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In this video, I’ll explain the key differences between polar protic and polar aprotic solvents and how each affects nucleophilicity and reaction mechanisms in organic chemistry. Understanding the role of solvents in reactions is crucial for predicting the outcome of nucleophilic substitution (SN1, SN2) and elimination reactions (E1, E2). You’ll learn: What polar protic and polar aprotic solvents are. How polar protic solvents (like water, alcohols, and acetic acid) stabilize ions and affect nucleophile strength. How polar aprotic solvents (like DMSO, acetone, and DMF) do not stabilize anions as much, leading to different reactivity patterns. How solvent choice impacts nucleophilicity, especially in SN1 and SN2 reactions. Examples of reactions in both solvent types, including how they affect reaction rates and mechanism pathways. By the end of this video, you’ll understand how solvent polarity and protic/aprotic nature can influence organic reactions and nucleophilic behavior, which is essential for mastering reaction mechanisms in organic chemistry. This video is perfect for students studying organic chemistry, reaction mechanisms, or anyone who wants to understand how solvents impact nucleophilic substitution and elimination reactions. Don’t forget to like, comment, and subscribe for more chemistry tutorials!