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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?Draw the structure(s) of the major organic product(s), for each of the following reactions. ELOH a) cat. H,SO4 Br 1) 2 eq. Li b) 2) PHCHO 3) NH,Cl(aq) Ph = Phenyl 2 eq. Li c) NH3(1) 1) Hg(0,CCF,)2, (CH,),COH d) 2) NaBH4, NAOH Os04 e) cat. NMO OH PB13 f) CH,Cl,Rank and explain the following compounds in order of increasing acidity
- Rank the following compounds in order of increasing basicity in aqueous solution, least basic first a) Propylamine, ammonium, dipropylamine b) Methyl-3-aminopropanoate, sectutylamine, NH3*CH2CH2NH2 c) Aniline, methyl m-aminobenzoate,, methy! p-aminobenzoateRank the following compounds in order of decreasing acidity. CH4 F3C- HO. H3C-S- HO. ОН A B C A: [ Select ] B: [ Select ] C: [Select] D: [ Select ]Rank each set of alcohols below in order of .increasing acidity. Explain your answers CI CI CI. CI .CI CI ÓH OH Он (a) (b) (c)
- Provide the major organic product of the following reaction. Ph NaOH, ARank the attached compounds in order of increasing acidity.Arrange the following substances according to their increasing acidity a) c) Fenol, p-metilfenol,p-(trifluorometil):fenol d) fenol, ácido p hidroxibenzoico CH3CHCH2CH2CH3 OCH3 CH3CH2O- CH₂OH CH3 c) Fenol, p-metilfenol,p-(trifluorometil): fenol fenol, ácido p-hidroxibenzoico