Chapter 5: Amines

These are organic derivatives of ammonia

Classification of animes

According to the number of alkyl groups attached to the nitrogen atom

(a) Primary amines: have only one alkyl group attached. i.e. RNH2
Examples

CH3NH2 methylamine
CH3CH2NH2 ethylamine
CH3CHCH2CH3 2-aminobutane
NH2

(b) Secondary amines: have two alkyl groups attached to a nitrogen atom, R2NH
Examples

CH3 N CH3 Dimethylamine

CH3NHCH2CH3 Ethylmethylamine

(in alphabetical order)

CH3 N CH3 Trimethylamine

CH3

Physical properties of amines

1. Boiling and melting points

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 (a) Amines are polar compounds and therefore have higher melting and boiling points than
non-polar compounds of similar molecular mass due to dipole-dipole intermolecular forces
or hydrogen bonding,
(b) Primary and secondary amines have higher melting points and boiling points than tertiary
amines because tertiary amine do not form intermolecular hydrogen bonds
(c) Primary amines have higher melting and boiling points than secondary amines because they
form many hydrogen bonds per molecule.

2. Solubility
Amines are soluble in water because they can form hydrogen bonds with water but the
solubility decrease with alkyl chain length. Generally, primary amines are stronger bases than
secondary amines than tertiary amines because they form many hydrogen bonds in water.

3. Basicity of amines

Like ammonia, amines dissolve in water to form alkaline solution.

RNH2 + H2O ↔ RN+H3 + OH-(aq)

The strength of the alkaline solution is measured by the function Kb

[ ][ ]
[ ]

The higher the Kb the stronger the base or the higher the hydroxyl ion concentrations.

The ability to form alkaline solution, by amines, is due to the presence of a lone pair of electron on
the nitrogen atom.

(i) Groups (such as alkyl groups) that donate electrons increase the electron density of the lone
pair on the nitrogen atom. This increases the ability of alkylamine to attract a proton from
water to release hydroxide ions.

Thus, secondary amines are stronger bases than primary amines than ammonia because
secondary amine has two electron donating groups, primary amines has one, whereas,
amines have none.

However, tertiary amines are weaker bases than either secondary or primary amines
because their iminium ions are poorly solvated or hydrated or are unstable.

(ii) Groups that withdraw electrons from nitrogen atoms like phenyl group, make amines
weaker bases because they reduce the ability of the lone pair of electron on the nitrogen
atom and its ability to attract a proton from water.

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 Exercise

Explain the following observations

(i) The basic strength of the following amine is in order.

< NH3
< (CH3)3N

Solution

Trimethylamine is a stronger base than ammonia because the methyl groups donate electrons to
the nitrogen atom. This increases the density of alone pair of electron on the nitrogen atom on
trimethylamine and its ability to attract a proton from water and form hydroxyl ions.

Phenylamine is a weaker base than ammonia because the phenyl group pulls electrons from the
nitrogen atom. The reduction of electron density of alone pair on the nitrogen atom reduces the
ability of the lone pair to attract a proton from water and form hydroxyl group.

(ii) The boiling points of the following amines are

Solutions

Propylamine has the highest boiling point has the highest boiling point because it has two
hydrogen atoms on the nitrogen atom which form many intermocular hydrogen bonding. The
hydrogen bonds necessitate high temperature to break; hence high boiling point.

Ethylmethylamine has one hydrogen bond on the nitrogen atom and thus forms fewer hydrogen
bonds leading to lower boiling point.

Trimethylamine lack a hydrogen atom on a nitrogen atom and is incapable of forming inter-
molecular hydrogen bond leading to the lowest boiling point.

