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- https://chem.libretexts.org/Ancillary_Materials/Reference/Organic_Chemistry_Glossary/Haworth_FormulaTraditionally, in carbohydrate chemistry, the furanose rings and the pyranose rings in carbohydrate molecules are shown in the planar conformation, placed on the plane perpendicular to the plane of th...Traditionally, in carbohydrate chemistry, the furanose rings and the pyranose rings in carbohydrate molecules are shown in the planar conformation, placed on the plane perpendicular to the plane of the paper. This representation of rings is known as the Haworth formula.
- https://chem.libretexts.org/Courses/Portland_Community_College/CH106%3A_Allied_Health_Chemistry_III/07%3A_Carbohydrates/7.02%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Chemistry_for_Allied_Health_(Soult)/05%3A_Properties_of_Compounds/5.02%3A_Carbohydrate_StructuresCarbohydrates are organic compounds that contain only carbon (C) , hydrogen (H) , and oxygen (O) . They contain a chain of carbons, an aldehyde or a ketone, and hydroxyl groups. Every carbon atom i...Carbohydrates are organic compounds that contain only carbon (C) , hydrogen (H) , and oxygen (O) . They contain a chain of carbons, an aldehyde or a ketone, and hydroxyl groups. Every carbon atom is attached to one oxygen atom. There are thousands of different carbohydrates, but they all consist of one or more smaller units called monosaccharides.
- https://chem.libretexts.org/Courses/Fullerton_College/Introductory_Chemistry_for_Allied_Health_(Chan)/13%3A_Carbohydrates/13.03%3A_Conformations_and_Stereochemistry/13.3.02%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_333_-_Organic_Chemistry_III_(Lund)/New_Page/3%3A_Conformations_and_Stereochemistry/3.8%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Courses/Nassau_Community_College/CHE200_-_Introduction_to_Organic_Chemistry_(Resch)/03%3A_Conformations_and_Stereochemistry/3.09%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Courses/SUNY_Oneonta/Chem_221%3A_Organic_Chemistry_I_(Bennett)/1%3ALecture_Textbook/03%3A_Conformations_and_Stereochemistry/3.09%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT_(Lund)%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)/03%3A_Conformations_and_Stereochemistry/3.08%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Bookshelves/General_Chemistry/Book%3A_Structure_and_Reactivity_in_Organic_Biological_and_Inorganic_Chemistry_(Schaller)/I%3A__Chemical_Structure_and_Properties/05%3A_Stereochemistry/5.11%3A_Carbohydrates_in_Cyclic_FormCarbohydrates are complicated molecules. In solution, they slowly change into different isomers. In water, most carbohydrates can change from one form to another quickly; they are described as being i...Carbohydrates are complicated molecules. In solution, they slowly change into different isomers. In water, most carbohydrates can change from one form to another quickly; they are described as being in equilibrium with different structures. That means they can change back and forth.
- https://chem.libretexts.org/Courses/University_of_West_Georgia/CCHEM_1152K%3A_Survey_of_Chemistry_II/04%3A_Aldehydes_Ketones_and_Chiral_Molecules/4.07%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_332_--_Organic_Chemistry_II_(Lund)/1%3A_Fall_term_review_sections/3%3A_Conformations_and_Stereochemistry/3.8%3A_Fischer_and_Haworth_projectionsWhile organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare...While organic chemists prefer to use the dashed/solid wedge convention to show stereochemistry, biochemists often use drawings called Fischer projections and Haworth projections to discuss and compare the structure of sugar molecules.
