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- Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the chloro with the para position in chlorobenzene. CI chlorobenzene You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. • []verse osis Consider the structures of the carbocations formed by ortho attack of the electrophile, *NO₂, on the given starting material. NH2 Part: 0/2 Part 1 of 2 + Draw all resonance structures for the carbocation formed by ortho attack of the electrophile "NO, on the given starting material. If applicable, include the resonance structure in which π bond electrons "move" to the more electronegative atom as a lone pair. Be sure to include all charges and relevant lone pairs. 00 al. Ar B KThis structure is considered to have 'aromatic character'. Using the provided starting and product structures, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps. Drawing Arrows e :O: Ⓡ14 Problem 7 of 21 + :O: Undo B Reset Done NH Submit Drag To Pan
- 2. Propose electron-pushing arrows for each step of the radical mechanism shown below. PhO,s.-so,Ph jor for > H [w-o [w-o Pho2s-sO,Ph HUse the curved-arrow formalism to show how the electrons flow in the resonance form on the left to give the one on the right. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions Submit Answer m H Try Another Version 2 item attempts remaining a Use curved arrows to show how the alkene below will react with HCI. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions NA ↔XT H HPls help ASAP
- ited Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. od m... • You do not have to consider stereochemistry. . Do not include anionic counter-ions, e.g., I', in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom Separate resonance structures using the → symbol from the drop-down menu. ● CH4 + ? HBrPlease help me this question. Thank youBe sure to answer all parts. One step in the synthesis of occidentalol, a natural product isolated from the eastern white cedar tree, involved the following reaction. + 8.0 CH3O Part 1 out of 2 2 attempts left A Check my work CH3O H draw structure ... B O several steps $ H Draw the structure of A (use hashed wedged onds to denote endo bonds and wedged bonds to denote exo bonds). "Кон OH Next part (-)-occidentalol G
- Draw both resonance structures of the most stable carbocation intermediate in the reactie 0 You do not have to consider stereochemistry. Do not include anionic counter-ions, e.g., in your answer.. • Draw one structure per sketcher. Add additional sketchers using the drop-down me • Separate resonance structures using the symbol from the drop-down menu. Submit Answer QNatal Fernandez 998) CH₂ Retry Entire Group Show Hin HBr VG+ 10120 [F 1 more group attempt Cengage Learning Cengage Technical suppo 199328= 91339 Client collected Vanita 94328 48036572Should the circled carbocation be included in the resonance structure bracket? It seems to be the same as the first one I drew, but I'm not sure.ranslate Bb Welcome, Kawtha... O Maps GE News Home [Review Topics] [References) Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. OH HO Br2 Br You do not have to consider stereochemistry. Include all valence lone pairs in youranswer. In cases where there is more than ore answer, just draw one. opy aste [* Previous Next Show Hint Email Instructor Save and Exit Cengage Learning | Cengage Technical Support