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A Manual of the Chemistry of the Carbon Compounds

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THE CABBON COMPOUNDS, 303<br />

taining Isopropene CBHg, boiling at 37°, and camUchaw C10Hl6, boiling<br />

at 171°.<br />

Gutta-percha, is <strong>the</strong> hardened milky juice <strong>of</strong> Isonandm Outlet, a<br />

tree growing in different parts <strong>of</strong> India. It is harder and less elastic<br />

than caoutchouc, but in warm water it becomes quite s<strong>of</strong>t, and can<br />

<strong>the</strong>n be formed into any shape. It has <strong>the</strong> same composition as<br />

caoutchouc, and dissolves in <strong>the</strong> same solvents as <strong>the</strong> latter. By<br />

destructive distillation, it yields isopropene, caoutchene, and a heavy<br />

oil called heveene, which appears to be polymeric with <strong>the</strong>se o<strong>the</strong>r<br />

hydrocarbons.<br />

CAMPHOBS,<br />

Common Camphor, or Japan Camphor C,0H WO, is obtained in China,<br />

and Japan by distilling <strong>the</strong> branches and leaves <strong>of</strong> Lawns Camphora<br />

with, water. It is a colourless, crystalline, translucent mass, having<br />

a powerful, peculiar odour and taste. By sublimation it may be<br />

obtained in brilliant crystal* It melts at 175°, and boils at 204°,<br />

Camphor is only sparingly soluble in water, but freely soluble in<br />

alcohol and acetic acid. Small pieces thrown on water move about<br />

with a revolving motion.<br />

When camphor is heated with concentrated hydriodio acid, several<br />

hydrocarbons are formed, as campkokne CBH,g, a liquid boiling at<br />

135°, and <strong>the</strong> compounds C10H18, boiling at 165 , and C10HM. By <strong>the</strong><br />

action <strong>of</strong> phosphorus pentasnlphide on camphor, cymme CwHlt<br />

(page 300) is formed ;—<br />

5C10H16O + P2S6 = 5C10Hu + P2O5 + 5SH8<br />

On heating a solution <strong>of</strong> camphor in toluene with sodium, two<br />

compounds, called sodium-camphor CwH15NaO and sodium camphylate<br />

CHNaO, are produced :—<br />

2O10HwO + Naa« C10H16NaO + CloHirNaO<br />

By <strong>the</strong> action <strong>of</strong> methyl iodide on this mixture, <strong>the</strong> sodium is<br />

CH 1<br />

replaced by methyl, and methyl-camphor „ TT 8 t 0, and camphylmethyl<br />

e<strong>the</strong>r ^ ^ 8 V 0 are produced. Ethyl iodide acts in an<br />

analogous way; ethyl-camphor is a liquid boiling at 230°.<br />

When <strong>the</strong> mixture <strong>of</strong> <strong>the</strong> two sodium-compounds is heated in a<br />

current <strong>of</strong> dry carbon dioxide to 100°, <strong>the</strong> sodium salts <strong>of</strong> campko-<br />

carbonic bi add id C^OCOH C^^O.COgH and d <strong>of</strong> f lborneol-carbonic l b i dd add CHOCO CI0HwO.CO2<br />

are formed. On dissolving <strong>the</strong>se salts in water, lactic acid is decomposed,<br />

and borneol or camphyl alcohol G^^Jb separates out:—<br />

1<br />

CO, + H,0 - CWHWO + jj } CO,

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