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Uses formula: = + for T = 0 to 36 °C = + for T = 36 to 170 °C Formula from Lange's Handbook of Chemistry , 10th ed. log 10 of acetic acid vapor pressure vs. temperature.
2.26 −12.9 –3.11 K b & K f [1] Formic acid: 101.0 2.4 8.0 –2.77 K b & K f [1] Naphthalene: 217.9 78.2 –6.80 Nitrobenzene: 210.8 5.24 5.7 –7.00 Phenol: 181.75 3.60 43.0 –7.27 K f [2] K b [1] Water: 100.00 0.512 0.00 –1.86 K b & K f [2] Ethyl Acetate: 77.1 [5] Acetic Anhydride: 139.0 [6] Ethylene Dichloride: 1.25 83.5 −35 [7 ...
acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...
The acetate anion, [CH 3 COO] −,(or [C 2 H 3 O 2] −) is one of the carboxylate family. It is the conjugate base of acetic acid. Above a pH of 5.5, acetic acid converts to acetate: [1] CH 3 COOH ⇌ CH 3 COO − + H + Many acetate salts are ionic, indicated by their tendency to dissolve well in water.
n-Butyl acetate is an organic compound with the formula CH 3 CO 2 (CH 2) 3 CH 3.A colorless, flammable liquid, it is the ester derived from n-butanol and acetic acid.It is found in many types of fruit, where it imparts characteristic flavors and has a sweet smell of banana or apple.
Octyl acetate, or octyl ethanoate, is an organic compound with the formula CH 3 (CH 2) 7 O 2 CCH 3. It is classified as an ester that is formed from 1-octanol (octyl alcohol) and acetic acid. It is found in oranges, grapefruits, and other citrus products. [10] Octyl acetate can be synthesized by the Fischer esterification of 1-octanol and ...
Methyl acetate, also known as MeOAc, acetic acid methyl ester or methyl ethanoate, is a carboxylate ester with the formula CH 3 COOCH 3. It is a flammable liquid with a characteristically pleasant smell reminiscent of some glues and nail polish removers.
Chloroacetic acid is mainly made by hydrolysing trichloroethylene in the presence of sulfuric acid: CCl 2 =CHCl + 2 H 2 O → CH 2 ClCOOH + 2 HCl; Dichloroacetic acid is manufactured in small quantities by reducing trichloroacetic acid. Trichloroacetic acid is made by directly reacting chlorine with acetic acid using a suitable catalyst.