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- 5. What reagents are needed to convert toluene (C,H,CH,) to each compound? a. C.H.COOH b. C.H₂CH₂Br c. p-bromotoluene d. o-nitrotoluene e. p-ethyltoluene f.Draw the products formed when ethylene oxide is treated with each reagent. a. HBr b. H2O(H2SO4) c. [1] CH3CH2O; [2] H2O d. [1] HC ≡ C−; [2] H2O e. [1] −OH; [2] H2O f. [1] CH3S−; [2] H2ODraw the organic product(s) formed when CH3CH2CH2OH is treated with each reagent. a.H2SO4 b.NaH c.HCl + ZnCl2 d.HBr e.SOCl2, pyridine f.PBr3 g.TsCl, pyridine h. [1] NaH; [2] CH3CH2Br [1] i.TsCl, pyridine; [2] NaSH j.POCl3, pyridine
- Synthesize each compound from cyclohexanone and organic halides having s4 C's. You may use any other inorganic reagents. OCH3 a. C. OH b. d.Synthesize each compound from toluene (CgH,CH3) and any other organic or inorganic reagents. a. CeHsCH2OC(CHa O,N H2N. b. CgH;CHO d. HOOC- -NO2 f. HO. -COOH CHO C. е. g. BrProvide the missing reactants and reagents. a is bis c is d is e is 11 V < Previous C 0 NHCH3 (R.S)-Methamphetamine
- a. b. C. d. e. type: OH type: type: OH 2 + OH TsOH cat. HÅH н Ἡ Acetal formation OH TsOH cat. SOCI₂ ܘ ܀ 1.2 equiv. NH3 2. LIAIH₂ 3. H₂O*1. Provide the major product for the following reactions. If the reaction creates a racemic mixture, draw only one of the stereoisomers (meaning put wedge and dash bonds on the structure). a. b. C. ZI OMe OH LOTS NaCN DMFDraw the structure of reactant A. CrO₂ H₂SO4 H₂O HO