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  2. Bicyclic molecule - Wikipedia

    en.wikipedia.org/wiki/Bicyclic_molecule

    In bridged bicyclic compounds, the two rings share three or more atoms, separating the two bridgehead atoms by a bridge containing at least one atom. For example, norbornane, also known as bicyclo[2.2.1]heptane, can be viewed as a pair of cyclopentane rings each sharing three of their five carbon atoms. Camphor is a more elaborate example.

  3. Norbornane - Wikipedia

    en.wikipedia.org/wiki/Norbornane

    Norbornane (also known as bicyclo[2.2.1]heptane) is an organic compound and a saturated hydrocarbon with chemical formula C 7 H 12. It is a crystalline compound with a melting point of 88 °C . The carbon skeleton is derived from cyclohexane ring with a methylene bridge in the 1,4- position, and is a bridged bicyclic compound.

  4. Bicycloaromaticity - Wikipedia

    en.wikipedia.org/wiki/Bicycloaromaticity

    Bicycloaromaticity has been studied by others in relation to the bicyclo[3.2.2]nonatrienyl cation [5] [6] and in relation to specific carbanions. [7] In 2017 experimental evidence was reported for bicycloaromaticity (dual aromaticity) to exist in a bicyclic porphyrinoid .

  5. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    Structures and names of common heterocyclic compounds Pyridine, a heterocyclic compound. A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1]

  6. Bredt's rule - Wikipedia

    en.wikipedia.org/wiki/Bredt's_rule

    Bicyclo[5.3.1]undecane-11-one-1-carboxylic acid undergoes decarboxylation on heating to 132 °C, but the similar compound bicyclo[2.2.1]heptan-7-one-1-carboxylic acid remains stable beyond 500 °C, because the decarboxylation proceeds through an anti-Bredt enol.

  7. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.

  8. endo–exo isomerism - Wikipedia

    en.wikipedia.org/wiki/Endo–exo_isomerism

    The prefix endo is reserved for the isomer with the substituent located closest, or "syn", to the longest bridge. The prefix exo is reserved for the isomer with the substituent located farthest, or "anti", to the longest bridge. Here "longest" and "shortest" refer to the number of atoms that comprise the bridge.

  9. Category:Bicyclic compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Bicyclic_compounds

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