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In organic chemistry, a ketene is an organic compound of the form RR'C=C=O, where R and R' are two arbitrary monovalent chemical groups (or two separate substitution sites in the same molecule). [1] The name may also refer to the specific compound ethenone H 2 C=C=O, the simplest ketene. [2] Although they are highly useful, most ketenes are ...
Chemical nomenclature, replete as it is with compounds with very complex names, is a repository for some names that may be considered unusual. A browse through the Physical Constants of Organic Compounds in the CRC Handbook of Chemistry and Physics (a fundamental resource) will reveal not just the whimsical work of chemists, but the sometimes peculiar compound names that occur as the ...
In chemistry, chemical stability is the thermodynamic stability of a chemical system, in particular a chemical compound or a polymer. [ 1 ] Thermodynamic stability occurs when a system is in its lowest energy state , or in chemical equilibrium with its environment.
Additionally, about 31 nuclides of the naturally occurring elements have unstable isotopes with a half-life larger than the age of the Solar System (~10 9 years or more). [ b ] An additional four nuclides have half-lives longer than 100 million years, which is far less than the age of the Solar System, but long enough for some of them to have ...
Antiaromaticity is a chemical property of a cyclic molecule with a π electron system that has higher energy, i.e., it is less stable due to the presence of 4n delocalised (π or lone pair) electrons in it, as opposed to aromaticity.
Francium is an alkali metal whose chemical properties mostly resemble those of caesium. [8] A heavy element with a single valence electron, [9] it has the highest equivalent weight of any element. [8] Liquid francium—if created—should have a surface tension of 0.05092 N/m at its melting point. [10]
the simplest aldehyde; an important precursor to many other chemical compounds, such as polymers and polyfunctional alcohols Formic acid: the simplest carboxylic acid; often used as a source of the hydride ion Grignard reagents: the most common application is for alkylation of aldehydes and ketones: [4] Hexamethylphosphoramide
1-Diazidocarbamoyl-5-azidotetrazole was produced by diazotizing triaminoguanidinium chloride with sodium nitrite in ultra-purified water. [6] Another synthesis uses a metathesis reaction between isocyanogen tetrabromide in acetone and aqueous sodium azide. [3]