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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 ...
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.
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
crotonic acid: 3724-65-0 C 4 H 6 O 2: diacetyl: C 4 H 6 O 2: diepoxybutane: C 4 H 6 O 2: 1,4-Dioxene: C 4 H 6 O 2: isocrotonic acid: C 4 H 6 O 2: methacrylic acid: 79-41-4 C 4 H 6 O 2: methyl acrylate: C 4 H 6 O 2: succinaldehyde: C 4 H 6 O 2: vinyl acetate: C 4 H 6 O 3: propylene carbonate: C 4 H 6 O 4: succinic acid: 110-15-6 C 4 H 7 BrO 2: 2 ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Acetic acid is the primary volatile acid in wine, but smaller amounts of lactic, formic, butyric, propionic acid, carbonic acid (from carbon dioxide), and sulfurous acid (from sulfur dioxide) may be present and contribute to VA; [2] [3] [4] in analysis, measures may be taken to exclude or correct for the VA due to carbonic, sulfuric, and sorbic ...
It can be prepared by treating a potassium-containing base such as potassium hydroxide or potassium carbonate with acetic acid: CH 3 COOH + KOH → CH 3 COOK + H 2 O. This sort of reaction is known as an acid-base neutralization reaction. At saturation, the sesquihydrate in water solution (CH 3 COOK·1½H 2 O) begins to form semihydrate at 41.3 ...
Acid strength is the tendency of an acid, symbolised by the chemical formula HA, to dissociate into a proton, H +, and an anion, A −. The dissociation or ionization of a strong acid in solution is effectively complete, except in its most concentrated solutions.