Definition

Alkyl halides (or tosylate) will react with the hydrosulfide anion (HS‾) to give thiols.

Structural reaction scheme for Thiol formation [HS(–)], diagram 1 of 2
Figure 1. Thiol formation [HS(–)]

Explanation

In a concerted process, nucleophilic attack and loss of a leaving group occur simultaneously. The attack of the nucleophile (hydrosulfide anion) is carried out on the opposite side of the leaving group (bromide). Because of this, backside attack results in inversion of configuration on the chiral center.

In the transition state dotted lines show the partial bonds which are breaking and forming.

Structural reaction scheme for Thiol formation [HS(–)], diagram 2 of 2
Figure 2. Thiol formation [HS(–)]