Draw a valid and complete reac stereochemistry for the reactio steps, arrows, and electrons inw (and/or transition states where non-zero formal charges. Also and all possible products, incluc needed). Please label these as minor" if needed) Vou m
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- Draw a valid and complete reaction mechanism for one (and only one) of the following reactions J, K, or L. Be sure to include any and all stereochemistry throughout the reaction mechanism. Include all appropriate steps, arrows, and electrons involved. Draw all of the intermediates (and/or transition states where discussed in lecture), and label all non-zero formal charges. For your reaction, also be certain draw the starting material, the reactant(s), and all possible products. Please label these as "major" and "minor" (and "very minor," if needed). You may use a label more than once, but each structure should only have one label. Reaction J OH H,SO4, A Reaction K 1. PB13, 2. NaCN OH Reaction L HI, ADraw the missing reactants for the reaction shown below. Be sure to include stereochemistry where appropriate.Choose one (and only one) of the reactions below and draw the complete mechanism for the major product(s) only, including the formation of the electrophile. You must also include all of the proper resonance structures for any intermediate species, but not for the starting material. Be sure to also include all arrows, charges, electrons, and any other mechanistic aspects discussed in lecture or within your textbook. Upload your answer (using any reasonable file format) within this question. Reaction I HO 1. AICI3 H 2. H-О H3C CI Reaction II H,SO4 NO2 Reaction III FeCl3 + Cl2 SO3H
- 1) Explain the formation of the MAJOR product for the reaction shown below. Your explanation should include a statement regarding substituent effects and an annotated mechanism (correct curved arrow notation, show all intermediates, include brief statements) H₂C-0 Br FeBr3 MAJOR PRODUCTThis content is protected and may nag shared t 4. Consider the following reaction. This reaction is a multi-step reaction. [1] Draw the mechanism for each step of this reaction using curved arrow notation, include all lone pairs of electrons if they are directly involved in the reaction. [2] Identify the arrow pushing pattern (mechanistic pattern: nucleophilic attack, loss of leaving group, or proton transfer) for each step. [3] Draw a transition state for each step. H-OSO3H CH3 00 H H3C-O-H Хосно H3C-O-H H9. Draw all four carbocation intermediates possible upon protonation of the diene below. Draw all halogenated products after nucleophilic attack of chloride (CI). Circle the product(s) expected to be the major product at elevated In temperatures. HCI 10. Draw a complete, detailed mechanism (curved arrows) of the following reaction based on the knowledge learned about the reactions of conjugated dienes. Include all resonance structures associated with the intermediate(s). HBr Br
- 16. Provide a curved arrow mechanism for the transformation shown below. Be sure to show the formation of all reactive intermediates (including the role of FeBr/Bra) and resonance forms and clearly show the movement of all electrons. Br2 Br FeBra Next, provide an energy vs. reaction coordinate diagram for the EAS mechanism above. Please only start with benzene and Br". Label all reaction intermediates, relative energies, and clearly show the rate-determining step.Select one activator & ortho para director to be on a benzene ring to start. You will then add a bromine to this group showing the COMPLETE mechanism, including all resonance structures. Put a box around the stabilizing resonance structure and explain why it is stabilizing.refer to image. Give the expected major product or products in each of the following transformations. Clearly show stereochemistry where appropriate (e.g., by using wedged or dashed bond lines, or by writing axial or equatorial bonds). If no reaction is expected, write “NR”. WILL RATE!
- Ochem help... What is the major product of the following reaction sequence? Provide the stepwise mechanism for each step (1, 2a, and 2b). (see attached image)6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap thanks 7. Draw a complete, detailed mechanism for the following reaction. Label the electron-rich and electron-poor sites in each step. H₂SO₂ OSOHUsing Curved Arrow Formalism, draw the reaction of 1-methylcyclopentanol treated with aqueous sulfuric acid and identify the rate determining step. If more than one product is formed, identify which is major, minor, very minor, etc. Thank you for the help with this question. I appreciate it.