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Reaction Sequences: Multistep synthesis involves sequential chemical reactions, each requiring its own work-up to isolate intermediates before proceeding to the next stage. [ 4 ] For example, the synthesis of paracetamol typically requires three separate reactions.
Using the twenty natural amino acids, for example, in a tripeptide creates 8,000 (20 3) possibilities. Solid-phase methods for small molecules were later introduced and Furka devised a "split and mix" approach [2] [4] In its modern form, combinatorial chemistry has probably had its biggest impact in the pharmaceutical industry. [5]
Also, some relatively minor additions to the reaction can be indicated above the reaction arrow; examples of such additions are water, heat, illumination, a catalyst, etc. Similarly, some minor products can be placed below the arrow, often with a minus sign. An example of organic reaction: oxidation of ketones to esters with a peroxycarboxylic acid
In the breakdown of a compound into its constituent parts, the generalized reaction for chemical decomposition is: AB → A + B (AB represents the reactant that begins the reaction, and A and B represent the products of the reaction) An example is the electrolysis of water to the gases hydrogen and oxygen: 2 H 2 O(l) → 2 H 2 (g) + O 2 (g)
These reactions are exothermic and the rise in temperature is usually in the order of the reactivity of the different metals. [5] If the reactant in elemental form is not the more reactive metal, then no reaction will occur. Some examples of this would be the reverse. + No Reaction
The Bray–Liebhafsky reaction is a chemical clock first described by W. C. Bray in 1921 with the oxidation of iodine to iodate: 5 H 2 O 2 + I 2 → 2 IO − 3 + 2 H + + 4 H 2 O. and the reduction of iodate back to iodine: 5 H 2 O 2 + 2 IO − 3 + 2 H + → I 2 + 5 O 2 + 6 H 2 O [4]
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).
Salt metathesis reaction; Salt-free reduction; Scavenger resin; Screaming jelly babies; SEA Native Peptide Ligation; Self-assembling peptide; Semiclassical transition state theory; Shiina esterification; Side reaction; Single displacement reaction; Small molecule sensors; Solid-state reaction route; Spin-forbidden reactions; Stripping reaction ...