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Examine the line angle structure of HNO integration of tos18,16, and 10. 5. A. Examine the line-angle structure of Molecule 1 below, Redraw it, correcting

Examine the line angle structure of HNO
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integration of tos18,16, and 10. 5. A. Examine the line-angle structure of Molecule 1 below, Redraw it, correcting a3 errors of structure flone pairs and bond anglest. B. Using the structure you drew above as Resonance contributor A, draw the other two resonance contributors (B and C) of Molecule 1 that have all closed-shell atomis and formal charges of +1,0, of - 1 : Be sure to include nonbonding electrons and any non-zero formal charges. You do not need to include curved arrows, but you can if it helps you complete the question. Be sure one of your contributors is labelend as B and the other as C C. Which of the three resonance contributors of Molecule 1 is the most significant contributor to the actual structure of Molecule 1 ( A,B, or C) ? Briefly explain your answer. The most significant contributor of all of the resonating structures is C. Because it has filed its a valance shet. D. Which of the three resonance contributors of Molecule 1 is the leost significant contributor to the actual structure of Molecule 1(A,B, or C) ? Briefly explain your answer. The least significant contributor is A. This structure is more electronegative. E. Re-draw the structure you drew in part A. Then, identify one atom for which resonance brings a change in its number of electronidense areas from 43/34 or 32/23. Label this atom your "atom of interest" and fill in the table below

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