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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Basic_Principles_of_Organic_Chemistry_(Roberts_and_Caserio)/05%3A_Stereoisomerism_of_Organic_Molecules/5.04%3A_Representation_of_Organic_StructureMany problems in organic chemistry require consideration of structures in three dimensions, and it is very helpful to use molecular models to visualize the relative positions of the atoms in space.
- 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/Workbench/Chemistry_LHS_Bridge/16%3A_Chirality/16.04%3A_Fischer_ProjectionsThe Fischer Projections allow us to represent 3D molecular structures in a 2D environment without changing their properties and/or structural integrity.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introduction_to_Organic_and_Biochemistry_(Malik)/05%3A_Carbohydrates/5.01%3A_What_are_carbohydratesCarbohydrates, monosaccharides, and polysaccharides are defined, and their general formula and functional groups and drawing Fisher projections are described.
- 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/Ancillary_Materials/Reference/Organic_Chemistry_Glossary/Fischer_ProjectionA Fischer projection or Fischer projection formula is a convention used to depict a stereoformula in two dimension without destroying the stereochemical information, i.e., absolute configuration, at c...A Fischer projection or Fischer projection formula is a convention used to depict a stereoformula in two dimension without destroying the stereochemical information, i.e., absolute configuration, at chiral centers.
- 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.
