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- When an alkene is treated with Hg(OAc)2 in EtOH, followed by reaction with basic NaBH4, what functional group is formed? alkane ether O syn diol O alkyne O epoxideHC CH CH3CO2H H,SO, H3C-C-O-C=CH2 H HgSO, Acetylene Acetic Acid Vinyl acetate Acetylene reacts with acetic acid in the presence of H,SO4 and HgSO4 to yield vinyl acetate, a monomer used in the production of poly(vinyl acetate). The reaction mechanism includes the following steps: 1. Formation of a bridged mercurinium ion intermediate between Hg- and acetylene; 2. Addition of acetic acid to open the three-membered ring; 3. Proton transfer to solvent to give an organomercury vinyl ester3; 4. Addition of H to the alkene to form a carbocation; 2+ 5. Expulsion of Hg²+ to form the alkene. Diagram the mechanism on a separate sheet of paper, and then draw the structure of the product(s) of step 3. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Draw organic species only. • Do not include counter-ions, e.g., Na, I, in your answer.When pent-1-ene is treated with mercury(II) acetate in methanol and the resulting product is reacted with NaBH4, what is the primary organic compound which results? 1-ethoxypentane 1-methoxypentane 3-ethoxypentane 2-ethoxypentane 2-methoxypentane
- Predict the major products formed when 2- methyl-1-butene reacts with: H2O, H+. Show the reaction mechanism of the given alkene reactionsConsider the following mechanism of reaction: CH3 CH, CH3 CH;C CH, + H-CI CH;CCH, + C: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic HCl and CI" are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI" are both electrophilic The alkene and CI" are both nucleophilic AMeving to another question will save this responseThe following product can be synthesized from the reaction of an alkene with Hg(OAc)2 followed by reduction with NaBH4. Draw all possible alkenes that will give the product shown
- The two reactants shown below are combined to bring about a nucleophilic substitution reaction O NaOCCH, Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding O b Oc Od O none + Br CH₂CH₂CHCH₂Provide the product and mechanism for the reaction: ОН Cro, H,SO, H,0Questão 10A certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis resulted in CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. What is the reasonable structure for this hydrocarbon? Hexadec-6,10-dino undec-1,5-dino Hept-1,5-dino hex-1,5-dino nah
- Which of the following reactions does not proceed? O Dehydration of 2-propanol with H;SO, catalyst Hydrogenation of benzene with H2/Pt o Oxidation of 2-propanol by H,Cro O Hydrobromination of 2-butene with HBr O Hydration of cyclohexene with H2O/H2SO4CoO7T07Q3769 Give the major product of the following reaction. H2 Ni CIPredict the product of the following reaction and name the product H₂C CH3 OH conc. H₂SO4 Explain the mechanism by which this reaction proceeds