They are yellowish-red solids, which behave as weak bases, their salts undergoing hydrolytic dissociation in aqueous solution.
Certain a-diketones condense to form benzenoid quinones, two molecules of the diketone taking part in the reaction; thus diacetyl, CH 3 CO CO CH 3, yields p-xyloquinone, C 6 H 2 (CH 3) 2 0 2 (Ber., 1888, 21, p. 1411), and acetylpropionyl, CH 3 CO CO C 2 H 5, yields duroquinone, or tetramethylquinone, C 6 (CH 3) 4 0 2, Oxymethylene compounds, characterized by the grouping > C:CH(OH), also give benzene derivatives by hydrolytic condensation between three molecules; thus oxymethylene acetone, or formyl acetone, CH 3 CO.
It appears to be synthesized in the plant tissues from carbon dioxide and water, formaldehyde being an intermediate product; or it may be a hydrolytic product of a glucoside or of a polysaccharose, such as cane sugar, starch, cellulose, &c. In the plant it is freely converted into more complex sugars, poly-saccharoses and also proteids.
Chem., 1892, 45, p. 604) observed acetic acid as a hydrolytic product.
On the other hand, they are much weaker bases than the aliphatic amines, their salts undergoing hydrolytic dissociation in aqueous solution.
The alkali and alkaline earth cyanides are soluble in water and in alcohol, and their aqueous solution, owing to hydrolytic dissociation, possesses an alkaline character.
P. 670) that the velocity of formation of the amino-azo compound depends only on the nature of the reagents and not on the concentration, and that in coupling the hydrochloride of a tertiary amine with diazobenzene suiphonic acid the reaction takes place between the acid and the base set free by the hydrolytic dissociation of its salt, for the formation of the amino-azo compound, when carried out in the presence of different acids, takes place most rapidly with the weakest acid (H.
The constitution of the diazonium groupN 2 -X, may be inferred from the following facts :-The group C6H6N2-behaves in many respects similarly to an alkali metal, and even more so to the ammonium group, since it is capable of forming colourless neutral salts with mineral acids, which in dilute aqueous solution are strongly ionized, but do not show any trace of hydrolytic dissociation (A.
Boric acid (q.v.) being only a weak acid, its salts readily undergo hydrolytic dissociation in aqueous solution, and this property can be readily shown with a concentrated aqueous solution of borax, for by adding litmus and then just sufficient acetic acid to turn the litmus red, the addition of a large volume of water to the solution changes the colour back to blue again.
The truxillic acids, C,8H1504, which result by the hydrolytic splitting of truxilline, C38H46N208, are phenyl derivatives of cyclo-butane.