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A Convenient Preparation of Volatile Acid Chlorides
A Convenient Preparation of Volatile Acid Chlorides

... very simple: the acid is mixed with an excess of The possibility of utilizing organic acid chlo- benzoyl chloride and the acid chloride desired is rides for the preparation of other acid chlorides distilled through a small column directly out of the has been neglected for the most part. Adams and re ...
chm238f02.pracexam2.ans
chm238f02.pracexam2.ans

... (b) What is the reactive electrophile in the above reaction? NO2+, nitronium ion. (c) If we used only pure (fuming) sulfuric acid, what would be the product(s)? mostly sulfonation of Cl benzene, both o and p, because SO3H+ becomes the superelectrophile and there is not as much protons for the dehydr ...
10 | Carbon: More Than Just Another Element
10 | Carbon: More Than Just Another Element

... Cis- and trans-2-butene are geometric isomers. Geometric isomerism in these compounds occurs as a result of the CPC double bond. Recall that the carbon atom and the attached groups cannot rotate around a double bond (page 420). Thus, the geometry around the CPC double bond is fixed in space. If iden ...
ALcohols CPP
ALcohols CPP

... • Identification using infra-red spectroscopy • Industrial preparation and uses of ethanol • Revision check list ...
Scoring Guidelines - AP Central
Scoring Guidelines - AP Central

... Write the formulas to show the reactants and the products for any FIVE of the laboratory situations described below. Answers to more than five choices will not be graded. In all cases, a reaction occurs. Assume that solutions are aqueous unless otherwise indicated. Represent substances in solution a ...
Compounds of Chlorine
Compounds of Chlorine

... The X-Cl bond is an electron pair covalent bond with a highly polar nature. In this regard, chlorine is similar to uorine. However, there are two key features with regard to chlorine's bonding that dierentiates it from uorine. 1. Unlike uorine, chlorine can form multiple covalent bonds, e.g., Cl ...
FULL PAPER Cobalt(II), Nickel(II), Copper(II), and Zinc
FULL PAPER Cobalt(II), Nickel(II), Copper(II), and Zinc

... compounds with a 1:1 metal/ligand stoichiometry: M(ClO4)2L·2H2O [M ⫽ Co (1), Ni (2), Zn (5); Cu(ClO4)2L·4H2O (3), and CuCl2L·4H2O (4)], while a compound with a 2:1 (M/L) stoichiometric ratio was isolated with zinc chloride: Zn2Cl4L (6). IR spectroscopic data (Table S1, Figure S1, Supporting Informat ...
Visible-Light Excitation of Infrared Lanthanide
Visible-Light Excitation of Infrared Lanthanide

... processes in the solid state. The complexes are photo-stable in dmso solution but undergo some photochemical decomposition in the solid state during photophysical experiments, as evidenced by gradual reduction of the absolute quantum yield in a series of consecutive experiments. At the same time, th ...
IE in C-H activation - The School of Life Sciences at Sussex
IE in C-H activation - The School of Life Sciences at Sussex

... Over the past 30 years or so, a number of examples of carbon-hydrogen bond activation by transition metals have appeared in the literature.1 This work took on greater significance in 1982, when Bergman reported a reaction in which a “simple” oxidative addition of cyclohexane to a photochemically gen ...
Chapter 18 Organic Chemistry - American Public University System
Chapter 18 Organic Chemistry - American Public University System

... • Alkanes composed of carbon atoms bonded in a straight chain without any branching—like the ones we have just seen—are called normal alkanes or n-alkanes. • In addition to linking together in straight chains to form the n-alkanes, carbon atoms can form branched structures called branched alkanes. T ...
- Thieme Connect
- Thieme Connect

... g-amino alcohols to aziridines and azetidines, conversion of carboxylic acid derivatives into acyl bromides, bromination or dehydration of carboxamide groups and epoxide opening to vicinal dibromides.2 Some of these resulting compounds have been reused in total syntheses of complex natural products ...
Nickel complexes of a diphosphine-ketone ligand: oxidation
Nickel complexes of a diphosphine-ketone ligand: oxidation

Chapter 1-
Chapter 1-

Sem-5 - NVPAS
Sem-5 - NVPAS

... Definition of stability, stepwise formation of complexes, Stepwise formation and overall formation constants, kinetic vs. thermodynamic stability, labile and inert octahedral complexes according to CFT, factors affecting on the stability of complexes, experimental determination of stability constant ...
6.3.1 Chromatography and Analysis
6.3.1 Chromatography and Analysis

... To calculate the concentration of each component in the curve it is necessary to complete external calibration curves to confirm concentrations of components. Known amounts of a pure component can be passed through the GC machine. The calibration curve will give the retention time of the component a ...
Exam 3 - Napa Valley College
Exam 3 - Napa Valley College

... mean that you would get a lot of by-products but you would end up getting more product also (SN1 major, E1 minor). 4) There are a number of ways of substituting a halogen for an alcohol group, but some ways are better than others. What advantage is there in using PCl3 rather than HCl in the chloride ...
Chapter 4 Quiz
Chapter 4 Quiz

... 7. Observe the structures of glucose and fructose. These two molecules are a. geometric isotopes. b. enantiomers. c. geometric isomers. d. structural isomers. e. nonisotopic isomers. 8. The two molecules shown in the following figure are best described as ...
Co-ordination compounds
Co-ordination compounds

... Q15. Why is geometrical isomerism not possible in tetrahedral complexes having two different types of unidentate ligands coordinated with central metal ion? Ans. Tetrahedral complexes do not show geometrical isomerism because the relative positions of the unidentate ligands attached to the central m ...
IOSR Journal of Applied Chemistry (IOSR-JAC)
IOSR Journal of Applied Chemistry (IOSR-JAC)

... rate constant of quenching of 1O2 by solvent-DMF.kr is the rate constant of chemical quenching of 1O2 by the substrate. Kq is the rate constant for chemical quenching by the probe [21,23]. The rate constant of reaction between singlet oxygen and substrate (A) were determined in solution containing a ...
1.4 The rate-determining step
1.4 The rate-determining step

... The slowest step of any multi-step reaction is known as the rate determining step and it is the species involved in this step that are found in the overall rate equation. Catalysts appear in the rate equation because they affect the rate but they do not appear in the stoichiometric equation because ...
Redox - SAVE MY EXAMS!
Redox - SAVE MY EXAMS!

... 40 Dilute sulphuric acid is electrolysed using inert electrodes. ...
STUDIES ON MERCURY(II), NICKEL(II) AND LEAD(II)
STUDIES ON MERCURY(II), NICKEL(II) AND LEAD(II)

ALCOHOLS, PHENOLS AND ETHERS
ALCOHOLS, PHENOLS AND ETHERS

synthesis, characterization and applications of metal complexes of 5
synthesis, characterization and applications of metal complexes of 5

... The development of new ligands is a very important step in the development of metal complexes. These metal complexes have unique properties and novel reactivities. The nature of these groups like steric properties, electronic properties, and the geometric properties affect the metal orbitals and thu ...
Chemdraw B&W - Chemistry Courses
Chemdraw B&W - Chemistry Courses

... CH3OH and alumina catalyst • Yields a mixture of monomethylated, dimethylated, and trimethylated products that are easily separated by distillation ...
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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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