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Encyclopedia Britannica - Main :: STE-SUS |
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STYROLENE, C6H5 .CH:CH2, also known as phenylethylene or vinylbenzene, an aromatic hydrocarbon found to the extent of I to 4% in storax; it also occurs with crude xylene in coal tar fractions. It may be obtained from storax by distillation with water, and synthetically by heating cinnamic acid with lime, by the action of aluminium chloride on a mixture of vinyl bromide and benzene, by removing the elements of hydrobromic acid from bromethylbenzene by means of alcoholic potash, or, best, by treating f9-bromhydrocinnamic acid with soda, when it yields styrolene, carbon dioxide and hydrobromic acid. It also results on condensing acetylene, and on reducing phenylacetylene by zinc dust and acetic acid. It is a clear, strongly refractive liquid, which has a pleasant odour; it boils at 144 and has a specific gravity of 0.925 at ()a. Styrolene is oxidized by nitric or chromic acids to benzoic acid; reduction gives ethylbenzene; hydrochloric and hydrobromic acids yield a-haloid ethylbenzenes, e.g. C6H5CHC1'CH3; whilst chlorine and bromine give a$-dihaloid ethylbenzenes,, e.g. C6H5CHC1-CH2CI. Tauern with the Hochgolling (9390 ft.), the Wolzer Alps with the Predigtstuhl (8349 ft.), the Rottenmanner Tauern with the Grosser Bosenstein (8032 ft.), and the Seckauer Alps or Zinken group, which culminates in the Zinkenkogel (7865 ft.). The principal ramifications of the primitive Alps of Carinthia and Styria are: the Stang Alps with the Konigsstuhl (7646 ft.) and Eisenhut (8007 ft.), the Judenburger or Seethaler Alps with the Zirbitzkogel (7862 ft.), and the Koralpen which culminates in the Grosser Speikkogel (7023 ft.). The Styrian Nieder Alps cover the country north and east
great
east
mineral
In spite of the irregular nature of the surface, but little of the soil can be called unproductive. Of its total area 4749% is covered with fine forests. About 19% is arable land, 12% pastures, 5.6o% meadows, while 1o6% is occupied by gardens and 1.4% by vineyards which produce wine of a good quality. Cattle-rearing has taken a great
mineral
special
Styrolene gives origin to three series of derivatives, two of which contain the substituents in the side chain, e.g. C6H6CCI:CH1 or a-compounds, and C6H6CH:CHCI, or w-compounds, whilst in the third the benzene nucleus is substituted. The a-halogen compounds are obtained by heating styrolene chloride (or bromide) with lime or alcoholic potash; they are liquids which have a penetrating odour, and yield acetophenone when heated with water to 180. The w-chlor compound results when 14-phenyl-a-chlorlactic acid (from hypochiorous acid and cinnamic acid) is heated with water; it has a hyacinthine odour and yields phenylacetaldehyde when heated with water. Nitrostyrolene results when styrolene is treated with fuming nitric acid.Related to styrolene is phenylacetylene, C6H5.CCH, which results when a-bromstyrolene or acetophenone chloride are heated to 130 with alcoholic potash, or phenylpropiolic acid with water to 120. It is a liquid, boiling at 139 and having a pleasant odour. It resembles acetylene in yielding metallic derivatives with ammoniacal copper and silver solutions. On solution in sulphuric acid, followed by dilution with water, it yields acetophenone. Stilbene or toluylene, C6H6'CH : CHCsH5, is symmetrical diphenylethylene. It may be obtained by distilling benzyl sulphide or disulphide, by the action of sodium on benzaldehyde or benzal chloride, by distilling fumaric and cinnamic phenyl esters: C6H5O.00CH:CHCO.006H63CO2+C6H6CH:CHCO-OC6H5 2CO2 +C6H6CH : CHC6H6 (Ber.,18, p.1945), and fromchlorasymmetrical diphenylethane derivatives which undergo a rearrangement when heated (Ber., 7. p. 1409). Stilbene (from Gr. vrt su^, to glisten) crystallizes in large, colourless, glistening monoclinic plates, which melt at 124 and boil at 306. On passing the vapour through red-hot tubes it yields anthracene and toluene. Reduction with hydriodic acid gives dibenzyl, and heating with sulphur
isomerism
cotton
diphenyl
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