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Acetylene (systematic name: ethyne) is the chemical compound with the formula C 2 H 2 and structure H−C≡C−H. It is a hydrocarbon and the simplest alkyne. [8] This colorless gas is widely used as a fuel and a chemical building block. It is unstable in its pure form and thus is usually handled as a solution. [9]
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2. It is a colourless, flammable gas with a faint "sweet and musky " odour when pure. [ 7 ] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds ).
Pages for logged out editors learn more. Contributions; Talk; Contents move to sidebar hide ... Acetic acid: 17.7098 0.1065 Acetic anhydride ... Ethane: 5.562 0.0638 ...
Natural gas from different gas fields varies in ethane content from less than 1% to more than 6% by volume. Prior to the 1960s, ethane and larger molecules were typically not separated from the methane component of natural gas, but simply burnt along with the methane as a fuel. Today, ethane is an important petrochemical feedstock and is ...
Phase behavior Triple point: 91 K (−182 °C), 1.1 Pa Critical point: 305.3 K (32.2 °C), 4.9 MPa Std enthalpy change of fusion, Δ fus H o: 9.76 kJ/mol at −182 °C
A 3D model of ethyne (), the simplest alkyneIn organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. [1] The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula C n H 2n−2.
In the presence of excess oxygen, hydrocarbons combust. With, however, careful conditions, which have been optimized for many years, partial oxidation results. Useful compounds can obtained in this way: maleic acid from butane, terephthalic acid from xylenes, acetone together with phenol from cumene (isopropylbenzene), and cyclohexanone from ...
Ethenone is a highly reactive gas (at standard conditions) and has a sharp irritating odour.It is only reasonably stable at low temperatures (−80 °C). It must therefore always be prepared for each use and processed immediately, otherwise a dimerization to diketene occurs or it reacts to polymers that are difficult to handle.