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- Identify compounds G,H,E in the following reaction sequences.Provide the complete mechanism using Curved Arrow Formalism for the reaction of (R)-3,3-dimethyl-2-hexanol treated with aqueous phosphoric acid. If more than one product is formed state which is major, minor, very minor, etc. Name the product(s).Please draw the mechanism (assuming an SN1pathway) for the reaction of cyclopentyl bromide with the cyanide anion (-CN) to yield cyclopentyl cyanide as the organic product Thank you
- Draw a detailed mechanism for the FeBr3@catalyzed reaction of ethylbenzene with bromine, and show why the sigma complex (and the transition state leading to it) is lower in energy for substitution at the ortho and para positions than it is for substitution at the meta position.The dehydration of pinacol can take place via two mechanisms, leading to the formation of thetwo products shown below: a) Draw detailed mechanisms for the formation of both products, including any resonancecontributors. b) Briefly explain why pinacolone formation is favored.5. Propose a plausible mechanism for the following transformation:
- Between E1 and E2, which reaction mechanism is most efficient to synthesize the (E) stereoisomer of this product on an industrial scale?Answer part a, b and c part a in image attached b) name the class of compound to which the phosphorus containing reagent belongs c) provide a detailed mechanism for transformation [5] to produce (11)Propose a mechanism for the following reaction that explains why the configuration of the asymmetric center in the reactant is retained in the product:
- Predict and draw the major product (C11H12O2) of the following reaction sequence.Provide a mechanistic explanation (using curly arrows) for theobserved mixture of products in the following dehydration reaction (addingH2SO4), circle the major product, and state why you think it is the majorproduct.Please state if the substrate below undergoes a carbocation rearrangement in an SN1 mechanism