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- which among the following alkenes will most likely undergo a hydride shift when reacting with HCl?.Which one of the following molecules can react as electrophile in reactions with alkenes? CH3OH NaCI HCI KCN NaCI O HCI O KCN O CH3OHwhich of the following alkenes will most likely undergo a hydride shift when reacting with HCl?
- Which of the following reactions results in Markovnikov addition of H2O to an alkene?When alkyne A is treated with NaNH2 followed by CH3I, a product havingmolecular formula C6H10O is formed, but it is not compound B. What isthe structure of the product, and why is it formed?Which alkene reacts with a red-brown solution of bromine to form 1,2-dibromo-1-ethylcyclohexane.
- Which represents an efficient synthetic route to go from an alkane to an alkene? O elimination with NaNH2, followed by a water workup O anti-Markovnikov hydrohalogenation, followed by elimination O radical bromination, followed by elimination O hydration, followed by elimination O hydration, followed by ozonolysis of the double bondWhen cyclohexene is reacted with hydrobromic acid in acetic acid, the major product is bromocyclohexane. There is a small amount of cyclohexyl acetate formed. What is the mechanism that forms both compounds? What is the purification procedure that isolates both compounds?Which of the following alkene reactions has a charged, cyclic reactive intermediate? Hydroboration Hydration Hydrohalogenation Halogenation Catalytic hydrogenation
- Which of the compounds will undergo a carbocation rearrangement upon heating in CH3CH2OH?Zaitsev's Rule refers to: which alkene is favored in a product mixture O how resonance contributors stabilize cations/anions/radicals O the stereochemistry of reaction intermediates/transition states O the stability of carbocation intermediatesEthers can often be prepared by SN2 reaction of alkoxide ions, RO*, with alkyl halides. Which of the two possible routes would be the better choice to synthesize the molecule shown below? Explain briefly.