Search results
Results from the WOW.Com Content Network
This requires mixing the compounds in a reaction vessel, such as a chemical reactor or a simple round-bottom flask. Many reactions require some form of processing ("work-up") or purification procedure to isolate the final product. [1] The amount produced by chemical synthesis is known as the reaction yield.
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol . This reaction was developed by Alexander Williamson in 1850. [ 2 ] Typically it involves the reaction of an alkoxide ion with a primary alkyl halide via an S N 2 reaction .
In a synthesis reaction, two or more simple substances combine to form a more complex substance. These reactions are in the general form: + Two or more reactants yielding one product is another way to identify a synthesis reaction.
Baeyer–Drewson indigo synthesis; Baeyer–Villiger oxidation, Baeyer–Villiger rearrangement [12]; Bakeland process (Bakelite) Baker–Venkataraman rearrangement, Baker–Venkataraman transformation [13] [14] [15] [16]
An example of a simple chain reaction is the thermal decomposition of acetaldehyde (CH 3 CHO) to methane (CH 4) and carbon monoxide (CO). The experimental reaction order is 3/2, [4] which can be explained by a Rice-Herzfeld mechanism. [5] This reaction mechanism for acetaldehyde has 4 steps with rate equations for each step :
Chemical synthesis, the execution of chemical reactions to form a more complex molecule from chemical precursors Organic synthesis, the chemical synthesis of organic compounds Total synthesis, the complete organic synthesis of complex organic compounds, usually without the aid of biological processes
[2] [3] This reaction is widely used for the synthesis of various phosphonates, phosphinates, and phosphine oxides. Several reviews have been published. Several reviews have been published. [ 4 ] [ 5 ] The reaction also occurs for coordinated phosphite ligands, as illustrated by the demethylation of {(C 5 H 5 )Co[(CH 3 O) 3 P] 3 } 2+ to give ...
The McMurry reaction of benzophenone. The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent. The reaction is named after its co-discoverer, John E. McMurry.