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One day, Wurtz took two identical Alkyl Halides and added some Sodium and Dry Ether . Suddenly, they doubled in size and became a symmetrical Alkane ! Reaction:

Finally, to see how beautiful his creations were, he used Tollen's Reagent . When he added it to an Aldehyde , a brilliant Silver Mirror formed on the walls of the test tube. 📝 Quick Revision List: "Must-Know" Reactions Reaction Name Key Reactants Key Reagent Wurtz Alkyl Halide / Dry Ether Alkane (Double Carbon) Finkelstein Alkyl Halide NaIcap N a cap I Alkyl Iodide Swarts Alkyl Halide AgFcap A g cap F Hg2F2cap H g sub 2 cap F sub 2 Alkyl Fluoride Reimer-Tiemann CHCl3cap C cap H cap C l sub 3 NaOHcap N a cap O cap H Salicylaldehyde Kolbe’s CO2cap C cap O sub 2 NaOHcap N a cap O cap H Salicylic Acid Hoffmann Bromamide Br2cap B r sub 2 NaOHcap N a cap O cap H Primary Amine (1 less C) Important Chemical Reactions for Class 12 Chemistry One day, Wurtz took two identical Alkyl Halides

Here is a short, fun story that weaves together several essential Class 12 organic reactions to help you remember the reactants and products. 🧪 The Tale of the Organic Laboratory When he added it to an Aldehyde ,

His brother Fittig didn't want to be left out, but he only worked with Aryl Halides (Benzene rings). He used the same Sodium and Dry Ether to join two rings together, creating a Biphenyl . He used the same Sodium and Dry Ether

It sounds like you're looking for a creative way to remember the for Class 12 Chemistry (often called "Naming Reactions"). Students frequently use stories or "tricks" to memorize these for their board exams.

Meanwhile, the village doctor, Dr. Sandmeyer , was busy. He took a Diazonium Salt and used Cuprous salts ( Cu2Cl2cap C u sub 2 cap C l sub 2 Cu2Br2cap C u sub 2 cap B r sub 2 ) to quickly transform it into Haloarene .