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  1. The simplest sugars contain three carbon atoms: one carbonyl group and two carbons bearing hydroxy groups. We call these sugars “trioses” (three-carbon sugars). There are two trioses: the aldose glyceraldehyde and the ketose dihydroxyacetone.

  2. 19 Μαρ 2015 · Hydrolysis of Sucrose. In the hydrolysis of any di- or poly saccharide, a water molecule helps to break the acetal bond as shown in red. The acetal bond is broken, the H from the water is added to the oxygen on the glucose. The -OH is then added to the carbon on the fructose. Figure \(\PageIndex{1}\): Hydrolosis of Sucrose

  3. 11 Μαΐ 2021 · In the case of disaccharides, one monosaccharide acts a the hemiacetal while the other monosaccharides acts as the alcohol. The formation of an acetal (or ketal) bond between two monosaccharides is called a glycosidic bond or glycosidic linkage.

  4. Disaccharides form when two monosaccharides undergo a dehydration reaction (a condensation reaction); they are held together by a covalent bond. Sucrose (table sugar) is the most common disaccharide, which is composed of the monomers glucose and fructose.

  5. 31 Μαΐ 2022 · Sucrose is a non-reducing sugar which gives a negative result in a Benedict’s test. When sucrose is heated with hydrochloric acid this provides the water that hydrolyses the glycosidic bond resulting in two monosaccharides that will produce a positive Benedict's test.

  6. The key point in carbohydrate numbering is to look for the carbon which is an aldehyde or a ketone (the carbonyl carbon). This will be the end of the monosaccharide which is numbered lowest. For aldoses, this carbon would be carbon 1.

  7. Disaccharides (C 12 H 22 O 11) are sugars composed of two monosaccharide units that are joined by a carbon–oxygen-carbon linkage known as a glycosidic linkage. This linkage is formed from the reaction of the anomeric carbon of one cyclic monosaccharide with the OH group of a second monosaccharide.

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