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- For the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Br H ***||||| CEN Select Draw Templates More / || | / C H N EraseFor the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Br. CEN Select Draw Templates / ||| |||| Y More C H N Erase Q2QFor 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
- Draw the organic product of the nucleophilic substitution reaction. Include the appropriate hydrogen atoms in your structural formula. CH₂CH₂CH₂Br + CH₂CH₂S¯ - Select Draw Templates More / |||||| C H S Br Q2 Erase Qited 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 + ? HBrDraw the structures of organic compounds A and B. Indicate stereochemistry where applicable HTC=C-H 1. NaNH, P 2. CH3CH₂CH₂Br (1 equiv.) Draw compound A. Select Draw Templates More / ||| ||| C H compound A Erase H₂ Lindlar's catalyst compound B Draw compound B. H₂O H3O+ Select Draw Templates More / ||| ||| C H OH Era.
- For the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. CI Br H Select Draw Templates More / // // / C H Br Cl ErasNoting the curved arrows, draw all the product(s), organic and inorganic, of the following reaction H Br -CH3 + . N-CH₂ • You do not have to consider stereochemistry. .. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in th right corner. Separate structures with + signs from the drop-down menu.Draw both resonance structures of the most stable carbocation intermediate in the reaction shown HCI - You do not have to consider stereochemistry. -Do not include anionic counter-1ons, e.g., I, in your answer. - Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. - Separate resonance structures using the symbol from the drop-down menu. y自ノ ee P. opy aste [F CH
- H₂C H H₁C Br NBS CH, CH₂ CC, hv **You may assume that Br-Br is formed by a side reaction that occurs (which we discussed in class). This is useful for one of the steps of the mechanism.Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HCI 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 right Separate resonance structures using the symbol from the drop-down menu. ← - CHA ? n ChemDoodleWhat is the Potential energy diagram for this reaction. Pls draw with as much detail as possible. labels and scale) 2-methylpropan-2-ol ---> 2-methylpropene +H2O Draw the potential energy diagram for the reaction of 2-methylpropan-2-ol ---> 2-methylpropene + H20 (1) Label the structures of the (a) reactants, (b) intermediates, (c) transition states, (d) products, and (e) activation energies (E.) for each step. (2) Which step is the rate-determining step? (3) Identify the electrophile and nucleophile in each step when applicable.