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![Are the following valid resonance structures of NCS?
[: N=C-S:] - and
Yes
No
[: N = C = S:] -](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9dd24c2e-6ed2-43a1-b29e-a378b8e284aa%2F97e2c851-9e08-4666-9ecf-172412860953%2F3cybsoh_processed.jpeg&w=3840&q=75)
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- Which of the following is a resonance structure of the compound below? 0=0 H CH₂CH3 || III ON H₂C H₂C 11 Нас-с CHOH CH3 HẠCHO CH E ||| :0 HC CH3 IVIm practicing drawing resonance structures. Can someone explain why this carbon's formal charge becomes negative? I calculated the formal charge to be: (ve-)-(bonds + dots) : 4- ( 2+2)= 0, so I'm confused .How would I draw all the important resonance structures for cyanate (NCO1-)?
- For each of the following pairs of resonance structures, cirele the one that would make greater contribution to the actual resonance hybrid. OCH, OCH, A- BI E =5. Do the following structures represent resonance structures? If yes, identify them by stating the more stable and less stable. ? H ? c=0 b) H FCH2 H. H ? ? H-CE d) HSpecify the formal charges on the atoms labeled a-c in each structure. b a:0: CH3CH2, CH2CH3 b H3CN-CH3 CH;CH2 CH2CH3 ČH3 a a b b
- How does the carbon in the right structure have a - formal charge? Explain how to calculate it.6. Which of the following does NOT depict resonance structures? (1) CH3-0-CH-CH3 CH3 0 CH CH3 (2) CH3 NO CH3-NO :O: (3) CH3 CH3- (4)11. Add curved arrows to the following structures to show how electron pairs must be moved to interconvert the structures, and locate any formal charges. This is the nitrate ion and it has three resona onance structures (RS). וך- :ó: :0: 1. supply formal charges 1. supply formal charges 2. draw e pushing arrows draw third RS here 2. draw e¯ pushing arrows that make second RS to make third RS
