b Use curved arrows to show the mechanism of the step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions :0=C=0: べ 2+ Mg Br
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- Be sure all major products appear on the right-hand side of the final step of your mechanism. And if there is more than one major product, be sure to use wedge and dash bonds to show the stereochemistry of each product. Draw the mechanism for the addition of HCI to the alkene below. : H-CI Add/Remove step X 5 C Click and drag to start drawing a structure. 00 مله Ar ดOrganic Chemistry presented by Macmillan Learning Maxwell Complete the electron-pushing mechanism for the given reaction of 3-pentanone in potassium cyanide and hydrogen cyanide. Add any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Details count. Step 1: add curved arrows. Select Draw Templates More C H H O|N|K] N N: Erase Step 2: complete the structure and add curved arrows. Select Draw Templates More : 0: C H O N H K N: EraseWrite a mechanism for the following reaction. You MUST use curved arrows to represent electron movement. Show the three possible termination steps as part of the mechanism. CH3 CH3 Br₂, heat Br
- Draw the least stable resonance form the intermediate in the following electophilic substitution reaction.b Assuming that halogens add to alkynes in the same manner that they add to alkenes, write a mechanism for the reaction step below. Use curved arrows to show electron reorganization. Arrow-pushing Instructions H3C C↔X ™ Br: CH3 BrPlease answer a-d.
