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Nucleophilic aromatic substitution reaction
The product is formed by a nucleophilic aromatic substitution reaction in which chloride is displaced by hydroxide ion. The product is ionized by -OH present in the reaction mixture; addition of acid (H3O+) forms the neutral phenol.
ClCH 2 CH 2 CH 2 COPh + Methanoic acid ----------------> CH2-(CH2)-CH2-CO-C 6 H 6
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The tris(monothiocarbamato)iron(III)complex shown to the right undergoes conversion from low to high spin state with an increase in temperature. This can be monitored by measurin
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