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Ferric acetates hydrates

Carboxy-3,5-dichlorophenyl diazo-nium chloride, 31, 97 Catalyst, ammonium acetate, 31, 25, 27 copper chromite, 31, 32 ferric nitrate, hydrated, 31, 53 piperidine, 31, 35 piperidine acetate, 31, 57 Catechol, 33, 74... [Pg.53]

Catalyst, alumina, 34, 79, 35, 73 ammonium acetate, 31, 25, 27 boron tnfluonde etherate, 38, 26 copper chromite, 31, 32, 36, 12 cupric acetate monohydrate, 38, 14 cuprous oxide silver oxide, 36, 36, 37 ferric nitrate, hydrated, 31, 53 phosphoric acid, 38, 25 piperidine, 31, 35 piperidine acetate, 31, 57 Raney nickel, 36, 21, 38, 22 sulfuric acid, 34, 26 Catechol, 33, 74 Cetylmalonic acid, 34, 16 Cetylmalonic ester, 34,13 Chlorination, by sulfuryl chloride, 33, 45, 37, 8... [Pg.97]

Ferric Acetates.—The normal salt, (Fea)(CsHsOii) , is obtained by adding slight excess of ferric sulfate to lead acetate, and decanting after twenty-four hours. It is dark red, nncrystallizable, very soluble in alcohol, and in HjO. If its solution be heated it darkens suddenly, gives off acetic acid, and contains a basic acetate. When boiled, it loses all its acetic acid, and deposits ferric hydrate. When heated in closed vessels to 100° (212° F.), and treated with a trace of mineral acid, it deposits the modified ferric hydrate. [Pg.156]

Besides acetophenone, this reaction was also applied to p-chloro- andp-methoxyacetophenone, and even to an aliphatic ketone, acetone (although the yield was stated to be only half as large as that obtained from mesityl oxide, i.e., less than 30%, Dorofeenko and co-workers reported a 45% yield of 2,4,6-trimethylpyrylium perchlorate from acetone, acetic anhydride, and perchloric acid), and is the standard method for preparing pyrylium salts with identical substituents in positions 2 and 4. The acylating agent may be an anhydride in the presence of anhydrous or hydrated ferric chloride, or of boron fluoride, or the acid chloride with ferric chloride.Schneider and co-workers ... [Pg.309]

A suspension of sodium amide2 (0.1 mole) in liquid ammonia is prepared in a 500-ml. three-necked, round-bottomed flask fitted with a West condenser, a ball and socket glass mechanical stirrer (Note 1), and a dropping funnel. In the preparation of this reagent a small piece of clean sodium metal is added to 350 ml. of commercial anhydrous liquid ammonia. After the appearance of a blue color, a few crystals of hydrated ferric nitrate are added, whereupon the blue color is discharged. The remainder of the 2.3 g. (0.1 mole) of sodium (Note 2) is then rapidly added as small pieces. After all the sodium has been converted to sodium amide (Note 3), a solution of 16.4 g. (0.1 mole) of ethyl phenyl-acetate (Note 4) in 35 ml. of anhydrous ethyl ether is added dropwise over a 2-minute period, and the mixture is stirred for 20 minutes. To the dark green suspension is added over an 8-minute period a solution of 18.5 g. (0.1 mole) of (2-bromo-... [Pg.72]

Ferric Phosphate occurs as a yellow-white to buff colored powder. It contains from one to four molecules of water of hydration. It is insoluble in water and in glacial acetic acid, but is soluble in mineral acids. [Pg.169]


See other pages where Ferric acetates hydrates is mentioned: [Pg.99]    [Pg.87]    [Pg.57]    [Pg.219]    [Pg.342]    [Pg.66]    [Pg.345]    [Pg.252]    [Pg.264]    [Pg.195]    [Pg.34]    [Pg.802]    [Pg.195]    [Pg.393]    [Pg.342]    [Pg.22]    [Pg.419]    [Pg.59]    [Pg.119]    [Pg.760]    [Pg.21]    [Pg.279]    [Pg.55]    [Pg.122]    [Pg.206]    [Pg.393]    [Pg.243]    [Pg.22]   
See also in sourсe #XX -- [ Pg.153 ]




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Catalyst, ammonium acetate ferric nitrate, hydrated

Ferric acetate

Ferric hydrate

Hydrate, Acetic

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