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- What product is obtained when the following compound undergoes two successive elimination reactions?The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?Which of the following compounds will react with methylamine to form the imine shown below? N.
- Draw the products formed when phenol (C6H5OH) is treated with following set of reagents. [1] CH3CH2Cl, AlCl3; [2] Br2, hνName and draw the structure of the major product in the following reactions of cyclohexanone: A) Reduction with NaBH4 in ethanol, followed by H+ B) Reaction with excess ethanol in the presence of H+Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. CH3COCl, AlCl3
- Draw the product formed when CH3CH2C=CH is treated with each of the following sets of reagents: (a) H2O, H2SO4, HgSO4; and (b) R2BH, followed by H2O2, HO−.Draw the products formed when each compound is treated with HNO3 and H2SO4.State whether the reaction occurs faster or slower than a similar reaction with benzene.Identify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. H2O, −OH
- Identify all carbonyl compounds that can undergo nucleophilic addition reactions from the following:Draw the products formed when phenol (C6H5OH) is treated with following set of reagents. [1] HNO3 , H2SO4; [2] Sn, HClWhat is the major organic product obtained from the following reaction? H HC A) 1 B) 2 HO H₂SO4 C) 3 OH 2 سل، ز. مل D) 4 OH