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- 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, hν
- Name 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, AlCl3Draw 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−.
- Identify all carbonyl compounds that can undergo nucleophilic addition reactions from the following:Identify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. H2O, −OHDraw 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.
- 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 OHWhy can’t 1-methylcyclohexanol be prepared from a carbonyl compound by reduction?