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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.
Acid strength is the tendency of an acid, symbolised by the chemical formula, to dissociate into a proton, +, and an anion, .The dissociation or ionization of a strong acid in solution is effectively complete, except in its most concentrated solutions.
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 ...
Where an acid has both a systematic and a common name (like CH 3 COOH, for example, which is known as both acetic acid and as ethanoic acid), its salts can be named from either parent name. Thus, KCH 3 CO 2 can be named as potassium acetate or as potassium ethanoate. The prefix form, is "carboxylato-".
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An acetate is a salt formed by the combination of acetic acid with a base (e.g. alkaline, earthy, metallic, nonmetallic or radical base). "Acetate" also describes the conjugate base or ion (specifically, the negatively charged ion called an anion) typically found in aqueous solution and written with the chemical formula C 2 H 3 O − 2.