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Octadecanal

Most of the theoretical predictions have now been substantially verified by a large series of experiments in a number of laboratories. Knobler and Scott and their coworkers (1977-1991) have studied a number of quasibinary mixtures, in particular ethane + (liexadecane + octadecane) for which the experimental n.2 = 17.6. Their experimental results essentially confimi the theoretical predictions shown in figure A2.5.31. [Pg.660]

By increasing the molar proportion of the monocarboxylic acid, the yield of (II) is improved. Thus electrolysis of a mixture of decanoic acid (n-decoic acid capric acid) (V) (2 mols) and methyl hydrogen adipate (VI) (1 mol) in anhydrous methanol in the presence of a little sodium methoxide gives, after hydrolysis of the esters formed, n-octadecane (VII), tetradecanoic or myristic acid (VIH) and sebacic acid (IX) ... [Pg.938]

Fig. 3. (a) Flame ionization detector (fid) response to an extract of commercially processed Valencia orange juice, (b) Gas chromatography—olfactometry (geo) chromatogram of the same extract. The abscissa in both chromatograms is a normal paraffin retention index scale ranging between hexane and octadecane (Kovats index). Dilution value in the geo is the -fold that the extract had to be diluted until odor was no longer detectable at each index. [Pg.6]

Related to the ladder polymers are the spiro polymers as typified by the reaction product of cyclo-octadecane-1, 10-dione with pentaerythritol Figure 29.22). [Pg.850]

In fact, this procedure can be used for any aliphatic series such as alcohols, amines, etc. Consequently, before dealing with a specific homologous series, the validity of using the methylene group as the reference group needs to be established. The source of retention data that will be used to demonstrate this procedure is that published by Martire and his group [5-10] at Georgetown University and are included in the thesis of many of his students. The stationary phases used were all n-alkanes and there was extensive data available from the stationary phase n-octadecane. The specific data included the specific retention volumes of the different solutes at 0°C (V r(To)) thus, (V r(T)) was calculated for any temperature (Ti) as follows. [Pg.55]

Similar substances were chosen to meet the assumptions of the theory that would offer approximately the same dispersive interactions but quite different polar interactions, for example di-n-octylmethylamine and n-octadecane. Consequently,... [Pg.79]

Observation, 2,15 Ocean, composition of, 440 Ocean water, composition, 439 n-Octadecane, properties, 341 Octahedral complex, 393 Octane, 46, 338 properties, 341 Octanamide, 339 Octanoic acid, 339 1-Octanol, 338 Octaves, Law of, 104 Octyl alcohol, 338 1-Octylamine, 338... [Pg.463]


See other pages where Octadecanal is mentioned: [Pg.424]    [Pg.425]    [Pg.427]    [Pg.337]    [Pg.941]    [Pg.71]    [Pg.1106]    [Pg.2]    [Pg.411]    [Pg.459]    [Pg.512]    [Pg.569]    [Pg.604]    [Pg.685]    [Pg.27]    [Pg.410]    [Pg.87]    [Pg.94]    [Pg.99]    [Pg.116]    [Pg.138]    [Pg.180]    [Pg.200]    [Pg.214]    [Pg.222]    [Pg.239]    [Pg.374]    [Pg.375]    [Pg.405]    [Pg.23]    [Pg.316]    [Pg.371]    [Pg.384]    [Pg.84]    [Pg.258]    [Pg.162]    [Pg.103]    [Pg.103]    [Pg.71]    [Pg.1106]    [Pg.1246]    [Pg.306]    [Pg.103]    [Pg.18]   
See also in sourсe #XX -- [ Pg.498 ]

See also in sourсe #XX -- [ Pg.498 ]




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N-Octadecane

N-octadecanal

Octadecane

Octadecane

Octadecane thiols

Octadecane, 7,8-dichloro

Octadecane, 7,8-epoxy-2-methylsynthesis

Octadecane, 7,8-epoxy-2-methylsynthesis via r-butyl 5-methylhexyl sulfoxide

Octadecane, 9,10-epoxy

Octadecane, oxidation

Octadecane-, sodium

Octadecane-1,2,3,4-tetrol

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