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A Manual of the Chemistry of the Carbon Compounds

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U THE CHEMISTRY OF<br />

exist in two modifications, one turning <strong>the</strong> polarized ray to <strong>the</strong> right,<br />

and <strong>the</strong> o<strong>the</strong>r to <strong>the</strong> left. In such a case <strong>the</strong> heraihedral faces are<br />

differently arranged, and when <strong>the</strong> two kinds <strong>of</strong> crystals are placed iu<br />

<strong>the</strong> same position it will be found that <strong>the</strong> hemihedral faces appear<br />

in one crystal on <strong>the</strong> right, and iu <strong>the</strong> o<strong>the</strong>r on <strong>the</strong> left side, or one <strong>of</strong><br />

<strong>the</strong> crystals looks like <strong>the</strong> image <strong>of</strong> <strong>the</strong> o<strong>the</strong>r in a mirror. These<br />

bodies are not only optically active in <strong>the</strong> solid state, but also in<br />

solution; and <strong>the</strong>re exist also many liquids having this property, as<br />

for instance, amyl alcohol, oil <strong>of</strong> turpentine, &c.<br />

This optical property has been made use <strong>of</strong> in <strong>the</strong> arts; it is used<br />

to determine <strong>the</strong> quantity <strong>of</strong> sugar contained in syrups. Under <strong>the</strong><br />

head <strong>of</strong> caDe-sugar it will be explained how, by simply measuring <strong>the</strong><br />

angle <strong>of</strong> deviation, <strong>the</strong> quantity <strong>of</strong> sugar contained in. a liquid can he<br />

ascertained.<br />

Colour <strong>of</strong> th <strong>Carbon</strong> <strong>Compounds</strong>.—Most carbon compounds are<br />

colourless, when in <strong>the</strong> pure state; but <strong>the</strong>re exist also a great number<br />

having characteristic colours, and many <strong>of</strong> <strong>the</strong>se are used as dye stuffs<br />

or for <strong>the</strong> preparation <strong>of</strong> pigments, such as indigo, <strong>the</strong> colours <strong>of</strong><br />

madder-root, cochineal, aniline colours, &c. It appears that <strong>the</strong> colour<br />

<strong>of</strong> <strong>the</strong>se bodies depends on <strong>the</strong>ir chemical constitution; <strong>the</strong>y contain<br />

certain elements, as oxygen and nitrogen, combined in a peculiar<br />

manner, as we shall see when we come to <strong>the</strong> study <strong>of</strong> <strong>the</strong>se bodies.<br />

Odour end Tmte.—~The odours <strong>of</strong> volatile carbon compounds vary<br />

very much, as <strong>the</strong> following examples show: spirits <strong>of</strong> wine, e<strong>the</strong>r, acetic<br />

e<strong>the</strong>r, acetic acid, chlor<strong>of</strong>orm, camphor, oil <strong>of</strong> cloves, &c. <strong>Compounds</strong><br />

having a similar constitution <strong>of</strong>ten possess a similar smell. Thus <strong>the</strong><br />

marsh-gas hydrocarbons all possess a.faint smell <strong>of</strong> flowers, which is<br />

more or less perceptible according to <strong>the</strong> volatility <strong>of</strong> <strong>the</strong> body. The<br />

compound e<strong>the</strong>rs <strong>of</strong> <strong>the</strong> fatty acids smell like various kinds <strong>of</strong> fruit,<br />

and are on that account used by confectioners and perfumers. Most<br />

sulphur compounds, in which this element is not combined with oxygen,<br />

are characterized by <strong>the</strong>ir disagreeable odour, and many chlorides<br />

have a smell similnr to that <strong>of</strong> chlor<strong>of</strong>orm.<br />

Delations between odour and chemical constitution certainly exist j<br />

but only a few such are known. Thus <strong>the</strong> amines or compound<br />

ammonias have an odour resembling that <strong>of</strong> ammonia, and many<br />

aldehydes, compounds which readily absorb oxygen from, <strong>the</strong> air,<br />

possess a peculiar suffbeatiug smell.<br />

The taste <strong>of</strong> carbon compounds is equally as varying as <strong>the</strong>ir<br />

odour; we find here also that analogous constitution produces a<br />

similar taste. The alkaloids, as quinine, strychnine, &c, have an<br />

intensely bitter taste, whilst <strong>the</strong> taste <strong>of</strong> <strong>the</strong> alcohols <strong>of</strong> polygenic<br />

radicals, as glycerin, mannite, and sugar, is pleasantly sweet,<br />

Solubility.—A. great number <strong>of</strong> carbon compouuds are soluble in<br />

water, o<strong>the</strong>rs only in alcohol, e<strong>the</strong>r, acetic acid, benzene, &c. These<br />

different solvents arc made use <strong>of</strong> in separating OT purifying <strong>the</strong>m.<br />

In homologous series <strong>the</strong> first members are generally more soluble in<br />

water than <strong>the</strong> higher ones. Thus in <strong>the</strong> seiies <strong>of</strong> <strong>the</strong> alcohols and

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