πŸ“šπŸ‘‰πŸ‘‰ PDF file for Wolff Rearrangement/ Arndt Eistert Synthesis of higher homologous acid

 


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At a glance :- The Wolff rearrangement is a reaction of Organic Chemistry where an alpha-diazocarbonyl compound is converted into a ketene by the loss of dinitrogen with accompanying 1,2-rearrangement.
     The reaction was discovered by  Ludwig Wolff in 1902.


Arndt Eistert reaction involves a series of chemical reactions and finally it synthesise a carboxylic acid from its homologue with one fewer carbon atoms. The Arndt Eistert Synthesis is a popular method for producing Ξ²- amino acids from Ξ±- amino acids.
    The reaction named after the German chemists Fritz Arndt and Bernd Eistert.

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