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Inversion of cane sugar

Specific acid Inversion of cane sugar C12H22O11 + H2o = c6h12o6 + c6h12o6... [Pg.222]

Since [H20] remain constant as in case of inversion of cane sugar, it does not effect the rate of reaction and reaction is simply first order with respect to ester. However, the hydrolysis of ester in presence of alkali... [Pg.5]

The reactions, in which molecularity and order are different due to the presence of one of the reactant in excess, are known as pseudo-order reactions. The word (pseudo) is always followed by order. For example, inversion of cane sugar is pseudo-first order reaction. [Pg.5]

Catalytic effects.—Within certain limits, the stimulating action exerted by the presence of hydrochloric acid upon the speed of inversion of cane sugar 28 is less the more dil. the acid. Thus, W. Ostwald found the velocity constant with a soln. containing a mol. of acid per 2 litres of soln. is 20 52 per 10 litres, 3 335 and per 100 litres, 0 3128. The action is favoured by the presence of neutral salts, and this the more, the lower the mol. wt. of the salt in the same family group of the periodic system. The temp, coeff. of the inversion is 17 92 at 100°, and. 0 04104 at 25°. W. Ostwald, R. Hopke, and H. Trey have likewise studied the accelerating influence of the acid on the hydrolysis of methyl and ethyl acetates. Similar studies have been made by W. Ostwald and A. Villiers on the hydrolysis of methyl and ethyl acetates, calcium oxalate, and ethyl bromide and iodide. [Pg.196]

The affinities of the acids deduced from their electrical conductivity, and their influence on the rates of hydrolysis of methyl acetate and of the inversion of cane sugar are nearly the same, as illustrated in Table XIV. [Pg.196]

Electrical conductivity. Hydrolysis of methyl acetate. Inversion of cane sugar. [Pg.196]

The electrical conductivity, the lowering of the f.p., the rate of hydrolysis of methyl acetate, and the inversion of cane-sugar, by W. Ostwald 2 have shown it to be one of the most powerful of the monobasic acids. It is therefore very active chemically and it usually behaves as an oxidizing agent, and is itself reduced. [Pg.582]

The chemical properties o orthophosphoric add.—W. Muller-Erzbach21 has discussed the affinity of the metals for phosphoric acid. J. Thomsen found the avidity of a mol. of phosphoric acid for one of sodium hydroxide to be a quarter of the value of that for hydrochloric acid. The affinity of phosphoric acid for the bases is greater than that of carbonic acid, boric acid, phosphorous acid, and hypophosphorous acid. The catalytic action of phosphoric acid on the reaction between bromic and hydriodic acids has been studied by W. Ostwald on the reaction between iodic and sulphurous acids, by R. Hopke and A. Purgotti and L. Zanichelli on hydrazine sulphate, N2H4.H2S04. According to W. Ostwald, the velocity constant for the inversion of cane sugar by phosphoric acid is 6-21 when the value for hydrochloric acid is 100 and J. Spohr showed that the presence of neutral salts at 25° retards, or at 40° completely suppresses,the activity of phosphoric acid. [Pg.962]

It is defined as, the total number of molecules of all the reactants taking part in a chemical reaction as represented by a simple equation. Examples, (i) Inversion of cane sugar (Molecularity = 2)... [Pg.212]

Reactions which are not unimolecular, but obey the first order rate expression are known as pseudo-unimolecular reactions. For example, hydrolysis of methyl acetate, inversion of cane sugar etc. are pseudo-unimolecular reactions. In general, when the order of reaction is generally less than the molecularity of a reaction, it is said to be a pseudo order reaction. [Pg.219]

Specific acid Inversion of cane sugar Hydrolysis of acetals Hydration of unsaturated aldehydes C12H22O11 +h2o = c6h12o6 +c6h12o6 R CH(OR2)2 + H20 = R CHO+ 2R2OH CH2 CH CH0 + H20 = CH20H CH2 CHO... [Pg.27]

In the beginnings of classical physical chemistry, starting with the publication of the Zeitschrift fUr Physikalische Chemie in 1887, we find the problem of chemical kinetics being attacked in earnest. Ostwald found that the speed of inversion of cane sugar (catalyzed by acids) could be represented by a simple mathematical equation, the so-called compound interest law. Nernst and others measured accurately the rates of several reactions and expressed them mathematically as first order or second order reactions. Arrhenius made a very important contribution to our knowledge of the influence of temperature on chemical reactions. His empirical equation forms the foundation of much of the theory of chemical kinetics which will be discussed in the following chapter. [Pg.2]

Whilst for this case, without the aid of the dissociation theory, there is hardly anything to be said, that theory pictures a mutual action of the two acids which explains that the properties of the solutions—conductivity, rate of inversion of cane sugar, c.—are not the mean between those of two solutions containing the acids separately. When one acid is mixed with another, the increased quantity of H-ions causes a displacement of equilibrium which can be followed out numerically. [Pg.120]

The early study of catalysis by acids and bases was concerned chiefly with the use of catalyzed reactions for investigating general problems of physical chemistry. For example, the first correct formulation of the kinetic laws of a first order reaction was made by Wilhelmy in 1850 in connection with his measurements of the catalytic inversion of cane sugar by acids (Wilhelmy, 1). Catalytic reactions also played an important... [Pg.151]

The study of catalysis by acids and bases played a very important part in the development of chemical kinetics, since many of the reactions studied in the early days of the subject were of this type. The early investigations of the kinetics of reactions catalyzed by acids and bases were carried out at the same time that,the electrolytic dissociation theory was being developed, and the kinetic studies contributed considerably to the development of that theory. The reactions considered from this, point of view were chiefly the inversion of cane sugar and the hydrolysis of esters. [Pg.417]

One of the fathers of chemical kinetics, Louis Jacques Thenard, discovered hydrogen peroxide and measured its decomposition rates. He demonstrated for the first time, that rates of chemical reactions varied with the concentrations of the reactants. In later study Ludwig Ferdinand Wilhelmy investigated the inversion of cane sugar in the presence of acids and... [Pg.8]

However, from about 1910 onwards the equation that gained general acceptance was the one used by Svante Arrhenius in a paper entitled, On the reaction velocity of the inversion of cane sugar by acids, published in 1889. The equation, which is now referred to as the Arrhenius equation, takes the form... [Pg.66]

Hudson CS. The inversion of cane sugar by invertase. III. J Am Chem Soc... [Pg.27]

In both cases M. A. Graham s results are lower than those of H. G. Denham. The hydrolyses calculated from the effect on the inversion of cane sugar for soln. with v=5 and 10, are respectively 8-39 and 6-84 per cent., but the results are not so... [Pg.323]

Historically, the first well-documented instance of a temperature-dependent Ea is provided by a hydrolysis reaction—the inversion of cane sugar, the very reaction which had served to establish the Arrhenius equation (9). [Pg.272]


See other pages where Inversion of cane sugar is mentioned: [Pg.2114]    [Pg.27]    [Pg.109]    [Pg.5]    [Pg.13]    [Pg.139]    [Pg.132]    [Pg.334]    [Pg.213]    [Pg.275]    [Pg.112]    [Pg.167]    [Pg.16]    [Pg.132]    [Pg.5]    [Pg.188]    [Pg.2114]    [Pg.209]    [Pg.84]    [Pg.384]    [Pg.120]    [Pg.270]    [Pg.318]    [Pg.322]   
See also in sourсe #XX -- [ Pg.514 ]




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