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  • ...ally prepared by the reaction between an amine group and a carboxylic acid halide group. Simple AB homopolymers may look like: ...sub>2</sub>)) to occupy the [[hydrogen bond]]s of the amide groups, and an organic component ([[Methylpyrrolidone|N-methyl pyrrolidone (NMP)]]) to dissolve th
    10 KB (1,313 words) - 10:07, 20 September 2010
  • ...nic Compounds (Recommendations 1993)] IUPAC, Commission on Nomenclature of Organic Chemistry, 1993, Blackwell Scientific</ref>). The difference in names betwe ...mist [[Karl Ziegler]] developed a catalytic system based on [[titanium]] [[halide]]s and organoaluminium compounds that worked at even milder conditions than
    20 KB (2,802 words) - 10:11, 20 September 2010
  • ...aracteristic of aromatic compounds. Aniline is colorless, but it slowly [[organic oxidation|oxidizes]] and resinifies in air, giving a red-brown tint to aged ...ediates, aniline can be conveniently converted to -OH, -CN, or a [[halogen|halide]] via [[Sandmeyer reaction]]s.
    14 KB (2,008 words) - 13:10, 20 September 2010
  • '''Ethylene oxide''', also called '''oxirane''', is the [[organic compound]] with the [[chemical formula|formula]] C<sub>2</sub>H<sub>4</sub> ...ref> Wurtz mistakenly assumed that ethylene oxide has the properties of an organic base. This delusion lasted until 1896 when [[Georg Bredig]] found that ethy
    82 KB (11,709 words) - 21:31, 20 September 2010
  • ...13>{{cite journal|author= David R. Lide, ed.|title= "Physical Constants of Organic Compounds", in CRC Handbook of Chemistry and Physics, Internet Version 2005 '''Benzene''' is an [[organic compound|organic]] [[chemical compound]] with the molecular formula [[Carbon|C]]<sub>6</sub>
    45 KB (6,444 words) - 21:33, 20 September 2010
  • ...ompounds that are usually called chlorides. Chlorine gas reacts with most organic compounds, and will even sluggishly support the combustion of [[hydrocarbon ..."|−1 || chlorides || align="center"|Cl<sup>−</sup> || ionic chlorides, organic chlorides, hydrochloric acid
    36 KB (5,155 words) - 21:35, 20 September 2010
  • ...lead are easily reduced to the metal. An example is heating PbO with mild organic reducing agents such as glucose. A mixture of the oxide and the sulfide hea ...acid|acetic]] acids, from which solutions it is possible to precipitate [[halide]], [[lead sulfate|sulfate]], [[lead chromate|chromate]], [[lead carbonate|c
    52 KB (7,694 words) - 21:36, 20 September 2010
  • ...salt. Another example involves iron(III) which forms weak complexes with [[halide]] and other anions, but not with [[perchlorate]] ions. ...the aqueous reaction mixture, so that the oxidation reaction occurs in the organic phase.
    50 KB (7,450 words) - 20:16, 21 September 2010
  • ...sub>2</sub>S]], [[hydrogen telluride|H<sub>2</sub>Te]], and the [[hydrogen halide|hydrohalic acids]]. However, Davy failed to develop a new theory, concludin ...s 1838</ref> based on his extensive works on the chemical composition of [[organic acid]]s. This finished the doctrinal shift from oxygen-based acids to hydro
    29 KB (4,415 words) - 20:17, 21 September 2010
  • ...tml}}</ref> The ligand may be atomic or polyatomic. Virtually all complex organic compounds can serve as bridging ligands, so the term is usually restricted * [[Halide]]s
    4 KB (576 words) - 20:18, 21 September 2010
  • ...chelate. Chelating ligands are commonly formed by linking donor groups via organic linkers. A classic ''bi''dentate ligand is [[ethylenediamine]], which is de ...de]], and [[water]] are particularly common charge-neutral ligands. Simple organic species are also very common, be they anionic ([[alkoxide|RO<sup><nowiki>&m
    25 KB (3,607 words) - 20:18, 21 September 2010
  • | SolubleOther = polar organic solvents '''Tris(2-aminoethyl)amine''' is the [[organic compound]] with the [[chemical formula|formula]] N(CH<sub>2</sub>CH<sub>2</
    4 KB (584 words) - 20:18, 21 September 2010
  • ...etallic]] complexes, but resembles the [[SN2 reaction|Sn2 mechanism]] in [[organic chemistry]]. The opposite pathway is [[dissociative substitution]], being The rate for the [[hydrolysis]] of cobalt(III) ammine halide complexes are deceptive, appearing to be associative but proceeding by an a
    6 KB (838 words) - 20:18, 21 September 2010
  • ...etallic]] complexes, but resembles the [[SN1 reaction|Sn1 mechanism]] in [[organic chemistry]]. The opposite pathway is [[associative substitution]], being a ...e for the [[hydrolysis]] of cobalt(III) ammine (NH<sub>3</sub>-containing) halide complexes are deceptive, appearing to be associative but proceeding by a pa
    4 KB (630 words) - 20:18, 21 September 2010
  • | Function = [[vinyl halide]] ...oethylene is an effective [[solvent]] for a variety of [[organic chemistry|organic]] materials.
    33 KB (4,639 words) - 21:02, 24 September 2010
  • '''Diethyl ether''', also known simply as ether, is the [[organic compound]] with the formula {{chem|({{chem|C|2|H|5}})|2|O}}. It is a color ...[wikt:immiscibility|immiscibility]] with water and the fact that non-polar organic compounds are highly soluble in it, ether is also used in the production of
    16 KB (2,212 words) - 21:03, 24 September 2010