Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Acids ethanoic

White crystals, m.p. 114" C. Manufactured by reacting aniline with excess ethanoic acid or ethanoic anhydride. Chief use is in the manufacture of dye intermediates such as p-nitro-acetanilide, p-nitroaniline and p-phenylene-diamine, in the manufacture of rubber, and as a peroxide stabilizer. [Pg.10]

Be40(02CCH3)e. The acetate is typical of the basic beryllium carboxylates (Be(OH)2 plus ethanoic acid). The structures have O at the centre of a tetrahedron of Be with carb-oxylate spanning each edge of the tetrahedron. Be(02CCH3)2 is formed from BeCl2 and glacial ethanoic acid. [Pg.58]

CH2Br COOH. White crystalline solid, m.p. 50"C, b.p. 208 C. Soluble in water and alcohol. Prepared by the action of dry bromine on dry ethanoic acid in presence of small amounts of red phosphorus. Produces sores upon the skin used in chemical syntheses. See Reformatski reaction. [Pg.68]

Trichloroethanoic acid, CCI3COOH. A crystalline solid which rapidly absorbs water vapour m.p. 58°C, b.p. 196-5" C. Manufactured by the action of chlorine on ethanoic acid at 160°C in the presence of red phosphorus, sulphur or iodine. It is decomposed into chloroform and carbon dioxide by boiling water. It is a much stronger acid than either the mono- or the dichloro-acids and has been used to extract alkaloids and ascorbic acid from plant and animal tissues. It is a precipitant for proteins and may be used to test for the presence of albumin in urine. The sodium salt is used as a selective weedkiller. [Pg.94]

Basic copper ethanoate arsenates(iii) prepared from verdigris (or other basic copper salt), sodium arsenate(m) and ethanoic acid. Used in insecticides for spraying fruit trees. Readily decomposed to soluble arsenic compounds so use is very restricted. [Pg.156]

Manufactured by the liquid-phase oxidation of ethanal at 60 C by oxygen or air under pressure in the presence of manganese(ii) ethanoate, the latter preventing the formation of perelhanoic acid. Another important route is the liquid-phase oxidation of butane by air at 50 atm. and 150-250 C in the presence of a metal ethanoate. Some ethanoic acid is produced by the catalytic oxidation of ethanol. Fermentation processes are used only for the production of vinegar. [Pg.164]

Ethyne is the starting point for the manufacture of a wide range of chemicals, amongst which the most important are acrylonitrile, vinyl chloride, vinyl acetate, ethanal, ethanoic acid, tri- and perchloro-ethylene, neoprene and polyvinyl alcohol. Processes such as vinylation, ethinylation, carbonylation, oligomerization and Reppe processes offer the possibility of producing various organic chemicals cheaply. Used in oxy-acetylene welding. [Pg.169]

C5H10O2, CHjCOOPr. Colourless liquid with a fragrant odour b.p. 88 C. Manufactured by leading propene into hot ethanoic acid containing sulphuric acid, or by heating isopropyl alcohol with ethanoic and sulphuric acids. Used as a solvent for cellulose nitrate and various gums. [Pg.227]

Kolbe reaction The pre >aration of saturated or unsaturated hydrocarbons by the electrolysis of solutions of the alkali salts of aliphatic carboxylic acids. Thus, ethanoic acid gives ethane,... [Pg.232]

Lead(fl) ethanoate, Pb(02CCH3)2,3H20, sugar of lead. Soluble in water (ethanoic acid and ethanoic anhydride plus Pb304). [Pg.237]

Used in ethanoic acid solution as a precipitating agent for nitrates. CI04 , PF , Re04 , W04 " also form precipitates. [Pg.279]


See other pages where Acids ethanoic is mentioned: [Pg.10]    [Pg.10]    [Pg.11]    [Pg.11]    [Pg.14]    [Pg.25]    [Pg.36]    [Pg.37]    [Pg.53]    [Pg.55]    [Pg.69]    [Pg.76]    [Pg.87]    [Pg.94]    [Pg.107]    [Pg.111]    [Pg.129]    [Pg.131]    [Pg.163]    [Pg.164]    [Pg.164]    [Pg.164]    [Pg.165]    [Pg.165]    [Pg.168]    [Pg.168]    [Pg.168]    [Pg.169]    [Pg.173]    [Pg.173]    [Pg.192]    [Pg.193]    [Pg.202]    [Pg.211]    [Pg.216]    [Pg.231]    [Pg.237]    [Pg.248]    [Pg.248]    [Pg.262]   
See also in sourсe #XX -- [ Pg.53 , Pg.54 ]

