he major product from the reaction of H20 with 2-methyl-2-butene in the presence of acid catalyst is O 2-methyl-2,3-butanediol O 2-methyl-2-butanol O 2-methyl-1,3-butanediol O 3-methyl-2-butanol 2-methyl-1-butanol
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- What is the final product of 1,2-dicyclohexylethene with Br2 followed by treatment with 2 equivalents of NaNH2? 1,2-dicyclohexylthyne 1,2-dibromo-1,2-diclohexylethane 1,2-dibromoethyne acetyleneOzonolysis (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-nonadieneReaction of HBr with 2-methylpropene yields 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction? Show the mechanism of the reaction.
- Which of the following statements best describes the stereospecificity of the resultingproduct of oxidation of an alkene using KmNO4? *Hydroxyl groups are found on opposite side.Alcohol groups undergo bond rotation.Alcohol groups are transformed into acids.Hydroxyl groups are found on the same side.What is the expected product from the hydrohalogenation of hex-1-ene using HCl? *1-chlorohexane1-chlorohex-1-ene1,2-dichlorohexane2-chlorohexaneDraw the major products obtained from the reaction of one equivalent of HCl with the following compounds. For each reaction, indicate the kinetic andthermodynamic products. a. 2,3-dimethyl-1,3-pentadiene b. 2,4-dimethyl-1,3-pentadieneDescribe the results you expect from each of the following test. a.) the reaction of an alkene with Br2: b.) the reaction of an aromatic compound with KMnO4: c.) the reaction of an aromatic compound with Br2 followed by AlCl3: d.) the reaction of an alkane with Br2: e.) the reaction of an alkane with Br2 followed by exposure to light
- For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yneShow the polarity on each halogenoalkane / alkyl halide. Show and name the mechanism of how the organic products are formed: CH3-CH2-CH2-I (g) + :CN- (aq) à CH3-CH2-CH2-CN (l) + :I- (aq) CH3-CH2-CH2-Br (g) + :OH- (aq) à CH3-CH2-CH2-OH (l) + :Br- (aq)Draw the products, including their configurations, obtained from the reaction of 1-ethylcyclohexene with the following reagents:a. HBr b. H2, Pd/C c. R2BH/THF, followed by HO– , H2O2, H2O d. Br2/CH2Cl2
- Give the major product for the reaction. (CH3)2CHCHBrCH3 + -OC(CH3)3For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne (b) hex-2-yneShow how you might use SN2 reactions to convert 1-chlorobutane into the followingcompounds.(a) butan-1-ol (b) 1-fluorobutane(c) 1-iodobutane