Friedel-Crafts reaction rearrangements during

Tne rearrangement of a primary to a tertiary artxxation during Friedel-Crafts reaction of betrzene with 1-chioro-ll-dimethyipi-opane eccurs by shift of an aikyl tnip with its electron. .jir. 

Yet a final limitation to the Friedel-Crafts reaction is that a skeletal rearrangement of the alkyl carbocation electrophile sometimes occurs during reaction, particularly when a primary alkyl halide is used. Treatment of benzene with 1-chlorobutane at 0 °C, for instance, gives an approximately 2 1 ratio of rearranged (sec-butyl) to unrearranged (butyl) products. 

Transalkylation and Dealkylation. In addition to isomerizations (side-chain rearrangement and positional isomerization), transalkylation (disproportionation) [Eq. (5.56)] and dealkylation [Eq. (5.57)] are side reactions during Friedel-Crafts alkylation however, they can be brought about as significant selective hydrocarbon transformations under appropriate conditions. Transalkylation (disproportionation) is of great practical importance in the manufacture of benzene and xylenes (see Section 5.5.4) ... 

Identification. The many possibilities for the formation of isomeric or anomalous products due to rearrangement, unusual orientation, or degradation of alkyl groups during the Friedel-Crafts reaction, coupled with the fact that the products are usually liquids, difficult to separate and identify, frequently necessitate particular care in establishing the structure and the purity of the products. The most effective method... 

Carbocations can rearrange during the Friedel-Crafts alkylation reaction, leading to the formation of unpredicted products. One example is the formation of isopropyl benzene by the reaction of propyl chloride with benzene. 

The present experiment demonstrates Friedel-Crafts alkylation and allows you to examine the following hypothesis The amount of alkyl rearrangement that occurs during a Friedel-Crafts alkylation of a series of arenes depends on the nucle-ophilicity of the arene, Ar-R. This hypothesis is derived as follows. The rate constant, ky is for a unimolecular process of 3 that does not involve the arene (Scheme 15.1), so its value is independent of the nucleophilicity of the arene. In contrast, 2 is the rate constant for a bimolecular reaction between 3 and the arene, so its value is dependent on the nucleophilicity of the arene. Substituents, R, that make the arene more nucleophilic yield higher values of the bimolecular rate constant k2, thereby increasing the overall rate of the electrophilic substitution. Consequently, formation of the product derived from rearrangement becomes a relatively less important reaction pathway. 

A successful preparation of 1,2,3-trimethylbenzene (not available by the Friedel-Crafts method) has been accomplished by use of the lif-feneau rearrangement which occurs during the reaction of benzyl-type Grignard reagents with formaldehyde. ... 

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