Alcohols, Phenols and Ethers
The total number of $$\sigma$$ and $$\pi$$ bonds present in azobenzene are:
Give the diazotisation reaction of aniline. Also give the chemical reaction involved in the preparation of red azo dye and light yellow azo dye.
The nitrosation of primary aromatic amines with nitrous acid (generated in situ from sodium nitrite and a strong acid, such as hydrochloric acid, sulfuric acid, or $$HBF_4$$) leads to diazonium salts.
Diazonium salts are important intermediates for the preparation of halides (Sandmeyer Reaction, Schiemann Reaction), and azo compounds.
Red Azo dye:
The naphthalen-2-ol ($$\beta$$-naphthol) is dissolved in sodium hydroxide solution and is cooled and mixed with the diazonium chloride solution.
An intense orange-red precipitate is formed.
Yellow azo dye:
The aniline is mixed with the diazonium chloride solution. An yellow colored precipitate is formed.
The total number of $$\sigma$$ and $$\pi$$ bonds present in azobenzene are:
Complete the following with appropriate structure: $$\displaystyle 2,3-\text{dinitroaniline}\xrightarrow [ (ii)Anisole ]{ (i){ NaNO }_{ 2 }\ and\ HCl\ at\ { 5 }^{ o }C } (A)$$
Diazo-coupling is use ful to prepare some
Coupling of benzene diazonium chloride with 1-napthol in alkaline medium will give:
Benzene diazonium chloride on reaction with aniline in the presence of dilute hydrochloric acid gives:
Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?
A compound $$X$$ has molecular formula $${C}_{7}{H}_{7}NO$$. On treatment with $${Br}_{2}$$ and $$KOH$$, $$X$$ gives an amine $$Y$$. The later gives carbylamine test. $$Y$$ upon diazotisation and coupling with phenol gives an azo dye. Thus, $$X$$ is :
Which statements are correct?
Complete the following.
Write short notes on Diazotisation