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- Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .What is the structure/s of the major organic product/s for the reaction below?in terms of ortho/para and meta directors, give the major products formed and indictae why Please Answer all the parts otherwise I'll downvote
- Please explain the reactions given below with the End orbital (FMO) method. Read the product/products stereochemically.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.predict the stating materials, reagents, or products of the followinf reactions
- Give a full curved arrow mechanism for the ring-opening reaction of an epoxide in aqueousacid shown below. Show ALL non-bonded electron pairs and all non-zero formal chargeswhere applicable. (Note: you will need to redraw the structures provided in order to showthe mechanism correctly; non-bonded electron pairs have not been shown, although nonzero formal charges are included.) Be sure to show any stereochemical elements in theproduct(s) correctly.One possible way of determining the identity of an alkene, is to let itundergo an oxidative cleavage reaction in the presence of hot basicpotassium permanganate. You are given two containers said to containdifferent alkenes. Container A is marked as cis / trans‐2‐butene andcontainer B as 2‐methyl‐1‐butene. Explain by referring to the formation ofproducts, how you would verify the identity of the alkenes.for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow mecanism. based on the reaction products, explain why a carbocation intermediate cannot be proposed
- How would you synthesize the followingcompounds from benzene using thereagents from the table? Each requires 3-4steps.Suppose you have compounds A–D at your disposal. Using thesecompounds, devise two different ways to make E. Which one of thesemethods is preferred, and why?All attempts to isolate primary and secondary nitroso compounds result solely in the formation of oximes. Tertiary nitroso compounds, however, are stable. Explain.