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- Benzene can be hydroxylated by treating it with hydrogen peroxide and a strong acid such as trifluoromethanesulfonic acid (TfOH). Propose amechanism for this reactionIbufenac, 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.Draw the organic products formed when cyclopentene is treated withfollowing reagent. [1] OsO4 + NMO; [2] NaHSO3, H2O
- An alkene is treated with OsO4 followed by H2O2. When the resulting diol is treated with HIO4, the only product obtained is an unsubstituted cyclic ketone with molecular formula C6H10O. What is the structure of the alkene?What is the basicity of H2SO4Draw the structure of a compound fitting each description: a.an aldehyde with molecular formula C4H8O b. ketone with molecular formulab C4H8O c. a carboxylic acid with molecular formula C4H8O2 d. an ester with molecular formula C4H8O2
- Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. NaNO2, HClDraw two enol forms of the following diketonewhat ate the structures for the following cinnamate reacts with methyl cinnamate reacts with ethyl cinnamate reacts with 1-propyl cinnamate reacts with 2-propyl
- An unknown compound A of molecular formula C10H18O reacts with H2SO4 to form two compounds (B and C)of molecular formula C10H16. B and C both react with H2 in the presence of Pd-C to form decalin. Ozonolysis of B forms D, and ozonolysis of C forms a diketone E of molecular formula C10H16O2. Identify the structures of compounds A, B, C, and E.Draw the organic products formed when cyclopentene is treated withfollowing reagent. [1] CH3CO3H; [2] H2O, HO−Draw the principal organic product for the reaction of 2-bromobutane with magnesium in diethyl ether, followed with benzaldehyde in diethyl ether, and then followed by dilute acid...