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Questa Cmap, creata con IHMC CmapTools, contiene informazioni relative a: MG_Addition, direct hydration involves alkynes, less substituted unsaturated carbon becomes a most stable most branched carbocation, direct hydration involves alkenes, electrophylic additions have second stage, two stages second being attack of a second radical, Addition reactions include radical additions, secondary enoles spontaneously transformed to ketones, attack by an electrophyle prefers less substituted unsaturated carbon, oxidative hydroboration generates less substituted alcohols, Addition reactions include catalytic hydrogenation, two stages first being attack of an halogen atom X·, attack of an halogen atom X· give rise to most branched more stable radical, attack of a second radical stabilizes most branched more stable radical, alkynes transformed in secondary enoles, second stage is the completion attack by the nucleophyle part of the reactant, Hydrogen molecule is summed up in cis position, Hydrogen molecule is summed up breaking of a pi-bond, alkenes hydrated to more substituted alcohols, hydration reaction can be oxidative hydroboration, electrophylic additions have first stage