A. Removal of a hydrogen atom from an alkane.
1 Answers 1 viewsYes.
1 Answers 1 viewsThe answer is compound A.If the mechanism of elimination is E1 then the reactivity of dehydrohalogenation is dependent on stability of carbocation. The more stable the carbocation the more readily...
1 Answers 1 viewsDehydrochlorination reaction proceeds most actively in the molecules with high numbers of substitutes around carbon atom which linked with a chlorine atom. Such structure makes final alkene molecule more stable...
1 Answers 1 views2-chloro-2-methylbutane will readily undergoes dehydrochlorination, since it will form the most stable carbocation after elimination of chlorine atom.
1 Answers 1 viewsThe answer is compound A.If the mechanism of elimination is E1 then the reactivity of dehydrohalogenation is dependent on stability of carbocation. The more stable the carbocation the more readily...
1 Answers 1 viewsPentan-3-ol gives 3- pentanone ( that is ketone ) is formed after oxidation . this is product A .Pentan-3-ol gives 2- pentene after reaction with H+ / Heat . THIS...
1 Answers 1 viewsMajor product is " p - nitroTolune . " Nitration have NO2+ electrophile .This will be attached at ortho and para .Major product at para position .
1 Answers 1 viewsCM (FeBr3) = n(FeBr3) / V (solution) V(H2O) = 900 mL = 0.9 L = V (solution) n(FeBr3) = CM (FeBr3) x V (solution) = 0.138 mol/L x 0.9 L...
1 Answers 1 viewsAnswer:PV = nRTP = 0.01*8.31*298 / 0.00381 = 6499.68 АТМ = 48.75 mm HgP final = 140.75 mm Hg
1 Answers 1 views