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The reaction is initiated by ZnCl2 or H2SO4. You can look up the structure of phthalic anhydride. The important part is one of the O-C=O's of phthalic anhydride. That O gets protonated, the ring opens, and next there is a (+)C=O hanging loose. That (+) attacks phenol (twice!) in nucleophilic aromatic sudstitution, which produces a (C6H4-OH)2 attached to the lactone of the newly formed phenolphthalein. The acid-base reaction (red-white) reaction results from the opening and closing of the lactone ring.

2007-08-12 10:48:11 · answer #1 · answered by steve_geo1 7 · 0 0

Synthesis Of Phenolphthalein

2016-12-10 16:08:29 · answer #2 · answered by ? 4 · 0 0

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