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Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.
Vapor pressure of acetone based on formula, = + from Lange's Handbook of Chemistry, 10th ed. vapor pressure of acetone (log scale) based on formula, log 10 P m m H g = 7.02447 − 1161.0 224 + T {\displaystyle \scriptstyle \log _{10}P_{mmHg}=7.02447-{\frac {1161.0}{224+T}}} from Lange's Handbook of Chemistry , 10th ed.
Acetone and acetic anhydride ((CH 3 C(O)) 2 O) upon the addition of boron trifluoride (BF 3) catalyst: [11] (CH 3 C(O)) 2 O + CH 3 C(O)CH 3 → CH 3 C(O)CH 2 C(O)CH 3 A second synthesis involves the base-catalyzed condensation (e.g., by sodium ethoxide CH 3 CH 2 O − Na + ) of acetone and ethyl acetate , followed by acidification of the sodium ...
Isophorone, derived from acetone, is an unsaturated, asymmetrical ketone that is the precursor to other polymers. Muscone , 3-methylpentadecanone, is an animal pheromone . Another cyclic ketone is cyclobutanone , having the formula (CH 2 ) 3 CO .
The production of acetone by acetoacetate decarboxylase-containing or clostridial bacteria was utilized in large-scale industrial syntheses in the first half of the twentieth century. In the 1960s, the industry replaced this process with less expensive, more efficient chemical syntheses of acetone from petroleum and petroleum derivatives. [ 6 ]
This unit is a statute measure in the United Kingdom, defined in the Weights and Measures Act 1985. [6] One link is a hundredth part of a chain, which is 7.92 inches (20.1168 cm). [7] The surveyor's chain first appears in an illustration in a Dutch map of 1607, [8] and in an English book for surveyors of 1610. [9]
The study analyzed lead levels in children’s blood from 1940 to 2015, and found that those born between 1966 and 1986 had the highest rate of lead-associated mental illnesses like depression, ...
A step-growth copolymer -(-A-A-B-B-) n - formed by the condensation of two bifunctional monomers A–A and B–B is in principle a perfectly alternating copolymer of these two monomers, but is usually considered as a homopolymer of the dimeric repeat unit A-A-B-B. [6] An example is nylon 66 with repeat unit -OC-( CH 2) 4-CO-NH-(CH 2) 6-NH ...