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

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

THE OASBON COMPOUNDS 91<br />

posed. The dry residue yields, on distillation with water, aqueous<br />

methyl alcohol, which ia dried ove* quicklime and again distilled<br />

from a water bath.<br />

The alcohol thus obtained is not quite pure. To prepare <strong>the</strong> pure<br />

compound, purified wood Bpirit is carefully mixed with its own weight<br />

<strong>of</strong> sulphuric acid, two parts <strong>of</strong> potassium binoxnlate are added, and<br />

<strong>the</strong> mixture distilled As soon as crystals <strong>of</strong> methyl oxalate appear<br />

in <strong>the</strong> neck <strong>of</strong> <strong>the</strong> retort, <strong>the</strong> receiver is changed and <strong>the</strong> distillation<br />

continued as long as this compound conies over. These crystals are<br />

finely powdered, pressed between filter paper, and dried over sulphuric<br />

acid. On distilling <strong>the</strong> pure e<strong>the</strong>r with water it splits up into methyl<br />

alcohol and oxalic acid:—<br />

The dilute methyl alcohol thus obtained is distilled from a water<br />

bath, to remove <strong>the</strong> greater part <strong>of</strong> <strong>the</strong> water, dried over quicklime,<br />

and rectiiied.<br />

The winter-green oil from GaiU<strong>the</strong>ria prommbens, a plant indigenous<br />

to North America, consists chiefly <strong>of</strong> <strong>the</strong> methyl e<strong>the</strong>r <strong>of</strong><br />

salicylic acid. On distilling this oil with caustic potash pure methyl<br />

alcohol is obtained.<br />

Methyl alcohol is a colourless, mobile liquid, possessing a pure<br />

spirituous smell; its specific gravity is 0-8142 at 0°, and it boils at<br />

66°. It burns with a bluish non-huninous flame, and is miscible<br />

with water in all proportions. With caustic baryta and with calcium<br />

chloride it forms crystalline compounds which are decomposed<br />

by water.<br />

Methyl alcohol is used instead <strong>of</strong> spirits <strong>of</strong> wino as a solvent for<br />

resins, essential oils, &c, for heating purposes, and in <strong>the</strong> manufacture<br />

<strong>of</strong> aniline colours.<br />

On oxidation it is converted into formic acid; this acid is also<br />

formed by passing <strong>the</strong> vapour over heated soda-lime:—<br />

CHyOH + NaOH = CHO.ONa + 2^<br />

Potassium and sodium dissolve in methyl alcohol with <strong>the</strong> evolution<br />

<strong>of</strong> hydrogen. On cooling, <strong>the</strong> compounds CH8.OK or CHs.ONa<br />

crystallize out, whicli are decomposed by water, methyl alcohol and<br />

caustic alkali being formed.<br />

Methyl Chloride CHSC1 is obtained by heating a mixture <strong>of</strong> one<br />

part <strong>of</strong> methyl alcohol and three ports <strong>of</strong> sulphuric acid with two<br />

parts <strong>of</strong> common salt :—<br />

CHyOH + NaCl + H(jSO4 « CH8C1 -t- NaHSO4 + H2O<br />

It is a colourless gas, possessing an e<strong>the</strong>real smell. When exposed<br />

to a low temperature it is condensed to a mobile liquid, boiliug at

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

Saved successfully!

Ooh no, something went wrong!