Yes. Within "The Chemical Reactions of Amino Acids / Reactions of Amino Groups" there are several examples - one of which is the ninhydrin reaction. A very widely applied reaction of the alpha amino group [that is the N in the peptide bond -CCN-CCN-], it is used to estimate the quantity of amino acids [in a sample] in very small amounts.
All amino acids and polypeptides with a free alpha group react with ninhydrin and yield [or produce] an intensely purple colored product - except for Proline and Hydroxyproline {both in which the alpha amino group is termed to be 'substituted' - something to do with carbon rings} which "yield derivatives with a characteristic yellow color."
See also 'Schiff's bases'.
Proline reacts with the ninhydrin reagent to form a yellow-colored complex. This complex is a result of a chemical reaction between proline and ninhydrin, leading to the formation of a chromophore that absorbs light in the visible spectrum, resulting in the yellow color.
When amino acids react with nitric acid, a yellow color may be observed due to the formation of nitro compounds. Nitric acid can nitrate amino acids, leading to the production of yellow-colored nitro derivatives. The specific yellow color observed can vary depending on the amino acid present and the reaction conditions.
You could get a mossy green colour (colour of the bag below) though it can change depending on how much yellow you put in.
Potassium superoxide is yellow in color.
The opposite of the colour purple on a colour wheel is yellow. To figure this out you need to understand the concept of primary and secondary colours. If the colour you have is a primary colour (one of red, yellow or blue) then the opposite colour is the secondary colour resultant from mixing the two remaining primary colours. If the colour you have is a secondary (purple, green or orange) then the opposite colour is the primary not involved in the making of the secondary colour.
Proline reacts with the ninhydrin reagent to form a yellow-colored complex. This complex is a result of a chemical reaction between proline and ninhydrin, leading to the formation of a chromophore that absorbs light in the visible spectrum, resulting in the yellow color.
When ammonia or primary and secondary amines are detected, a deep blue or purple color known as Ruhemann's purple is produced. Ninhydrin can also be used to monitor deprotection in solid phase peptide synthesis (Kaiser Test). The chain is linked via its C-terminus to the solid support, with the N-terminus extending off it. When that nitrogen is deprotected, a ninhydrin test yields blue. Amino-acid residues are attached with their N-terminus protected, so if the next residue has been successfully coupled onto the chain, the test gives a colorless or yellow result.
The amino group (-NH2) present in the amino acids/proteins is responsible for the ninhydrin reaction. Ninhydrin reacts with this group to form a colored compound, which is used in assays to detect amino acids.
Casein is a protein that contains amino acids, and when subjected to the ninhydrin test, it will generally produce a yellow or orange color due to the reaction between the amino acids in casein and ninhydrin. This color change is characteristic of the presence of proteins and can be used as a qualitative test for the detection of proteins like casein.
Well, the best I could come up with is it's either:C9H6O2orC4H3O2If someone knows any different please correct me.jman63: it is actually C9H6O4
butt colour and reaction - yellow slant colour and reaction - yellow carbohydrate fermented - glucose only H2S production :- blackening- NO H2S - (-) negative
yellow and green
yellow yellow yellow yellow
yellow it was also his favorite colour.
Yellow = Amarillo
Bcs its in yellow colour
It Makes the Colour Orange