Informacion para experimento de arrastre de vapor

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a) Propiedades físicas, químicas y tóxicas del eugenol, acetileugenol, éter etílico, cloroformo, sulfato de sodio, cloruro de benzoilo, cloruro férrico y benzoato de eugenol. Usos del eugenol.

Benzoyl Chloride

Monograph Number: 1113

Title: Benzoyl Chloride

CAS Registry Number: 98-88-4

Additional Names: Benzenecarbonyl chloride

MolecularFormula: C7H5ClO

Molecular Weight: 140.57.

Percent Composition: C 59.81%, H 3.59%, Cl 25.22%, O 11.38%

Literature References: Prepd by partial hydrolysis of benzotrichloride: Davies, Dick, J. Chem. Soc. 1932, 2808; by chlorination of benzaldehyde: Wöhler, Ann. 3, 262 (1832); from benzoic acid and PCl5 or from benzoic acid and phosgene: Uwarow, Stepanow, SU 56693 (1936). Labprepn from benzoic acid and thionyl chloride: A. I. Vogel, Practical Organic Chemistry (Longmans, London, 3rd ed., 1959) p 792; Gattermann-Wieland, Praxis des organischen Chemikers, (de Gruyter, Berlin, 40th ed., 1961) p 112.

Properties: Liquid. Penetrating odor. d425 1.2070. mp -1.0°. bp760 197.2°; bp35 100°; bp15 82.3°; bp9 71°; bp3 49°. nD20 1.55369. Dipole moment 3.28. Flash pt 88°C(190.4°F). Parachor 289.8. Dec by water and alc. Miscible with ether, benzene, carbon disulfide, oils.

Melting point: mp -1.0°

Boiling point: bp760 197.2°; bp35 100°; bp15 82.3°; bp9 71°; bp3 49°

Flash point: Flash pt 88°C (190.4°F)
Index of refraction: nD20 1.55369

Density: d425 1.2070

CAUTION: Lacrimator. Irritating to skin, eyes, mucous membranes.
Use: For acylation,i.e., introduction of the benzoyl group into alcohols, phenols, and amines (Schotten-Baumann reaction); in the manuf of benzoyl peroxide and of dye intermediates. In organic analysis for making benzoyl derivatives for identification purposes.

Ethyl ether

Monograph Number: 3840

Title: Ethyl Ether

CAS Registry Number: 60-29-7

CAS Name: 1,1¢-Oxybisethane

Additional Names:ethoxyethane; ether; diethyl ether; ethyl oxide; diethyl oxide; sulfuric ether; anesthetic ether

Molecular Formula: C4H10O

Molecular Weight: 74.12.

Percent Composition: C 64.82%, H 13.60%, O 21.59%

Line Formula: C2H5OC2H5

Literature References: Produced on a large scale by dehydration of ethanol or by hydration of ethylene, both processes being carried out in thepresence of sulfuric acid. Review of mfg processes: Himmler in Ullmann's Encyklopädie der Technischen Chemie, vol. 5 (1954) pp 777-782; D. E. Keeley in Kirk-Othmer Encyclopedia of Chemical Technology vol. 9 (Wiley-Interscience, New York, 3rd ed., 1980) pp 381-393.
Properties: Mobile, very volatile, highly flammable liq. Explosive! Vapor heavier than air. Characteristic, sweetish, pungent odor,more agreeable than chloroform. Burning taste. Tends to form explosive peroxides under the influence of air and light, esp when evaporation to dryness is attempted. Peroxides may be removed from ether by shaking with 5% aq ferrous sulfate soln. Addition of naphthols, polyphenols, aromatic amines, and aminophenols has been proposed for the stabilization of ethyl ether. d40 0.7364; d410 0.7249;d420 0.7134; d430 0.7019. Vapor density 2.55 (air = 1.0). mp -116.3° (stable crystals); mp -123.3° (metastable crystals). bp760 34.6°; bp400 17.9°; bp200 +2.2°; bp100 -11.5°; bp10 -48.1°; bp1.0 -74.3°. Satd vapor press. at 0°: 184.9 mm; at 10°: 290.8 mm; at 20°: 439.8 mm; at 50°: 1276 mm; at 70°: 2304 mm. Critical temp 192.7°; crit press. 35.6 atm. Flash pt, closed cup: -49°F (-45°C).Air-ether mixtures containing more than 1.85 volume-% of ether vapor, are explosive hazards.

Autoignition temp 180-190°. nD15 1.35555. Dielectric constant at 26.9° and 85.8 kilocycles = 4.197; good insulator. When shaken under absolutely dry conditions ether can generate enough static electricity to start a fire. Surface tension at 20°: 17.06 dynes/cm. Viscosity at 20°: 0.2448 cp. Heat...
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