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  2. Nierenstein reaction - Wikipedia

    en.wikipedia.org/wiki/Nierenstein_reaction

    The unreactive diazoketone can be re-activated and reacted by treatment with hydrogen chloride to give the normal Nierenstein product. The Nierenstein reaction mechanism. In some cases, even limiting the amount of diazomethane gives a reaction process that stalls via the neutral diazoketone pathway, requiring the addition of HCl gas to rescue ...

  3. Biological carbon fixation - Wikipedia

    en.wikipedia.org/wiki/Biological_carbon_fixation

    This is known as carbon isotope discrimination and results in carbon-12 to carbon-13 ratios in the plant that are higher than in the free air. Measurement of this isotopic ratio is important in the evaluation of water use efficiency in plants, [32] [33] [34] and also in assessing the possible or likely sources of carbon in global carbon cycle ...

  4. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    The general mechanism is shown below. The resonating arrow (1) shows a resonance contributor of the diazo compound with a lone pair of electrons on the carbon adjacent to the nitrogen. The diazo compound then does a nucleophilic attack on the carbonyl-containing compound (nucleophilic addition), producing a tetrahedral intermediate (2).

  5. Carbon-carbon bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon-carbon_bond_activation

    Carbon-carbon bond activation refers to the breaking of carbon-carbon bonds in organic molecules. This process is an important tool in organic synthesis , as it allows for the formation of new carbon-carbon bonds and the construction of complex organic molecules. [ 1 ]

  6. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    The mechanism for the Pd-catalyzed C-H activation reactions of 2-phenylpyridine involves a metallacycle intermediate. The intermediate is oxidized to form a Pd IV species, followed by reductive elimination to form the C-O bond and release the product. [18] Mechanism for Pd-catalyzed C-H activation

  7. Insertion reaction - Wikipedia

    en.wikipedia.org/wiki/Insertion_reaction

    The oxidative addition reaction of methyl iodide with (1) involves the formal insertion of the iridium(I) centre into the carbon-iodine bond, whereas step (3) to (4) is an example of migratory insertion of carbon monoxide into the iridium-carbon bond.

  8. CH2N2 - Wikipedia

    en.wikipedia.org/wiki/CH2N2

    CH 2 N 2 may refer to: . Cyanamide, an organic compound; Diazirine, class of organic molecules with a cyclopropene-like ring, 3H-diazirene; Diazomethane, chemical compound discovered in 1894

  9. Carbon cycle - Wikipedia

    en.wikipedia.org/wiki/Carbon_cycle

    Ocean mixed layer carbon, c m, is the only explicitly modelled ocean stock of carbon; though to estimate carbon cycle feedbacks the total ocean carbon is also calculated. [ 107 ] Current trends in climate change lead to higher ocean temperatures and acidity , thus modifying marine ecosystems. [ 108 ]