Search results
Results from the WOW.Com Content Network
1-Ethynylcyclohexanol (ECX) is an alkynyl alcohol derivative which is both a synthetic precursor to, and an active metabolite of the tranquilizer ethinamate, and has similar sedative, anticonvulsant and muscle relaxant effects. It has been sold as a designer drug, first being identified in the UK in March 2012. [1] [2] [3] [4]
Number of C atoms Number of isomers [3] [4] Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl ...
1-Hexanol (IUPAC name hexan-1-ol) is an organic alcohol with a six-carbon chain and a condensed structural formula of CH 3 (CH 2) 5 OH. This colorless liquid is slightly soluble in water, but miscible with diethyl ether and ethanol .
decacarbonyl-1κ 3 C,2κ 3 C,3κ 4 C-di-μ-hydrido-1:2κ 2 H;1:2κ 2 H-triangulo-(3 Os—Os), (Decacarbonyldihydridotriosmium). decacarbonyl-1κ 3 C,2κ 3 C,3κ 4 C shows that there are three carbonyl groups on two osmium atoms and four on the third. di-μ-hydrido-1:2κ 2 H;1:2κ 2 H specifies that the two hydride bridge between the osmium atom ...
The hexatriynyl radical, C 6 H, is an organic radical molecule consisting of a linear chain of six carbon atoms terminated by a hydrogen (H−C≡C−C≡C−C≡C•). The unpaired electron is located at the opposite end to the hydrogen atom, as indicated. Both experimental work and computer simulations on this species was done in the early ...
The double bond of an alpha olefin is between the #1 and #2 (IUPAC) or α and β (common) carbon atoms. In organic chemistry , terminal alkenes ( alpha-olefins , α-olefins , or 1-alkenes ) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula C x H 2 x , distinguished by having a double bond at the ...
The destruction of ethynyl is dominantly through neutral-neutral reactions with O 2 (producing carbon monoxide and formyl, HCO), or with atomic nitrogen (producing atomic hydrogen and C 2 N). Ion-neutral reactions can also play a role in the destruction of ethynyl, through reactions with HCO + and H + 3. The dominant destruction reactions are ...
The polarity of C=O bond also enhances the acidity of any adjacent C-H bonds. Due to the positive charge on carbon and the negative charge on oxygen, carbonyl groups are subject to additions and/or nucleophilic attacks. A variety of nucleophiles attack, breaking the carbon-oxygen double bond, and leading to addition-elimination reactions.