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Alkyl groups in carbocations

The carbocations that are formed to generate these two products are shown on the left. You will recall that alkyl groups can exert a positive inductive effect (see p. 59), i.e. they can push electrons towards the positively charged carbon atom in the carbocation and so stabilise it. Therefore carbocation A will be more stable than carbocation B because it has two alkyl groups directly attached to the positively charged carbon atom, whereas there is only one alkyl group in carbocation B. [Pg.65]


See other pages where Alkyl groups in carbocations is mentioned: [Pg.513]    [Pg.820]   
See also in sourсe #XX -- [ Pg.160 , Pg.161 , Pg.181 , Pg.342 ]

See also in sourсe #XX -- [ Pg.160 , Pg.161 , Pg.181 , Pg.342 ]

See also in sourсe #XX -- [ Pg.193 ]

See also in sourсe #XX -- [ Pg.160 , Pg.161 , Pg.181 , Pg.342 ]

See also in sourсe #XX -- [ Pg.140 , Pg.143 , Pg.162 , Pg.317 ]




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