Which of the above is a reasonable resonance structure of the molecule below?
Answer can only be one of the options.
Please explain why? And show transfer of p orbital or lone pair electrons.
Will rate and give thumbs up if explanation is clear.
Thank you
Which of the above is a reasonable resonance structure of the molecule below? Answer can only...
3) Consider the following structure: a) (6 pts) Draw two additional resonance structures for the following compound. Show curved arrows to convert between the resonance structures. (You need to redraw the molecule below) b) (4 pts) Circle the major contributor above. Explain your choice 4) (5 pts) For the following compound draw in the lone pairs, indicate if each lone pair is localized or delocalized and identify what type of orbital each lone pair is in
(i) Resonance involving only two p-orbitals: Lone pair next to a vacant orbital Both lewis structures are valid. Only one is a contributing resonance structure (CRS). Which one? Why?
Propose a reasonable resonance structure for the molecule shown below. A end end N -z = IL IV O IV None of these
please help in all sections asap! The following two drawings are resonance structures of one compound. a-o But the following two drawings are not resonance structures Not resonance structures They are, in fact, two different compounds. Choose the correct explanation(s). Select all that apply. Benzene does not have three C-C single bond and three C-C double bonds. In fact, all six C-C bonds of the ring have the same bond order and same length. Benzene have three C- single bond...
A molecule that can be described by multiple resonance forms: Select the correct answer below: possesses an electronic structure described by only one of the resonance forms O will rapidly fluctuate in electronic structure between the resonance forms will have an electronic structure that is an average of the resonance forms none of the above
Draw the Lewis structure of H3CNCO (the arrangement of atoms in the molecule is shown below). You must draw the "most stable resonance structure in the box provided and all lone pairs of electrons and formal charges that are not zero must be shown. Do not show formal charges that are zero: i.e. do not type in "0" I-U-I
3.Fill in the table below - only 1 Lewis structure for eaclh is necessary, no resonance structures: Formula à HCNNO FICl, (exception to sulfite ion the octet rule) 3-D Lewis structure including bonding and lone pairs, and formal charges (each atom in the structure) electron pair geometry molecular geometry (with bond angles) Hybridization of the central atom(s) Polar?- Yes/No
5. Resonance provides the basis for a large portion of organic chemistry and helps us identify sites of high and low electron density. We will see that the electron source (nucleophile) is attracted to the site of electron sinks or deficiency (electrophile). For the following, draw the curved arrow that shows the movement of electrons that takes you from one resonance structure to the other. Remember to always start your arrow at the source of electrons (r-bond or lone pair)....
3. Draw the important resonance contributors for each structure below (Hint - only 3-4 required for each). Include resonance arrows as necessary, and use the curved arrows to show electron movement. Also be sure to show all relevant lone pairs and formal charges. :0: H3CNCH CH3
I need help with questions 1-8 POST-LAB: LABORATORY 11 Complete on a separate sheet of paper. 1. Indicate whether the molecule is an ion. Then, indicate whether the molecule is polar m. I n. H,PO o. BrO, p. IF q CO2 a. HCN b. H,SO c. HNO, d. BF H,CO, i. SF j. BeCl k. PO, 1. SO, e. XeF f H,O Calculate the number of valence electrons in each structure in question 1 2. Draw a correct Lewis dot...