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GLUCOSE (from Gr. - twais, sweet)

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Originally appearing in Volume V12, Page 142 of the 1911 Encyclopedia Britannica.
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See also:

GLUCOSE (from Gr. - twais, sweet)  , a See also:carbohydrate of the See also:formula C5H12O6; it may be regarded as the aldehyde of sorbite . The name is applied in See also:commerce to a complex mixture of carbohydrates obtained by boiling See also:starch with dilute See also:mineral acids; in See also:chemistry, it denotes, with the prefixes d, 1 and d+l (or i), the dextro-rotatory, laevo-rotatory and inactive forms of the definite chemical See also:compound defined above . The d modification is of the commonest occurrence, the other forms being only known as synthetic products; for this See also:reason it is usually termed See also:glucose, simply; alternative names are dextrose, See also:grape See also:sugar and diabetic sugar, in allusion to its right-handed See also:optical rotation, its occurrence in large quantity in grapes, and in the urine of diabetic patients respectively . In the See also:vegetable See also:kingdom glucose occurs, always in admixture with See also:fructose, in many fruits, especially grapes, cherries, bananas, &c.; and in See also:combination, generally with phenols and See also:aldehydes belonging to the aromatic See also:series, it forms an extensive class of compounds termed glucosides . It appears to be synthesized in the plant tissues from See also:carbon dioxide and See also:water, formaldehyde being an intermediate 'product; or it may be a hydrolytic product of a See also:glucoside or of a polysaccharose, such as See also:cane sugar, starch, See also:cellulose, &c . In the plant it is freely converted into more complex sugars, poly-saccharoses and also proteids . In the See also:animal kingdom, also, it is very widely distributed, being some-times a normal and sometimes a pathological constituent of the fluids and tissues; in particular, it is See also:present in large amount in the urine of those suffering from See also:diabetes, and may be present in nearly all the See also:body fluids . It also occurs in See also:honey, the See also:white See also:appearance of candied honey being due to its separation . Pure d-glucose, which may be obtained synthetically (see SUGAR) or by adding crystallized cane sugar to a mixture of 8o % See also:alcohol and See also:volume of fuming hydrochloric See also:acid so See also:long as it dissolves on shaking, crystallizes from water or alcohol` at See also:ordinary temperatures in nodular masses, composed of See also:minute six-sided plates, and containing one See also:molecule of water of See also:crystallization . This product melts at 86° C., and becomes anhydrous when heated to 11o° C . The anhydrous compound can also be prepared, as hard crusts melting at 146°, by crystallizing concentrated aqueous solutions at 30° to 35° . It is very soluble in water, but only slightly soluble in strong alcohol .

Its See also:

taste Chemistry.—In its chemical properties glucose is a typical oxyaldehyde or aldose . The aldehyde See also:group reacts with hydrocyanic acid to produce two stereo-isomeric cyanhydrins; this See also:isomerism is due to the See also:conversion of an originally non-See also:asymmetric carbon See also:atom into an asymmetric one . The cyanhydrin is hydrolysable to an acid, the lactone of which may be reduced by See also:sodium See also:amalgam to a glucoheptose, a non-fermentable sugar containing seven carbon atoms . By repeating the See also:process a non-fermentable gluco-octose and a fermentable glucononose may be prepared . The aldehyde group also reacts with phenyl See also:hydrazine to See also:form two phenylhydrazones; under certain conditions a hydroxyl group adjacent to the aldehyde group is oxidized and glucosazone is produced ; this glucosazone is decomposed by hydrochloric acid into phenyl hydrazine and the keto-aldehyde glucosone . These transformations are fully discussed in the See also:article SUGAR . On reduction glucose appears to yield the hexahydric alcohol d-sorbite, and on oxidation d-gluconic and d-saccharic acids . Alkalis partially convert it into d-mannose and d-fructose . Baryta and See also:lime yield saccharates, e.g . C6Hi2O6•BaO, precipitable by alcohol . The constitution of glucose was established by H . Kiliani in 1885–1887, who showed it to be See also:CH2OH•(CH•OH)4•CHO .

The subject was taken up by Emil See also:

Fischer, who succeeded in synthesizing glucose, and also several of its stereo-isomers, there being 16 according to the Le See also:Bel-See also:van't Hoff theory (see STEREO-ISOMERISM and SUGAR) .. This open See also:chain structure is challenged in the views put forward by T . M . Lowry and E . F . See also:Armstrong . In 1895 C . Tanret showed that glucose existed in more than one form, and he isolated a, $ and y varieties with specific rotations of 105°, 52.5° and 22° . It is now agreed that the B variety is a mixture of the a and y . This See also:discovery explained the mutarotation of glucose . In a fresh See also:solution a-glucose only exists, but on See also:standing it is slowly trans-formed into 7-glucose, See also:equilibrium being reached when the a and y forms are present in the ratio 0.368:0.632 (Tanret, Zeit. physikal . Chem., 1905, 53, p .

