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- Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation. My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not???Step 4c: Draw the resulting structure or structures indicated by the curved‑arrow mechanism shown. Include formal charges, but not lone pairs.kindly answer from C to E
- How do I get to my target molecule (1st image) with the following uncomplete reaction (2nd image)Carbocations often rearrange, as shown below. Draw in the hydrogens on the two carbons involved in the rearrangement, and show formal arrow-pushing to illustrate the transformation.The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.
- 1. Which absorbs at higher frequencies: a C-H or C-D bond? Explain. 2. Predict which alkene will predominate at equilibrium. Explain.#6). Second picture shows instructions on how the arrows must be shown as.Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?