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Examples of anions
Examples of anions

... 3. Esterification - organic acid and alcohol forms an ester and water • e.g. acetic acid and ethanol : CH3COOH + C2H5OH  CH3COOC2H5 + H2O 4. Addition : A C=C bond is broken and atoms are attached to the carbon atoms ...
Review Answers - cloudfront.net
Review Answers - cloudfront.net

... b. What change, if any, will occur in ΔG° for the reaction as the temperature is increased? Explain your reasoning in terms of thermodynamics principles. Since when Temp is increased there are more molecules of PCl3 and Cl2, this reaction is endothermic and ∆H is positive. ∆G = ∆H-T∆S: = + - T(+). A ...
Reaction of niobium and tantalum neutral clusters with low pressure
Reaction of niobium and tantalum neutral clusters with low pressure

Why Do Vanadium Atoms Form Multiple-Decker Sandwich Clusters with Benzene
Why Do Vanadium Atoms Form Multiple-Decker Sandwich Clusters with Benzene

... 9; therefore, when the number of valence electrons is less than or equal to 18, the metal-ligand bonds are formed strongly without antibonding electrons. The numbers of valence electrons are 16, 17, and 18 for Ti(C6H6)2, V(C6H6)2, and Cr(C6H6)2, respectively, and it is expected that these complexes ...
Document
Document

... Equilibrium exists between an undissolved solute and its saturated solution when the rate of precipitation equals the rate of dissolution. An aqueous solution containing aqueous NaCl and solid NaCl contains the following equilibrium. NaCl(s) → Na+(aq) + Cl-(aq) Ksp = [Na+][Cl-] This equilibrium is d ...
5 - ChemWeb (UCC)
5 - ChemWeb (UCC)

... element centre, so need 6 hybrid orbitalsformed from one s, three p, and two d a.o.’s so the T.E. is sp3d2 hybridised. e.g. [Fe(NH3)6]Cl2 Fe is sp3d2 hybridised. Tetrahedral complexes Four electron pairs around the transition element centre, so need 4 hybrid orbitals – formed from one s, and three p ...
A COMPUTATIONAL STUDY OF CRYSTAL VIOLET
A COMPUTATIONAL STUDY OF CRYSTAL VIOLET

Carbenes and Nitrenes: Structure, generaNon and reacNvity
Carbenes and Nitrenes: Structure, generaNon and reacNvity

... 1991,  Arduengo,  first  X-­‐ray  structure  of  a  carbene)  that  NHCs  have  become  ubiquitous both  as  ligands  in  organometallic  chemistry  and  as  organocatalysts. ...
Chapter 21: Carboxylic Acids and Their Derivatives
Chapter 21: Carboxylic Acids and Their Derivatives

... Amines are more basic than alcohols, and they react with the carboxylic acid by acidbase reaction. The resulting ammonium ions do not have lone pairs, and therefore do not act as nucleophiles. This prevents the amine from reacting with the carbonyl (C=O) carbon and forming the amide. ...
ch18 by dr. dina
ch18 by dr. dina

... synthesis of 5- and 6-membered rings anhydrides by heating the appropriate diacid ...
Essential Oils Composition
Essential Oils Composition

... Essential Oils Composition Component of Essential Oils can be classified into 4 major groups : • ALIPHATIC COMPOUNDS • TERPENE AND TERPENE DERIVATIVES • BENZENE DERIVATIVES • MISCELLANEOUS COMPOUNDS ...
COVER SHEET
COVER SHEET

... in Figure 6, while selected bond distances and angles can be found in Table 1 and data collection and structure solution parameters are in Table 2. In comparison to 1, the geometry of the molecule changes somewhat upon oxidation; the P - C - P angle opens further to 128° and 125° in the two unique m ...
Stereoisomers
Stereoisomers

... Structural integrity: The three dimensional architecture of proteins and nucleic acids depends upon zinc and manganese as well as iron and copper. These metals bind and hold large molecules in active configurations. An example is the requirement of zinc for proper conformation of the taste- bud prot ...
Co(NH 3 ) 5 (NO 2 ) - Department of Chemistry
Co(NH 3 ) 5 (NO 2 ) - Department of Chemistry

... Tests revealed the compound had prevented cell division, but not other growth processes in the bacteria. It was approved for cancer treatment in 1978. ...
Co(NH
Co(NH

View/Open - Minerva Access
View/Open - Minerva Access

... decarboxylative cross-coupling reactions of allyl acetate and related esters are then reviewed. These studies have explored the role of the metal carboxylate complex in the gas phase decarboxylative coupling of allyl acetate proceeding via a simple twostep catalytic cycle. In Step 1, an organometall ...
New System of Deprotection Step for the Hydroxide Radicals: Boron
New System of Deprotection Step for the Hydroxide Radicals: Boron

... into ester, halogenated hydrocarbon, aldehydes, ketone, carboxylic acid and unsaturated hydrocarbon easily. It is necessary to protect the hydroxide radical from transforming when we do not want the hydroxide radical change into others. Alkylation of a hydroxyl moiety is regarded as one of the most ...
Oxidation catalytic system and oxidation process using the same
Oxidation catalytic system and oxidation process using the same

... N-hydroxyphthalimide), and a co-catalyst (except phospho vanadomolybdic acid) containing an element selected from the group consisting of Group 2A elements of the Periodic Table of Elements, transition metals (Group 3A to 7A elements, Group 8 elements, Group 1B elements and Group 2B elements of the ...
Synthesis and structure of copper(II) complexes: Potential cyanide
Synthesis and structure of copper(II) complexes: Potential cyanide

... The copper complexes under N2 O2 coordination sphere where the ligands had ortho or para alkyl sulfanyl substituent as spectator, in terms of coordination to the metal centre, and both the O-donors were phenolato oxygen and both the N-donors were aldimino-N had exhibited GO activity.59 Encouraged by ...
Student Review packet
Student Review packet

... What is the solubility of MgF2 in molarity? ...
Complexes. X-ray Structure of Rh1[C6H,(CH2NMe2),-o ,o`
Complexes. X-ray Structure of Rh1[C6H,(CH2NMe2),-o ,o`

... rhodium(1) complexes were performed under an atmosphere of analogous rhodium(1) and iridium(1) species having aryl dry nitrogen using Schlenk techniques. Solvents were carefully ligands that are either mono- or bis-ortho-chelated by dried and distilled prior to use. Reactions were carried out a t ni ...
mechanistic investigations of transition metal catalyzed reactions
mechanistic investigations of transition metal catalyzed reactions

Some more basic organic (more naming, reactions, polymers)
Some more basic organic (more naming, reactions, polymers)

... 1,1,2,2-tetrachloropropane CH3CHBrCH3 2-bromopropane ...
IUPAC nomenclature of organic chemistry
IUPAC nomenclature of organic chemistry

... Numbering of the various substituents and bonds with their locants. If there is more than one of the same type of substituent/double bond, the prefix (di-, tri-, etc.) is added. The numbers for that type of side chain will be grouped in ascending order and written before the name of the side-chain. ...
lecture 9 nucl_electro_add_abs
lecture 9 nucl_electro_add_abs

...  As 1e reagents, organic free radicals can also give addition and abstraction reactions, but these reactions are less well understood.  Radical addition and abstraction also tends to occur only as part of a larger reaction scheme in which radicals are formed and quickly react.  We briefly looked ...
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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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