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NICKEL(II) PINCER COMPLEXES SUPPORTED BY 2,6
NICKEL(II) PINCER COMPLEXES SUPPORTED BY 2,6

... nickel(II) pincer complexes in various chemical processes it was realized that this could be a potential area to explore. So, the first plan was to synthesize a new set of ligand, pyrrolyl pyridine [2,6-bis(3,5-di-tolylpyrrol-2-yl)pyridine] that could be used to prepare ...
Chapter 9
Chapter 9

... Fluorine is too reactive to give mono-fluorinated products For Iodine, an oxidizing agent such as hydrogen peroxide or a copper salt such as CuCl2 must be added to the reaction • These substances oxidize I2 to the electrophilic species that reacts as if it were I+ • The aromatic ring reacts with the ...
Solvation Effects on Transition Metal Hydricity
Solvation Effects on Transition Metal Hydricity

Microsoft Word - Ethesis@nitr
Microsoft Word - Ethesis@nitr

... diazo compounds onto triple bonds26. The former process, considered to be the best method for the preparation of pyrazoles, involves the double condensation of 1, 3diketones with hydrazine or its derivatives.27 This method has a wide scope not only because of the readily availability of 1, 3-diketon ...
Lecture № 20
Lecture № 20

... Imidazole was first synthesized by Heinrich Debus in 1858, but various imidazole derivatives had been discovered as early as the 1840s. His synthesis, as shown below, used glyoxal and formaldehyde in ammonia to form imidazole. This synthesis, while producing relatively low yields, is still used for ...
Photosystem II: Its Function, Structure, and Implications for Artificial
Photosystem II: Its Function, Structure, and Implications for Artificial

Coordination number 4 - INTEC Chemistry Blog
Coordination number 4 - INTEC Chemistry Blog

... (c), the 3+ ion (Co also in +III) state will go on to produce [Co(H2O)6]2+ . It is quite a strong oxidizing agent. (c) will actually react with the surrounding water. O 2 is produced. A blue/green precipitate of Co(OH)2 will slowly turn into [Co(NH3)6]3+ over time. Note about Copper: Copper I oxide ...
Mechanisms of Alkenes
Mechanisms of Alkenes

... goal is NOT to memorize the steps of a mechanism of a SPECIFIC molecule. When you do that, typically you become too focused on the structures provided in a single example. • If that happens, you will get confused when the next mechanism problem has a ...
Hydrogenation for Low Trans and High Conjugated Fatty Acids
Hydrogenation for Low Trans and High Conjugated Fatty Acids

... 0.25 to 60 Hz had no effect on current efficiencies. The combination of increased oil feed flow rate and inserted nickel turbulence promoter into the oil stream increased the current efficiency of oil hydrogenation. An and others (1999) also reported the effects of cathode designs and reactor operat ...
Chapter 24. Amines
Chapter 24. Amines

...  Most amines that have 3 different substituents on N are not resolved because the molecules interconvert by pyramidal inversion ...
Chapter 24. Amines - Houston Community College System
Chapter 24. Amines - Houston Community College System

...  Most amines that have 3 different substituents on N are not resolved because the molecules interconvert by pyramidal inversion ...
rev3
rev3

... 3. Amines have lower boiling points than their corresponding alcohols. Why? How water-soluble are they? 4. Amines smell “fishy”. Many drugs are amines. Alkaloids are natural amines from plants, like opium alkaloids. 5. Amines are weak bases. They will produce OH- in water to make a basic solution. A ...
© NCERT not to be republished
© NCERT not to be republished

Guess Paper – 2008 Class – X Subject
Guess Paper – 2008 Class – X Subject

... solution containing [ii] __________ ions. The article to be plated is placed at the [iii] _________ of the cell in which the plating is carried out. The [iv] ___________ of the cell is made from pure nickel. The ions which are attracted to the negative electrode and discharged are called [v] _______ ...
Alkyne metathesis - University of Windsor
Alkyne metathesis - University of Windsor

