Predict the product formed when the compound shown below undergoes a reaction in the presence of light (hv) Interactive 3D display mode -CH3 H;C honds). Atoms, and Advanced Template shed or
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- 2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and explain why it's unusual. Please be sure to include all structures (use line angle notation or perspective diagrams as appropriate to illustrate the stereochemistry of the process), resonance forms, intermkediates, transition states, curved arrows, formal charges, or lone pairs as necessary. Please don't cheat. Br HBr SCH3 SCH + ENDraw the structure of the organic product that is formed when the compound shown below is treated with the following reagents: 1) TsCl, pyridine; 2) NaCN. Interactive 3D display mode H₂Cl OH Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single beTROVIOW Topicaj (References) Draw the major organic product of the reaction shown below. HO, NANH2 You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include cationic counter-ions, e.g., Na" in your answer, but draw them in their own sketcher. (Review Top Draw the major organic product of the reaction shown below. OH K2Cr207 H2SO4, H20 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.
- A full arrow pushung mechanism for the reactions and show their intermediatesProvide a mechanism including relevant resonance forms, intermediates, reaction arrows, and curved arrows showing electron flow.Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the intermediates and product of the following reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Mg. Br: CO₂ > :O: Q Atoms, Bonds and Rings Draw or tap a new bond to
- 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. Then draw the organic product of the reaction. Include all lone pairs in the structures. Ignore inorganic byproducts and + counterions. Drawing Arrows NaNH2 Select to Draw Product H H I I O:Z: + S :O: H Undo H Na+ EP ResetCurved 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. Drawing Arrows (CH3)3ONA, (CH3)3OH heat HO :Br:O K+ H :Br: HO +5 'H ΚΘ = Undo Reset DoneCurved 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. يتو H:CE HH Select to Add Arrows H₂O H heat H Please select a drawing or reagent from the question area
- D 1. a)Please show the mechanism for the below (b) indicate the parts that can be labeled products. as E and electrophilic addition. () Show the potential energy diagrams for the last two steps of the meintinism assuming the kinetic and thermodynamic products are the Saume. GM H₂J Oy> #₂0 для низои хат ха Product A bp 104°C Product B bp 101-102°tWhat 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.Which reaction or statement regarding nucleophilic substitutions is incorrect? A) C₁ + 2 H2O ноттон + 2 HCI B) ta CI+MeOH to + HCI C) D) The rate-limiting step in SN1 reactions is the initial step, loss of the leaving group. Nucleophilic substitution reactions that follow second-order kinetics involve complete inversion of configuration.