For the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Hi... CEN + CI Organic product + Inorganic product
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- Write down major r producto), or other recietent6) and/or fallawine the reactionconditions for the Ht Na BH (OAC)S +(CH2)2NH 1. CH3 CH2 Mg Br 2. H30+ CH2CN CH30 OEt 1.NaOH, tho A 2. H3ot 3. ADraw the final organic product of the following three-step reaction of bromomethylbenzene. Br 1. NaCN 2. CH3MgBr 3. H3O*, H₂O Select Draw / ||| ||| Templates с H More N Erase Q2 QFor the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Н..... C=N Organic product Inorganic product CI Draw the organic product. Erase Select Draw Rings More |||| с H N Cl Erase Draw the inorganic product. Select Draw Rings More /// с H N Cl
- Pls help ASAP. Pls do all asked questions. Pls identify the reaction below.In Part 1. choose the most "electron-rich" atom in the reaction below, In Part 2. identify the elementary mechanistic step. Part 1 sitnl See Periodic Table See Na-ö: H,C-ö: Na-r: Part 2 Select the elementary mechanistic step: Choose one: O nucleophilic elimination O nucleophilic substitution O carbocation rearrangement O electrophilic addition4. Please choose either Reaction A or Reaction B, and then provide the complete mechanism. The mechanism MUST include the formation of the "super electrophile." Then provide the reaction coordinate pathway starting from benzene + super electrophile. Be sure to include an energy access and labels for reactants, products, intermediates, energies of activation, and transition states. Reaction A NO2 Reaction B HNO3, H2SO4 CH3COCI, AICI3
- 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 + ? HBrComplete the mechanism for the given base-catalyzed formation of a hemiacetal from cyclopentanecarbaldehyde and sodium methoxide in methanol by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. Step 1: complete the structure and add Step 2: complete the structure and add curved arrows. curved arrows. Select Draw Rings More Erase Select Draw Rings More Erase C H C H H. 1L :o - I :o :Consider the reaction below: Br H₂O heat OH to 1. The reaction mechanism for the reaction is choose your answer... 2. The nucleophile in the reaction is a choose your answer... ✓nucleophile.
- Pls help ASAP, thank you! “Synthesis. Provide the steps to obtain the product from the reactant for the reaction below.”a) Give a detailed (arrow pushing) mechanism for the following reaction, where appropriate label the Lewis/Bronsted Acids/bases b) On the provided axes, draw a reaction energy diagram for the reaction above, indicate the rate determining step and its activation energy, indicate the positions of any transition states and draw structures for all transition states. To preview the image click here HBr + CCl4 (solvent) BrQ-I: Determine the product(s) of the rxn and llustrate the mechanism. AlCl3 ? Q-II: Determine which reagent would complete the rxn and illustrate the reaction mechanism. F3C F;C (Br2 ) (HBR ) (Br2 + Fe) (None of the Above) Q-III: Determine which reagents are needed to conduct the synthesis. OH NO, 1) NANO2 II) R-COOH I) HNO3/H2SO4 II) KMN04/HCI I) R-COOH II) NANO2 1) R-COOH II) HNO3/H2S04