6.5.2

Basicity & Nucleophilicity (A2 Only)

Test yourself

Basicity and Nucleophilicity

Amines display both basic and nucleophilic behaviour. We also will look at quaternary ammonium salts.

Illustrative background for BasicityIllustrative background for Basicity ?? "content

Basicity

  • Amines contain a lone pair of electrons. This makes the amine attracted to positive charge and, in particular, to protons.
    • This gives them the basic property of being able to accept protons - as shown above.
Illustrative background for NucleophilictyIllustrative background for Nucleophilicty ?? "content

Nucleophilicty

  • The lone pair on the nitrogen also makes amines nucleophilic.
    • It is attracted to positive charge.
    • They react with halogenoalkanes, acyl chlorides and acid anhydrides in nucleophilic reactions.
Illustrative background for Quaternary ammonium saltsIllustrative background for Quaternary ammonium salts ?? "content

Quaternary ammonium salts

  • Quaternary ammonium salts can be used as cationic surfactants.
  • Surfactants lower the surface tension of a liquid.
    • They can act as detergents, wetting agents, emulsifiers, foaming agents, and dispersants.
  • The cationic surfactant has a hydrophilic head, which is able to interact with water, and a hydrophobic tail, which interacts with organic matter such as oils or fats.

Strength of Basicity

We can evaluate the strength of an amine's basicity by considering its -R groups.

Illustrative background for Strength of basicityIllustrative background for Strength of basicity ?? "content

Strength of basicity

  • The basic strength of an amine depends on the availability of electrons.
    • If the molecule's electron pair is more available, it will be a stronger base.
  • This availability is often affected by whether the -R groups push or pull electron density.
    • We can use ammonia (NH3) as a reference and evaluate whether specific -R groups will increase or decrease the electron availability in comparison to ammonia.
Illustrative background for Aliphatic aminesIllustrative background for Aliphatic amines ?? "content

Aliphatic amines

  • Alkylated amines are more basic than ammonia.
    • Any alkyl -R group will increase basicity.
    • Alkyl -R groups push electron density towards the nitrogen.
    • This increases the electron density on nitrogen, making the lone pair more available.
Illustrative background for Aliphatic aminesIllustrative background for Aliphatic amines ?? "content

Aliphatic amines

  • So we can say aliphatic amine basicity strength is of the order:
    • 3o > 2o > 1o
Illustrative background for Aromatic aminesIllustrative background for Aromatic amines ?? "content

Aromatic amines

  • Aromatic amines are less basic than ammonia.
    • An aromatic -R group will decrease basicity.
    • Aromatic -R groups pull electron density away from the nitrogen.
    • This decreases the electron density on nitrogen, making the lone pair less available.

Jump to other topics

1Physical Chemistry

2Physical Chemistry 2 (A2 Only)

3Inorganic Chemistry

4Inorganic Chemistry 2 (A2 Only)

5Organic Chemistry 1

6Organic Chemistry 2 (A2 Only)

6.1Optical Isomerism (A2 Only)

6.2Aldehydes & Ketones (A2 Only)

6.3Carboxylic Acids & Esters (A2 Only)

6.4Aromatic Chemistry (A2 Only)

6.5Amines (A2 Only)

6.6Polymers (A2 Only)

6.7Biological Organic (A2 Only)

6.8Organic Synthesis (A2 Only)

6.9NMR Spectroscopy (A2 Only)

6.10Chromatography (A2 Only)

6.11A-A* (AO3/4) - Organic 2

Go student ad image

Unlock your full potential with GoStudent tutoring

  • Affordable 1:1 tutoring from the comfort of your home

  • Tutors are matched to your specific learning needs

  • 30+ school subjects covered

Book a free trial lesson