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Question
How will you carry out the following conversions?
toluene `->` p-toluidine
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Solution
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Illustrate the following reaction giving suitable example in each case: Diazotisation
Write equations of the following reactions:
Acetylation of aniline
Why is benzene diazonium chloride not stored and is used immediately after its preparation?
Why does acetylation of –NH2 group of aniline reduce its activating effect?
Predict the product of reaction of aniline with bromine in non-polar solvent such as \[\ce{CS2}\].
Why is aniline soluble in aqueous HCl?
How will you carry out the following conversions?
p-toluidine diazonium chloride `→` p-toluic acid
Match the compounds given in Column I with the items given in Column II.
| Column I | Column II | ||
| (i) | Benzene sulphonyl chloride | (a) | Zwitter ion |
| (ii) | Sulphanilic acid | (b) | Hinsberg reagent |
| (iii) | Alkyl diazonium salts | (c) | Dyes |
| (iv) | Aryl diazonium salts | (d) | Conversion to alcohols |
A colourless substance ‘A’ \[\ce{(C6H7N)}\] is sparingly soluble in water and gives a water soluble compound ‘B’ on treating with mineral acid. On reacting with \[\ce{CHCl3}\] and alcoholic potash ‘A’ produces an obnoxious smell due to the formation of compound ‘C’. Reaction of ‘A’ with benzenesulphonyl chloride gives compound ‘D’ which is soluble in alkali. With \[\ce{NaNO2}\] and \[\ce{HCl}\], ‘A’ forms compound ‘E’ which reacts with phenol in alkaline medium to give an orange dye ‘F’. Identify compounds ‘A’ to ‘F’.
Predict the reagent or the product in the following reaction sequence.
In order to distinguish between C2H5NHz and C6H5NHz, which of the following reagents is useful?
Benzene diazonium chloride is a ______.
Aniline dissolved in dilute HCl is reacted with sodium nitrate at 0 °C. This solution was added dropwise to a solution containing equimolar mixture of aniline and phenol in dil. HCl. The structure of the major product is:
Identify A and B for the following reaction:
What are polymers?
How will the following be converted? (Give chemical equation)
Aniline to benzene diazonium chloride.
Given below are two statements:
Statement I: Benzenediazonium salt is prepared by the reaction of aniline with nitrous acid at 273-278 K. It decomposes easily in the dry state.
Statement II: Insertion of iodine into the benzene ring is difficult and hence, iodobenzene is prepared through the reaction of benzenediazonium salt with KI.
In the light of the above statements, choose the most appropriate answer from the options given below:
