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Radical chlorosulfonyl

The 2-chloro/l-chloro ratio in chlorination of 2,3-dimethylbutane, for instance, is 12.0 with sulfuryl chloride versus 4.2 in photochlorination. The chlorosulfonyl radical, however, easily decomposes under reaction conditions to yield a chlorine atom [Eq. (10.19)], which also participates in chlorination ... [Pg.587]

A variety of chemical modifications result Irom radical additions or cyclo-additions to the (CH) backbone, e.g. with chlorosulfonyl isocyanate. The ring of the adduct thus formed can be opened by alkalis. The reaction scheme for cyclo-addition of chlorosulfonyl isocyanate and ring opening to substituted hydrophilic polyacetylene is as follows ... [Pg.100]


See other pages where Radical chlorosulfonyl is mentioned: [Pg.196]    [Pg.7]    [Pg.587]    [Pg.588]    [Pg.985]    [Pg.164]    [Pg.985]    [Pg.72]    [Pg.157]    [Pg.269]    [Pg.275]    [Pg.172]   
See also in sourсe #XX -- [ Pg.587 ]




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