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- In the information provided,-see photo, we read that the axial attack is preferred for the reaction. Explain this preference for the axial attack and the trans product formedin Figure 1. Be sure to comment on the steric factors of the substituents, their placement onthe ring, and the hydride delivery agentDraw the (pericyclic) reaction (reaction 1), including all mechanistic steps, that lead from the starting materials to the intermediate product. Show all isomers that can be formed and provide an explanation as to why that is. Determine the configuration of all chiral centers. I included the molecule, the retrosynthesis of the molecule, and reaction 1 to help solve this question.Please complete both subpart reactions in clear handwritten answer on a paper!
- For the following reactions, what is its (a) type of alkyl halide, (b) type of Nu, (c) type of solvent, (d) if is it substitution is it inverted or not if not substitution is it not applicable and (e) what is the mechanism?which is more reactive in E2 reaction?Fill in the blank for this reaction by using the E1 mechanism that includes rearrangemnt
- Draw a detailed mechanism, showing appropriate bonds forming and breaking, for the reaction between cyclopentadiene and methyl acrylate3) If the product of an SN1 or Free radical reaction contains a stereocenter then a _______________ mixture occurs. Complete the sentence above and explain why this occurs. 4) List and explain the 3 steps of a free radical reaction.as a follow-up question can explain this mechanism