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Unlike many compounds with the acet-prefix which have a 2-carbon chain, acetone has a 3-carbon chain. That has caused confusion because there cannot be a ketone with 2 carbons. The prefix refers to acetone's relation to vinegar (acetum in Latin, also the source of the words "acid" and "acetic"), rather than its chemical structure. [28]
Liquid properties Std enthalpy change of formation, Δ f H o liquid: −249.4 kJ/mol Standard molar entropy, S o liquid: 200.4 J/(mol K) Enthalpy of combustion, Δ c H o –1785.7 kJ/mol Heat capacity, c p: 125.5 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: −218.5 kJ/mol Standard molar entropy, S o gas: 295.35 J ...
Isopropylidene acetone. Identifiers CAS Number. 141-79-7 ... This compound is a colorless, volatile liquid with a honey-like odor. [3] Synthesis
It resembles an inverted eutectic, with the δ phase combining with the liquid to produce pure austenite at 1,495 °C (2,723 °F) and 0.17% carbon. At the peritectic decomposition temperature the compound, rather than melting, decomposes into another solid compound and a liquid. The proportion of each is determined by the lever rule.
Flubber, also commonly known as slime, is a non-Newtonian fluid, easily made from polyvinyl alcohol–based glues (such as white "school" glue) and borax. It flows under low stresses but breaks under higher stresses and pressures. This combination of fluid-like and solid-like properties makes it a Maxwell fluid.
The fractional distillation of organic substances played an important role in the 9th-century works attributed to the Islamic alchemist Jabir ibn Hayyan, as for example in the Kitāb al-Sabʿīn ('The Book of Seventy'), translated into Latin by Gerard of Cremona (c. 1114–1187) under the title Liber de septuaginta. [1]
The feather is adjusted and made ever smaller by adding increasing amounts of oxygen to the flame. A welding feather is measured as 2X or 3X, with X being the length of the inner flame cone. The unburned carbon insulates the flame and drops the temperature to approximately 5,000 °F (2,760 °C).
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 ...