Oxidation States of Organic Compounds

Oxidation States of Organic Chemical Compounds, Oxidation Numbers in Organic Chemical Compounds, and Organic Chemical Redox Reactions... 

Some Oxidation States of Sulfur Compounds and Their Organic Analogues (Only compounds with one or two sulfur atoms in the molecule are listed.)... 

Given a nitrogen containing organic compound such as an amide a nitnle or a nitro compound how is the correct oxidation state of the desired amine to be achieved" ... 

Many mercury compounds are labile and easily decomposed by light, heat, and reducing agents. In the presence of organic compounds of weak reducing activity, such as amines (qv), aldehydes (qv), and ketones (qv), compounds of lower oxidation state and mercury metal are often formed. Only a few mercury compounds, eg, mercuric bromide/77< 5 7-/7, mercurous chloride, mercuric s A ide[1344-48-5] and mercurous iodide [15385-57-6] are volatile and capable of purification by sublimation. This innate lack of stabiUty in mercury compounds makes the recovery of mercury from various wastes that accumulate with the production of compounds of economic and commercial importance relatively easy (see Recycling). 

The most common oxidation state of niobium is +5, although many anhydrous compounds have been made with lower oxidation states, notably +4 and +3, and Nb can be reduced in aqueous solution to Nb by zinc. The aqueous chemistry primarily involves halo- and organic acid anionic complexes. Virtually no cationic chemistry exists because of the irreversible hydrolysis of the cation in dilute solutions. Metal—metal bonding is common. Extensive polymeric anions form. Niobium resembles tantalum and titanium in its chemistry, and separation from these elements is difficult. In the soHd state, niobium has the same atomic radius as tantalum and essentially the same ionic radius as well, ie, Nb Ta = 68 pm. This is the same size as Ti ... 

The most common oxidation states and the corresponding electronic configuration of mthenium are +2 and +3 (t5 ). Compounds are usually octahedral. Compounds in oxidations states from —2 and 0 (t5 ) to +8 have various coordination geometries. Important appHcations of mthenium compounds include oxidation of organic compounds and use in dimensionally stable anodes (DSA). 

The +3 oxidation state is exhibited by bismuth in the vast majority of its compounds. A few inorganic and a variety of organic compounds, however, contain the element in the +5 state. Other rarer oxidation states reported for bismuth include +2, +1, and —3. Bismuth also forms polynuclear ionic species with oxidation states that ate usually fractional and range from —1 to +1. 

Indeed, these reactions proceed at 25 °C in ethanol-aqueous media in the absence of transition metal catalysts. The ease with which P-H bonds in primary phosphines can be converted to P-C bonds, as shown in Schemes 9 and 10, demonstrates the importance of primary phosphines in the design and development of novel organophosphorus compounds. In particular, functionalized hydroxymethyl phosphines have become ubiquitous in the development of water-soluble transition metal/organometallic compounds for potential applications in biphasic aqueous-organic catalysis and also in transition metal based pharmaceutical development [53-62]. Extensive investigations on the coordination chemistry of hydroxymethyl phosphines have demonstrated unique stereospe-cific and kinetic propensity of this class of water-soluble phosphines [53-62]. Representative examples outlined in Fig. 4, depict bidentate and multidentate coordination modes and the unique kinetic propensity to stabilize various oxidation states of metal centers, such as Re( V), Rh(III), Pt(II) and Au(I), in aqueous media [53 - 62]. Therefore, the importance of functionalized primary phosphines in the development of multidentate water-soluble phosphines cannot be overemphasized. 

The various oxidation states of sulfur have been determined by polarography. The electrochemical oxidation of sulfide ions in aqueous solution may lead to the production of elementary sulfur, polysulfides, sulfate, dithionate, and thiosulfate, depending on the experimental conditions. Disulfides, sulfoxides, and sulfones are typical polarographically active organic compounds. It is also found that thiols (mer-captans), thioureas, and thiobarbiturates facilitate oxidation of Hg resulting thus in anodic waves. 

At pulp and paper mills, air emissions from both process and combustion units are regulated under the National Ambient Air Quality Standards (NAAQS) and the State Implementation Plans (SIP) that enforce the standards. States may implement controls to limit emissions of particulate matter (PM), nitrogen oxides (NO ), volatile organic compounds (VOCs), and sulfur dioxide (S02). 

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