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A Manual of the Chemistry of the Carbon Compounds

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10 THE CHEMISTRY OF<br />

two atoms <strong>of</strong> chlorine for hydrogen ia <strong>the</strong> members <strong>of</strong> <strong>the</strong> methane<br />

series:—<br />

DSSSESSL.<br />

2C18» 08H6Clg + 2HC1<br />

The chlorine or bromine in <strong>the</strong>se compounds can, as is <strong>the</strong> case<br />

with <strong>the</strong> chlorides <strong>of</strong> <strong>the</strong> monad radicals, be displaced by o<strong>the</strong>r elements<br />

or radicals, and thus we obtain alcohols, amines, &c, <strong>of</strong> dyad<br />

radicals:—<br />

E<strong>the</strong>ne Alcohol. E<strong>the</strong>ne-diamine.<br />

H<br />

0H P T /<br />

If two atoms <strong>of</strong> chlorine are replaced by one atom <strong>of</strong> oxygen, <strong>the</strong><br />

oxides <strong>of</strong> <strong>the</strong>se dyad radicals are obtained, and by <strong>the</strong> substitution <strong>of</strong><br />

oxygen for hydrogen in <strong>the</strong> alcohols, acids are formed containing<br />

oxygenated dyad radicals:—<br />

E<strong>the</strong>ne Oxide. Ethane Alcohol. Olycollic Acid. Oxalic Acid.<br />

The hydrocarbons <strong>of</strong> <strong>the</strong> ethine series can ei<strong>the</strong>r combine with<br />

two or with four atoms <strong>of</strong> chlorine, and play <strong>the</strong> part <strong>of</strong> dyad as well<br />

as <strong>of</strong> tetrad radicals.<br />

In o<strong>the</strong>r compounds we have to assume <strong>the</strong> existence <strong>of</strong> triad,<br />

pentad, hexad, &&, radicals. Thus glycerin C.H6(OH)8 is <strong>the</strong> alcohol<br />

<strong>of</strong> <strong>the</strong> radical propenyl CgHj, which contains three atoms <strong>of</strong> hydrogen<br />

less than propane, and is <strong>the</strong>refore a triad radical in which <strong>the</strong> carhon<br />

atoms are linked toge<strong>the</strong>r exactly as <strong>the</strong>y are in propane; whilst in<br />

<strong>the</strong> monad radical allyl, which has <strong>the</strong> same composition as propenyl,<br />

<strong>the</strong> carbon atoms are combined in <strong>the</strong> same manner as in propene<br />

CgHfl. Propenyl and allyl compounds are nearly related to <strong>the</strong> propyl<br />

and propene compounds, and from a member <strong>of</strong> one group, compounds<br />

belonging to ano<strong>the</strong>r group may be easily obtained. Thus, by <strong>the</strong><br />

action <strong>of</strong> chlorine upon propane <strong>the</strong> chloride's <strong>of</strong> propyl, propene, and<br />

propenyl are formed :—<br />

C8H8+ Cl3 = C8H7Cl +HC1<br />

8 8 + 8 8 a 8 f<br />

C8H8 + SClj = C^Cl, + 3HC1<br />

When propyl alcohol is heated with sulphuric acid, propene and<br />

water are prodnced:—<br />

By <strong>the</strong> action <strong>of</strong> iodine and phosphorus on glycerin, allyl iodide is<br />

formed :—<br />

fOH<br />

C3H5] OH + P + I - C8H6I + P0sH,<br />

(OH

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