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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.
Alkanes have the general chemical formula C n H 2n+2. The alkanes range in complexity from the simplest case of methane (CH 4), where n = 1 (sometimes called the parent molecule), to arbitrarily large and complex molecules, like pentacontane (C 50 H 102) or 6-ethyl-2-methyl-5-(1-methylethyl) octane, an isomer of tetradecane (C 14 H 30).
The formula for acyclic saturated hydrocarbons (i.e., alkanes) is C n H 2n+2. [1]: 623 The most general form of saturated hydrocarbons, (whether linear or branched species, and whether with or without one or more rings) is C n H 2n+2(1-r), where r is the number of rings. Those with exactly one ring are the cycloalkanes.
Carboxylic acids, ketones, epoxides, and alcohols are often obtained by partial oxidation of alkanes and alkenes with dioxygen. These intermediates are essential to the production of consumer goods. Partial oxidation is challenging because the most favored reaction between oxygen and hydrocarbons is combustion.
The naming of polycyclic alkanes such as bicyclic alkanes and spiro alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings ( "bicyclo-" or "spiro-"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of ...
Alkanes as substituents are called alkyl groups Subcategories. This category has the following 5 subcategories, out of 5 total. B. Butane (2 C, 11 P) E. Ethane (1 C ...
Dehydrogenation is important, both as a useful reaction and a serious problem. At its simplest, it's a useful way of converting alkanes, which are relatively inert and thus low-valued, to olefins, which are reactive and thus more valuable. Alkenes are precursors to aldehydes (R−CH=O), alcohols (R−OH), polymers, and aromatics. [1]
Alkenes react with hydrogen chloride (HCl) to give alkyl chlorides. For example, the industrial production of chloroethane proceeds by the reaction of ethylene with HCl: H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 ...
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