Rhodium-catalyzed hydrogenation: Rhodium catalyzed hydrogenation is a chemical reaction that typically involves the addition of pairs of hydrogen atoms to another compound or element in the presence of a Rhodium complex catalyst. The addition of hydrogen to double or triple bonds in hydrocarbons is a type of redox reaction that can be thermodynamically favorable without a catalyst.Iridium(III) chlorideRhodium(III) chlorideOrganoruthenium chemistry: Organoruthenium chemistry is the chemistry of organometallic compounds containing a carbon to ruthenium chemical bond.Synthesis of Organometallic Compounds: A Practical Guide Sanshiro Komiya Ed.Acid catalysis: In acid catalysis and base catalysis a chemical reaction is catalyzed by an acid or a base. The acid is the proton donor and the base is the proton acceptor.Sharpless asymmetric dihydroxylation: Sharpless asymmetric dihydroxylation (also called the Sharpless bishydroxylation) is the chemical reaction of an alkene with osmium tetroxide in the presence of a chiral quinine ligand to form a vicinal diol.Hydroacylation: Hydroacylation is a type of organic reaction in which an aldehyde is added over an alkene or alkyne bond. The reaction product is a ketone.Aluminium phosphide poisoning: Acute aluminium phosphide poisoning (AAlPP) is a large, though under-reported, problem in the Indian subcontinent. Aluminium phosphide (AlP), which is readily available as a fumigant for stored cereal grains, sold under various brand names such as QuickPhos and Celphos, is highly toxic, especially when consumed from a freshly opened container.Hexene: Hexene is an alkene with a molecular formula C6H12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the "-ene" suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond.Palladium(II) chloridePrimary alcoholAlkyne: In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond between two carbon atoms.Alkyne.DiketoneNitrenium ion: A nitrenium ion (also called: aminylium ion) in organic chemistry is a reactive intermediate based on nitrogen with both an electron lone pair and a positive charge and with two substituents (R2N+).Reactive Intermediate Chemistry, Moss, Platz, & Jones (eds.Organosulfur compounds: Organosulfur compounds are organic compounds that contain sulfur. They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.Outline of organic chemistry: The following outline is provided as an overview of and topical guide to organic chemistry:Hydrogen gas porosity: Hydrogen gas porosity is an aluminium casting defect under the form of a porosity or void in an aluminium casting caused by a high level of hydrogen gas (H2) dissolved in the aluminium at liquid phase. Because the solubility of hydrogen in solid aluminium is much smaller than in liquid aluminium, when the aluminium freezes, the dissolved hydrogen gas creates porosity in solid aluminium.Fatty aldehyde: A fatty aldehyde is an aldehyde with a "fatty" aliphatic carbon chain attached that is typically eight carbon or more in length. In contrast, phenolic aldehydes are aromatic.Phylactolaemata: PhylactolaemataBiological Greek: phylax, "protect, guard" + laema, "throat": "provided with a protective throat" is a class of the phylum Bryozoa whose members live only in freshwater environments. Like all bryozoans, they filter feed by means of an extensible "crown" of ciliated tentacles called a lophophore.Lithium 12-hydroxystearateLepidineConvergent synthesis: In chemistry a convergent synthesis is a strategy that aims to improve the efficiency of multistep synthesis, most often in organic synthesis. In this type of synthesis several individual pieces of a complex molecule are synthesised in stage one and then in stage two these pieces are combined to form the final product Organic Synthesis, 3th Ed.Outline of chemical engineering: The following outline is provided as an overview of and topical guide to chemical engineering:Stilbene photocyclization: Stilbene photocyclization is the coupling of two aromatic carbons in stilbenes upon ultraviolet irradiation. The reaction can be used to form polycyclic aromatic hydrocarbons and heteroaromatics.DopastinMetallocene: A metallocene is a compound typically consisting of two cyclopentadienyl anions (Cp, which is C5H5−) bound to a metal center (M) in the oxidation state II, with the resulting general formula (C5H5)2M. Closely related to the metallocenes are the metallocene derivatives, e.