3. Problem: Outlined below is a synthesis of the gypsy moth sex attractant E (a type of pheromone). Give the structure of the gypsy moth sex attractant E and of the intermediates in the synthesis. CH3 NaNH, HC CNa - A(C9H16) B (C9H15Na) C6H5CO₂H H₂ E(C19H380) D(C19H38) C (C19H36) Lindlar's Catalyst
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- From the following sequences which one allows for this synthetic transformation to occur? Please answer very soon will give rating surelyplease show the mechanism for the acid-catalyzed conversion of this ketone (carvone) to cumyl alcohol with arrow moment of electrons for every step. Assume that sulfuric acid acts as a catalyst, donating + ions.Write a plausible mechanism for this transformation. Only two sequential pericyclic reactions are required.
- Could you show the structural formulas of the compounds A-C, whitch of these compounds is the most likely to form if the reaction occures via a chair conformation intermediate and why?.(A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?The phenyl group, C6H5, is known to be an ortho/para-directing group. (a) With that in mind, predict theproduct of the reaction shown here. (b) Justify why it is an ortho/para director by examining the ortho, meta,and para arenium ion intermediates that would beformed during the course of the reaction.