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Both the oxidation and reduction steps are pH dependent. Figure 1 shows the standard potentials at pH 0 (strongly acidic) as referenced to the normal hydrogen electrode (NHE). 2 half reactions (at pH = 0) Oxidation 2H 2 O → 4H + + 4e − + O 2 E° = +1.23 V vs. NHE Reduction 4H + + 4e − → 2H 2 E° = 0.00 V vs. NHE
In organic chemistry, an addition reaction is an organic reaction in which two or more molecules combine to form a larger molecule called the adduct. [1] [2] An addition reaction is limited to chemical compounds that have multiple bonds. Examples include a molecule with a carbon–carbon double bond (an alkene) or a triple bond (an alkyne).
Oxidative additions of nonpolar substrates such as hydrogen and hydrocarbons appear to proceed via concerted pathways. Such substrates lack π-bonds, consequently a three-centered σ complex is invoked, followed by intramolecular ligand bond cleavage of the ligand (probably by donation of electron pair into the sigma* orbital of the inter ligand bond) to form the oxidized complex.
Adding the hydrogen ion to one carbon atom in the alkene creates a positive charge on the other carbon, forming a carbocation intermediate. The more substituted the carbocation, the more stable it is, due to induction and hyperconjugation. The major product of the addition reaction will be the one formed from the more stable intermediate.
Reductive elimination is an elementary step in organometallic chemistry in which the oxidation state of the metal center decreases while forming a new covalent bond between two ligands. It is the microscopic reverse of oxidative addition, and is often the product-forming step in many catalytic processes. Since oxidative addition and reductive ...
The Mukaiyama aldol addition is a Lewis acid-mediated addition of enol silanes to carbonyl (C=O) compounds. In this reaction, compounds with various organic groups can be used (see educts). [3] A basic version (R 2 = H) without the presence of chiral catalysts is shown below. Simplified overview with a stereocenter. A racemic mix of enantiomers ...
The first and second steps are electrophilic addition that breaks the aromatic ring in benzene (A) and forms two hydroxyl groups (–OH) in intermediate C. Later an ·OH grabs a hydrogen atom in one of the hydroxyl groups, producing a radical species (D) that is prone to undergo rearrangement to form a more stable radical (E).
In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.