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  2. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    The oldest organic reactions are combustion of organic fuels and saponification of fats to make soap. Modern organic chemistry starts with the Wöhler synthesis in 1828. In the history of the Nobel Prize in Chemistry awards have been given for the invention of specific organic reactions such as the Grignard reaction in 1912, the Diels–Alder ...

  3. Saturated and unsaturated compounds - Wikipedia

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

    alkene (unsaturated) vs alkane (saturated) 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 ...

  4. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    Combustion of hydrocarbons is the main source of the world's energy. Petroleum is the dominant raw-material source for organic commodity chemicals such as solvents and polymers. Most anthropogenic (human-generated) emissions of greenhouse gases are either carbon dioxide released by the burning of fossil fuels , or methane released from the ...

  5. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. [1] Alkanes have the general chemical formula C n H 2n+2.

  6. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In certain kinds of alkene polymerization reactions, chain walking is an isomerization process that introduces branches into growing polymers. [citation needed] The trans isomer of resveratrol can be converted to the cis isomer in a photochemical reaction. [6] Thermal rearrangement of azulene to naphthalene has been observed. [7]

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    A 3D model of ethylene, the simplest alkene. In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. [1] The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins.

  8. Organic redox reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_redox_reaction

    Organic redox reactions: the Birch reduction. Organic reductions or organic oxidations or organic redox reactions are redox reactions that take place with organic compounds.In organic chemistry oxidations and reductions are different from ordinary redox reactions, because many reactions carry the name but do not actually involve electron transfer. [1]

  9. Combustion - Wikipedia

    en.wikipedia.org/wiki/Combustion

    The flames caused as a result of a fuel undergoing combustion (burning) Air pollution abatement equipment provides combustion control for industrial processes.. Combustion, or burning, [1] is a high-temperature exothermic redox chemical reaction between a fuel (the reductant) and an oxidant, usually atmospheric oxygen, that produces oxidized, often gaseous products, in a mixture termed as smoke.