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. Select to Add Arrows Br: a Select to Add Arrows > H₂C Br Select to Add Arrows :Br: a Problem 33
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- Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing Instructions H. +0: H H H-C-C–H :br: -c-Br: H H H. Submit Answer Retry Entire Group 9 more group attempts remaining (Previou MAR 30 étv MacBook Air 888 DII DD F4 F5 F6 F8 F9 F10 F11 & * 4 6 7 8 Y U10:11 AM Thu Mar 23 :0: :CI: 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. Al Select to Add Arrows :0: CFCI: Problem 8 of 23 Select to Add Arrows :0: :0: • C. CIFCI: Select to Add Arrows Ⓒ @ : 66% CICI: Submit Select to Add Arrows63°F Partly sunny Predict the product of the following reaction. H₂O Heat Draw the molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. NN ● [1] A осо A H₂CrO4 H₂SO4 Submit Request Answer 1 H 12D EXP. CONT. L CONT. ?** Im Marvin JS by ChemAxon Search PRE H C N O S CI Br - P F Ty I -- O
- 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. esc F1 •N. H H Select to Add Arrows @ 2 :O: O:CEN: F2 KCN, HCI !!!! ΚΘ KO # 3 F3 $ 4 000 F4 % 5 F5 MacBoo 6 E1. .CI HC C: Li HC CH LICI 2. -CH3 OH Aqueous HO-S- -CH3 acetone g = SN1 Nucleophilic substitution Electrophilic a = Proton transfer addition h = SN2 Nucleophilic substitution b = Lewis acid/base e = El Elimination c = Radical chain f= E2 Elimination substitution Identify the mechanism by which each of the reactions above proceeds from the mechanisms listed. Use the letters a - i for your answers. among 1. 2.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. Be bond-breaking and bond-making steps. sure to account for all esc H ! 1 O F1 Drawing Arrows ♡ NaNha Na Bre 2 Na Ⓒ Select to Add Arrows 143,177 ☀ F2 # 3 31 6 80 F3 $ 4 a F4 % 5 stv 0 F5 A 6 NAA c F6 & 7 ‹ F7 Na Ⓒ 40 8 :Br: DII F8 ← than Undo ( 9 F9 Reset P se Ⓒ Done ) F10 0 F11 Ⓒ:№: (1) { F12 -8 Drag To Pan del
- Please help with the following ochem reaction I've included the starting compound's bond line structure and need to figure out how it reacts with the included reagents. Thank you!Draw the arrows on the structures in the first two boxes to show the mechanism of a-halogenation under basic conditions. All necessary atoms and formal charges are drawn on the structures. See Periodic Table O See Hint H. H. :Br: :Br: 一 Add curved arrow notation to show the reaction between the two compounds. H C P. H. CI H-O: H' :Br: Br :ロ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 step(s). Be sure to account for all bond-breaking and bond-making steps. kš. Br Drawing Arrows I.O. HBr Your Aktiv Learning trial expires on 01/19/24 at 11:59 PM J I OO :Br: G Select to Add Arrows r: 01 Br: G Select to Add Arrows Problem 21 of 35 :O: + Undo H Activate Now Submit Br. 177 Reset Done Drag To Pan
- Alec wanted to prepare to diene B to use in a subsequent Diels-Alder reaction. He thought he could prepare it via the reaction shown below. However, treatment of the diol (A) with acid yield either ketone (C) as the major product. H,SO, HO IPh Нeat Ph Ph OH B C a. Give a detail account of how you would determine whether product of the reaction was B or C. Assume that the only method available to you is FT-IR. You must give values for all features of all spectra. b. Provide a detail mechanism as to how compound B and C are formed under the reaction conditions. ..1.Draw the structures of all 3 resonance hybrid forms of the benzenonium intermediatefor both o and p attack for the case of activating groups an indicate which one in eachcase is the most stable form.Draw the structure of all 3 resonance hybrid forms of the benzenonium intermediatefor m attack in the case involving a deactivating group. 2.Halogens are deactivating groups but direct electrophilic attack at the o and ppositions. Why is this the case?Identify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОН