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Download as PDF; Printable version; In other projects ... Well-known reactions and reagents in organic chemistry include 0-9. 1,2-Wittig rearrangement; 1,3-Dipolar ...
Carbonyl α-substitution reaction; Carboxylation; Carbylamine reaction; Coarctate reaction; Concerted reaction; Conia-ene reaction; Copper-free click chemistry; Cracking (chemistry) Crich beta-mannosylation; Cycloisomerization
Open Reaction Database ORD consortium Organic reactions machine-readable reaction schemes "ORD" [8] 2,000,000 OrgSyn Organic Syntheses: Organic Syntheses, Inc. Reliable chemical reactions Searchable experimental procedures Peer reviewed "OrgSyn search". PDB PDBe Protein Data Bank in Europe EMBL-EBI: has some chemicals as well as proteins "PDBe".
Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).
The Darzens reaction (also known as the Darzens condensation or glycidic ester condensation) is the chemical reaction of a ketone or aldehyde with an α-haloester in the presence of a base to form an α,β-epoxy ester, also called a "glycidic ester". [1] [2] [3] This reaction was discovered by the organic chemist Auguste Georges Darzens in 1904 ...
A mnemonic is a memory aid used to improve long-term memory and make the process of consolidation easier. Many chemistry aspects, rules, names of compounds, sequences of elements, their reactivity, etc., can be easily and efficiently memorized with the help of mnemonics.
Many redox reactions in organic chemistry have coupling reaction reaction mechanism involving free radical intermediates. True organic redox chemistry can be found in electrochemical organic synthesis or electrosynthesis. Examples of organic reactions that can take place in an electrochemical cell are the Kolbe electrolysis. [3] In ...
Allylic oxidation can be predicted by the substitution pattern on the olefin. In the case of 1,2-disubstituted olefins, reaction rates follow CH > CH 2 > CH 3: Geminally-substituted olefins react in the same order of reaction rates as above: [2] Trisubstituted alkenes experience reactivity at the more substituted end of the double bond.