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  2. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...

  3. Tautomer - Wikipedia

    en.wikipedia.org/wiki/Tautomer

    Tautomerization is pervasive in organic chemistry. [ 2 ] [ 7 ] It is typically associated with polar molecules and ions containing functional groups that are at least weakly acidic. Most common tautomers exist in pairs, which means that the hydrogen is located at one of two positions, and even more specifically the most common form involves a ...

  4. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    Isomers do not necessarily share similar chemical or physical properties. Two main forms of isomerism are structural (or constitutional) isomerism, in which bonds between the atoms differ; and stereoisomerism (or spatial isomerism), in which the bonds are the same but the relative positions of the atoms differ. Isomeric relationships form a ...

  5. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    In organic chemistry, a rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule. [1] Often a substituent moves from one atom to another atom in the same molecule, hence these reactions are usually intramolecular. In the example below ...

  6. Metamerism (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Metamerism_(Chemistry)

    The isomers which have been cited as examples of metamers in chemical literature consist primarily of ethers; [3] but this could by the same reasoning be extended to thioethers, secondary as well as tertiary amines, esters, secondary as well as tertiary amides, (mixed) acid anhydrides etc. Metamers in organic chemistry

  7. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    In organic chemistry, two molecules are valence isomers when they are constitutional isomers that can interconvert through pericyclic reactions. [ 1 ] [ 2 ] Benzene

  8. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In chemistry, isomerization or isomerisation is the process in which a molecule, polyatomic ion or molecular fragment is transformed into an isomer with a different chemical structure. [1] Enolization is an example of isomerization, as is tautomerization. [2] When the isomerization occurs intramolecularly it may be called a rearrangement reaction.

  9. Isotopomer - Wikipedia

    en.wikipedia.org/wiki/Isotopomer

    Isotopomers or isotopic isomers are isomers with isotopic atoms, having the same number of each isotope of each element but differing in their positions in the molecule. The result is that the molecules are either constitutional isomers or stereoisomers solely based on isotopic location.