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Barfoed's test is a chemical test used for detecting the presence of monosaccharides. It is based on the reduction of copper(II) acetate to copper(I) oxide (Cu 2 O), which forms a brick-red precipitate. [1] [2] RCHO + 2Cu 2+ + 2H 2 O → RCOOH + Cu 2 O↓ + 4H + (Disaccharides may also react, but the reaction is much
Well-known reactions and reagents in organic chemistry include ... Barfoed's test; Bargellini reaction; Bartoli indole synthesis, Bartoli reaction [19] [20] [21]
Christen Thomsen Barfoed. Christen Thomsen Barfoed (16 June 1815 – 30 April 1889) was a Danish chemist credited with the development of a method to detect monosaccharide sugars in a solution, now known as the Barfoed's test. [1] [2] Barfoed is also credited with having introduced systematic chemical analyses in Danish agricultural sciences. [3]
Additionally, protein binding triggers a metachromatic reaction, evidenced by the emergence of a species that absorbs light around 595 nm, indicative of the unprotonated form [10] This dye creates strong noncovalent bonds with the proteins, via electrostatic interactions with the amino and carboxyl groups, as well as Van Der Waals interactions ...
Molisch test (using α-napthol) indicating a positive result (see purple ring). Molisch's test is a sensitive chemical test, named after Austrian botanist Hans Molisch, for the presence of carbohydrates, based on the dehydration of the carbohydrate by sulfuric acid or hydrochloric acid to produce an aldehyde, which condenses with two molecules of a phenol (usually α-naphthol, though other ...
The dehydrated ketose then reacts with two equivalents of resorcinol in a series of condensation reactions to produce a molecule with a deep cherry red color. Aldoses may react slightly to produce a faint pink color. Fructose and sucrose are two common sugars which give a positive test. Sucrose gives a positive test as it is a disaccharide ...
Phosphomolybdic acid is also occasionally used in acid-catalyzed reactions in organic synthesis. It has been shown to be a good catalyst for the Skraup reaction for the synthesis of substituted quinolines. [6] Bismuth phosphomolybdate catalyzes ammoxidation in the Sohio process. [7]
The reaction order is 1 with respect to B and −1 with respect to A. Reactant A inhibits the reaction at all concentrations. The following reactions follow a Langmuir–Hinshelwood mechanism: [4] 2 CO + O 2 → 2 CO 2 on a platinum catalyst. CO + 2H 2 → CH 3 OH on a ZnO catalyst. C 2 H 4 + H 2 → C 2 H 6 on a copper catalyst. N 2 O + H 2 ...