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- (A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?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?4. Give the structure of compounds A to E in the following reaction sequence.
- Two of the following will give the same dimethylcyclooctatriene prod (A) while the third one will give the different dimethylcyclooctatriene (B) Preditc which of the ffg gives prod A or BProvide a detailed step-wise mechanism for the following reaction. Be sure to show all intermediates, formal charges, and show the movement of electrons with curved arrows.Draw a detailed step-wise mechanism for the following reactions. Be sure to show all steps, formal charges, and show the movement of electrons with curved arrows.
- Give typed full explanation nothing should be hand written otherwise leave it indicate which hydrogens are prochiral and give them their correct notation (Pro-R or Pro-S)Illsutrate the Energy diagram for carbocation formation in two different SN1 reactions ?Draw out the complete mechanism (curved arrow formalism) for the preparation of benz-alacetophene