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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS, 348<br />

action <strong>of</strong> acids, it is decomposed into benzene and a mercuric salt'<br />

and when it is heated with iodine, according to <strong>the</strong> proportion <strong>of</strong> <strong>the</strong><br />

two bodies present, ei<strong>the</strong>r iodobenzene and phenylmercuric iodide<br />

C 6 H 1<br />

j J- Hg are formed, or iodobenzene and mercuric iodide.<br />

CHI<br />

Stannifrphcnyl Triethide ,Q A . 6 ^ Sn is obtained by <strong>the</strong> action ol<br />

sodium upon a mixture <strong>of</strong> bromobenzene and triethyl-stannic iodide.<br />

It is a colourless, strongly refractive liquid, boiling at 254°; its vapour<br />

slowly absorbs oxygen. By <strong>the</strong> action <strong>of</strong> iodine, it is resolved into<br />

iodobenzene and triethyl-stannic iodide.<br />

ADDITIVE 'COMPdDMDS OF BENZENE.<br />

Benzene HexacMoride CpHgCl^ is obtained, by <strong>the</strong> action <strong>of</strong> chlorine<br />

on benzene, in <strong>the</strong> sunshine or at <strong>the</strong> boiling-point, in colourless<br />

crystals, melting at lS'T, and boiling, with partial decomposition, at<br />

288°. On heating it -with alkalis, it is resolved into hydrochloric<br />

acid and trichlorobenzene.<br />

A similar compound is Benzene Eexabromide CjHjBr,.<br />

Bmxm Triehlorhydrin CLHJGgXOHJg is formed by shaking<br />

benzene with aqueous hydrochlorous acid. It is slightly soluble in<br />

water, and freely in alcohol and benzene, and crystallizes at a low<br />

temperature in small plates, melting at 10°. By <strong>the</strong> action <strong>of</strong> a dilute<br />

solution <strong>of</strong> sodium carbonate, an amorphous deliquescent mass called<br />

phenose C6H0(OH)6 is obtained, which, as well as <strong>the</strong> triehlorhydrin,<br />

yields, when heated with hydriodic acid, mdniodobenzolene COHUI, a<br />

heavy, colourless liquid, which boils without decomposition.<br />

Tricliforophenomalic Add C0H0CL05 is produced, toge<strong>the</strong>r with<br />

oxalio acid, chlorinated benzenes, and quinones,

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