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Ethane (US: / ˈ ɛ θ eɪ n / ETH-ayn, UK: / ˈ iː-/ EE-) is a naturally occurring organic chemical compound with chemical formula C 2 H 6. At standard temperature and pressure, ethane is a colorless, odorless gas. Like many hydrocarbons, ethane is isolated on an industrial scale from natural gas and as a petrochemical by-product of petroleum ...
When comparing a polar and nonpolar molecule with similar molar masses, the polar molecule in general has a higher boiling point, because the dipole–dipole interaction between polar molecules results in stronger intermolecular attractions. One common form of polar interaction is the hydrogen bond, which is also
Ethyl group (highlighted blue) as part of a molecule, as the ethyl radical, and in the compounds ethanol, bromoethane, ethyl acetate, and ethyl methyl ether.. In organic chemistry, an ethyl group (abbr. Et) is an alkyl substituent with the formula −CH 2 CH 3, derived from ethane (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 hydride; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H 14: n-hexane: dipropyl; Gettysolve-B; hexyl hydride; Skellysolve B 7 9 11 C 7 H 16: n-heptane
Dimethyl ether (DME; also known as methoxymethane) is the organic compound with the formula CH 3 OCH 3, (sometimes ambiguously simplified to C 2 H 6 O as it is an isomer of ethanol).
A cyclic ether, one of the most polar simple ethers that is used as a solvent. Anisole (methoxybenzene) An aryl ether and a major constituent of the essential oil of anise seed. Crown ethers: Cyclic polyethers that are used as phase transfer catalysts. Polyethylene glycol (PEG) A linear polyether, e.g. used in cosmetics and pharmaceuticals.
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
For example, CH 3-CH 3 is the alkane ethANe. The name of CH 2 =CH 2 is therefore ethENe. For straight-chain alkenes with 4 or more carbon atoms, that name does not completely identify the compound. For those cases, and for branched acyclic alkenes, the following rules apply: Find the longest carbon chain in the molecule.