Properties of amines
The lower aliphatic amines (C1 -C2 ) are colourless gases and have ammonia like smell and those with four or more carbons are volatile liquids with fish like smell.
Aniline and other arylamines are usually colourless but when exposed to air they become coloured due to oxidation.
Due to the polar nature of primary and secondary amines, can form intermolecular hydrogen bonds using their lone pair of electorn on nitrogen atom. There is no such H-bonding in tertiary amines.
The boiling point of various amines follows the order,
Amines have lower boiling point than alcohols because nitrogen has lower electronegative value than oxygen and hence the N-H bond is less polar than -OH bond.
Table Boiling points of amines, alcohols and alkanes of comparable molecular weight.
Lower aliphatic amines are soluble in water, because they can form hydrogen bonds with water molecules. However, solubility decreases with increase in molecular mass of amines due to increase in size of the hydrophobic alkyl group. Amines are insoluble in water but readily soluble in organic solvents like benzene, ether etc.
The lone pair of electrons on nitrogen atom in amines makes them basic as well as nucleophilic. They react with acids to form salts and also react with electrophiles.
They form salts with mineral acids
In the aqueous solutions, the following equilibrium exists and it lies far to the left, hence amines are weak bases compared to NaOH .
The basicity constant Kb gives a measure of the extent to which the amine accepts the hydrogen ion (H+ ) from water,
we know that,
Larger the value of Kb or smaller the value of pKb, stronger is the base.
Table : pKb values of Amines in Aqueous solution. (pKb for NH3 is 4.74)
The factors which increase the availability of electron pair on nitrogen for sharing with an acid will increase the basic character of an amine. When a +I group like an alkyl group is attached to the nitrogen increase the electron density on nitrogen which makes the electron pair readily available for protonation.
a) Hence alkyl amines are stronger bases than ammonia.
Consider the reaction of an alkyl amine ( ) with a proton
The electron – releasing alkyl group R pushes electron towards nitrogen in the amine ( ) and provide unshared electron pair more available for sharing with proton.
Therefore, the expected order of basicity of aliphatic amines (in gas phase) is
The above order is not regular in their aqueous solution as evident by their pKb values given in the table.
To compare the basicity of amines, the inductive effect, solvation effect, steric hindrance, etc., should be taken into consideration.
In the aqueous solution, the substituted ammonium cations get stabilized not only by electron releasing (+I) effect of the alkyl group but also by solvation with water molecules. The greater the size of the ion, lesser will be the solvation. The order of stability of the protonated amines is greater the size of the ion, lesser is the solvation and lesser is the stability. In case of secondary and tertiary amines, due to steric hindrance, the alkyl groups decrease the number of water molecules that can approach the protonated amine. Therefore the order of basicity is,
Based on these effects we can conclude that the order of basic strength in case of alkyl substituted amines in aqueous solution is
The resultant of +I effect, steric effect and hydration effect cause the 20 amine, more basic.
In aniline, the NH2 group is directly attached to the benzene ring. The lone pair of electron on nitrogen atom in aniline gets delocalised over the benzene ring and hence it is less available for protonation makes the, aromatic amines (aniline) less basic than NH3 .
In case of substituted aniline, electron releasing groups like -CH3,-OCH3,-NH2 increase the basic strength and electron withdrawing group like - NO2,-X,-COOH decrease the basic strength.
Table pKb’s of substituted anilines (pKb value of aniline is 9.376)
The relative basicity of amines follows the below mentioned order
Alkyl amines > Aralkyl amines > Ammonia > N – Aralkyl amines > Aryl amines
Amines reacts with alkyl halides to give successively 2º and 3º amines and quaternary ammonium salts.
Aliphatic / aromatic primary and secondary amines react with acetyl chloride (or) acetic anhydride in presence of pyridine to form N – alkyl acetamide.
Aniline reacts with benzoylchloride (C6 H5COCl) in the presence of NaOH to give N – phenyl benzamide. This reaction is known as Schotten – Baumann reaction. The acylation and benzoylation are nucleophilic substitutions.
Three classes of amines react differently with nitrous acid which is prepared in situ from a mixture of NaNO2 and HCl .
a) primary amines
i) Ethylamine reacts with nitrous acid to give ethyl diazonium chloride, which is unstable and it is converted to ethanol by liberating N2 .
ii) Aniline reacts with nitrous acid at low temperature (273 – 278 K) to give benzene diazonium chloride which is stable for a short time and slowly decomposes even at low temperatures. This reaction is known as diazotization.
b) secondary amines
Alkyl and aryl secondary amines react with nitrous acid to give N – nitroso amine as yellow oily liquid which is insoluble in water.
This reaction is known as Libermann’s nitroso test,
c) Teritiary amine
i) Aliphatic tertiary amine reacts with nitrous acid to form trialkyl ammonium nitrite salt, which is soluble in water.
ii) Aromatic tertiary amine reacts with nitrous acid at 273K to give p – nitroso compound.
Aliphatic (or) aromatic primary amines react with chloroform and alcoholic KOH to give isocyanides (carbylamines), which has an unpleasant smell. This reaction is known as carbylamine test. This test used to identify the primary amines.
i) When primary amines are treated with carbon disulphide (CS2), N - alkyldithio carbomic acid is formed which on subsequent treatment with HgCl2 , give an alkyl isothiocyanate.
ii) When aniline is treated with carbon disulphide, or heated together, S- diphenylthio urea is formed, which on boiling with strong HCl , phenyl isothiocyanate (phenyl mustard oil), is formed.
These reactions are known as Hofmann – Mustard oil reaction. This test is used to identify the primary amines.
The group is a strong activating group. In aniline the NH2 is directly attached to the benzene ring, the lone pair of electrons on the nitrogen is in conjugation with benzene ring which increases the electron density at ortho and para position, thereby facilitating the electrophilic attack at ortho and para positions.
Aniline reacts with Br2 / H2O to give 2,4,6 – tribromo aniline a white precipitate.
To get mono bromo compounds, - NH2 is first acylated to reduce its activity.
When aniline is acylated, the lone pair of electron on nitrogen is delocalised by the neighbouring carbonyl group by resonance. Hence it is not easily available for conjugation with benzene ring.
The acetylamino group is thus less activating than the amino group in electrophilic substitution reaction.
Direct nitration of aniline gives o and p – nitro aniline along with dark coloured ‘tars’ due to oxidation. Moreover in a strong acid medium aniline is protonated to form anilinium ion which is m – directing and hence m – nitro aniline is also formed.
To get para product, the - NH2 group is protected by acetylation with acetic anhydride.
Then, the nitrated product is hydrolysed to form the product.
Aniline reacts with Conc. H2 SO4 to form anilinium hydrogen sulphate which on heating with H2 SO4 at 453 – 473K gives p- aminobenzene sulphonic acid, commonly known as sulphanilic acid, as the major product.
It does not under go Friedel – Crafts reaction (alkylation and acetylation) we know aniline is basic in nature and it donates its lone pair to the lewis acid AlCl3 to form an adduct which inhibits further the electrophilic substitution reaction.