Search results
Results from the WOW.Com Content Network
A structural formula is a simplified model that cannot represent certain aspects of chemical structures. For example, formalized bonding may not be applicable to dynamic systems such as delocalized bonds. Aromaticity is such a case and relies on convention to represent the bonding. Different styles of structural formulas may represent ...
Orthoformic acid or methanetriol is a chemical compound with the formula H C(OH) 3. In this molecule, the central carbon atom is bound to one hydrogen and three hydroxyl groups. Orthoformic acid was long held to be a hypothetical chemical compound , as it was expected to decompose instantly into formic acid and water, making it too unstable to ...
By adding a correction factor, known as the activity (, the activity of the i th component) to the liquid phase fraction of a liquid mixture, some of the effects of the real solution can be accounted for. The activity of a real chemical is a function of the thermodynamic state of the system, i.e. temperature and pressure.
The skeletal formula of the antidepressant drug escitalopram, featuring skeletal representations of heteroatoms, a triple bond, phenyl groups and stereochemistry. The skeletal formula, line-angle formula, bond-line formula or shorthand formula of an organic compound is a type of molecular structural formula that serves as a shorthand representation of a molecule's bonding and some details of ...
The chemical formula for TEOS is given by Si(OC 2 H 5) 4, or Si(OR) 4, where the alkyl group R = C 2 H 5. Alkoxides are ideal chemical precursors for sol–gel synthesis because they react readily with water. The reaction is called hydrolysis, because a hydroxyl ion becomes attached to the silicon atom as follows: Si(OR) 4 + H 2 O → HO−Si ...
[2] [3] In aqueous solution, it exists as a mixture of at least four species, which rapidly interconvert. [4] Structures and distribution of glycolaldehyde as a 20% solution in water. Notice that the free aldehyde is a minor component. In acidic or basic solution, the compound undergoes reversible tautomerization to form 1,2-dihydroxyethene. [5]
In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.
The crystal structure called Form I is a disappearing polymorph that cannot be produced by researches anymore while Form II and III still exist. [6] The reason for this is that Form I is converted to another polymorph upon contact with a seed crystal and most places are contaminated with tiny amounts of Form II or III that are enough to prevent any viable amounts of Form I to be produced.