요 CECH H2O, H2SO4 HgSO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions nno XT HO HO C=CH2 H-OH2 cho C-CH3 H2O
CECH H20, H2SO4 HgSO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions nn QoXT HO HO C=CH H20 H-OH2 C=CH2 Hg2+ Hg
요 CECH H2O, H2SO4 HgSO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presenc
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요 CECH H2O, H2SO4 HgSO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presenc
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