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Among the two modifications of Wittig discussed herein, the first one is the Wittig-Horner reaction, and the second one is the Schlosser modification. The first modification can eliminate the disadvantage of the insolubility of the side product (phosphine oxide), and the second one enables the selective formation of E-alkenes. Important books to be followed: Peter Sykes; Graham Solomons; Clayden, Greeves, Warren & Wothers; Carey, Sundberg. Playlist link of all the videos of Nucleophilic Addition to carbonyl: • Introduction | Nucleophilic Addition to Ca... Playlist link of all the videos of Nucleophilic Addition to C-C Multiple bond: • Introduction & Cyanoethylation | Nucleophi... Playlist link of all the videos of Electrophilic Addition to C-C Multiple bond: • Introduction | Electrophilic Addition to C... Playlist link of all the videos of Nucleophilic Aromatic Substitution: • Introduction to mechanism | Addition-Elimi... Playlist link of all the videos of Electrophilic Aromatic Substitution: • Arenium Ion Mechanism | Energy Profile Dia... Playlist link of all the videos of Elimination reaction: • Introductory idea of Elimination reaction ... Playlist link of all the videos of Substitution reaction: • NGP and SNi/SNi' with examples | Aliphatic... #reactionmechanism #HornerWittig #ImprovedWittig #Phosphonateester #phosphonatecarbanion #HornerWadsworthEmmons #SchlosserModification #ealkenes #betaine #lithiobetaine