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Hint: Azo dyes are mainly formed by the reaction between an aromatic compound and the intermediate formed during Sandmeyer's reaction. Now try to identify the different types of dyes that can be formed with this reaction. With this, you can figure out the name of the azo dye that imparts red colour to the solution.
Complete step by step solution:
Azo compounds are compounds consisting of the functional group diazinyl. The functional group is mentioned below:
Where,
R and R' are alkyl or aryl groups
Stable azo compounds usually contain two aryl groups.
Azo dyes are organic compounds bearing the diazene functional group as defined by the International Union of Pure and Applied Chemistry(IUPAC). Azo dyes are widely used to treat textiles, leather articles and few foods as well.
One characteristic feature of azo dyes is their unique colour. They impart colour to the solution due to the alternating single and double bonds, known as a conjugated system. One such dye is the red dye.
The IUPAC name for red azo dye is p-N, N-dimethyl amino azo benzene. The structure for the compound is given below:
Note: Although many azo pigments are non-toxic, some compounds such as dinitroaniline orange, ortho-nitroaniline orange are found to be mutagenic. Along with that several case studies have reported azo pigments with basal cell carcinoma. Due to this, the European Union has prohibited the manufacture and sale of azo pigments since September 2003.
Complete step by step solution:
Azo compounds are compounds consisting of the functional group diazinyl. The functional group is mentioned below:
Where,
R and R' are alkyl or aryl groups
Stable azo compounds usually contain two aryl groups.
Azo dyes are organic compounds bearing the diazene functional group as defined by the International Union of Pure and Applied Chemistry(IUPAC). Azo dyes are widely used to treat textiles, leather articles and few foods as well.
One characteristic feature of azo dyes is their unique colour. They impart colour to the solution due to the alternating single and double bonds, known as a conjugated system. One such dye is the red dye.
The IUPAC name for red azo dye is p-N, N-dimethyl amino azo benzene. The structure for the compound is given below:
Note: Although many azo pigments are non-toxic, some compounds such as dinitroaniline orange, ortho-nitroaniline orange are found to be mutagenic. Along with that several case studies have reported azo pigments with basal cell carcinoma. Due to this, the European Union has prohibited the manufacture and sale of azo pigments since September 2003.
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