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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 299<br />

The camphors contain oxygen, and most <strong>of</strong> <strong>the</strong>m exhibit <strong>the</strong><br />

character <strong>of</strong> alcohola<br />

Most <strong>of</strong> <strong>the</strong> terpenes, as well as camphors, exist in plants as essential<br />

or volatile oik.<br />

OIL OF TURPENTINE Ol0H10.<br />

All <strong>the</strong> trees belonging to <strong>the</strong> order Coniferse contain resins and<br />

liquid hydrocarbons; a mixture <strong>of</strong> both exudes as an oleo-resinous<br />

juice from <strong>the</strong> barks <strong>of</strong> <strong>the</strong>se trees, and is called turpentine. When<br />

turpentine is distilled; ei<strong>the</strong>r alone or with -water, <strong>the</strong> hydrocarbons<br />

volatilize, and resin is left behind.<br />

Oil <strong>of</strong> turpentine is obtained from different species <strong>of</strong> Pinus and<br />

Abies; it is a limpid, mobile liquid, with <strong>the</strong> specific gravity 0,89,<br />

and boiling at 160°. It is almost insoluble in water, bat readily<br />

dissolves in strong alcohol and glacial acetic acid; with e<strong>the</strong>r and<br />

absolute alcohol it mixes in any proportion, Oil <strong>of</strong> turpentine<br />

dissolves sulphur, phosphorus, resins, and many o<strong>the</strong>r bodies which<br />

are insoluble in water. It readily absorbs oxygen, converting it into<br />

ozone, which gradually oxidizes <strong>the</strong> oil, forming resinous products.<br />

The oils <strong>of</strong> turpentine <strong>of</strong> different origin exhibit considerable<br />

diversities in <strong>the</strong>ir optical properties. The French oil (from Pinus<br />

maritima), as well as <strong>the</strong> oils from Pinus Laricc a.nd Abies pectinata,<br />

tarn <strong>the</strong> plane <strong>of</strong> polarization to <strong>the</strong> left, whilst English turpentineoil<br />

(from Pinus auMralis) turns it to <strong>the</strong> right.<br />

These different varieties are converted into new optical modifications,<br />

by repeated distillation or by <strong>the</strong> action <strong>of</strong> acids. It also appears<br />

that <strong>the</strong> oil contained in <strong>the</strong> plants is different from that which is<br />

obtained by distillation. Thus, on distilling <strong>the</strong> young branches <strong>of</strong><br />

<strong>the</strong> pine with water, an oil is obtained possessing an agreeable<br />

odour, which is ohanged into that <strong>of</strong> <strong>the</strong> common oil by distilling it<br />

over potash.<br />

When oil <strong>of</strong> turpentine is boiled with dilute nitric acid, it is<br />

oxidized to acetic acid, propionte acid, butvrio acid, oxalic acid, terebio<br />

acid, and o<strong>the</strong>r compounds. Terebie acid C7HloO4 crystallizes in<br />

colourless prisms, and is resolved by heat into carbon dioxide and<br />

pyrotmbk acid C8HBO2 (see page 270).<br />

Terpin or ffydmte <strong>of</strong> Turpentine-oil C1OH2OO2 + H?O.-r-Ofl <strong>of</strong><br />

turpentine slowly oombineswith water, forming terpin; this combination<br />

takes place more quickly if an acid he present. To prepare this<br />

compound, eight volumes <strong>of</strong> <strong>the</strong> oil are mixed with two volumes <strong>of</strong><br />

weak nitrio acid and one volume <strong>of</strong> alcohol; <strong>the</strong> mixture ia exposed<br />

to <strong>the</strong> sunlight, and frequently shaken. Terpin crystallizes in large<br />

iliombio prisms, melting at 100° with loss <strong>of</strong> one molecule <strong>of</strong> water;<br />

<strong>the</strong> anhydrous compound sublimes at 150° ia needles, It is sparingly<br />

soluble in cold water, but dissolves freely in alcohol and in boiling<br />

water.

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