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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 ...
Phase behavior Triple point: 289.8 K (16.7 °C), ? Pa Critical point: 593 K (320 °C), 57.8 bar Eutectic point with water –26.7 °C Std enthalpy change
Carboxylic acids are organic acids characterized by a carboxyl (-COOH) functional group. The naming of these compounds is governed by IUPAC nomenclature, which ensures systematic and consistent naming of chemicals.
As an eardrop it is used to treat infections of the ear canal. [1] It may be used with an ear wick. [2] As a liquid it is used to flush the bladder in those who have a urinary catheter in an attempt to prevent infection or blockage. [3]
Glycolaldehyde is the organic compound with the formula HOCH 2 −CHO.It is the smallest possible molecule that contains both an aldehyde group (−CH=O) and a hydroxyl group (−OH).
Glucose (C 6 H 12 O 6), ribose (C 5 H 10 O 5), Acetic acid (C 2 H 4 O 2), and formaldehyde (CH 2 O) all have different molecular formulas but the same empirical formula: CH 2 O.This is the actual molecular formula for formaldehyde, but acetic acid has double the number of atoms, ribose has five times the number of atoms, and glucose has six times the number of atoms.
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