How many of the transformations given below would result in aromatic amines?
How many of the transformations given below would result in aromatic amines?
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Correct Answer: 3
Solution and Explanation
The correct answer is 3.
Top Questions on Amines
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
How can you convert the following:
(i) Ethanoic acid to methanamineAmines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Arrange the following in increasing order of their basic strength in aqueous solution:
CH$_3$–NH$_2$, (CH$_3$)$_2$NH, (CH$_3$)$_3$NAmines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Why is the pK$_b$ value of aniline more than that of methylamine?- How can you obtain the following?
(a) Aniline from ammonium benzoate
(b) Benzene diazonium chloride from nitrobenzene
(c) 2,4,6-Tribromoaniline from aniline - An amine 'X' reacts with Hinsberg reagent and the product obtained is soluble in alkali. The amine 'X' is:
Questions Asked in JEE Main exam
- CrCl\(_3\).xNH\(_3\) can exist as a complex. 0.1 molal aqueous solution of this complex shows a depression in freezing point of 0.558°C. Assuming 100\% ionization of this complex and coordination number of Cr is 6, the complex will be:
- JEE Main - 2025
- Colligative Properties
- Suppose that the number of terms in an A.P. is \( 2k, k \in \mathbb{N} \). If the sum of all odd terms of the A.P. is 40, the sum of all even terms is 55, and the last term of the A.P. exceeds the first term by 27, then \( k \) is equal to:
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- Arithmetic Progression
- If \( \alpha + i\beta \) and \( \gamma + i\delta \) are the roots of the equation \( x^2 - (3-2i)x - (2i-2) = 0 \), \( i = \sqrt{-1} \), then \( \alpha\gamma + \beta\delta \) is equal to:
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- Complex numbers
- Let \( [x] \) denote the greatest integer function, and let \( m \) and \( n \) respectively be the numbers of the points, where the function \( f(x) = [x] + |x - 2| \), \( -2<x<3 \), is not continuous and not differentiable. Then \( m + n \) is equal to:
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- Differential Equations
- Let \( f(x) = \frac{x - 5}{x^2 - 3x + 2} \). If the range of \( f(x) \) is \( (-\infty, \alpha) \cup (\beta, \infty) \), then \( \alpha^2 + \beta^2 \) equals to.
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- Functions
Concepts Used:
Amines - Chemical Properties
There are many chemical properties of amines.
The primary and secondary amines, including several amine derivatives, have a direct impact on their properties due to the presence of hydrogen bonding. The compounds containing phosphorus have a lower boiling point and the compounds containing amines and alcohol have a higher boiling point. The structure of alkanols is immensely similar to that of amine except the presence of the hydroxyl group. In such a case, oxygen has a higher electronegativity than that of nitrogen, so alkanol compounds are more acidic in nature in comparison to the amines.
On account of the ability to form hydrogen bonds, the amines have tendencies of high solubility in water. The amine molecules such as Ethyl, diethyl, triethyl, and Methyl are gaseous in nature. Whereas, higher weight amines have a solid structure and alkyl amines have a liquid structure. There is an ammonia smell to gaseous amines and a fishy smell to liquid amines. The solubility of amines entirely depends upon the number of carbon atoms in the molecule.