A Lewis acid is an electron-pair acceptor, while a Lewis base is an electron-pair donor. When they react, the Lewis base donates both electrons that form a new coordination bond.
This is Additional Higher Level content in Reactivity 3.4, Electron-pair sharing reactions.
How the reaction works
A Lewis base must have an available electron pair, usually a lone pair. A Lewis acid must have somewhere to accept that pair, such as an incomplete valence shell, a vacant orbital, or a positive charge.
For example, ammonia reacts with boron trifluoride:
Nitrogen in donates its lone pair, so is the Lewis base. Boron in has only six electrons around it and accepts the pair, so is the Lewis acid.
The resulting species is a Lewis acid-base adduct. Although the new bond is described as a coordination bond because both bonding electrons originated from nitrogen, after formation it behaves like an ordinary covalent bond. The distinction describes the bond’s origin, not a permanently different bond type.
| Species | Lewis behavior | Reason |
|---|---|---|
| Base | Nitrogen donates a lone pair | |
| Base | Oxygen donates a lone pair | |
A common misconception is that all acid-base reactions require proton transfer. That describes BrønstedtoLowry reactions, but Lewis acid-base theory is broader: no proton needs to be transferred. For example, is a Lewis acid even though it cannot donate a proton.
Exam technique
If asked to identify a Lewis acid or base, state both the role and the evidence: “ is a Lewis base because it donates a lone pair.” In a mechanism, draw the curly arrow from the lone pair on the Lewis base toward the atom accepting the pair; reversing the arrow loses chemical accuracy.