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- Propose a series of reactions to synthesize each molecule below and show the structure of the intermediate compounds formed following each step you propose. Do not give handwriting solution.Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys fir and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.give the reagents for parts a-p
- 2-bromo-2-methylbutane undergoes hydrolysis reaction with water, H2O toform compound W. Compound X and compound Y are produced when 2-bromo-2-methylbutane undergoes elimination reaction with alcoholic ofsodium hydroxide, NaOH. (i) Draw the structural formula of compounds W, X and YIbufenac, a para-disubstituted arene with the structure HO2CCH2C6H4CH2CH(CH3)2, is a much more potent analgesic than aspirin, but it was never sold commercially because it caused liver toxicity in some clinical trials. Devise a synthesis of ibufenac from benzene and organic halides having fewer than five carbons.Synthesize each compound from benzonitrile (C6H5CN) as the only organic starting material; that is, every carbon in the product must originate in benzonitrile.
- 1 Provide step by step analysis of each reagent and final product clearly indicated17. Provide a synthesis of CH3CH2CH2 CH2 SH from any alkyl halide. Show the structure of all reactants and products.Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys r and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.
- 7.56 Below are two potential methods for preparing the same ether, but only one of them is successful. Identify the successful approach and explain your choice.Prepare the following compounds : 1-Starting with benzene or any other reagents , prepare 3-phenyl -1-propanolUndecanal is commercially available, but 6-methyl-1-bromoheptane is not. Propose two methods for the synthesis of 6-methyl-1-bromoheptane using precursors containing fewer than five carbon atoms (Cn n < 5). A protecting group will probably be required.