Phoenix-squares

692) . It is convenient to refer to these two forms as a and 0 . Lowry and See also:

Arm-strong represent these compounds by the following spatial formulae which postulate a 7-oxidic structure, and 5 asymmetric carbon atoms, i.e. one more than in the Fischer formulae . These formulae are supported by many considerations. especially by the selective H2OH CH2OH C CH•OH CH•OH CH O CH (CH•OH)2 ~(CH•OH)2 HC OH HO•CH a-glucose $-glucose See also:action of enzymes, which follows similar lines with the a- and 0-glucosides, i.e. the compounds formed by the interaction of glucose with substances generally containing hydroxyl See also:groups (see GLUCOSIDE) . See also:Fermentation of Glucose.—Glucose is readily fermentable . Of the greatest importance is the alcoholic fermentation brought about by yeast cells (Saccharomyces cerevisiae seu vini); this follows the See also:equation C6H1206=2C2H60+2CO2, See also:Pasteur considering 94 to95 %of the sugar to be so changed . This See also:character is the See also:base of the See also:plan of adding glucose to See also:wine and See also:beer wort before fermenting, the alcohol content of the liquid after fermentation being increased . Some fusel oil, See also:glycerin and succinic acid appear to be formed simultaneously, but in small amount . Glucose also undergoes fermentation into lactic acid (q.v.) in the presence of the lactic acid bacillus, and into butyric acid if the action of the preceding ferment be continued, or by other bacilli . It also yields, by the so-called mucous fermentation, a mucous, gummy See also:mass, mixed with mannitol and lactic acid . We may here See also:notice the frequent See also:production of glucose by the action of enzymes upon other carbohydrates . Of especial See also:note is the transformation of maltose by maltase into glucose, and of cane sugar by invertase into a mixture of glucose and fructose (invert sugar) ; other instances are: lactose by lactase into galactose and glucose; trehalose by trehalase into glucose; melibiose by melibiase into galactose and glucose; and of melizitose by melizitase into touranose and glucose, touranose yielding glucose also when acted upon by the See also:enzyme touranase .

Commercial Glucose . The glucose of commerce, which may be regarded as a mixture of grape sugar, maltose and dextrins, is pre-pared by hydrolysing starch by boiling with a dilute mineral acid . In See also:

Europe, See also:potato starch is generally employed; in See also:America, See also:corn starch . The acid employed may be hydrochloric, which gives the best results, or sulphuric, which is used in See also:Germany; sulphuric acid is more readily separated from the product than hydrochloric, since the addition of powdered See also:chalk precipitates it as See also:calcium sulphate, which may be removed by a See also:filter See also:press . The processes of manufacture have much in See also:common, although varying in detail . The following is an outline of the process when hydrochloric acid is used: Starch (" See also:green " starch in America) is made into a " See also:milk " with water, and the milk pumped into boiling dilute acid contained in a closed " converter," generally made of See also:copper or See also:cast See also:iron; See also:steam is led in at the same See also:time, and the pressure is kept up to about 25 lb to the sq. in . When the converter is full the pressure is raised some-what, and the See also:heating continued until the conversion is See also:complete . The liquid is now run into neutralizing tanks containing sodium carbonate, and, after settling, the supernatant liquid, termed " See also:light liquor," is run through bag filters and then on to See also:bone-See also:char filters, which have been previously used for the " heavy liquor." The colourless or See also:amber-coloured filtrate is concentrated to 27° to 28°B., when it forms the " heavy liquor," just mentioned . This is filtered through fresh bone-char filters, from which it is discharged as a practically colourless liquid . This liquid is concentrated in vacuum pans to a specific gravity of 40° to 44° B., a small quantity of sodium bisulphite solution being added to bleach it, to prevent fermentation, and to inhibit See also:browning . " See also:Syrup glucose " is the commercial name of the product; by continuing the concentration further solid glucose or grape sugar is obtained . Several brands are recognized: " Mixing glucose " is used by syrup and See also:molasses manufacturers, " jelly glucose " by makers of jellies, " confectioners' glucose " in See also:confectionery, " brewers' glucose" in See also:brewing, &c .

End of Article: GLUCOSE (from Gr. - twais, sweet)
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