Diazo coupling reactions produce azo dyes, with colours dependent on the structure of the aromatic compounds involved.
This is an example of a diazo coupling reaction, where a diazonium salt reacts with 1-naphthylamine to form an azo dye. The product is red in colour due to the extensive conjugation in the azo compound.
The correct answer is (C) : Red
Alcohols undergo a number of reactions involving the cleavage of C – OH bond. However, phenols do not undergo reactions involving the cleavage of C – OH bond. Alcohols are weaker acids than water. Alcohols react with halogen acids to form the corresponding haloaklanes. Phenols are stronger acids than alcohols. A charac- teristic feature of phenols is that they undergo electrophilic substitution reactions such as halogenation, nitration, etc. Since –OH group is a strong activating group, phenol gives trisubstituted products during halogenation, nitration, etc.
Let $ P_n = \alpha^n + \beta^n $, $ n \in \mathbb{N} $. If $ P_{10} = 123,\ P_9 = 76,\ P_8 = 47 $ and $ P_1 = 1 $, then the quadratic equation having roots $ \alpha $ and $ \frac{1}{\beta} $ is:
Alcohol is formed when a saturated carbon atom bonds to a hydroxyl (-OH) group. It is an organic compound that contains a hydroxyl functional group attached to a carbon atom.
Phenol is formed when the -OH group replaces the hydrogen atom in benzene. It is an organic compound in which a hydroxyl group directly attaches to an aromatic hydrocarbon.
Ether is formed when oxygen atom bonds to two alkyl or aryl groups. It is an organic compound that has an oxygen atom that is connected to two aryl and alkyl groups.
Read More: Alcohol, Phenol, and Ethers