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About 29 results
  • https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/04%3A_Organic_Compounds_-_Cycloalkanes_and_their_Stereochemistry/4.03%3A_Cis-Trans_Isomerism_in_Cycloalkanes
    Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one cla...Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one class of molecules that exhibit stereoisomerism.  Di-substituted cycloalkane stereoisomers are designated by the nomenclature prefixes cis (Latin, meaning on this side) and trans (Latin, meaning across).
  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Morsch_et_al.)/04%3A_Organic_Compounds_-_Cycloalkanes_and_their_Stereochemistry/4.02%3A_Cis-Trans_Isomerism_in_Cycloalkanes
    Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one cla...Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one class of molecules that exhibit stereoisomerism.  Di-substituted cycloalkane stereoisomers are designated by the nomenclature prefixes cis (Latin, meaning on this side) and trans (Latin, meaning across).
  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Basic_Principles_of_Organic_Chemistry_(Roberts_and_Caserio)/05%3A_Stereoisomerism_of_Organic_Molecules/5.01%3A_Prelude_to_Stereoisomerism
    Thus, four single bonds to a carbon form a tetrahedral arrangement; two single bonds and one double bond to a carbon give a planar array with bond angles near 120o, while one single bond a...Thus, four single bonds to a carbon form a tetrahedral arrangement; two single bonds and one double bond to a carbon give a planar array with bond angles near 120o, while one single bond and one triple bond (or two double bonds) to a carbon are arranged linearly:
  • https://chem.libretexts.org/Bookshelves/General_Chemistry/Map%3A_Chemistry_-_The_Central_Science_(Brown_et_al.)/24%3A_Chemistry_of_Life-_Organic_and_Biological_Chemistry/24.07%3A_Chirality_in_Organic_Chemistry
    Stereoisomers are isomers that differ in spatial arrangement of atoms, rather than order of atomic connectivity. One of their most interesting type of isomer is the mirror-image stereoisomers, a non-s...Stereoisomers are isomers that differ in spatial arrangement of atoms, rather than order of atomic connectivity. One of their most interesting type of isomer is the mirror-image stereoisomers, a non-superimposable set of two molecules that are mirror image of one another. The existence of these molecules are determined by concept known as chirality.
  • https://chem.libretexts.org/Courses/SUNY_Oneonta/Organic_Chemistry_with_a_Biological_Emphasis_(SUNY_Oneonta)/03%3A_Conformations_and_Stereochemistry/3.04%3A_Chirality_and_stereoisomers
    We turn now to concept of chirality that formed the basis of the story about Louis Pasteur in the beginning of this chapter. Recall that the term chiral, from the Greek work for 'hand', refers to anyt...We turn now to concept of chirality that formed the basis of the story about Louis Pasteur in the beginning of this chapter. Recall that the term chiral, from the Greek work for 'hand', refers to anything which cannot be superimposed on its own mirror image.
  • https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/04%3A_Organic_Compounds_-_Cycloalkanes_and_their_Stereochemistry/4.03%3A_Cis-Trans_Isomerism_in_Cycloalkanes
    Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one cla...Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one class of molecules that exhibit stereoisomerism.  Di-substituted cycloalkane stereoisomers are designated by the nomenclature prefixes cis (Latin, meaning on this side) and trans (Latin, meaning across).
  • https://chem.libretexts.org/Courses/Fullerton_College/Introductory_Chemistry_for_Allied_Health_(Chan)/13%3A_Carbohydrates/13.03%3A_Conformations_and_Stereochemistry/13.3.01%3A_Chirality_and_stereoisomers
    We turn now to concept of chirality that formed the basis of the story about Louis Pasteur in the beginning of this chapter. Recall that the term chiral, from the Greek work for 'hand', refers to anyt...We turn now to concept of chirality that formed the basis of the story about Louis Pasteur in the beginning of this chapter. Recall that the term chiral, from the Greek work for 'hand', refers to anything which cannot be superimposed on its own mirror image.
  • https://chem.libretexts.org/Courses/can/CHEM_231%3A_Organic_Chemistry_I_Textbook/04%3A_Organic_Compounds_-_Cycloalkanes_and_their_Stereochemistry/4.04%3A_Cis-Trans_Isomerism_in_Cycloalkanes
    Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one cla...Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one class of molecules that exhibit stereoisomerism.  Di-substituted cycloalkane stereoisomers are designated by the nomenclature prefixes cis (Latin, meaning on this side) and trans (Latin, meaning across).
  • https://chem.libretexts.org/Courses/Chandler_Gilbert_Community_College/Fundamental_Organic_ala_Mech/03%3A_Representations_of_Molecules/3.04%3A_Conformations_of_Cycloalkanes/3.4.02%3A_Cis-Trans_Isomerism_in_Cycloalkanes
    Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one cla...Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one class of molecules that exhibit stereoisomerism.  Di-substituted cycloalkane stereoisomers are designated by the nomenclature prefixes cis (Latin, meaning on this side) and trans (Latin, meaning across).
  • https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_331_-_Organic_Chemistry_(Lund)/04%3A_Conformations_and_Stereochemistry/4.03%3A_Chirality_and_stereoisomers
    We turn now to concept of chirality that formed the basis of the story about Louis Pasteur in the beginning of this chapter. Recall that the term chiral, from the Greek work for 'hand', refers to anyt...We turn now to concept of chirality that formed the basis of the story about Louis Pasteur in the beginning of this chapter. Recall that the term chiral, from the Greek work for 'hand', refers to anything which cannot be superimposed on its own mirror image.
  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/04%3A_Organic_Compounds_-_Cycloalkanes_and_their_Stereochemistry/4.02%3A_Cis-Trans_Isomerism_in_Cycloalkanes
    Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one cla...Stereoisomers are molecules that have the same molecular formula, the same atom connectivity, but they differ in the relative spatial orientation of the atoms.  Di-substituted cycloalkanes are one class of molecules that exhibit stereoisomerism.  Di-substituted cycloalkane stereoisomers are designated by the nomenclature prefixes cis (Latin, meaning on this side) and trans (Latin, meaning across).

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