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. Drawing Arrows :0: 0:0 KO
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- OChem help with the following reaction schemes (see attached image) Please provide the bond line structures for the products obtained in the following reaction schemes... Notice in question #1 that A, B, and C are actually shown as C, B, and finally A in the actual reaction scheme so C correlates with PCC, and so on Question #2 is in order.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. + Drawing Arrows ON. 8: H ·0: I+ + Undo :CI: H U Reset H © Done 'H Drag ToDraw structural formulas for the alkode son and the alkylarybromide that may le ed in a Willmn yhei CH, CH-O-C CH, • You de mot have to consader stereochemistry • Do not inchude counter ions, eg. NaT, in your answer • Draw one structure per skrtcher. Add additional sketchees uing the drop-down menu in the hemo right com Separate structures with signs fipm the drop down menw.
- Electron pairs CH3 .. Erase H3C - С — СІ: H3C – S- CH3 CH3 CH, CH3 THF/H,0 + H,C--CH, CH C- CH CHs CH, Use curved arrows to write the first step of this nucleophilic substitution mechanism. :ö: | :ö:Rewrite the entire reaction in Full Structure Format with the Ending Products [The second image is an example of Full Structure Format ] THANKSSSSSSSSSSSSComplete the following both subpart reactions with missing information. In clear handwritten!
- Part A Predict the product and propose a mechanism for the elimination reaction that results when (S)-(1-chloropropylibenzene, - CH, is heated in the presence of HOCH, CH,, Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron-fiow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H. BrSee the Attachment & solev the followings (a) Add curved arrows to show how the starting material A is convertedto the product B. (b) Draw all reasonable resonance structures for B. (c) Draw the resonance hybrid for B.The curved-arrow convention depicts the flow of electrons, including bond-forming and breaking events. Draw the outcome of the following reaction based on the provided curved arrow. Be vigilant regarding formal charges. :ci: B. Ci: Draw three additional resonance structures of acetamide (below) and use curved arrow notation to show how the resonance structures are formed. Label the resonance contributors alphabetically (ex. A, B, C, D) and rank them from most to least significant contributor. •oº• Ⅱ. H3C 0°• H N H
- Show all He steps necessay, inorder to make each of the followring compoundS, Starting with benzene Br BrCurved 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. Drawing Arrows H H₂O e :0: Na Ⓒ H H H. * H H H H :0: + ← Undo :0: 1 Reset Na Done Drag To PanDraw 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