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Traduzione e analisi delle parole da parte dell'intelligenza artificiale
In questa pagina puoi ottenere un'analisi dettagliata di una parola o frase, prodotta utilizzando la migliore tecnologia di intelligenza artificiale fino ad oggi:
- come viene usata la parola
- frequenza di utilizzo
- è usato più spesso nel discorso orale o scritto
- opzioni di traduzione delle parole
- esempi di utilizzo (varie frasi con traduzione)
- etimologia
Cosa (chi) è oxidation dye - definizione
CHEMICAL COMPOUND
Ley oxidation; Ley Oxidation
oxidation number
NUMBER THAT DESCRIBES DEGREE OF OXIDATION OF AN ATOM IN A CHEMICAL COMPOUND; THE HYPOTHETICAL CHARGE THAT AN ATOM WOULD HAVE IF ALL BONDS TO ATOMS OF DIFFERENT ELEMENTS WERE FULLY IONIC
Oxidation states; Oxidation State; Metal oxidation state; Oxidation number; Oxidation numbers; List of oxidation numbers by element; List of oxidation states by element; Elementary state; List of oxidation states; Oxidation value; List of oxidation states of the elements
(also oxidation state)
¦ noun Chemistry a number representing the number of electrons lost or gained by an atom of a particular element when chemically combined.
Oxidation state
NUMBER THAT DESCRIBES DEGREE OF OXIDATION OF AN ATOM IN A CHEMICAL COMPOUND; THE HYPOTHETICAL CHARGE THAT AN ATOM WOULD HAVE IF ALL BONDS TO ATOMS OF DIFFERENT ELEMENTS WERE FULLY IONIC
Oxidation states; Oxidation State; Metal oxidation state; Oxidation number; Oxidation numbers; List of oxidation numbers by element; List of oxidation states by element; Elementary state; List of oxidation states; Oxidation value; List of oxidation states of the elements
In chemistry, the oxidation state, or oxidation number, is the hypothetical charge of an atom if all of its bonds to different atoms were fully ionic. It describes the degree of oxidation (loss of electrons) of an atom in a chemical compound.
Triarylmethane dye
![[[Methyl violet]] 2B](https://commons.wikimedia.org/wiki/Special:FilePath/Methyl Violet 2B.png?width=200 "[[Methyl violet]] 2B")
![[[Methyl violet]] 6B](https://commons.wikimedia.org/wiki/Special:FilePath/Methyl Violet 6B.png?width=200 "[[Methyl violet]] 6B")
![Methyl violet 10B]]](https://commons.wikimedia.org/wiki/Special:FilePath/Methyl Violet 10B.png?width=200 "Methyl violet 10B]]")
![[[Pararosaniline]]](https://commons.wikimedia.org/wiki/Special:FilePath/Pararosaniline.png?width=200 "[[Pararosaniline]]")
![[[Fuchsine]] (hydrochloride salt)](https://commons.wikimedia.org/wiki/Special:FilePath/Rosaniline hydrochloride.svg?width=200 "[[Fuchsine]] (hydrochloride salt)")
![[[New fuchsine]] (As chloride)](https://commons.wikimedia.org/wiki/Special:FilePath/Neofuchsin.svg?width=200 "[[New fuchsine]] (As chloride)")
![[[Fuchsine acid]]](https://commons.wikimedia.org/wiki/Special:FilePath/Fuchsine acid vector.svg?width=200 "[[Fuchsine acid]]")
![[[Phenolphthalein]]](https://commons.wikimedia.org/wiki/Special:FilePath/Phenolphthalein-low-pH-2D-skeletal.svg?width=200 "[[Phenolphthalein]]")
![[[Phenol red]]](https://commons.wikimedia.org/wiki/Special:FilePath/Phenol-red-zwitterionic-form-2D-skeletal.png?width=200 "[[Phenol red]]")
![[[Chlorophenol red]]](https://commons.wikimedia.org/wiki/Special:FilePath/Chlorophenol red.png?width=200 "[[Chlorophenol red]]")
![[[Cresol red]]](https://commons.wikimedia.org/wiki/Special:FilePath/Structure of cresol red.png?width=200 "[[Cresol red]]")
![[[Bromocresol purple]]](https://commons.wikimedia.org/wiki/Special:FilePath/Structure of Bromocresol purple.png?width=200 "[[Bromocresol purple]]")
![[[Bromocresol green]]](https://commons.wikimedia.org/wiki/Special:FilePath/Bromocresol green.svg?width=200 "[[Bromocresol green]]")
![[[Malachite green]]](https://commons.wikimedia.org/wiki/Special:FilePath/Malachite green structure.svg ?width=200 "[[Malachite green]]")
![[[Brilliant green (dye)]]](https://commons.wikimedia.org/wiki/Special:FilePath/Structure of the dye brilliant green.png?width=200 "[[Brilliant green (dye)]]")
![[[Brilliant blue FCF]], a common food colorant](https://commons.wikimedia.org/wiki/Special:FilePath/Brilliant Blue FCF(2).svg?width=200 "[[Brilliant blue FCF]], a common food colorant")
![[[Victoria blue B]]](https://commons.wikimedia.org/wiki/Special:FilePath/Victoria blue B with charge.svg?width=200 "[[Victoria blue B]]")
![[[Victoria blue FBR]]](https://commons.wikimedia.org/wiki/Special:FilePath/Victoria blue FBR revised.svg ?width=200 "[[Victoria blue FBR]]")
![[[Victoria blue BO]]](https://commons.wikimedia.org/wiki/Special:FilePath/Victoria blue BO.svg?width=200 "[[Victoria blue BO]]")
![[[Victoria blue FGA]]](https://commons.wikimedia.org/wiki/Special:FilePath/Victoria pure blue FGA revised.svg?width=200 "[[Victoria blue FGA]]")
![[[Victoria blue 4 R]]](https://commons.wikimedia.org/wiki/Special:FilePath/Victoria blue 4 R revised.svg?width=200 "[[Victoria blue 4 R]]")
![[[Victoria blue R]]](https://commons.wikimedia.org/wiki/Special:FilePath/Victoria blue R revised.svg?width=200 "[[Victoria blue R]]")
![[[Eosin B]]](https://commons.wikimedia.org/wiki/Special:FilePath/EosinB.png?width=200 "[[Eosin B]]")
![[[Eosin Y]]](https://commons.wikimedia.org/wiki/Special:FilePath/EosinY.png?width=200 "[[Eosin Y]]")
![[[Rhodamine B]]](https://commons.wikimedia.org/wiki/Special:FilePath/rhodamine B.svg?width=200 "[[Rhodamine B]]")
![[[Rhodamine 123]]](https://commons.wikimedia.org/wiki/Special:FilePath/Rhodamine 123.svg?width=200 "[[Rhodamine 123]]")
![[[Fluorescein]]](https://commons.wikimedia.org/wiki/Special:FilePath/Fluorescein 2.svg ?width=200 "[[Fluorescein]]")
CLASS OF DYE
Triphenylmethane Dye; Triphenylmethane dye; Victoria blue dye
Triarylmethane dyes are synthetic organic compounds containing triphenylmethane backbones. As dyes, these compounds are intensely colored.
Wikipedia
Tetrapropylammonium perruthenate
Tetrapropylammonium perruthenate (TPAP or TPAPR) is the chemical compound described by the formula N(C3H7)4RuO4. Sometimes known as the Ley–Griffith reagent, this ruthenium compound is used as a reagent in organic synthesis. This salt consists of the tetrapropylammonium cation and the perruthenate anion, RuO−4.
