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Chlorides s. a. Halides

Chlorides s. a. Halides, Hydrochlorides, Replacement Chlorination s. a. Halogenation, Replacement of hydrogen by halogen... [Pg.247]

Characterization of compounds s. subentry derivatives Chelates s. Complex salts, inner Chloranil as reagent 16, 524 Chlorides s. a. Halides, Replacement... [Pg.239]

Wilkinson s catalyst has also been reported to decarbonylate aromatic acyl halides at 180°C (ArCOX ArX). This reaction has been carried out with acyl iodides, bromides, and chlorides. Aliphatic acyl halides that lack an a hydrogen also give this reaction, but if an a hydrogen is present, elimination takes place instead (17-16). Aromatic acyl cyanides give aryl cyanides (ArCOCN—> ArCN). Aromatic acyl chlorides and cyanides can also be decarbonylated with palladium catalysts. °... [Pg.944]

Reaction VI. (b) Action of Aluminium and Mercuric Chloride on a Mixture of an Aromatic Hydrocarbon and an Alkyl Halide. (J. C. S., 117,... [Pg.60]


See other pages where Chlorides s. a. Halides is mentioned: [Pg.261]    [Pg.308]    [Pg.296]    [Pg.227]    [Pg.261]    [Pg.308]    [Pg.296]    [Pg.227]    [Pg.297]    [Pg.357]    [Pg.311]    [Pg.279]    [Pg.289]    [Pg.409]    [Pg.390]    [Pg.149]    [Pg.285]    [Pg.456]    [Pg.89]    [Pg.290]    [Pg.125]    [Pg.55]    [Pg.114]    [Pg.168]    [Pg.276]    [Pg.74]    [Pg.235]    [Pg.91]    [Pg.174]    [Pg.314]    [Pg.149]    [Pg.520]    [Pg.79]    [Pg.618]    [Pg.416]    [Pg.390]    [Pg.149]    [Pg.744]    [Pg.58]    [Pg.623]    [Pg.1021]   


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Halides Chlorides

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