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- III. Give a detailed mechanism for the following reaction: OH ОН1.When 2-methyl-1-butanol is dehydrated in an acid medi- um to an alkene, it yelds mainly 2-methyl-2-butene rather than 2-methyl-1-butene. This indicates that the dehydra- tion to an alkene is at least a two-step reaction. Suggest a mechanism to explain the reaction.What major organic product would you expect to obtain when acetic anhydride reacts with CH;CH;CH;OH? А. СH,COОН + CH,CH,OH В. СН:CH:COОН + СH:CH2OН С. СH:COOCН.CH-CH; + CH:СООН D. CH;COOCH2CH¿CH3 + CH3CH2OH
- What reagents are needed to synthesize the following bromides? Br Br Provide the major organic products obtained from the following reactions. a) SN1 CH;OH methanol b) DMF TsO Et CH;COONA SN2 Br, lightIf anhydrides react like acid chlorides with the nucleophiles, draw the products formed when each of the following nucleophiles reacts with benzoic anhydride [(C6H5CO)2O]: (a) CH3MgBr (2 equiv), then H2O; (b) LiAlH4, then H2O; (c) LiAlH[OC(CH3)3]3, then H2O.Predict the product(s) and provide the mechanism. d Br for
- Provide the product and mechanism for the reaction: ОН Cro, H,SO, H,0(c) Write a mechanism to account for the products of the following reactions: CH3 CH, H3C. H3C. -H,0 OH -CH3 H,SO, H;C CH3OH - NH, Br2/KOH →product; 1. (a-hydroxy amide) Product of this Hoffmann bromamide reaction is : OH (a) Ph – Ĉ-CH3 (Ъ) Ph — CHO (c) Ph- CH3 (d) Ph – CH2 -NH2 NO2