19.06.2013 Views

A Manual of the Chemistry of the Carbon Compounds

A Manual of the Chemistry of the Carbon Compounds

A Manual of the Chemistry of the Carbon Compounds

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

320 THE GHMMJSTSY OF<br />

consists in <strong>the</strong> decomposition <strong>of</strong> a salt <strong>of</strong> diazobenzene with hydriodic<br />

acid. Substitution-products <strong>of</strong> beuzene are also produced by<br />

treating silver benzoate with iodine chloride -.—<br />

C6H6.CO2Ag + IC1 = C6H5I + AgCl + CO,<br />

Mon<strong>of</strong>iuobenzene CSH6F, is produced by distilling fluobenzoic acid<br />

with quicklime. It is a scaly, crystalline mass, melting at 40°, and<br />

boiling at 180°. Its odour resembles that <strong>of</strong> benzene,<br />

Mtrdbenzem C6H6NO8.—Benzene dissolves in concentrated nitric<br />

acid with <strong>the</strong> evolution <strong>of</strong> heat; on <strong>the</strong> addition <strong>of</strong> water, nitrobenzene<br />

is precipitated as a heavy oily liquid:—<br />

CA + NO^OH - C6H8N02 + H2O<br />

Nitrobenzene has generally a brown colour, but when quite pure it<br />

is a pale yellow, strongly refractive liquid, boiling at 220°. It has a<br />

burning sweet taste, and a smell resembling that <strong>of</strong> oil <strong>of</strong> bitter<br />

almonds, and <strong>of</strong> cinnamon.<br />

Mnitrobmzme C6H.(FOj)2 is formed by boiling nitrobenzene with<br />

strong nitric acid, or by acting upon benzene with a mixture <strong>of</strong> concentrated<br />

sulphuric and nitric acids. It crystallizes from nitric acid<br />

or from alcohol in long, glistening, colourless needles, melting at 86°.<br />

"When mono- or dinitrobenzene, or o<strong>the</strong>r nitro-compounds are<br />

heated with potash, <strong>the</strong>y are decomposed, yielding potassium cyanide,<br />

and o<strong>the</strong>r products which have not been examined!<br />

By <strong>the</strong> action <strong>of</strong> strong nitric acid upon <strong>the</strong> substitution-products<br />

<strong>of</strong> benzene, already described, nitro-compounds <strong>of</strong> <strong>the</strong> latter are<br />

obtained.<br />

Benzenesulpkmic Add C8H?.SOa.OH.—When benzene is shaken<br />

with concentrated sulphuric acid, it is dissolved :—<br />

SO8 j ° | =; C6H6.SOyOH + H8O<br />

On neutralizing <strong>the</strong> diluted solution with carbonate <strong>of</strong> barium or<br />

lead, <strong>the</strong> excess <strong>of</strong> sulphuric acid is removed, and <strong>the</strong> solution contains<br />

<strong>the</strong> benzenesulphonates <strong>of</strong> <strong>the</strong>se metals. To obtain <strong>the</strong> free<br />

aoid, <strong>the</strong> salts are decomposed ei<strong>the</strong>r by sulphuric acid or hydrogen<br />

sulphide, and <strong>the</strong> filtered solution is evaporated, Benzeuesulphouio<br />

acid forms small colourless deliquescent plates.<br />

fienzcncsulphonic Chloride C6H5.SOaCl is obtained by<strong>the</strong> action <strong>of</strong><br />

phosphorus puntachloride upon sodium benzenesulphouate; it is an<br />

oily liquid boiling at 246°, which ia decomposed by boiling water.<br />

By <strong>the</strong> action <strong>of</strong> ammonia it is converted into Senzenesulplwnamidc<br />

ORH..SO a colourless crystalline solid,<br />

f SO OH<br />

Bemmedimlplwnia Add CeH4-J gQ^nH ^ produced by heating<br />

<strong>the</strong> monosulphonic acid with fuming sulphuric acid. It forms ,i<br />

crystalline deliquescent mass. Tde barium-salt ia very soluble in<br />

water, but <strong>the</strong> lead-salt less so.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!