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- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_333_-_Organic_Chemistry_III_(Lund)/New_Page/3%3A_Conformations_and_Stereochemistry/3.7%3A_Meso_CompoundsThe levorotatory and dextrorotatory forms of tartaric acid studied by Louis Pasteur were, as we now know, the (S,S) and (R,R) enantiomers.
- https://chem.libretexts.org/Courses/University_of_Illinois_Springfield/UIS%3A_CHE_267_-_Organic_Chemistry_I_(Morsch)/Chapters/Chapter_05%3A_Stereochemistry/4.06%3A_Fischer_Projections_and_Meso_CompoundsA meso compound is an achiral compound that has chiral centers. It is superimposed on its mirror image and is optically inactive although it contains two or more stereocenters.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT_(Lund)%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)/03%3A_Conformations_and_Stereochemistry/3.07%3A_Meso_CompoundsThe levorotatory and dextrorotatory forms of tartaric acid studied by Louis Pasteur were, as we now know, the (S,S) and (R,R) enantiomers.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Wade)_Complete_and_Semesters_I_and_II/Map%3A_Organic_Chemistry_I_(Wade)/06%3A_Stereochemistry_at_Tetrahedral_Centers/6.05%3A_Meso_CompoundsA meso compound is an achiral compound that has two or more chiral centers. Molecular symmetry allows the mirror images to super-impose so that they are not enantiomers.
- https://chem.libretexts.org/Workbench/Pick_Your_Poison%3A_Introduction_to_Materials_Toxicology/22%3A_Stereochemistry_at_Tetrahedral_Centers/22.08%3A_Meso_CompoundsA meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive altho...A meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive although it contains two or more stereocenters. Remember, an internal plane of symmetry was shown to make a molecule achiral.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.07%3A_Meso_CompoundsA meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive altho...A meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive although it contains two or more stereocenters. Remember, an internal plane of symmetry was shown to make a molecule achiral.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Morsch_et_al.)/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.07%3A_Meso_CompoundsA meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive altho...A meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive although it contains two or more stereocenters. Remember, an internal plane of symmetry was shown to make a molecule achiral.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.07%3A_Meso_CompoundsA meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive altho...A meso compound is an achiral compound that has chiral centers. A meso compound contains an internal plane of symmetry which makes it superimposable on its mirror image and is optically inactive although it contains two or more stereocenters. Remember, an internal plane of symmetry was shown to make a molecule achiral.
- https://chem.libretexts.org/Courses/SUNY_Oneonta/Organic_Chemistry_with_a_Biological_Emphasis_(SUNY_Oneonta)/03%3A_Conformations_and_Stereochemistry/3.08%3A_Meso_CompoundsThe levorotatory and dextrorotatory forms of tartaric acid studied by Louis Pasteur were, as we now know, the (S,S) and (R,R) enantiomers.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Book%3A_Organic_Chemistry_with_a_Biological_Emphasis_v2.0_(Soderberg)/03%3A_Conformations_and_Stereochemistry/3.08%3A_Meso_CompoundsThe levorotatory and dextrorotatory forms of tartaric acid studied by Louis Pasteur were, as we now know, the (S,S) and (R,R) enantiomers.
- https://chem.libretexts.org/Courses/Brevard_College/CHE_201%3A_Organic_Chemistry_I/05%3A_Stereochemistry/5.06%3A_Meso_CompoundsA meso compound is an achiral compound that has two or more chiral centers. Molecular symmetry allows the mirror images to super-impose so that they are not enantiomers.
