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  2. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    As such, cyclobutane is unstable above about 500 °C. The four carbon atoms in cyclobutane are not coplanar; instead, the ring typically adopts a folded or "puckered" conformation. [2] This implies that the C-C-C angle is less than 90°. One of the carbon atoms makes a 25° angle with the plane formed by the other three carbons.

  3. Ring strain - Wikipedia

    en.wikipedia.org/wiki/Ring_strain

    The simplest examples of angle strain are small cycloalkanes such as cyclopropane and cyclobutane. Ring strain energy can be attributed to the energy required for the distortion of bond and bond angles in order to close a ring. [3] Ring strain energy is believed to be the cause of accelerated rates in altering ring reactions.

  4. Bent bond - Wikipedia

    en.wikipedia.org/wiki/Bent_bond

    Cyclobutane is a larger ring, but still has bent bonds. In this molecule, the carbon bond angles are 90° for the planar conformation and 88° for the puckered one. Unlike in cyclopropane, the C–C bond lengths actually increase rather than decrease; this is mainly due to 1,3-nonbonded steric repulsion.

  5. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    An example of a common name is terpineol, the name of which can tell us only that it is an alcohol (because the suffix "-ol" is in the name) and it should then have a hydroxyl group (–OH) attached to it. The IUPAC naming system for organic compounds can be demonstrated using the example provided in the adjacent image.

  6. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    Rings may vary in size from three to many atoms, and include examples where all the atoms are carbon (i.e., are carbocycles), none of the atoms are carbon (inorganic cyclic compounds), or where both carbon and non-carbon atoms are present (heterocyclic compounds with rings containing both carbon and non-carbon).

  7. Cope rearrangement - Wikipedia

    en.wikipedia.org/wiki/Cope_rearrangement

    The transition state of the molecule passes through a boat or chair like transition state. An example of the Cope rearrangement is the expansion of a cyclobutane ring to a cycloocta-1,5-diene ring: In this case, the reaction must pass through the boat transition state to produce the two cis double bonds.

  8. Are Seed Oils Really Unhealthy? Dietitians Explain. - AOL

    www.aol.com/seed-oils-really-unhealthy...

    For example, oil might undergo a bleaching and refining phase to remove any odors and colors, but that doesn't mean you're finding bleach in your oil.

  9. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron.The bond angles are arccos(− ⁠ 1 / 3 ⁠) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane (CH 4) [1] [2] as well as its heavier analogues.