Big Chemical Encyclopedia

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

Articles Figures Tables About

Characterisation 12 point

These are formed by less electropositive elements. They are characterised by the existence of discrete molecules which exist even in the solid state. They have generally lower melting and boiling points than the ionic halides, are more volatile and dissolve in non-polar solvents. [Pg.344]

To reiterate a point that we made earlier, these problems of accurately calculating the free energy and entropy do not arise for isolated molecules that have a small number of well-characterised minima which can all be enumerated. The partition function for such systems can be obtained by standard statistical mechanical methods involving a summation over the mini mum energy states, taking care to include contributions from internal vibrational motion. [Pg.329]

Being crystalline compounds which usually have sharp melting-points, they are used to characterise the parent aldehydes and ketones. [Pg.93]

Identification of Amines. Picric acid combines with many amines to give crystalline picrates, of general formula B,(NO )aCeHjOH, where B is a molecule of a monacidic base. These picrates have usually sharp melting- or decomposition-points, and serve to characterise the amines concerned. They may be formed either by (a) direct union of the acid and the base in a suitable solvent, or (6) by the interaction of sodium picrate and a salt of the amine in aqueous solution. [Pg.174]

It is clear from the figure that the presence of a stable compound is characterised by (i) a maximum point on the liquidus, (ii) a meeting... [Pg.30]

Chakactkrisation of Unsaturatkd Aliphatic Hydrocarbons Unlike the saturated hydrocarbons, unsaturated aliphatic hydrocarbons are soluble in concentrated sulphuric acid and exhibit characteristic reactions with dUute potassium permanganate solution and with bromine. Nevertheless, no satisfactory derivatives have yet been developed for these hydrocarbons, and their characterisation must therefore be based upon a determination of their physical properties (boiling point, density and refractive index). The physical properties of a number of selected unsaturated hydrocarbons are collected in Table 111,11. [Pg.241]

The low reactivity of aliphatic ethers renders the problem of the preparation of suitable crystalline derivatives a somewhat difficult one. Increased importance is therefore attached to the physical properties (boding point, density and refractive index) as a means for providing preliminary information. There are, however, two reactions based upon the cleavage of the ethers which are useful for characterisation. [Pg.315]

AUphatic nitriles are usually liquids or low melting point sohds. The most important reaction of a nitrile is its hydrolysis either by an alkaU or by an acid to the corresponding ahphatic acid characterisation of the acid enables the identity of the original nitrile to be established. [Pg.410]

The sulphides (I) can be readily oxidised in glacial acetic acid solution by potassium permanganate to the corresponding sulphones (II) the latter exhibit a wide range of melting points and are therefore particularly valuable for the characterisation of mercaptans ... [Pg.500]

The refractive index of a liquid is recorded as where t is the temperature at which the measurement is made, and D refers to the wave length of the D line of sodium. As already pointed out, it is usual to determine both the refractive index and the density of the liquid at 20° in any case they should be determined at the same temperatme. These two constants are useful in assisting the characterisation of a pure hquid they are particularly valuable for ahphatic hydrocarbons and similar compounds where the methods of characterisation by the formation of solid derivatives are not entirely satisfactory. [Pg.1034]

Sulphonic acids. The aromatic sulphonic acids and their alkali metal salts are soluble in water, but insoluble in ether (Solubility Group II). They are best characterised by conversion into crystalline S-benzyl-iso-thiuronium salts (see Section IV,33,2 and 111,85,5), which possess characteristic melting points. A more time-consuming procedure is to treat the well-dried acid or... [Pg.1077]

The methods of preparation of some of the more important derivatives of a number of classes of organic compounds are described in the various Sections dealing with their reactions and characterisation. These Sections conclude with tables incorporating the melting points and boiling points of the compounds themselves, and also the melting points of selected derivatives. For convenience, the references to the various tables are collected below. [Pg.1082]

Proof stress (F/Aq at a permanent strain of 0.1%) (0.2% proof stress is often quoted instead. Proof stress is useful for characterising yield of a material that yields gradually, and does not show a distinct yield point.)... [Pg.84]

The situation presented in fig. 29 corresponds to the sudden limit, as we have already explained in the previous subsection. Having reached a bend point at the expense of the low-frequency vibration, the particle then cuts straight across the angle between the reactant and product valley, tunneling along the Q-direction. The sudden approximation holds when the vibration frequency (2 is less than the characteristic instanton frequency, which is of the order of In particular, the reactions of proton transfer (see fig. 2), characterised by high intramolecular vibration frequency, are being usually studied in this approximation [Ovchinnikova 1979 Babamov and Marcus 1981]. [Pg.71]

The Melt Flow Rate Test is a method used to characterise polymer melts. It is, in effect, a single point ram extruder test using standard testing conditions (BS... [Pg.373]

A-methylanonaine, prepared from the natural alkaloid by the action of formaldehyde and formic acid, was isolated as the hydriodide, m.p. 246-7° (dec.). dZ-A-methylanonaine was also synthesised and characterised as the hydriodide, m.p. 244° (dec.), and methiodide, m.p. 210-1°. It is regarded as identical with dZ-rcemerine (p. 314), and it may be noted that the melting-point of the Hofmann degradation product of rcemerine is very similar to that of anonaine (IV NMe NH) (Barger and Weitnauer). "... [Pg.318]

Both from the experimental or theoretical point of view, clusters studies present many difficulties due to their typical size (1-10 nm), usually larger than current systems studied in chemistry, but also too small for many physical standard techniques of characterisation and manipulation. [Pg.129]

Sehlogl has shown that para-aminophenylglycine, para-amino-phenyloxamic acid, and para-aminoacetanilide form compounds with aldehydes, which have sharp melting-points and are suitable for the characterisation of aldehydes. With p-aminophenylglycine condensation takes place when the glycine, mixed with alcohol and the aldehyde in question, is warmed. For the purpose of condensing with p-aminophenyloxamic acid and with p-aminoacetaldehyde the alcoholic suspension of the amino-hody is acidulated slightly with hydrochloric acid and the solution is warmed after the aldehyde has heen added. This method yields the hydrochloride of the condensation products. [Pg.180]

When submitted to oxidation by a 2 per cent, solution of permanganate, pinononic acid, CgHj Og, melting at 128° to 129° C., the semi-carbazone of which melts at 204° C. Lastly the constitution of verbenone, as expressed by the above formula, is further confirmed by the fact that the bicyclic system is convertible into a monocyclic system by boiling with 25 per cent, sulphuric acid, with the formation of acetone and 3-methylcyclohexene-(2)-one-(l). This cyclohexenone has been characterised by its semi-carbazone (melting-point 198° C.) and by its conversion into y-acetobutyric acid (melting-point 36° C). The oily liquid, which did not react with sulphite, was submitted to benzoylation after dilution with pyridine. It thus gave rise to a benzoate from which was... [Pg.228]


See other pages where Characterisation 12 point is mentioned: [Pg.290]    [Pg.64]    [Pg.40]    [Pg.41]    [Pg.240]    [Pg.302]    [Pg.519]    [Pg.727]    [Pg.243]    [Pg.17]    [Pg.262]    [Pg.342]    [Pg.455]    [Pg.1028]    [Pg.1037]    [Pg.1136]    [Pg.64]    [Pg.65]    [Pg.495]    [Pg.153]    [Pg.216]    [Pg.270]    [Pg.13]    [Pg.46]    [Pg.190]    [Pg.219]    [Pg.349]    [Pg.677]    [Pg.100]    [Pg.69]    [Pg.183]    [Pg.354]   
See also in sourсe #XX -- [ Pg.113 ]




SEARCH



© 2024 chempedia.info