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1 -
1 -

... propyne 4-methoxyhex-2-yne ...
Substitution reactions
Substitution reactions

Chemistry of Carbon Compounds (Module 1)
Chemistry of Carbon Compounds (Module 1)

... a) understand that all organic compounds ultimately come from crude oil b) understand that crude oil is a mixture of organic compounds c) know that fractional distillation is used to obtain various fractions which would contain alkanes and alkenes d) list at least three fractions that are obtained f ...
Forming Ligand in Homo-and Heterometallic Complexes - Hal-CEA
Forming Ligand in Homo-and Heterometallic Complexes - Hal-CEA

... In the overwhelming majority of the known structures containing H4thftc or its anions, either free or complexed, the molecule retains the achiral trans,cis,trans (2R*,3R*,4S*,5S*) isomeric form of the single species shown to be present in the commercially available acid. 14 In principle, six diaster ...
Rh(acac)(CO)(PR1R2R3) - University of the Free State
Rh(acac)(CO)(PR1R2R3) - University of the Free State

... Rhodium (Rh), a transition metal, which often has a red-pink colour,1 was named after rhodon, the Greek term for rose. It is one of the least abundant metals in the earth’s crust and was discovered by William Hyde Wollaston (1803-04) in crude platinum ore from South America. Rhodium is often used as ...
Document
Document

... Alkyl ammonium ions, R3NH+ X-, have pKa values in the range of 10-11 (ammonium ion, H4N+ X-, has a pKa ~ 9.3) The ammonium ions of aryl amines and heterocyclic aromatic amines are considerably more acidic than alkyl amines (pKa < 5). The nitrogen lone pair is less basic if it is in an sp2 hybridized ...
Mechanism of intra - Chemical Engineering Labs
Mechanism of intra - Chemical Engineering Labs

... of inter- and intra-molecular C@C bond formation that involve bimolecular coupling of propanal and unimolecular deoxygenation steps, respectively. The inter-molecular C@C bond formation proceeds via mechanistic steps resembled the acid-catalyzed aldol condensation reactions in the homogeneous phase, ...
amine
amine

... • Name the longest chain attached to the nitrogen. • Replace the final –e with –amine. • Number the chain so the carbon bonded to the nitrogen has the lowest possible number. • Number the other substituents on the carbon chain. • An italic “N” is used as a prefix for a substituent on nitrogen. Examp ...
Design of Nanostructured Catalysts for H2 Production
Design of Nanostructured Catalysts for H2 Production

... catalysts has a profound effect on the catalytic activity. A heterogeneous catalytic reaction begins with the adsorption of the reacting gases or liquids on the surface of the catalyst, where intramolecular bonds are broken or weakened. Next, the adsorbed species react on the surface, often in sever ...
Catalytic decomposition of N2O over Rh/Zn–Al2O3 catalysts
Catalytic decomposition of N2O over Rh/Zn–Al2O3 catalysts

... ozone layer depletion has raised much concern. The concentration of N2O in the atmosphere has been increasing at an annual rate of 0.2–0.3% since the industrial revolution.1 Anthropogenic N2O emission comes from several chemical processes (e.g., nitric acid and adipic acid production) and fossil fue ...
14_Aldehydes_and_Ketones
14_Aldehydes_and_Ketones

...  with one to four carbons are soluble in water.  with five or more carbons are not very soluble in water.  form hydrogen bonds with water between the carbonyl oxygen and hydrogen atoms of water. ...
Chapter 20: Carboxylic Acids and Nitriles
Chapter 20: Carboxylic Acids and Nitriles

... Heating in either aqueous acid or aqueous base produces a carboxylic acid and amine  Acidic hydrolysis by nucleophilic addition of water to the protonated amide, followed by loss of ammonia ...
+ 2 KI + 2 H3P04 + 2 RI + 2 KHzPOI + H2O
+ 2 KI + 2 H3P04 + 2 RI + 2 KHzPOI + H2O

Sample pages 6 PDF
Sample pages 6 PDF

... Apparently, the oxidation takes place in the organic phase, where such substrates are present in a very low concentration. • The oxidation can be substantially accelerated by the addition of quaternary ammonium salts as a phase-transfer catalyst. Thus, while in the absence of phase-transfer catalyst ...
+ CH - Loreto Chemistry from 2015
+ CH - Loreto Chemistry from 2015

... Base hydrolysis requires hot aqueous alkali. This reaction is not reversible. Because it is done in alkali conditions, instead of producing the carboxylic acid the carboxylate salt is made. This process is called saponification because if you hydrolysed a large ester such as those found in animal fa ...
Alcohols
Alcohols

... Primary (1º) alcohol contains –OH group on carbon atom that is bonded to one R group Secondary (2º) alcohol contains –OH group on carbon atom that is bonded to two R groups Tertiary (3º) alcohol contains –OH group on carbon atom that is bonded to three R groups ...
Practice Exercise
Practice Exercise

... has an octahedral geometry. Like [Co(NH3)4Cl2 ]+ (Figure 24.1), it has four ligands of one type and two of another. Consequently, it possesses two isomers: one with the Cl – ligands across the metal from each other (trans-Fe(CO)4Cl2) and one with the Cl– ligands adjacent (cis-Fe(CO)4Cl2). In princip ...
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... ○ Cofactors of pyruvate DH and a-KG DH complexes  Tender loving Care for Nobody  Tiamine pyrophosphate, lipoic acid, CoA, FAD, NAD ...
Common Incompatible Chemicals
Common Incompatible Chemicals

... A wide variety of chemicals react dangerously when mixed with certain other materials. Some of the more widely-used incompatible chemicals are given below, but the absence of a chemical from this list should not be taken to indicate that it is safe to mix it with any other chemical! ...
Catalytic, Enantioselective Alkylations of N,O- and
Catalytic, Enantioselective Alkylations of N,O- and

... Conclusion. In summary, we have developed the first practical method for catalytic, enantioselective alkylation of N,O- and N, N-acetals. Stable, readily available acetals la-i can be alkylated with a variety of nucleophiles in up to 96% ee with as little as 1 mol % of catalyst 2. This research has ...
Ex. 29 Answer
Ex. 29 Answer

... derived from gum benzoin (the resinous product from styrax trees), which was for a long time the only source for benzoic acid. ...
lecture 5 ligand substitution
lecture 5 ligand substitution

... CO, CN-, NO C2H4 > PR3, H- > CH3-, S=C(NH2)2 > PhNO2- SCN-, I-, > Br- > Cl- > Py, NH3, OH- H2O ...
The Preparation and Analysis of a Coordination
The Preparation and Analysis of a Coordination

... When the 26 year-old Swiss chemist Alfred Werner began his study of the compounds formed by cobalt(III) with aqueous ammonia and chloride ion at the end of the 19th century, very little was understood about the nature of the chemical bonds and molecular geometry of these substances. By 1913 he had b ...
chm238f02.exam2
chm238f02.exam2

... (b) Given pKas: CH3OH = 45; CH3OH = 16; H2 = 38; H2O = 16; PhOH = 10: Predict the direction and Keq of the reaction above. ...
CHM238-01 EXAM 2 October 14, 2002 103
CHM238-01 EXAM 2 October 14, 2002 103

< 1 ... 110 111 112 113 114 115 116 117 118 ... 359 >

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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