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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 13<br />

The monad group Uranyl UO exists in a number <strong>of</strong> uranium<br />

compounds:—<br />

Uranyl Chloride UO Cl<br />

Uranyl Nitrate UO NO8<br />

Uranyl Sulphate , uo{ SO *<br />

Uranyl Sulphide UO { S<br />

Such compound radicals are nothing but groups <strong>of</strong> atoms which<br />

remain unchanged in a great number <strong>of</strong> reactions, and so far act like<br />

a single atom ; it is <strong>the</strong>refore quite a matter <strong>of</strong> indifference whe<strong>the</strong>r<br />

compound radicals can exist m <strong>the</strong> free state or not Thus <strong>the</strong><br />

monad and triad alcohol radicals cannot be isolated, but dyad and<br />

tetrad radicals exist in <strong>the</strong> free state, as for example <strong>the</strong> hydrocarbons<br />

<strong>of</strong> <strong>the</strong> e<strong>the</strong>ne and ethine series.<br />

Whilst in a great number <strong>of</strong> metamorphoses <strong>the</strong> compound radicals<br />

remain unaltered, <strong>the</strong>y undergo by o<strong>the</strong>r reactions manifold changes.<br />

In some <strong>of</strong> <strong>the</strong>se <strong>the</strong> carbon group is left intact: thus ethyl alcohol<br />

yields by oxidation acetic aoid, <strong>the</strong> radical ethyl C2H6 being con*<br />

verted into acefcyl C2H8O :~<br />

O + O8 = °» H 8g J-0 + H.O<br />

When we act with chlorine upon propyl chloride, <strong>the</strong> monad radical<br />

propyl is changed into dyad propene:—<br />

HC1<br />

The dyad radical e<strong>the</strong>ne combines with hydroiodio acid, <strong>the</strong> iodide<br />

<strong>of</strong> monad ethyl being formed :—<br />

But in many o<strong>the</strong>r chemical changes <strong>the</strong> group <strong>of</strong> carbon atoms<br />

is broken up into two or more fragments: thm by heating acetic<br />

aoid with an excess <strong>of</strong> caustio soda, it splits up into carbon dioxide<br />

and methane s—<<br />

C 4 4<br />

By <strong>the</strong> action <strong>of</strong> <strong>the</strong> galvanic cvinent, succinio acid is decomposed<br />

into e<strong>the</strong>ne, carbon dioxide, and hydrogen:—<br />

CaH< + 2CO4 + Ha<br />

Such a breaking up <strong>of</strong> groups <strong>of</strong> carbon atoms takes place most<br />

easily in those derivatives <strong>of</strong> hydrocarbons in which hydrogen has<br />

been displaced by oxygen.<br />

On <strong>the</strong> o<strong>the</strong>r hand, by joining two carbon atoms toge<strong>the</strong>r, we are<br />

able to bxiild up more complicated compounds from simple ones.<br />

By heating methyl iodide with ziuc, <strong>the</strong> iodine combines with <strong>the</strong>

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