C H,C ncorrect Aspect Octet exceeded Formal charge e- movement Atom movement No problems :0=0

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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K 10:13 Problem 92 of 20 5G+ 5G+ Select to Draw Draw a resonance structure that places a pi bond in a different position. Include all lone pairs in your structure. Submit 0
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For each highlighted bond (shown in red), select the arrow that indicates the direction of bond polarity (leave the box blank for a completely nonpolar bond).
For resonance structures, I am confused how many arrows are necessary to produce a necessary resonance structure. The first/white picture represents an example given by the textbook (utilizing one arrow). The second picture/in pen is my own work (utilizing three arrows). Both produce a positive and negative charge. Are they both correct? Or is one supposed to use the least amount of arrows when producing resonance structures?
Question 2 Initial Knowledge Check Shown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. c+ .C. H. Click and drag to start drawing a H H structure. H. I Don't Know Submit Accessibil 2022 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center BANNHA MacBook Air HIN: HIC II
Order the following bonds from most polar to least polar: Q-E D-R L-J *picture attached* Answer Options: A.) L-J > Q-E > D-R B.) D-R > Q-E > L-J C.) Q-E > D-R > L-J D.) L-J > D-R > Q-E *I think its D?
◄ Search 7:42 PM Mon Jan 23 ← Draw an equivalent resonance structure that minimizes charge. Include all lone pairs in your structure. Drawing CH₂ Problem 10 of 20 Atoms, Bonds and Rings Charges and Lone Pairs Draw or tap a new bond to see suggestions. Undo X › Ish 90% Reset Drag To Pan Remove Done Submit
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K 9:55 Problem 42 of 56 Draw a resonance structure that places a pi bond in a different position. Include all lone pairs in your structure. :O: 4 Submit 0
5. Formal Charge: Formal charge a. **Try before lecture** Calculate the formal charge on each carbon and oxygen (all valence electrons are shown). Which structure(s) have an "unfilled octet"? (First example in each row completed for you) H-C-H H FC = (4)-(3) - (0) = +1 HỘH H FC = (6)-(3)-(2) = +1 H-C-H H-O-H H-C-H H H-N-H H H-Ö: b. Add the missing nonbonding (lone pair) electrons to each nitrogen (all formal charges are shown) H 10 H-N-H H H-N