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Why isn't ortho isomer of aminobenzenesulfonic acid a major product?

In the second paragraph of the image you can see that p-aminobenzenesulfonic acid is more stable.

In the second paragraph of the image you can see that p-amino-benzenesulphonic acid is more stable.

But according to me, o-aminobenzenesulfonic acid should be more stable as there is six-member cycle of H-bonding.

Am I wrong in my claim?

Swastik
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