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Wohl–Ziegler Bromination
The Wohl–Ziegler reaction is a chemical reaction that involves the allylic or benzylic bromination of hydrocarbons using an ''N''-bromosuccinimide and a radical initiator. : Best yields are achieved with ''N''-bromosuccinimide in carbon tetrachloride solvent. Several reviews have been published. In a typical setup, a stoichiometric amount of ''N''-bromosuccinimide solution and a small quantity of initiator are added to a solution of the substrate in CCl4, and the reaction mixture is stirred and heated to the boiling point. Initiation of the reaction is indicated by more vigorous boiling; sometimes the heat source may need to be removed. Once all ''N''-bromosuccinimide (which is denser than the solvent) has been converted to succinimide (which floats on top) the reaction has finished. Due to the high toxicity and ozone-depleting nature of carbon tetrachloride, trifluorotoluene Trifluorotoluene is an organic compound with the formula of C6H5CF3. This colorless fluorocarbon ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Alfred Wohl
Alfred Wohl (3 October 1863 – 25 December 1939) was a German chemist. Several chemical reactions are named after him, including the Wohl degradation, Wohl-Aue reaction and the Wohl-Ziegler reaction. Life Wohl studied chemistry at the University of Heidelberg from 1882 until 1886. He received his Ph.D 1886 for work on Hexamethylenetetramine with August Wilhelm von Hofmann. He became an assistant of Hermann Emil Fischer at the University of Berlin from 1886 until 1891, where he also received his habilitation. He became professor at the University of Berlin in 1901, but he left for the Technical University of Danzig in 1904. He retired because of antisemitic pressure in 1933, but worked in his lab until 1937. He emigrated to Sweden in 1938, where he died in 1939. His son Kurt Wohl (1896-1962) - who also became a renowned chemical scientist - emigrated to Great Britain in 1939 and some years later to the United States. [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Carbon Tetrachloride
Carbon tetrachloride, also known by many other names (such as tetrachloromethane, also recognised by the IUPAC, carbon tet in the cleaning industry, Halon-104 in firefighting, and Refrigerant-10 in HVACR) is an organic compound with the chemical formula CCl4. It is a colourless liquid with a "sweet" smell that can be detected at low levels. It is practically incombustible at lower temperatures. It was formerly widely used in fire extinguishers, as a precursor to refrigerants and as a cleaning agent, but has since been phased out because of environmental and safety concerns. Exposure to high concentrations of carbon tetrachloride (including vapor) can affect the central nervous system and degenerate the liver and kidneys. Prolonged exposure can be fatal. Properties In the carbon tetrachloride molecule, four chlorine atoms are positioned symmetrically as corners in a tetrahedral configuration joined to a central carbon atom by single covalent bonds. Because of this symmetri ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Halogenation Reactions
In chemistry, halogenation is a chemical reaction that entails the introduction of one or more halogens into a compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. This kind of conversion is in fact so common that a comprehensive overview is challenging. This article mainly deals with halogenation using elemental halogens (F2, Cl2, Br2, I2). Halides are also commonly introduced using salts of the halides and halogen acids. Many specialized reagents exist for and introducing halogens into diverse substrates, e.g. thionyl chloride. Organic chemistry Several pathways exist for the halogenation of organic compounds, including free radical halogenation, ketone halogenation, electrophilic halogenation, and halogen addition reaction. The nature of the substrate determines the pathway. The facility of halogenation is influenced by the halogen. Fluorine and chlorine are more electrophilic and are ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Free-radical Halogenation
In organic chemistry, free-radical halogenation is a type of halogenation. This chemical reaction is typical of alkanes and alkyl-substituted aromatics under application of UV light. The reaction is used for the industrial synthesis of chloroform (CHCl3), dichloromethane (CH2Cl2), and hexachlorobutadiene. It proceeds by a free-radical chain mechanism. General mechanism The chain mechanism is as follows, using the chlorination of methane as a usual example: :1. Initiation: Splitting or homolysis of a chlorine molecule to form two chlorine atoms, initiated by ultraviolet radiation . A chlorine atom has an unpaired electron and acts as a free radical. :: :2. chain propagation (two steps): a hydrogen atom is pulled off from methane leaving a primary methyl radical. The methyl radical then pulls a Cl• from Cl2. :: This results in the desired product plus another chlorine radical. This radical will then go on to take part in another propagation reaction causing a chain reaction. If t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Addition Vs
Addition (usually signified by the plus symbol ) is one of the four basic operations of arithmetic, the other three being subtraction, multiplication and division. The addition of two whole numbers results in the total amount or '' sum'' of those values combined. The example in the adjacent image shows a combination of three apples and two apples, making a total of five apples. This observation is equivalent to the mathematical expression (that is, "3 ''plus'' 2 is equal to 5"). Besides counting items, addition can also be defined and executed without referring to concrete objects, using abstractions called numbers instead, such as integers, real numbers and complex numbers. Addition belongs to arithmetic, a branch of mathematics. In algebra, another area of mathematics, addition can also be performed on abstract objects such as vectors, matrices, subspaces and subgroups. Addition has several important properties. It is commutative, meaning that the order of the ope ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Goldfinger And Bloomfield Mechanisms
