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  2. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    [citation needed] The π-bond in the ethylene molecule is responsible for its useful reactivity. The double bond is a region of high electron density, thus it is susceptible to attack by electrophiles. Many reactions of ethylene are catalyzed by transition metals, which bind transiently to the ethylene using both the π and π* orbitals.

  3. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Shell OMEGA technology (Only Mono-Ethylene Glycol Advantage) is a two-step synthesis of ethylene carbonate using a phosphonium halide as a catalyst. The glycol yield is 99–99.5%, with other glycols practically absent. The main advantage of the process is production of pure ethylene glycol without the need for further purification.

  4. Electrochemical reduction of carbon dioxide - Wikipedia

    en.wikipedia.org/wiki/Electrochemical_reduction...

    The electrochemical reduction of carbon dioxide, also known as CO2RR, is the conversion of carbon dioxide (CO 2) to more reduced chemical species using electrical energy. It represents one potential step in the broad scheme of carbon capture and utilization.

  5. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    Another key step in the Wacker process is the migration of the hydrogen from oxygen to chloride and formation of the C-O double bond. This step is generally thought to proceed through a so-called β-hydride elimination with a cyclic four-membered transition state: Wacker hydride elimination

  6. Methanizer - Wikipedia

    en.wikipedia.org/wiki/Methanizer

    Methanizer is an appliance used in gas chromatography (GC), which allows the user to detect very low concentrations of carbon monoxide and carbon dioxide.It consists of a flame ionization detector, preceded by a hydrogenating reactor, which converts CO 2 and CO into methane CH 4.

  7. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    The minimum energy to produce a 360° bond rotation is called the rotational barrier. Ethane gives a classic, simple example of such a rotational barrier, sometimes called the "ethane barrier". Among the earliest experimental evidence of this barrier (see diagram at left) was obtained by modelling the entropy of ethane. [ 16 ]

  8. Ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/Ethylenediamine

    Ethylenediamine (abbreviated as en when a ligand) is the organic compound with the formula C 2 H 4 (NH 2) 2.This colorless liquid with an ammonia-like odor is a basic amine.It is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998. [6]

  9. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    Instead, the slow step involves two molecules of NO 2. A possible mechanism for the overall reaction that explains the rate law is: 2 NO 2 → NO 3 + NO (slow) NO 3 + CO → NO 2 + CO 2 (fast) Each step is called an elementary step, and each has its own rate law and molecularity. The sum of the elementary steps gives the net reaction.