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  2. C4H8 - Wikipedia

    en.wikipedia.org/wiki/C4H8

    The molecular formula C 4 H 8 (molar mass: 56.11 g/mol) may refer to: Butenes (butylenes) 1-Butene, or 1-butylene; 2-Butene; Isobutylene; Cyclobutane; Methylcyclopropane

  3. Isobutylene - Wikipedia

    en.wikipedia.org/wiki/Isobutylene

    Isobutylene is used in the production of a variety of products. It is alkylated with butane to produce isooctane or dimerized to diisobutylene (DIB) and then hydrogenated to make isooctane, a fuel additive.

  4. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    alkyne (unsaturated) vs alkane (saturated) arene (unsaturated) vs cycloalkane (saturated) For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are: carbonyl, e.g. ketones, aldehydes, esters, carboxylic acids (unsaturated) vs alcohol or ether (saturated) nitrile ...

  5. 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.

  6. Butadiene - Wikipedia

    en.wikipedia.org/wiki/Butadiene

    Overall, there is a barrier of 24.8 kJ/mol (5.9 kcal/mol) for isomerization between the two conformers. [23] This increased rotational barrier and strong overall preference for a near-planar geometry is evidence for a delocalized π system and a small degree of partial double bond character in the C–C single bond, in accord with resonance theory.

  7. Degree of unsaturation - Wikipedia

    en.wikipedia.org/wiki/Degree_of_unsaturation

    For hydrocarbons, the DBE (or IHD) tells us the number of rings and/or extra bonds in a non-saturated structure, which equals the number of hydrogen pairs that are required to make the structure saturated, simply because joining two elements to form a ring or adding one extra bond (e.g., a single bond changed to a double bond) in a structure reduces the need for two H's.

  8. Artist behind DJ Burns mural at NC State celebrates an ... - AOL

    www.aol.com/news/artist-behind-dj-burns-mural...

    The mural, painted outside the Free Expression Tunnel on campus, is based on a portrait of Burns taken by a News & Observer photojournalist. Artist behind DJ Burns mural at NC State celebrates an ...

  9. N-Acylethanolamine - Wikipedia

    en.wikipedia.org/wiki/N-Acylethanolamine

    General chemical structure of N-acylethanolamines. An N-acylethanolamine (NAE) is a type of fatty acid amide where one of several types of acyl groups is linked to the nitrogen atom of ethanolamine, and highly metabolic formed by intake of essential fatty acids through diet by 20:4, n-6 and 22:6, n-3 fatty acids, [1] [2] and when the body is physically and psychologically active,.