Predict the product of the following reaction and then draw a stepwise mechanism for its formation: Part 1 Part 2 out of 3 OH H₂SO4 +- complete the structure view structure edit structure A. HSO4 B. H₂O C. H₂SO4 D. SO₂
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- Amines are converted into alkenes by a two-step process called Hofmann elimination. SN2 reaction of the amine with an excess of CH3I in the first step yields an intermediate that undergoes E2 reaction when treated with silver oxide as base. Pentylamine, for example, yields 1-pentene. Propose a structure for the intermediate, and explain why it readily undergoes elimination.7. When butan-2-ol undergoes acid catalysed dehydration reaction, a mixture of products, B and C, are formed.Compound C shows cis-trans isomerism. Ozonolysis of compound B yields D and E. Draw the structure of Band C, and determine the major product. Draw cis-trans isomers of C. Write the reaction equation for theozonolysis of compound B that yields D and E. Show the preparation of butan-2-ol via a Grignard reagent byusing a suitable alkyl halide and compound D and E.Predict the product of the following reaction and classify the reaction. Pb(NO3)2+FeSO4--->PbSO4+________
- Ozonolysis (O3 in CH2Cl2) of compound A under reducing conditions (Zn /acetic acid) gives formaldehyde, 2-butanone, and compound B. Catalytic hydrogenation (H2/Pd) of A gives 2,7-dimethylnonane. What is a possible structure for compound A? a. 2,7-Dimethyl-2,8-nonadieneb. 2,7-Dimethyl-1,8-nonadienec. 2,7-Dimethyl-1,6-nonadiened. 2,7-Dimethyl-1,7-nonadieneWhich of the following reagent/s will efficiently convert isopropylbenzene to 2- and 4-chloro-1-isopropylbenzene? Select one: a. HCl in the presence of peroxides b. SOCl2 c. PCl3 d. Cl2, FeCl3 e. Cl2, initiated by heat or lightChoose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) Br2, FeBr3 Na/NH3, -33 degrees C NBS, light KMnO4, H3O+ Mg metal, ether KOH, EtOH, heat
- Rank the species below in order of increasing nucleophilicity in protic solvent. I. H2O II. CH3S— III. CH3COO— IV. t-BuO— I, II, IV, III I, III, II, IV I, III, IV, II I, II, III, IVProvide the reagents necessary to convert 3-methyl-2-butanol to 2-bromo-3-methylbutane. CHOOSE FROM THE FOLLOWING REAGRENTS BELOW conc. HBr NaBr, H2SO4 PBr3 HBr, peroxide Br2When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.
- Give the product/s for the following reaction and indicate what mechanism is involved in the formation of such product/s as SN1, SN2, E1, E2. CH3CH=CHCl + NaNH2A. In the synthesis of 1-bromobutane, what is the inorganic by-product left in the reaction flask following the distillation? Why was the bromoalkane the bottom layer in the separatory funnel? B. Predict the product when 1-methylcyclohexanol reacts with H2SO4 and KBr. Show the mechanism.Draw the organic products formed when cyclopentene is treated with each reagent. With some reagents, no reactionoccurs.a. H2 + Pd-Cb. H2 + Lindlar catalystc. Na, NH3d. CH3CO3He. [1] CH3CO3H; [2] H2O, HO–f. [1] OsO4 + NMO; [2] NaHSO3, H2Og. KMnO4, H2O, HO–h. [1] LiAlH4; [2] H2Oi. [1] O3; [2] CH3SCH3j. (CH3)3COOH, Ti[OCH(CH3)2]4, (–)-DETk. mCPBAl. Product in (k); then [1] LiAlH4; [2] H2O