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A Manual of the Chemistry of the Carbon Compounds

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130 THE CHEMISTRY OF<br />

C»H4O.CNH, which boils at 180°, with partial decomposition. On<br />

aiding oonoentrated hydrochloric acid to this body ammonium<br />

chloride and lactic acid are formed (compare lactic acid).<br />

Phosphorus pentachloride acts violently upon aldehyde; <strong>the</strong><br />

products <strong>of</strong> <strong>the</strong> reaction being phosphorus oxychloride and dicMorethcme<br />

C2H4Clj,<br />

A great number <strong>of</strong> substances, such as hydrochloric acid, sulphuric<br />

acid, carbonyl chloride, &c, even if present only in very minute<br />

quantities, cause <strong>the</strong> condensation <strong>of</strong> <strong>the</strong> aldehyde into paraldehyde<br />

C8HJ9Ofl, a liquid boiliug at 124°, and solidifying at a low temperature<br />

into crystals melting at + 10-5°. On distilling paraldehyde with <strong>the</strong><br />

above substances, it again splits up into three molecules <strong>of</strong> acetaldehyde.<br />

Ano<strong>the</strong>r polymeride called 7netaldehydet <strong>the</strong> molecular weight <strong>of</strong><br />

which is not known, is produced when <strong>the</strong> above-mentioned substances<br />

are brought into contact with aldehyde at a temperature<br />

below 0". It crystallizes in colourless needles or prisms, which when<br />

quickly heated sublime, When metaldehyde is heated in a closed<br />

vessel to 115°, it again changes after a few hours into common<br />

aldehyde.<br />

On heating aldehyde with a solution <strong>of</strong> zinc chloride or some o<strong>the</strong>r<br />

salts, water is eliminated, and crotan, aldehyde C4H0O is formed, a<br />

compound whioh will be described hereafter!<br />

ACKTIC ACID C2H4O2.<br />

Dilute acetic acid, or vinegar, has been known from very early<br />

times, The different modes <strong>of</strong> <strong>the</strong> formation <strong>of</strong> this acid have<br />

already been fully described. On <strong>the</strong> large scale acetic acid is<br />

produced by <strong>the</strong> oxjdation <strong>of</strong> alcohol, or by <strong>the</strong> destructive distillation<br />

<strong>of</strong> wood. Pure alcohol, even when very dilute, is not<br />

oxidized in contact with air, but in <strong>the</strong> presence <strong>of</strong> platinum black<br />

and air it is converted into aldehyde and acetic acid. The same<br />

change occurs when dilute alcohol ooutains certain nitrogenous<br />

organic bodies. For this reason wine, beer, &o., in which such bodies<br />

are contained, turn sour on exposure to <strong>the</strong> air.<br />

In <strong>the</strong> manufacture <strong>of</strong> vinegar a mixture <strong>of</strong> wine, beer, or diluted<br />

spirits, with some vinegar and yeast, is kept in loosely covered vafca,<br />

at a temperature <strong>of</strong> about 24—27°, for about fourteen days, after<br />

which time <strong>the</strong> liquid is changed into vinegar. On increasing <strong>the</strong><br />

surface <strong>of</strong> <strong>the</strong> liquid, <strong>the</strong> oxidation goes on much quicker. To effect<br />

this <strong>the</strong> liquid is made to run slowly over shavings <strong>of</strong> beechwood<br />

saturated with vinegar, contained in large vats, through which a<br />

current <strong>of</strong> air is made to pass.<br />

Acetic acid is found in nature in <strong>the</strong> form <strong>of</strong> acetic e<strong>the</strong>rs in several<br />

plants; it has also been found in small quantities in animal juices.

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