... which were recovered unchanged. Likewise, a butynoate failed to afford the desired product. Comparison of different tungsten alkylidyne complexes showed there to be no major improvement in terms of yield or reaction rate by choosing either different alkylidyne substituents or by replacing the tertbu ...
BIOC371 (2-Carbohydrates)
BIOC371 (2-Carbohydrates)

... Reducing sugars: • Reducing sugars is when the oxygen on the anomeric carbon (the carbonyl group) of a sugar is not attached to any other structure. ...
Production of Distillate Fuels from Biomass
Production of Distillate Fuels from Biomass

Coordination Numbers and Structures
Coordination Numbers and Structures

Coordination Nature of 4-Mercaptoaniline to Sn(II) Ion: Formation of
Coordination Nature of 4-Mercaptoaniline to Sn(II) Ion: Formation of

... and the reduction of carbon dioxide [17] and NOx [18]. Tin oxides [19] and tin sulfides [20] are well known and characterized for their structures and activities. Previously Eichhöfer and co-workers reported the synthesis of a one dimensional polymer compound (2) that was formed by one tin(II) and t ...
02. Titration method
02. Titration method

... complexation The use of a monodentate ligand, such as Cl– and CN–, however, limited the utility of complexation titrations to those metals that formed only a single stable complex. • The utility of complexation titrations improved following the introduction by Schwarzenbach, in 1945, of aminocarboxy ...
Alkyl Aryl Ether Bond Formation with PhenoFluor
Alkyl Aryl Ether Bond Formation with PhenoFluor

... owing to low reactivity and undesired side reactions, such as elimination.[2] Transition-metal-catalyzed or -mediated crosscoupling reactions, exemplified by Ullmann,[3] Chan–Lam– Evans,[4] and Buchwald–Hartwig couplings,[5] are powerful methods for ether bond formation. Functionally complex seconda ...
CHM102 - National Open University of Nigeria
CHM102 - National Open University of Nigeria

... easily explained by considering the molecules to be formed by sharing of electron pairs between the atoms. Another approach to formation of molecules is the molecular orbital method. Organic chemists have for many years employed a bonding model that combines elements of molecular orbital theory with ...
ORGANOHALIDES + Nucleophilic Reactions (SN1
ORGANOHALIDES + Nucleophilic Reactions (SN1

... • ZAITZEV’S RULE: base-induced eliminations will form more stable alkene ...
Preparation of metal complexes
Preparation of metal complexes

... values in DMF fall in the range (145130 S.cm2.mol-1) . These values of ratio are well consistent with the expected range for electrolyte (2:1). The molar ratio method was followed to determine the M:L ratio .The results of complexes in ethanol (solvent) , suggest that the metal to ligand ratio was 1 ...
britannica article
britannica article

... carbon-carbon double bonds under mild conditions to form polymers of high molecular weight and highly ordered (stereoregular) structures. Certain of these polymers are of great commercial importance because they are used to make many kinds of fibres, films, and plastics. Other technologically impor ...
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Hydroformylation



Hydroformylation, also known as oxo synthesis or oxo process, is an important homogeneously catalyzed industrial process for the production of aldehydes from alkenes. This chemical reaction entails the addition of a formyl group (CHO) and a hydrogen atom to a carbon-carbon double bond. This process has undergone continuous growth since its invention in 1938: Production capacity reached 6.6×106 tons in 1995. It is important because the resulting aldehydes are easily converted into many secondary products. For example, the resulting aldehydes are hydrogenated to alcohols that are converted to plasticizers or detergents. Hydroformylation is also used in specialty chemicals, relevant to the organic synthesis of fragrances and natural products. The development of hydroformylation, which originated within the German coal-based industry, is considered one of the premier achievements of 20th-century industrial chemistry.The process typically entails treatment of an alkene with high pressures (between 10 to 100 atmospheres) of carbon monoxide and hydrogen at temperatures between 40 and 200 °C. Transition metal catalysts are required.
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