7. Draw the mechanism and predict all major regiochemical and stereochemical products of the following reaction. Be sure to explain your answer in some format (partial charges, resonance structures, etc.). Heat + HO
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- 4. For the following reaction, draw a reasonable mechanism showing stereochemistry Br-Br6. 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 OSOH3. Draw the major product in the following reaction and reaction mechanism. Remember when drawing a reaction mechanism, you need to show all nonbonding electron pairs, formal charges, electron flow arrows, and all resonance structures. What is the name of this mechanism? Determine and circle whether the substituent is an activator or deactivator. Explain what is meant by being an activator or deactivator and circle the single resonance structure that supports your decision regarding the substituent in the starting material. OH CH₂CH₂CH₂Br FeBr
- Draw a curved arrow mechanism that accounts for the cyclisation of 2 into F [ please make sure your mechanism takes into account stereochemical considerations including the stereoselectivity of the reaction and clearly indicate if a conrotatory or a disrotatory process is responsible for each of the transformations]. can you please explain how you decide and select the stereoselectivty and how to see if its conrotatory or disrotatory so that i can apply to similar questions. thank you2. Draw the product(s) of the following reaction and a mechanism. Include all resonance structures of the intermediate. AICI32. For each of the following molecules, draw all possible products of an allylic bromination. .d 3. Can you think of an alkene that undergos allylic bromination to produce only 3 products (do not count stereoisomers as different products)?
- I labeled one of the atoms incorrectly, but I am not sure which. Would the H in HBr be considered a nucleophile as well ?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. Drawing Arrows N :Br: NaⒸ N: C:O NaⒸ Br.ochem help please Predict the major product(s) for the following reaction sequences and provide the stepwise mechanism for both steps 1 and 2 .... (see attached image)
- Draw the missing reactants for the reaction shown below. Be sure to include stereochemistry where appropriate.5. Complete the following reaction and propose a mechanism to justify your ane 1. Ög ? 2. Reductive workThe carbocation intermediate formed in the first step is resonance-stabilized. Draw the other resonance structure (by modifying the provided drawing) and add curved arrow(s) to convert the first resonance structure into the second one. Use the +/- tools to add/remove charges, and use the single bond tool to interconvert between double and single bonds. ÇH3 CH3 H3C. H,C. CH3 CH3 ČH3 ČH3 ČH3 ČH3 Edit Drawing