Bondline / Reactions

Epoxide ring opening (acid)

Under acid the epoxide oxygen is protonated first; the nucleophile then attacks the more substituted carbon, which carries more positive charge.

Substitution · 3 steps

Conditions

Dilute acid in an alcohol or water (compare base, which attacks the less hindered carbon).

Mechanism in 3 steps

Red curly arrows show where each pair of electrons moves.

OHOH2+HO+HO++
Step 1The epoxide oxygen is protonated.
HO+HOHO+OHH2OMeOH++
Step 2Methanol attacks the more substituted carbon, opening the ring.
HO+OHH2OOOHH3O+++
Step 3Loss of a proton gives the neutral ether-alcohol.

About substitution reactions

In a substitution, a nucleophile replaces a leaving group on a saturated carbon. Whether it happens in one step (SN2) or through a carbocation (SN1) depends on the substrate, the nucleophile and the solvent.

Practise this mechanismDraw the curly arrows yourself and Bondline checks each one. Or add it to your notes and watch it in 3D.

Open in Bondline