(iii) The acid constants Ka for the following amines are:

(CH3)3N 9.70

CH3CH2CH2NH2 10.67

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Solution

Trimethylamine (CH3)3N is a weaker base than propylamine because it form unstable aqueous
ammonium ions

Chemical properties

1. They react with acids to form salts

CH3NH2 + HCl CH3N+H3Cl-

2. Primary and secondary amines react with alkanoyl halides to form amides

Example

O O

CH3NH2 + CH3 C CH3C

Cl NHCH3

Mechanism

O O
O

-HCl
CH3C CH3C
CH3C Cl NCH3
Cl
H2NCH3
H
H2NCH3

Exercise

Complete and write a mechanism

CH3COBr + CH3CH2NH2

3. Primary amines undergo condensation reaction with carbonyl compounds between pH 4 -5 to

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 Example

CH3CH2NH2 + CH3CHO H+ CH3CH2N=CHCH3

MECHANISM

O OH OH
H
+
H Proton shift
CH3C CH3C CH3C NCH2CH3
H H

H
CH3CH2NH2 H

Then

OH2
H H

CH3C NHCH2CH3 CH3C NHCH2CH3

H
H

Then,

OH2
H
-H+
CH3C NHCHCH3
CH3C NHCH2CH3
H
H

NB: Take note of the movement of the proton

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 Exercise

Complete the following equations and write appropriate mechanism.

1. CH3COCH3 + RNH2 H+

2. CH3CH2CHO + H+
H2NH NO2

NO2

3. CH3COCH3 + H2NH H+

Distinguishing between primary, secondary and tertiary amines

A. Reagent: nitrous acid (NaNO2, HCl (0-50C))

Observation
(i) Primary amine: effervescence

Equation

RNH2 + NaNO2 + 2HCl RCl + N2(g) +H2O + NaCl

(ii) Secondary amines: yellow oil liquid

Equation

R2NH + NaNO2 + HCl R2N-NO + NaCl + H2O

(iii) Tertiary amines: no observable change du to the formation of soluble diazonium salts

Equation

R3N + NaNO2 + 4HCl RN2Cl + 2RCl + NaCl + 2H2O

(iv) Aromatic amine: no observable change du to the formation of soluble diazonium salts

Equation

ArNH2 + NaNO2 + 2HCl ArN2Cl + NaCl + 2H2O

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 Reaction of aromatic diazonium salts

Cu2O, Cu2+, H2O Ar-OH

CuI
Ar-Cl

CuBr
Ar-Br

Ar-N2 CuCN
Ar-CN

KI
Ar-I

H3PO2, H2O Ar-H

B. The Hinsberg test

Procedure: a mixture of small amount of the amine and benzenesuplfonyl chloride is shaken
potassium hydroxide, time allowed for the reaction to take place and then the mixture is
acidified.

Primary amine for a colorless solution with potassium hydroxide, forming a precipitate when the
mixture is acidified.

Secondary amine: forms a precipitate with potassium hydroxide insoluble when the mixture is
acidified

Tertiary amine: no observable change

Preparation of amines
1. Reaction of alkyl halides with ammonia
Example
NH3
CH3CH2Cl CH3CH2NH2

Mechanism
H H H

-H+
CH3 C Cl CH3 C NH3 CH3 C NH2

H H H

:NH3

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 2. By reduction of nitroalkane

NO2
NH2
Sn/HCl

Or

NO2
NH2
1. Fe, HCl

2. OH

3. By Hofmann degradation
Amides with no substituent on the nitrogen atom react with solution of bromine or chlorine
in sodium hydroxide to yield amines.
O

H2O
R C NH2 + Br2 + 4NaOH RNH2 + 2NaBr + 2Na2CO3 + 2H2O

Example
Br2 / -OH
CH3CONH2 CH3NH2

4. By reduction of nitriles
i.e. RCN LiAlH4, dry ether RCH2NH2
nitrile

Example
LiAlH4, dry ether
CH3CN CH3CH2NH2

Nitrile can be obtained by reacting alkyl halides with potassium cyanide.

i.e. RCl + KCN RCN +KCl

5. By reduction of oximes
i.e. RCH=NOH LiAlH4, dry ether RCH2NH2.
Example
CH3CH=NOH LiAlH4, dry ether CH3CH2NH2
Thank you
Dr. Bbosa Science

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