Birch reduction of anisole delivers the hydrogens to its a) ortho- and para- positions c) ipso- and para- positions b) ortho- and meta- positions d) ipso- and m

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The Birch reduction of anisole is thought to proceed by the formation of the radical anion which is protonated to give a cyclohexadienyl radical. The observed product, 2,5 dihydroanisole, can be formed from two possible cyclohexadienyls, one arising by ortho protonation of the anisole anion and the other by meta attack.

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could you please explain about 'ipso' position

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https://www.thoughtco.com/ipso-meso-and-peri-substitutions-608695 meghna see the difference

The attachment of an entering group to a position in an aromatic compound already carrying a substituent group (other than hydrogen). ...This position is ipso position where already substituent is present

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option B is correct

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