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  2. Heat of combustion - Wikipedia

    en.wikipedia.org/wiki/Heat_of_combustion

    That is, the heat of combustion, ΔH° comb, is the heat of reaction of the following process: C c H h N n O o (std.) + (c + h ⁄ 4 - o ⁄ 2) O 2 (g) → c CO 2 (g) + h ⁄ 2 H 2 O (l) + n ⁄ 2 N 2 (g) Chlorine and sulfur are not quite standardized; they are usually assumed to convert to hydrogen chloride gas and SO 2 or SO

  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. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    In organic chemistry, the cycloalkanes (also called naphthenes, but distinct from naphthalene) are the monocyclic saturated hydrocarbons. [1] In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains ), and all of the carbon-carbon bonds are single .

  5. Self-propagating high-temperature synthesis - Wikipedia

    en.wikipedia.org/wiki/Self-propagating_high...

    Reactions have been conducted in a vacuum and under both inert or reactive gases. The temperature of the reaction can be moderated by the addition of inert salt that absorbs heat in the process of melting or evaporation, such as sodium chloride, or by adding "chemical oven"—a highly exothermic mixture—to decrease the ratio of cooling. [9]

  6. Strain (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Strain_(chemistry)

    The simplest examples of angle strain are small cycloalkanes such as cyclopropane and cyclobutane, which are discussed below. Furthermore, there is often eclipsing or Pitzer strain in cyclic systems. These and possible transannular interactions were summarized early by H.C. Brown as internal strain, or I-Strain. [10]

  7. Cyclopropane - Wikipedia

    en.wikipedia.org/wiki/Cyclopropane

    One theory invokes σ-aromaticity: the stabilization afforded by delocalization of the six electrons of cyclopropane's three C-C σ bonds to explain why the strain of cyclopropane is "only" 27.6 kcal/mol as compared to cyclobutane (26.2 kcal/mol) with cyclohexane as reference with E str =0 kcal/mol, [18] [19] [20] in contrast to the usual π ...

  8. 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.

  9. Thermochemistry - Wikipedia

    en.wikipedia.org/wiki/Thermochemistry

    Thermochemistry is the study of the heat energy which is associated with chemical reactions and/or phase changes such as melting and boiling. A reaction may release or absorb energy, and a phase change may do the same. Thermochemistry focuses on the energy exchange between a system and its surroundings in the form of heat. Thermochemistry is ...