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In organic chemistry, Fehling's solution is a chemical reagent used to differentiate between water-soluble carbohydrate and ketone (>C=O) functional groups, and as a test for reducing sugars and non-reducing sugars, supplementary to the Tollens' reagent test. The test was developed by German chemist Hermann von Fehling in 1849. [1]
Hermann von Fehling was born in Lübeck.With the intention of taking up pharmacy he entered Heidelberg University about 1835. After graduating he went to Gießen as preparateur to Justus von Liebig, with whom he elucidated the composition of paraldehyde and metaldehyde.
The standard method of determining the dextrose equivalent is the Lane-Eynon titration, based on the reduction of copper(II) sulfate in an alkaline tartrate solution, [1] an application of Fehling's test. Examples: A maltodextrin with a DE of 10 would have 10% of the reducing power of dextrose which has a DE of 100.
Various explicit approximations of the related Darcy friction factor have been developed for turbulent flow. Stuart W. Churchill [5] developed a formula that covers the friction factor for both laminar and turbulent flow. This was originally produced to describe the Moody chart, which plots the Darcy-Weisbach Friction factor against Reynolds ...
Formula IUPAC Name Common name Monohydric alcohols: CH 3 OH: Methanol: Wood alcohol C 2 H 5 OH: Ethanol: Alcohol, Rubbing alcohol C 3 H 7 OH: Propan-2-ol: Isopropyl alcohol, Rubbing alcohol C 4 H 9 OH: Butan-1-ol: Butanol, Butyl alcohol C 5 H 11 OH: Pentan-1-ol: Pentanol, Amyl alcohol C 16 H 33 OH: Hexadecan-1-ol Cetyl alcohol: Polyhydric ...
Before choosing a formula it is worth knowing that in the paper on the Moody chart, Moody stated the accuracy is about ±5% for smooth pipes and ±10% for rough pipes. If more than one formula is applicable in the flow regime under consideration, the choice of formula may be influenced by one or more of the following: Required accuracy
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.
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