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Chapter 8 Alkenes and Alkynes II
Chapter 8 Alkenes and Alkynes II

... Boron becomes attached to less substituted carbon of double bond l Bulkier boron group approaches the less hindered carbon more easily l This orientation also allows a δ+ charge in the transition state to ...
H1- Functional Groups Theory Sheet Alcohol An alcohol group
H1- Functional Groups Theory Sheet Alcohol An alcohol group

... An alcohol group contains an oxygen with a single bond to a hydrogen. One or more of the H atoms in the alkane is replaced by an OH. Alcohols can be primary secondary or tertiary, depending on how many other carbons are attached to the carbon with the alcohol group: (1C = Primary; 2C = Secondary; 3C ...
Chapter 8
Chapter 8

... Reduction: decreases # C-O bonds and increases the # C-H bonds Common reagents: chromic acid, chromate salt, dichromate salt, permanganate  Oxidation of a 1° alcohol to a carboxylic acid is commonly carried out using potassium dichromate, K2Cr2O7, in aqueous sulfuric acid. ...
Seminar_1 1. Classification and nomenclature of organic
Seminar_1 1. Classification and nomenclature of organic

... Whilst many of the alkanes present in crude oil are aliphatic, having straight–or branched–chain molecules, some of them form rings – they are alicyclic. These compounds are denoted as cycloalkanes. These cycloalkanes have the general formula CnH2n instead of CnH2n+2 for the chain molecules. Cycloal ...
Investigation of Nickel and Copper Coordination Complexes
Investigation of Nickel and Copper Coordination Complexes

... Typically, as ligand is added to the solution of metal ion, ML is formed first. As the addition of ligand is continued, the ML2 concentration rises, while the ML concentration drops. Then ML3 becomes dominant with ML and ML2 becoming unimportant. This process continues until the highest complex, ML6 ...
Chapter 4
Chapter 4

... Found in the nonliving world Example: NaCl ...
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... •Reaction of the d block with water - a redox reaction - to form metal hydroxides The d block elements, unlike group I elements and Group II elements, react very slowly if at all with water to form hydrogen and metal hydroxides. Even those with negative Eo values , do so only slowly due to the oxid ...
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... Prepared  by  José  Laboy,  MS   http:  www.chem.wisc.edu/areas  /clc  (Resource  page)   Reactions  of  Alcohols  #5:  Oxidation  of  Primary  Alcohols  to  Aldehydes   ...
Atom efficiency and catalysis in organic synthesis
Atom efficiency and catalysis in organic synthesis

... Acid-catalyzed rearrangement of epoxides to carbonyl compounds is another widely used reaction in fine chemicals manufacture. Lewis acids such as ZnCl2 are generally used, often in stoichiometric amounts, to perform such transformations. According to recent reports [14–16], zeolites can be used as r ...
CM1121 - ORGANIC CHEMISTRY 1
CM1121 - ORGANIC CHEMISTRY 1

... Stability of phases; phase transitions; phase diagrams of pure substances; chemical potential; effect of temperature and pressure on phase stability; Clapeyron equation; Clausius-Clapeyron equation. Partial molar quantities; thermodynamics of mixing; chemical potentials of liquids; ideal solutions, ...
paper 14 organic synthesis: disconnection approach - e
paper 14 organic synthesis: disconnection approach - e

... An introduction to synthons and synthetic equivalents, disconnection approach, functional group inter- conversions, the importance of the order of events in organic synthesis, one group C-X and two group C-X disconnections, chemoselectivity, reversal of polarity, cyclisation reactions , amine synthe ...
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... WHICH ONE IS AN ALKYNE? ...
Alcohols, Ethers, and Epoxides
Alcohols, Ethers, and Epoxides

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Biology 2B-1 - secondary

... – Organic compounds are based on carbon and its unusual bonding characteristics, They all contain carbon, most organic compounds under natural circumstances are the product of biosynthesis – Inorganic substances are derived from nonliving material and lack carbon ...
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name Page 1 of 6 Multiple Choice. Choose the best answer for the

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Thermodynamics Test Study Guide—AP _____ 1. The entropy

... beneath each species, what is the standard free energy change for this reaction at 298 K? C3H8(g) --------> CH4(g) ...
The Baylis–Hillman reaction is an organic reaction of an aldehyde
The Baylis–Hillman reaction is an organic reaction of an aldehyde

... The Henry Reaction is a base-catalyzed C-C bond-forming reaction between nitroalkanes and aldehydes or ketones. It is similar to the Aldol Addition, and also referred to as the Nitro Aldol Reaction. If acidic protons are available (i.e. when R = H), the products tend to eliminate water to give nitr ...
Experiment 2 Synthesis of macrocyclic complexes of nickel(II)
Experiment 2 Synthesis of macrocyclic complexes of nickel(II)

New process of low-temperature methanol synthesis from CO/CO2
New process of low-temperature methanol synthesis from CO/CO2

... low-temperature methanol synthesis impossible. It is well known that for methanol synthesis from CO/CO2/H2 over supported copper-based catalysts formate was the key intermediate, which was further hydrogenated to produce methanol[3]. The hydrogenolysis of formate has two ways: direct hydrogenolysis ...
BiochemistryMolecules
BiochemistryMolecules

... 4. As discussed in class, condensation reactions form the basis for the formation of most biopolymers. These reactions are named “condensation” because they generate H2O as a product. In this exercise, you are shown the reactants and products. Your task is to identify which atoms in the reactants fo ...
reactions of alcohols
reactions of alcohols

... Secondary alcohols are alcohols where 2 carbon are attached to the carbon adjoining the oxygen Tertiary alcohols are alcohols where 3 carbon are attached to the carbon adjoining the oxygen ...
Chapter 18 - people.vcu.edu
Chapter 18 - people.vcu.edu

... Considerations: You want alkyl halide to be methyl or primary because they are best for SN2 ...
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... Amides and carboxylic acids both contain carbonyl groups. Amides have the carbonyl carbon bonded to a nitrogen atom, but carboxylic acids have the carbonyl carbon bonded to a hydroxyl group. 19. What happens to the double bond of a monomer participating in the formation of an addition polymer? One o ...
l - CMatthews
l - CMatthews

... 6. a) Draw the formula for the polymer made from a two carbon double acid and a three carbon double alcohol. b) Draw the structural formula for the polymer formed from monomer units of 1,1-fluoro ethene. 7. Order the substance form the lowest boiling point to the highest for the following compounds: ...
Unit 2 Natural Products
Unit 2 Natural Products

... (a) Olive oil can be hardened using a nickel catalyst to produce a fat. (i) What type of catalyst is nickel in this reaction? (ii) In what way does the structure of a fat molecule differ from that of an oil molecule? (b) Olive oil can be hydrolysed using sodium hydroxide solution to produce sodium s ...
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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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