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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/25%3A_Biomolecules-_Carbohydrates/25.05%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThe only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determin...The only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determine whether the molecule is alpha or beta. The lower energy conformation is the one in which four of the five substituents are equatorial, but the presence of the one axial hydroxyl group means that the alpha isomer is, overall, less stable than the beta isomer.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/25%3A_Biomolecules_-_Carbohydrates/25.05%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThis section explains the cyclic structures of monosaccharides, focusing on the formation of anomers. When monosaccharides undergo cyclization, they form two different configurations at the anomeric c...This section explains the cyclic structures of monosaccharides, focusing on the formation of anomers. When monosaccharides undergo cyclization, they form two different configurations at the anomeric carbon, designated as alpha (α) and beta (β). This transformation is crucial in carbohydrate chemistry, as it influences the properties and reactivity of sugars. Understanding anomers is essential for studying carbohydrate metabolism and their biological functions.
- https://chem.libretexts.org/Courses/Martin_Luther_College/Organic_Chemistry_-_MLC/05%3A_Biomolecules/5.01%3A_Biomolecules-_Carbohydrates/5.1.06%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThe only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determin...The only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determine whether the molecule is alpha or beta. The lower energy conformation is the one in which four of the five substituents are equatorial, but the presence of the one axial hydroxyl group means that the alpha isomer is, overall, less stable than the beta isomer.
- https://chem.libretexts.org/Ancillary_Materials/Reference/Organic_Chemistry_Glossary/AnomersAnomers are cyclic monosaccharides or glycosides that are epimers, differing from each other in the configuration of C-1 if they are aldoses or in the configuration at C-2 if they are ketoses. The epi...Anomers are cyclic monosaccharides or glycosides that are epimers, differing from each other in the configuration of C-1 if they are aldoses or in the configuration at C-2 if they are ketoses. The epimeric carbon in anomers are known as anomeric carbon or anomeric center.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_III_(Morsch_et_al.)/25%3A_Carbohydrates/25.05%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThe only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determin...The only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determine whether the molecule is alpha or beta. The lower energy conformation is the one in which four of the five substituents are equatorial, but the presence of the one axial hydroxyl group means that the alpha isomer is, overall, less stable than the beta isomer.
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/25%3A_Biomolecules-_Carbohydrates/25.06%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersNote that an –OH group on the right in a Fischer projection is on the bottom face of the pyranose ring, and an –OH group on the left in a Fischer projection is on the top face of the ring. The pyranos...Note that an –OH group on the right in a Fischer projection is on the bottom face of the pyranose ring, and an –OH group on the left in a Fischer projection is on the top face of the ring. The pyranose form results from addition of the –OH at C6 to the carbonyl group, while the furanose form results from addition of the –OH at C5 to the carbonyl group (Figure 25.6).
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/25%3A_Biomolecules-_Carbohydrates/25.06%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThe only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determin...The only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determine whether the molecule is alpha or beta. The lower energy conformation is the one in which four of the five substituents are equatorial, but the presence of the one axial hydroxyl group means that the alpha isomer is, overall, less stable than the beta isomer.
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/11%3A_Biomolecules-_Carbohydrates/11.06%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThe only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determin...The only differences between the Haworth Projection of the alpha or beta form of a single carbohydrate, is how the OH (and carbon 1 if furanose ring) is arranged around the anomeric carbon to determine whether the molecule is alpha or beta. The lower energy conformation is the one in which four of the five substituents are equatorial, but the presence of the one axial hydroxyl group means that the alpha isomer is, overall, less stable than the beta isomer.
- https://chem.libretexts.org/Workbench/Pick_Your_Poison%3A_Introduction_to_Materials_Toxicology/24%3A_Biomolecules_-_Carbohydrates/24.06%3A_Cyclic_Structures_of_Monosaccharides_-_AnomersThis section explains the cyclic structures of monosaccharides, focusing on the formation of anomers. When monosaccharides undergo cyclization, they form two different configurations at the anomeric c...This section explains the cyclic structures of monosaccharides, focusing on the formation of anomers. When monosaccharides undergo cyclization, they form two different configurations at the anomeric carbon, designated as alpha (α) and beta (β). This transformation is crucial in carbohydrate chemistry, as it influences the properties and reactivity of sugars. Understanding anomers is essential for studying carbohydrate metabolism and their biological functions.
