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Activation by n Donors X and C Substituents

The first reaction provides a route for the reduction of alkyl halides since the carbo-cation (isopropyl, in Rl) may be prepared from action of AICI3 on the corresponding alkyl halide. Reactions of the type Rl are also important in the process, catalytic cracking, in the manufacture of gasoline. They have also been studied in mass spectro-metric experiments [235]. Reaction R2 is one route to the preparation of carbocations under stable ion conditions. Reaction R3 is employed in the laboratory synthesis of the tropylium cation. Reaction R4, the (crossed) Cannizzaro reaction, is unusual in that it takes place under strongly basic conditions. The oxy dianion is an intermediate in the reaction of concentrated hydroxide with the aldehyde, R HO. None of R1, R2, or R3 may have hydrogen atoms a to the carbonyl groups. Formaldehyde (R1 = H) is readily [Pg.146]


See other pages where Activation by n Donors X and C Substituents is mentioned: [Pg.145]    [Pg.145]    [Pg.145]    [Pg.145]    [Pg.145]    [Pg.145]    [Pg.124]    [Pg.124]    [Pg.180]    [Pg.124]    [Pg.124]    [Pg.46]    [Pg.4130]    [Pg.1511]    [Pg.138]    [Pg.316]    [Pg.123]    [Pg.274]    [Pg.134]    [Pg.61]   


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Activating substituents

C-Substituents

Donor substituent

Donor substituents

N activation

N activity

N donors

X: substituents

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