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About 12 results
  • https://chem.libretexts.org/Courses/Chandler_Gilbert_Community_College/Fundamental_Organic_ala_Mech/03%3A_Representations_of_Molecules/3.06%3A_A_Review_of_Isomerism
    We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another (Figure 5.15). There are two fundamental types of isomers, both o...We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another (Figure 5.15). There are two fundamental types of isomers, both of which we’ve now encountered: constitutional isomers and stereoisomers. Among the kinds of constitutional isomers we’ve seen are skeletal, functional, and positional isomers. Among the kinds of stereoisomers we’ve seen are enantiomers, diastereomers, and cis–trans isomers of cycloalkanes.
  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Morsch_et_al.)/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.09%3A_A_Review_of_Isomerism
    b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the...b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the pi bond between carbons 2 & 3, there is not free rotation between the C2-C3 bond so the structure on the left has the carbon chains on the same side of the double bond (cis) and the structure on the right has the carbon chains on opposite sides of the double bond (trans).
  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.09%3A_A_Review_of_Isomerism
    As noted on several previous occasions, isomers are compounds with the same chemical formula but different structures. We’ve seen several kinds of isomers in the past few chapters, and it’s a good ide...As noted on several previous occasions, isomers are compounds with the same chemical formula but different structures. We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another.
  • https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.10%3A_A_Review_of_Isomerism
    We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another (Figure 5.15). There are two fundamental types of isomers, both o...We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another (Figure 5.15). There are two fundamental types of isomers, both of which we’ve now encountered: constitutional isomers and stereoisomers. Among the kinds of constitutional isomers we’ve seen are skeletal, functional, and positional isomers. Among the kinds of stereoisomers we’ve seen are enantiomers, diastereomers, and cis–trans isomers of cycloalkanes.
  • https://chem.libretexts.org/Ancillary_Materials/Worksheets/Worksheets%3A_Inorganic_Chemistry/Structure_and_Reactivity_in_Organic_Biological_and_Inorganic_Chemistry/Chem_125_Worksheets/13%3A_Conformations_(Workshop)
    To get the correct stereochemistry, the substituents must be in the correct order around the ring AND in the correct Up/Down position. The student looked up the structures in CSB stockroom inventory a...To get the correct stereochemistry, the substituents must be in the correct order around the ring AND in the correct Up/Down position. The student looked up the structures in CSB stockroom inventory and found more than one entry for 1,3 cyclohexanediol shown below. (The “diol” portion of the name indicates that there are two OH groups attached to the ring.)
  • https://chem.libretexts.org/Courses/Smith_College/CHM_222_Chemistry_II%3A_Organic_Chemistry_(2025)/13%3A_Stereochemistry_at_Tetrahedral_Centers/13.10%3A_A_Review_of_Isomerism
    b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the...b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the pi bond between carbons 2 & 3, there is not free rotation between the C2-C3 bond so the structure on the left has the carbon chains on the same side of the double bond (cis) and the structure on the right has the carbon chains on opposite sides of the double bond (trans).
  • https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introduction_to_Organic_and_Biochemistry_(Malik)/03%3A_Stereochemistry/3.02%3A_Confirmations
    Representing conformations of simple organic molecules, including ethane and butane, by Sawhorse and Newman projections, drawing chair conformations of cyclohexane and substituted cyclohexane, and rel...Representing conformations of simple organic molecules, including ethane and butane, by Sawhorse and Newman projections, drawing chair conformations of cyclohexane and substituted cyclohexane, and relative stability of the conformational isomers are described.
  • https://chem.libretexts.org/Courses/Thompson_Rivers_University/CHEM_1500%3A_Chemical_Bonding_and_Organic_Chemistry/08%3A_Organic_Chemistry_II_-_Stereochemistry/8.01%3A_Types_of_Isomers
    b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the...b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the pi bond between carbons 2 & 3, there is not free rotation between the C2-C3 bond so the structure on the left has the carbon chains on the same side of the double bond (cis) and the structure on the right has the carbon chains on opposite sides of the double bond (trans).
  • https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.10%3A_A_Review_of_Isomerism
    b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the...b) ) Since both structures have the same formula (C 4 H 8 ) and the same connectivity they are stereoisomers since they differ in what is known as cis/trans isomerism (covered more in Ch 7).Due to the pi bond between carbons 2 & 3, there is not free rotation between the C2-C3 bond so the structure on the left has the carbon chains on the same side of the double bond (cis) and the structure on the right has the carbon chains on opposite sides of the double bond (trans).
  • https://chem.libretexts.org/Courses/can/CHEM_231%3A_Organic_Chemistry_I_Textbook/05%3A_Stereochemistry_at_Tetrahedral_Centers/5.10%3A_A_Review_of_Isomerism
    We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another (Figure \PageIndex1). There are two fundamental types of is...We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another (Figure \PageIndex1). There are two fundamental types of isomers, both of which we’ve now encountered: constitutional isomers and stereoisomers. Among the kinds of stereoisomers we’ve seen are enantiomers, diastereomers, and cis–trans isomers of cycloalkanes.
  • https://chem.libretexts.org/Workbench/Pick_Your_Poison%3A_Introduction_to_Materials_Toxicology/22%3A_Stereochemistry_at_Tetrahedral_Centers/22.10%3A_A_Review_of_Isomerism
    As noted on several previous occasions, isomers are compounds with the same chemical formula but different structures. We’ve seen several kinds of isomers in the past few chapters, and it’s a good ide...As noted on several previous occasions, isomers are compounds with the same chemical formula but different structures. We’ve seen several kinds of isomers in the past few chapters, and it’s a good idea at this point to see how they relate to one another.

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