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Sugar in coffee

We see capillary action at work in many phenomena. If a paintbrush is dipped into water, the water rises into the narrow spaces between the bristles by capillary action. Hang your hair in the bathtub, and water seeps up to your scalp in the same way. This is how oil moves up a lamp wick and how water moves up a bath towel when one end hangs in water. Dip one end of a lump of sugar in coffee, and the entire lump is quickly wet. The capillary action occurring between soil particles is important in bringing water to the roots of plants. [Pg.267]

What is this about entropy really decreasing " I didn t know how to answer my family, worried by some preposterous news report. My best try was, "I don t know the words that you and I can use in the same way. I tell you what. Let me give you examples of where you see entropy changing, as when you put cream and sugar in coffee. You think a while about these examples. Then we can answer your question together."... [Pg.393]

In the course of a day, you use or make solutions many times. Your morning cup of coffee is a solution of solids (sugar and coffee) in a liquid (water). The gasoline you fill your gas tank with is a solution of several different liquid hydrocarbons. The soda you drink at a study break is a solution containing a gas (carbon dioxide) in a liquid (water). [Pg.259]

Sugar dissolving in coffee involves dispersal of molecules. Sugar molecules are distributed more widely in solution than they are in the solid crystal. [Pg.975]

Trihydroxybenzene carboxylic acid esters with a sugar are characteristic of hydrolyzable tannins .37 These, too, may be present in coffee... [Pg.117]

The chemical origin of free radicals in coffee is attributed to the sugars or carbohydrates, rather than phenolic constituents100. [Pg.141]

The purple speck disease of soybeans is caused by the fungus Cercospora kikuchii, and additional cash crops such as tobacco, com, sugar, and coffee are damaged by fungi from the genus Cercospora [3]. Cercosporin (3, Chart 7.1), initially isolated in 1957 from Cercospora kikuchii and subsequently from other Cercospora species, was found to be the phototoxin responsible for the destructive nature of the pathogen [4]. For these reasons, the natural product was extensively studied, yet its structure was not elucidated until the 1970s [5]. [Pg.158]

Pyrroles are found in the volatiles of most heated foods [29], although they have received less attention than some other classes of aroma volatiles. Some pyrroles may contribute desirable aromas, e.g. 2-acetylpyrrole has a caramel-like aroma, and pyrrole-2-carboxaldehyde is sweet and corn-like, but alkylpyrroles and ac-ylpyrroles have been reported to have unfavourable odours [22]. Many more volatile pyrroles have been found in coffee than in other foods [30], and they are common products of amino acid-sugar model systems. Pyrroles are closely related in structure to the furans, and they are probably formed in a related manner from the reaction of a 3-deoxyketose with ammonia or an amino compound followed by dehydration and ring closure (cf Scheme 12.2). [Pg.277]

Furfural comes from pentose sugars in cereal straws and brans. Furfural is the precursor of furfuryl mercaptan and its disulfide, difurfuryl disulfide, which are both important chemicals for coffee, meat and roasted flavours. They are prepared by the reaction of furfural and hydrogen sulfide (Scheme 13.15). [Pg.298]

We report this molarity as 0.146 M C12H22On(aq). The (aq) indicates an aqueous solution. If we were to dissolve 20.0 g of cane sugar instead of 10.0 g, the sugar in the coffee would be twice as concentrated its molarity would be 0.292 M C12H22021(aq). [Pg.93]

Uses systemic insecticide and acaricide to control pests in cotton, sugar cane, coffee, tobacco, olives, rice hops, sorghum, maize, deciduous fruits, citrus fruits, potatoes, sugar beet, tomatoes, soya beans, and ornamentals. [Pg.742]

The degree of roasting influenced the magnitude of degradation of sucrose, the major sugar present in coffee, Table XIII. [Pg.227]

If you ve had a cup of coffee and your brain is functioning normally, you may have already guessed that /3-ribose is the sugar in the backbone of ribonucleic acids (RNA), while /3-2-deoxyribose forms the skeletal structure of deoxyribonucleic acid (DNA). In both types of polymers, these sugars are strung together by condensation reactions (remember those ) involving phosphoric... [Pg.272]

A sugar cube dissolves in a cup of coffee in an endothermic process, (a) Is the entropy change of the system (sugar plus coffee) greater than, less than, or equal to zero ... [Pg.645]

If you keep adding sugar to your coffee, eventually you reach a point where the maximum amount has dissolved, and adding more sugar leaves solid sugar on the bottom of the cup. At this point, you have reached the solubility limit of sugar in your coffee solution. Let s try to visualize what this means at the molecular level. [Pg.592]

Sucrose is used as a sweetener in teas, coffee, and a host of soft drinks. The solvent in all of these beverages is water, a polar molecule. The rule "like dissolves like" implies that sucrose must also be a polar molecule. Without even knowing the formula or structure of sucrose, we can infer this important information from a simple experiment—dissolving sugar in our morning cup of coffee. [Pg.196]

The authors observed that an exhaustive list of all the chemicals present in coffee flavor had not yet been compiled, but they believed they had identified the components that are present at the higher ratio of weight, and those which principally control the odor note. Most of the substances identified were well-known compounds present in other roasted products as well, for instance in caramel sugar, cocoa, baked bread and—partially—even in wood tar. However, some of the chemicals detected were new and, obviously, characteristic of roasted coffee. Traces of methyl mercaptan, which was already known at that time and which smells even worse, were also detected in coffee aroma. Commenting on this observation, Reichstein and Staudinger note that it is generally known that many popular raw materials and synthetic perfume compounds owe their characteristic note, which is extremely pleasant to the olfactory sense, to their content of small quantities in additives which carry a rather unpleasant odor in themselves but prove very attractive in thinned solutions and in admixture with other oils. The authors tried to reconstitute coffee aroma, and only by combining over 40 of the substances extracted from coffee... [Pg.62]


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See also in sourсe #XX -- [ Pg.8 , Pg.280 ]




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