8. Consider the two structures shown below. о CH3COH CH3CO + H Structure A Structure B (a) Which structure is favored at equilibrium? Explain. 9. Draw all possible resonance structures for the given molecule. Each correct resonance structure will be awarded 2 marks. (a) -0-0 (b) (c)
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- To preview image Click here For the following bonds indicated below, choose which one would have the smallest and highest bond dissociation energy. 1. Smallest Bond Dissociation Energ: ✔ [Select] 2. Highest Bond Dissociation Energy :0 C B C H ΤῊ H A BPlease give the best resonance and second best resonance for SO2. Please explain why the best resonance is the "best" and why the second best resonance is the "second best".pls help
- 13) Which pairs are resonance structures of one compound? X-X and A) X B) and Y-Y D) All (A, B, C)Determining the Relative Energy of Resonance Structures and the Hybrid Draw a second resonance structure for carbocation A, as well as the hybrid of both resonance structures. Then use Rules [1]–[3] to rank the relative stability of both resonance structures and the hybrid.Including reasonance structures, draw most stable allylic cation for both
- Put curved arrows to show the forming and breaking of bonds in the reaction below.Part A Draw the product formed when the compound shown below undergoes a reaction with HCI in CH₂Cl₂- Interactive 3D display mode H₂C CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. DOCR HEX CONT? 1 hul HPredict Product
- Which line (A or B) corresponds to the energy change for an ortho/para substitution?Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bond-making steps. :OH: Select to Add Arrows H₂O 3 H₂ H HH H :Br:Ⓒ HH Select to Add Arrows H₂O 17 :Br: H H Please select a drawing or reagent from the question area13. Aniline and nitrobenzene are two substituted benzene compounds that contain nitrogen atoms. A) Use resonance structures to identify all carbon atoms that are electron rich on aniline. Mark the appropriate carbons in the figure below with a d-. NH₂ nitrobenzene aniline Note: this is benzene B) Use resonance structures to identify all carbon atoms that are electron deficient on nitrobenzene. Mark the appropriate carbons in the figure below with a dª.