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    • https://espanol.libretexts.org/Quimica/Libro%3A_Qu%C3%ADmica_Org%C3%A1nica_con_%C3%A9nfasis_Biol%C3%B3gico_(Soderberg)/09%3A_Reacciones_de_sustitucion_nucleofilica%2C_parte_II/9.6%3A_Problems_for_Chapter_9
      In the methionine biosynthesis reaction, the 5-methyl group from 5-methyltetrahydrofolate ends up on methionine, with overall retention of stereochemical configuration about the methyl carbon (this ca...In the methionine biosynthesis reaction, the 5-methyl group from 5-methyltetrahydrofolate ends up on methionine, with overall retention of stereochemical configuration about the methyl carbon (this can be demonstrated by using 2 H- and 3 H-labels on the methyl group- see section 9.1A).. Propose a likely mechanism for this process, taking into account the stereochemical outcome (you will need to infer the precursor to methionine).

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