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Fructose sugars

But here is what Philip Brown did He took a different tack on the question. He set up and performed an experiment wherein he took different sugars (fructose, glucose, and sucrose) and made up solutions by dissolving them in water, each at five different concentration levels, and made solutions using all combinations of concentrations. That gave an experimental design with 125 samples. He then measured the spectra of all of those samples. Since the samples were all clear solutions there were no extraneous effects due to optical scatter. [Pg.464]

It was found98 that the amount of sucrose consumed could be accounted for entirely as levan and reducing sugars. Fructose formed part of the reducing sugars produced, and there was no appreciable interconversion of aldose and ketose. When raffinose was used as substrate, the products were levan, melibiose and D-fructose (but not sucrose and D-galactose). The following equation expresses fully the net result of the action of the autolyzate ... [Pg.246]

Sugar Fructose Mannose Xylose Dextrose Galactose Sorbitol... [Pg.23]

The separation of the two sugars fructose and glucose, is currently perhaps the industrial separation of biomolecules performed on the largest scale. Since it is a typical two-component separation, the advantages of utilizing an SMB for this purpose are obvious and glucose/fructose separations by SMB are well estab-... [Pg.224]

The food fiavorist also must be aware of metal complexes, which carbohydrates are capable of forming, Iron salts not only form complexes with dietary fiber, but with nearly all of the known natural sugars. Fructose, maltitol. sorbitol, and xylitol can easily form complexes with the ferric... [Pg.649]

The reactant concentrations of 48 g of sodium aluminate and 105 g of lactose are equivalent to a mol ratio of two mols of aluminate to one mol of lactose. The mixture was then heated to 50°C and 100 ml aliquots were removed at periodic intervals to determine the level of conversion. The reaction was terminated after three hours by adding sufficient 30% HCI to lower the pH to 4.2. The pH was then raised to neutrality, i.e., 6.5 to 7.0, with ammonium hydroxide so as to completely precipitate insoluble aluminum hydroxide. The precipitate was then removed by vacuum filtration and the filtrate was analyzed for the presence of ketose sugar by chromatographic analysis. The chromatographic analysis of the filtrate confirmed that the main component of the filtrate was lactulose and not the monosaccharide ketose sugar, fructose. [Pg.2008]

Sugars (fructose) Reaction Intermediate 4-Hydroxy-5-Methyl -3-(2H)-Furanone+ Methanal... [Pg.243]

Chemists have known about racemates since Pasteur, at 26 years of age, told the Paris Academy of Sciences how he used tweezers to separate two types of crystals of salts of tartaric acid, which rotate polarized light clockwise (d, dextro) or counterclockwise (l, levo). Unfortunately, this correspondence does not always hold true. In fact, the magnitude and even the direction of optical rotation are complicated functions of the electronic structure surrounding the chiral center. For example, the common enantiomer of the sugar fructose is termed d because of the stereochemical orientation about the chiral atom. But this enantiomer actually rotates the plane of polarization to the left, and its mirror image, L-fructose, rotates the plane of polarization to the right. [Pg.294]

The sugar fructose is an isomer of glucose. Like glucose, fructose forms a cyclic hemiacetal, but in this case the ring is five membered rather than six membered. Show the structure for the hemiacetal formed from fructose and show a mechanism for its formation in acidic solution. [Pg.799]

Two structures of the sugar fructose are shown next. The cyclic stmcture predominates in aqueous solution. [Pg.875]

Fructose is very soluble and is hence a very hygroscopic product - for this reason fructose is usually used as a syrup. Attempts to crystallise fructose by normal methods do not work, and for many years it was referred to as the uncrystallisable sugar. Fructose in a form which is described as crystalline is now available commercially and could well be produced by spray drying. [Pg.27]

The empirical formula of a compound is the formula that gives the lowest whole-number ratio of atoms of all the elements. For example, the empirical formula of fruit sugar, fructose, C6H12O6, is CH2O. The simplest ratio of carbon... [Pg.204]

Calculate the mass of a sample of fruit sugar, fructose, CgHi20g, containing 2.65 X 10 ° molecules. [Pg.215]

Okay, neat, but so what To answer that, we have to investigate the molecules we re dealing with. There are two kinds of sugars—fructose (in the corn syrup) and glucose. They both have the molecular formula but... [Pg.130]

It will be observed that the hypothesis of intramolecular transformation advanced by us to explain the interconversion of glucose, fructose and mannose should be modified or rather extended. It would seem appropriate to postpone these theoretical considerations until the constitution of the new sugars has been established. It is to be noted, however, that the theory takes into consideration the existence of a great number of ketoses, it being possible for an intramolecular transformation of the kind indicated to take place among several carbons in the chain of the sugar. Fructose, for example, can produce in this way two new ketoses with a C==0 on carbon 3, which can be transformed, by reduction, into four different hexitols, and yet can form one and the same osazone. [Pg.115]


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See also in sourсe #XX -- [ Pg.7 , Pg.104 ]

See also in sourсe #XX -- [ Pg.2 , Pg.329 , Pg.330 , Pg.331 ]




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Carbohydrates/sugar fructose

Fructose invert sugar

Fructose—Levulose—Fruit Sugar

Fruit Sugar (Fructose)

Sucrose Invert Sugar Fructose

Sugar transporters fructose

Sugars high-fructose corn syrup

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