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  2. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    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. Four-carbon molecule - Wikipedia

    en.wikipedia.org/wiki/Four-carbon_molecule

    Four-carbon molecules are based on a skeleton made from four carbon atoms. They may be in a chain, branched chains, cycles or even bicyclic compounds C 4 H 4 isomers with CAS registry numbers

  4. Chemical equation - Wikipedia

    en.wikipedia.org/wiki/Chemical_equation

    A chemical equation is the symbolic representation of a chemical reaction in the form of symbols and chemical formulas.The reactant entities are given on the left-hand side and the product entities are on the right-hand side with a plus sign between the entities in both the reactants and the products, and an arrow that points towards the products to show the direction of the reaction. [1]

  5. Hydroperoxyl - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxyl

    The molecule has a bent structure. [3] The superoxide anion, • O − 2, and the hydroperoxyl radical exist in equilibrium in aqueous solution: • O − 2 + H 2 O ⇌ HO • 2 + HO −. The pK a of HO 2 is 4.88. Therefore, about 0.3% of any superoxide present in the cytosol of a typical cell is in the protonated form. [4] It oxidizes nitric ...

  6. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The numbering of the molecule is based on the ketone groups. When numbering from left to right, the ketone groups are numbered 3 and 9. When numbering from right to left, the ketone groups are numbered 15 and 21. 3 is less than 15, therefore the ketones are numbered 3 and 9. The smaller number is always used, not the sum of the constituents ...

  7. Decarboxylation - Wikipedia

    en.wikipedia.org/wiki/Decarboxylation

    Decarboxylations are pervasive in biology. They are often classified according to the cofactors that catalyze the transformations. [11] Biotin-coupled processes effect the decarboxylation of malonyl-CoA to acetyl-CoA. Thiamine (T:) is the active component for decarboxylation of alpha-ketoacids, including pyruvate: T: + RC(O)CO 2 H → T=C(OH)R ...

  8. Chemical synthesis - Wikipedia

    en.wikipedia.org/wiki/Chemical_synthesis

    Chemical synthesis employs various strategies to achieve efficient, precise, and molecular transformations that are more complex than simply converting a reactant A to a reaction product B directly. These strategies can be grouped into approaches for managing reaction sequences. Reaction Sequences:

  9. Ribbon diagram - Wikipedia

    en.wikipedia.org/wiki/Ribbon_diagram

    Ribbon diagrams are simple yet powerful, expressing the visual basics of a molecular structure (twist, fold and unfold). This method has successfully portrayed the overall organization of protein structures, reflecting their three-dimensional nature and allowing better understanding of these complex objects both by expert structural biologists ...