Hydroxylic oxygen is obtained by subtracting the molecular refractions of acetic acid and acetaldehyde.
Thus oxygen varies according as whether it is linked to hydrogen (hydroxylic oxygen), to two atoms of carbon (ether oxygen), or to one carbon atom (carbonyl oxygen); similarly, carbon varies according as whether it is singly, doubly, or trebly bound to carbon atoms.
Normal values of K were given by nitrogen peroxide, N204, sulphur chloride, S 2 C1 21 silicon tetrachloride, SiC1 4, phosphorus chloride, PC1 3, phosphoryl chloride, POC1 31 nickel carbonyl, Ni(CO) 4, carbon disulphide, benzene, pyridine, ether, methyl propyl ketone; association characterized many hydroxylic compounds: for ethyl alcohol the factor of association was 2.74-2.43, for n-propyl alcohol 2.86-2.72, acetic acid 3.62 -2.77, acetone 1 .
How much of the hydrogen and oxygen are in the hydroxylic (OH) form cannot be absolutely stated, but from the study of the acetates at least three hydroxyl groups may be assumed.
ESTERS, in organic chemistry, compounds formed by the condensation of an alcohol and an acid, with elimination of water; they may also be considered as derivatives of alcohols, in which the hydroxylic hydrogen has been replaced by an acid radical, or as acids in which the hydrogen of the carboxyl group has been replaced by an alkyl or aryl group. In the case of the polybasic acids, all the hydrogen atoms can be replaced in this way, and the compounds formed are known as "neutral esters."
The subject has been especially studied by Skraup, Konigs, and von Miller; Kiinigs and von Miller have proposed formulae consisting of a piperidine ring substituted with a vinyl group; in the former that is a bridge of CH 2 C(OH) from the nitrogen atom to the -y-carbon atom, connexion with the quinoline residue being made at the hydroxylic carbon atom through a CH2 group: whilst in the latter the piperidine ring is substituted by a methyl group in addition to the vinyl group and the bridge is simply C(OH), with which connexion is made as before.
It crystallizes from benzene in prisms, which melt at 97° C. Sodium nitrite in the presence of excess of acid converts it into the corresponding hydroxylic compound flavenol.
reactions it shows the properties of a hydroxylic substance.
The /3 compound is hydroxylic in character, whilst the a and -y derivatives behave frequently as if they possess the tautomeric ketostructure, yielding according to the conditions of the experiment either N- or 0-ethers (H.
It crystallizes from benzene in prisms, which melt at 97Ã‚° C. Sodium nitrite in the presence of excess of acid converts it into the corresponding hydroxylic compound flavenol.
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