See also in sourсe #XX -- [ Pg.102 ]

See also in sourсe #XX -- [ Pg.114 , Pg.156 , Pg.158 , Pg.162 , Pg.164 , Pg.174 , Pg.233 , Pg.234 , Pg.241 , Pg.254 , Pg.267 , Pg.271 , Pg.351 , Pg.358 ]

See also in sourсe #XX -- [ Pg.53 , Pg.54 ]

See also in sourсe #XX -- [ Pg.30 , Pg.36 ]

See also in sourсe #XX -- [ Pg.15 , Pg.728 ]

See also in sourсe #XX -- [ Pg.189 ]

See also in sourсe #XX -- [ Pg.290 ]

See also in sourсe #XX -- [ Pg.120 , Pg.235 , Pg.237 , Pg.260 ]

See also in sourсe #XX -- [ Pg.104 ]

See also in sourсe #XX -- [ Pg.65 ]

See also in sourсe #XX -- [ Pg.217 ]

See also in sourсe #XX -- [ Pg.77 , Pg.941 , Pg.982 ]

See also in sourсe #XX -- [ Pg.544 ]

See also in sourсe #XX -- [ Pg.131 , Pg.135 ]

See also in sourсe #XX -- [ Pg.6 ]

See also in sourсe #XX -- [ Pg.339 , Pg.409 , Pg.444 ]

See also in sourсe #XX -- [ Pg.105 , Pg.105 ]

See also in sourсe #XX -- [ Pg.488 ]

See also in sourсe #XX -- [ Pg.113 , Pg.128 , Pg.129 ]

See also in sourсe #XX -- [ Pg.80 ]

See also in sourсe #XX -- [ Pg.189 ]

See also in sourсe #XX -- [ Pg.238 , Pg.259 , Pg.316 , Pg.379 ]

See also in sourсe #XX -- [ Pg.238 , Pg.259 , Pg.316 , Pg.379 ]

See also in sourсe #XX -- [ Pg.3 , Pg.190 ]

See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.338 ]

See also in sourсe #XX -- [ Pg.26 ]

See also in sourсe #XX -- [ Pg.284 ]

See also in sourсe #XX -- [ Pg.326 ]

See also in sourсe #XX -- [ Pg.98 , Pg.815 , Pg.818 , Pg.819 , Pg.821 , Pg.822 , Pg.824 , Pg.825 ]

See also in sourсe #XX -- [ Pg.145 , Pg.772 ]

See also in sourсe #XX -- [ Pg.18 , Pg.96 , Pg.98 , Pg.100 , Pg.113 ]

See also in sourсe #XX -- [ Pg.243 ]

See also in sourсe #XX -- [ Pg.555 ]

See also in sourсe #XX -- [ Pg.1122 ]

See also in sourсe #XX -- [ Pg.672 , Pg.681 ]

See also in sourсe #XX -- [ Pg.210 , Pg.218 , Pg.230 , Pg.239 , Pg.246 , Pg.256 , Pg.265 , Pg.419 , Pg.657 , Pg.679 , Pg.726 , Pg.872 , Pg.892 , Pg.993 ]

See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.670 , Pg.671 ]

See also in sourсe #XX -- [ Pg.1026 ]

See also in sourсe #XX -- [ Pg.9 ]

See also in sourсe #XX -- [ Pg.142 , Pg.780 ]

See also in sourсe #XX -- [ Pg.722 ]

See also in sourсe #XX -- [ Pg.476 , Pg.615 , Pg.618 , Pg.625 ]

See also in sourсe #XX -- [ Pg.54 , Pg.57 , Pg.58 ]

See also in sourсe #XX -- [ Pg.104 ]

See also in sourсe #XX -- [ Pg.81 ]

See also in sourсe #XX -- [ Pg.229 ]

See also in sourсe #XX -- [ Pg.174 , Pg.419 , Pg.473 , Pg.477 , Pg.480 , Pg.497 ]

See also in sourсe #XX -- [ Pg.98 ]




SEARCH



2- ethano

Ethanal Ethanoic Acid

Ethanoates

Ethanoic acid Ethanol, ion

Ethanoic acid Ethyl ester

Ethanoic acid enolization with

Ethanoic acid esterification

Ethanoic acid solution, properties

Ethanoic acid, molecular structure

Ethanol with ethanoic acid

Reactions of ethanoic acid

© 2019 chempedia.info