Goldfinger may refer to: ''James Bond'' * ''Goldfinger'' (novel), a 1959 James Bond novel written by Ian Fleming ** ''Goldfinger'' (film), a 1964 James Bond film starring Sean Connery *** ''Goldfinger'' (soundtrack), the soundtrack to the film composed by John Barry *** "Goldfinger" (Shirley Bassey song), the title song of the film performed by Shirley Bassey ** Auric Goldfinger, the eponymous villain of the novel and film ''Goldfinger'' ** ''Goldfinger'' (adventure), for the role-playing game ''James Bond 007'' Music * Goldfinger (band), a Los Angeles punk rock band ** ''Goldfinger'' (album), the 1996 first album by Goldfinger * "Goldfinger" (Ash song), 1996 * "Goldfinger", a song by Die Krupps from ''Volle Kraft voraus!'' * " Goldfinger 2019", a song by Japanese musician Koda Kumi Other uses * Goldfinger (surname) * ''Goldfinger'' (dragster), an early slingshot dragster * Goldfinger banana, a banana cultivar developed in Honduras * '' Goldfinger v. Feintuch'', a 19 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Trifluorotoluene
Trifluorotoluene is an organic compound with the formula of C6H5CF3. This colorless fluorocarbon is used as a specialty solvent in organic synthesis and an intermediate in the production of pesticides and pharmaceuticals.Banks, R.E. Organofluorine Chemicals and their Industrial Applications, Ellis Horwood LTD, Chichester, 1979. Synthesis For small-scale laboratory preparations, trifluorotoluene is synthesized by coupling an aromatic halide and trifluoromethyl iodide in the presence of a copper catalyst: :PhX + CF3I → PhCF3 (where X = I, Br) Industrial production is done by reacting benzotrichloride with hydrogen fluoride in a pressurized reactor.Siegemund, Günter "Aromatic Compounds with Fluorinated Side-Chains" in Ullmann’s Encyclopedia of Industrial Chemistry 2005, Wiley-VCH. . :PhCCl3 + 3 HF → PhCF3 + 3 HCl Uses Trifluorotoluene has a variety of niche uses. Low toxicity alternative to dichloromethane According to Ogawa and Curran, trifluorotoluene is similar to ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Succinimide
Succinimide is an organic compound with the formula (CH2)2(CO)2NH. This white solid is used in a variety of organic syntheses, as well as in some industrial silver plating processes. The compound is classified as a cyclic imide. It may be prepared by thermal decomposition of ammonium succinate. Succinimides Succinimides refers to compounds that contain the succinimide group. These compounds have some notable uses. Several succinimides are used as anticonvulsant drugs, including ethosuximide, phensuximide, and methsuximide. Succinimides are also used to form covalent bonds between proteins or peptides and plastics, which is useful in a variety of assay techniques. See also * Succinic anhydride Succinic anhydride, is an organic compound with the molecular formula (CH2CO)2O. This colorless solid is the acid anhydride of succinic acid. Preparation In the laboratory, this material can be prepared by dehydration of succinic acid. Such dehy ... * ''N''-Hydroxysuccinimide * ''N' ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chem , a place in Finland
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Chem may refer to: * Chemistry practical waali mam * Chemistry * Chemical * ''Chem'' (journal), a scientific journal published by Cell Press *Post apocalyptic slang for "drugs", medicinal or otherwise in the Fallout video game series. In Ancient Egyptian usage: * ''Khem'' (also spelt ''Chem''), the Egyptian word for "black" * Min (god), in the past erroneously named ''Khem'' CHEM may refer to : *A metabolic panel: for instance, CHEM-7, which is the basic metabolic panel *CHEM-DT, a Canadian television channel See also *Chemo (other) *Kemi Kemi (; sme, Giepma ; smn, Kiemâ; sms, Ǩeeʹmm; Swedish (historically): ''Kiemi'') is a town and municipality of Finland. It is located very near the city of Tornio and the Swedish border. The distance to Oulu is to the south and to Rovani ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
NBS Allylic Bromination Scheme
NBS may refer to: Business * National Bank of Samoa * National Bank of Serbia * National Bank of Slovakia * National Book Store, in the Philippines * Nationwide Building Society, UK * NBS (Natal Building Society), former bank in South Africa * NBS Bank, Malawi * Nelson Building Society, New Zealand * Newcastle Building Society, UK Science and technology * Nature-based solutions, use of nature for addressing societal challenges * ''N''-Bromosuccinimide, a chemical reagent * Newborn screening, a series of medical tests given to newborn babies * Nijmegen breakage syndrome, a genetic medical condition Schools * National Broadcasting School, UK * NUST Business School, of the National University of Sciences and Technology, Pakistan Telecommunications * Nagano Broadcasting Systems, Japan * National Broadcasting Service, former name of National Broadcasting Network (Trinidad and Tobago) * National Broadband Plan (United States) * NBS Television (Uganda) * Nippon Broadcasting Syste ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Karl Ziegler
Karl Waldemar Ziegler (26 November 1898 – 12 August 1973) was a German chemist who won the Nobel Prize in Chemistry in 1963, with Giulio Natta, for work on polymers. The Nobel Committee recognized his "excellent work on organometallic compounds hich..led to new polymerization reactions and ... paved the way for new and highly useful industrial processes". He is also known for his work involving free-radicals, many-membered rings, and organometallic compounds, as well as the development of Ziegler–Natta catalyst. One of many awards Ziegler received was the Werner von Siemens Ring in 1960 jointly with Otto Bayer and Walter Reppe, for expanding the scientific knowledge of and the technical development of new synthetic materials. Biography Early life and education Karl Ziegler was born on 26 November 1898 in Helsa near Kassel, Germany and was the second son of Karl Ziegler, a Lutheran minister, and Luise Rall Ziegler. He attended Kassel-Bettenhausen in elementary school. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
