OCR A-Level Chemistry B H433
Development of Practical Skills in Chemistry
Elements of Life
Developing Fuels
Elements From the Sea
The Ozone Story
What's in a Medicine?
The Chemical Industry
Polymers and Life
Oceans
Developing Metals
Colour by Design
Chemical Literacy
Mathematical Skills in Chemistry
Polymers and Life
Basicity of amines
- 3 things to know
- Components 01, 02 and 03
Overview
Recall questions on why the nitrogen lone pair makes an amine basic, the salt formed with an acid, and the smell and solubility of short-chain amines.
What you need to know
Answer each one before you reveal it.
What is seen when a volatile amine meets hydrogen chloride fumes, why do short-chain amines dissolve well in water, and why is the amino group of an amino acid protonated at low pH?
Why is an amide much less basic than an amine?
Questions from this subtopic
Each one with the model answer underneath.
- 1
Give the formula of the primary amine functional group.
Model answer
The primary amine group is –NH₂.
- 2
Why is the amino group basic?
Model answer
The nitrogen atom has a lone pair of electrons that can be donated to a proton, so the group accepts H⁺.
- 3
What is formed when an amine accepts a proton?
Model answer
A positively charged alkylammonium cation, RNH₃⁺.
- 4
Which orbital on nitrogen holds the electron pair that is donated?
Model answer
The fourth orbital in the roughly tetrahedral arrangement around the nitrogen, holding the pair left over once the three bonds have been formed.
- 5
Write an equation for methylamine reacting with water.
Model answer
CH₃NH₂ + H₂O ⇌ CH₃NH₃⁺ + OH⁻.
- 6
Why is a solution of an amine in water alkaline?
Model answer
The amine takes a proton from water, leaving hydroxide ions in solution.
Other ways to work this
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