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  2. Bicyclobutane - Wikipedia

    en.wikipedia.org/wiki/Bicyclobutane

    The intermediate 1-bromo-3-chlorocyclobutane can also be prepared via a modified Hunsdiecker reaction from 3-chlorocyclobutanecarboxylic acid using mercuric oxide and bromine: [4] A synthetic approach to bicyclobutane derivatives involves ring closure of a suitably substituted 2-bromo-1-(chloromethyl)cyclopropane with magnesium in THF. [5]

  3. Bicyclic molecule - Wikipedia

    en.wikipedia.org/wiki/Bicyclic_molecule

    The numbers are sometimes omitted in unambiguous cases. For example, bicyclo[1.1.0]butane is typically called simply bicyclobutane. The heterocyclic molecule DABCO has a total of 8 atoms in its bridged structure, hence the root name octane. Here the two bridgehead atoms are nitrogen instead of carbon atoms.

  4. Intermediate agricultural product - Wikipedia

    en.wikipedia.org/wiki/Intermediate_agricultural...

    Applied to trade policy, intermediate products are one of three categories of agricultural products used by the Foreign Agricultural Service to report export and import data under its BICO system (the others are bulk and consumer-oriented agricultural products).

  5. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    Cyclobutane is a cycloalkane and organic compound with the formula (CH 2) 4.Cyclobutane is a colourless gas and is commercially available as a liquefied gas.Derivatives of cyclobutane are called cyclobutanes.

  6. Category:Bicycloalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Bicycloalkanes

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  7. Cyclobutanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclobutanecarboxylic_acid

    Cyclobutanecarboxylic acid is an intermediate in organic synthesis. For example, it is a precursor to cyclobutylamine. For example, it is a precursor to cyclobutylamine. [ 3 ]

  8. Ring strain - Wikipedia

    en.wikipedia.org/wiki/Ring_strain

    In alkanes, optimum overlap of atomic orbitals is achieved at 109.5°. The most common cyclic compounds have five or six carbons in their ring. [6] Adolf von Baeyer received a Nobel Prize in 1905 for the discovery of the Baeyer strain theory, which was an explanation of the relative stabilities of cyclic molecules in 1885.

  9. Cyclobutanol - Wikipedia

    en.wikipedia.org/wiki/Cyclobutanol

    Cyclobutanol is an organic compound with the chemical formula C 4 H 8 O; it is defined as a cyclobutyl group with a hydroxyl group pendant and thus a cycloalkanol. Physically, it is a yellowish clear liquid [1] that crystallizes orthorhombically at low-temperatures.