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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 87<br />

Dimethyl Cnfbinol. Dimethyl Ketono.<br />

CH8<br />

CH8<br />

CH.OH - H, . CO<br />

CH8<br />

CH8<br />

The ketones contain two alcohol radicals combined with carbonyl;<br />

<strong>the</strong>y may be obtained by different o<strong>the</strong>r reactions besides <strong>the</strong> oxidation<br />

<strong>of</strong> secondary alcohols.<br />

(1) By <strong>the</strong> action <strong>of</strong> <strong>the</strong> zinc compounds <strong>of</strong> <strong>the</strong> alcohol radicals<br />

upon <strong>the</strong> chlorides <strong>of</strong> <strong>the</strong> fatty acids. Thus zinc methide and acetyl<br />

chloride yield dimethyl carbinol, and by acting upon <strong>the</strong> same chloride<br />

with zinc ethide, methyl-ethyl ketoue is produced :—<br />

ZnCl2<br />

(2) Ketones are also formed by <strong>the</strong> destructive distillation <strong>of</strong> <strong>the</strong><br />

calcium- and o<strong>the</strong>r salts <strong>of</strong> fatty acids, or by passing <strong>the</strong> vapours <strong>of</strong><br />

<strong>the</strong>se acids through a red-hot tube:—<br />

CH8<br />

CO.OH |<br />

= CO + CO, + H2O<br />

CO.OH<br />

CH4<br />

The ketones are capable <strong>of</strong> combining with nascent hydrogen like<br />

<strong>the</strong> aldehydes, a secondary alcohol being again formed; but on<br />

fur<strong>the</strong>r oxidation <strong>the</strong>y do not yield like <strong>the</strong> aldehydes an acid<br />

containing <strong>the</strong> same number <strong>of</strong> onrbon atoms, bnt <strong>the</strong> molecule is<br />

broken up into two fragments according to tho following law. The<br />

most simple alcohol radical remains combined with <strong>the</strong> carboxyl and<br />

forms a fatty acid, whilst tho o<strong>the</strong>r alcohol radical is oxidked exactly<br />

in <strong>the</strong> same way as <strong>the</strong> alcohol corresponding to it would be. Tims<br />

dimethyl Jcelone Q5 S [ CO yields acetic acid and formic acid (or carbon<br />

CII 1<br />

dioxide); methyl-ethyl ketone X, | [CO yields only acetic acid, and<br />

iiethjl ketonc ^ 2 S 6 \ CO acetic and propionic acids, and <strong>the</strong> same<br />

CH ><br />

two acids are obtained from mdhyl-propyl ketone ^ j£> S-CO, whilst<br />

CII } .<br />

mthyl-i&opropiil MOM ,nr( s ^rf \ CO is first resolved into acetic<br />

^ • r " (uncoil,)

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