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A Manual of the Chemistry of the Carbon Compounds

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210 THE OBEM18TRY OF<br />

+ 3HJJO is prepared by dissolving iron filings hi sour whey. It<br />

forms nearly colourless crystalline crusts; it is but sparingly soluble<br />

in water, and is used in medicine.<br />

When a mixture <strong>of</strong> lactic acid and phosphorus di-iodide FtJt is introduced<br />

in water, a iodopropionic add is formed, an oily liquid<br />

insoluble in water, which, when heated with strong hydriodic acid<br />

to 160°, is converted into propionic acid. This transformation <strong>of</strong><br />

laotio acid into propionic acid is explained by <strong>the</strong> following equations<br />

:—<br />

CH8<br />

CH3<br />

(1) CH.OH + HI = CHI +H4O<br />

CO.OH CO.OH<br />

CHa<br />

CHS<br />

(2) CHI +HI = CHj + T2<br />

CO.OH CO.OH<br />

Lacbyl OMoride C8H,OC1,.—This compound is obtained by distilling<br />

two molecules <strong>of</strong> phospnorus pentaohloride with one molecule <strong>of</strong><br />

calcium lactate. It is a fuming liquid, which has not been obtained<br />

quite free from phosphorus oxychloride. It is decomposed by cold<br />

water with <strong>the</strong> formation <strong>of</strong> hydrochloric acid and a elUoropropionic<br />

add, a colourless liquid, boiling at 186°.<br />

CHa<br />

CH3<br />

HC1 + HaO = CHC1 + HC1<br />

IOC1 CO.OH<br />

ETHERS OP UCTIC ACID.<br />

Ethyl Lactate, a colourless neutral liquid boiling at 156°, is produced<br />

by heating lactic acid with absolute alcohol It is soluble in water;<br />

its aqueous solution soon turns acid, being decomposed into alcohol<br />

and lactic acid. Sodium dissolves in ethyl lactate with <strong>the</strong> evolution<br />

<strong>of</strong> hydrogen. On heating <strong>the</strong> sodium compound thus formed with<br />

ethyl iodide, diethyl lactate is formed, a liquid possessing an agreeable<br />

odour, and boiling, like <strong>the</strong> monolactate, at 156°. By <strong>the</strong> action<br />

<strong>of</strong> hot potash-solution it yields potassium etliyllactate; <strong>the</strong> free<br />

ethyllaetic acid is as yet very little known. The constitution <strong>of</strong><br />

<strong>the</strong>se e<strong>the</strong>rs is shown by <strong>the</strong> following formula?:—

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