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Carbocations, continued methyl migration

Having participated, the methyl group continues to migrate to carbon 1 because by doing so it allows the formation of a stable tertiary carbocation, which then captures water in a step reminiscent of the second half of an S l reaction. [Pg.979]

As the methyl group migrated in part (b), the hydrogen migrates here, forming the more stcible 3 carbocation. This migration is called a 1,2-hydride shift. We now continue as in part (b) and obtain the expected products ... [Pg.475]


See other pages where Carbocations, continued methyl migration is mentioned: [Pg.940]    [Pg.1094]    [Pg.304]    [Pg.1101]    [Pg.1099]    [Pg.1014]    [Pg.297]   
See also in sourсe #XX -- [ Pg.96 , Pg.192 ]




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