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Welcome to Part 3 – Nucleophilic Addition Reactions of Alkynes 🧪🔥 This is one of the most scoring yet heavily misunderstood topics in Organic Chemistry for JEE Main, JEE Advanced, NEET UG & Boards. Part 1 – Introduction & Preparation of Alkynes 🔥 Part 2 – Physical Properties & Electrophilic Additions ⚡ Part 3 – Nucleophilic Addition Reactions 🧪 Part 4 – Oxidation Reactions of Alkynes 🔷➡️🔶 Part 5 – Substitution Reactions of Alkynes ♻️ Part 6 – Isomerization, Polymerization & Misc. reactions, Uses & Laboratory tests 🔄✨ In this session, we break things down so simply that you’ll never fear alkyne mechanisms again! You’ll finally understand why alkynes—especially terminal alkynes—behave like powerful nucleophile magnets⚡, how the acidic terminal hydrogen (H⁺) drives the mechanism, and what makes alkynes more reactive than alkenes in several nucleophilic pathways. 🚀 What You’ll Learn Today: 👉 Formation of Acetylide Ions — the real game-changers in nucleophilic chemistry 👉 CN⁻ Addition (Cyanide attack) explained like never before 👉 Grignard Reagent & Organolithium additions 🔥 👉 Metal-catalysed hydrogenation that proceeds via nucleophilic mechanisms 👉 How nucleophiles attack the electron-deficient triple bond 👉 Step-by-step mechanism breakdown + product prediction hacks 🎯 This session focuses on deep understanding, not mugging up. Perfect for concept building, top-rank preparation, and MCQ accuracy improvement. #AlkyneReactions #organicchemistry #organicchemistryclass11 #chemistrymadeeasy #reactionmechanisms