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- Provide the an efficient synthesis for the following transformation:Which of the following most readily forms a cyclic hemiacetal with acid catalysis? You are wreen dharing Stop Share A' но но CH3 CH3 но ноPropose a synthesis pathway for the production of the following compounds a) to e) from the givenstarting materials plus necessary organic and inorganic reagents.
- Propose an efficient synthesis for each of the following transformations он OMe O;N.Devise concise syntheses for the following transformations. Clearly show the reagent and product foreach step.Mustard gas, Cl¬CH2CH2¬S¬CH2CH2¬Cl, was used as a poisonous chemical agentin World War I. Mustard gas is much more toxic than a typical primary alkyl chloride. Itstoxicity stems from its ability to alkylate amino groups on important metabolic enzymes,rendering the enzymes inactive.(a) Propose a mechanism to explain why mustard gas is an exceptionally potent alkylatingagent
- Propose the synthesis for the following transformations.Devise concise syntheses for the following transformations. Clearly show the reagent andproduct for each step. All syntheses can be accomplished in two steps.Ibufenac, a para-disubstituted arene with the structureHO2CCH2C6H4CH2CH(CH3)2 , is a much more potent analgesic thanaspirin, but it was never sold commercially because it caused livertoxicity in some clinical trials. Devise a synthesis of ibufenac frombenzene and organic halides having fewer than five carbons.
- Which of the following compounds will react with methylamine to form the imine shown below? N.Ibufenac, 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.2) Propose a suitable synthesis to accomplish the following transformation. о H₂N