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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS, 383<br />

forma colourless crystals. This e<strong>the</strong>r is decomposed by alkalis, <strong>the</strong><br />

alcohol being formed, a heavy liquid, boiling at 225°, and possessing<br />

an aromatic odour.<br />

StyrolyUthyl E<strong>the</strong>r OJ^H'OH *" P 10 '* 1106 ' 1 bv heating <strong>the</strong><br />

bromide with alcoholic potash or ammonia;—<br />

C6H6.C2H4Br + GftOH + NH8 = r H &5*} 0 + NH4Br<br />

It is a mobile, fragrant liquid, boiling at 187°.<br />

Plwnylacetic or Alphatoluic Add C6H&.CHg.C02H.—This acid was<br />

first obtained by boiling vulpinic acid (see below) with baryta-water.<br />

It has been prepared syn<strong>the</strong>tically from its nitrile, and by heating<br />

bromobenzene and ethyl chloracetate with silver-dust:—<br />

CsH, +C,H,ftp + Ag2 -<br />

A + AgCl + AgBr<br />

Phenylacetic acid forms thin, brilliant plates, melting at 76°*5, and<br />

boiling at 261°, Chromic acid oxidizes it to benzoic acid, and when<br />

heated with lime it yields toluene. With chlorine, bromine, fuming<br />

nitric acid, it gives substitution-products, resembling those <strong>of</strong> benzoic<br />

acid.<br />

Pkenylaeetonitrik CjHpCHyCN is a liquid resembling benzoaitrile,<br />

and boiling at 229°, It is obtained by distilling benzyl chloride with<br />

potassium cyanide,<br />

Vidpinie Acid C^H^Oj exists in Cetraria vulpina, Parmlia.<br />

parietina, and o<strong>the</strong>r lichens, and may be extracted from <strong>the</strong>m by<br />

chlor<strong>of</strong>orm. It crystallizes in lemon-yellow thick prisms, melting<br />

at 110°, Boiling baryta-water resolves it into methyl alcohol, oxalic<br />

acid, and phenylacetio acid;—<br />

CIBHMO6 + 4H8O = CH4O + CaH204 + SCgHgO,,<br />

When it is boiled with dilute potash, it yields methyl alcohol,<br />

carbon dioxide, and oxatohiic acid ;-~<br />

Oxatolwie Add forms four-sided prisms, melting at 154°, and is<br />

monobasic like vulpinic acid. Concentrated boiling potash resolves<br />

it into oxalic acid and toluene:—<br />

CMH16OS + II2O = CjHgC^ + 20,118<br />

Methyl'phenyl Ketone, or Acetyl-bemenc C0H«.CO.CH3, is obtained<br />

by distilling a mixtuie <strong>of</strong> calcium benzoate ana acetate.<br />

It ia a limpid liquid, boiling at 198°. By dissolving it in cold<br />

concentrated nitric acid, it ia converted iuto methyl-mowniitrophaiyl<br />

kctone CJH^NOJCO.CHJ, wl.ich crjstnllizea in needlos. An isomeride

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