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- Which alkyl halide will react the fastest in an SN2 reaction (CH3)3CI CH3CH2Br CH3CH2I CH3I CH3BrBicyclo[2.2.1]heptan-7-one + PCC (in CH₂Cl₂) => A.) Bicyclo[2.2.1]heptan-7-ol B.) Bicyclo[2.2.1]heptanoic acid C.) Cyclohexanecarbaldehyde D.) All the given choices are possible products E.) No reactionWhat is the major E2 elimination product formed from each halide?
- The Hofmann product is favored by the E2 mechanism when 2-bromo-3-methylbutane is added: A. MeOH B. MeO:- in MeOH C. Nal in acetona D. (CH 3)3 CO:- in (CH 3),COHDraw Sn1/E1 products of both reactions below or fill in the blank with appropriate stuffs for Sn1/E1what is the product of 1-Hexyne reacting with 1 equivalent of HBr? Include E/Z if necessary.
- Choose the appropriate reagent for the following reaction. A) TsCl/pyridine B) SOCl2/pyridine C) ZnCl2 D) PBr3 E) HIThe molecule, 2-bromo-1,3-diethyl-1,4-dimethylcyclohexane undergoes an SN1/E1 reaction in the solvent ethanol. i) Draw the intermediate resulting from the first step of this reaction. ii) Draw the two most favorable intermediates resulting from carbonation iii) From the intermediate(s) in (ii) draw all the possible E1 products and circle the product(s) that is(are) most favorable. iv) Name the most favorable product(s). v) Draw an SN1 product from an intermediate in (ii).What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict the major product.