Nucleophilic substitution reactions
8:32
Khan AcademyRevathi Ramachandran
Nucleophilic substitution reactions
In this video, we’ll explore nucleophilic substitution reactions, a fundamental concept in organic chemistry. These are reactions where a nucleophile, or a species rich in electrons, attacks an electrophilic carbon, usually bonded to a leaving group like a halide.\nAs the nucleophile comes in, the leaving group gets kicked out, a molecular ...
2 months ago
Substitution Nucleophile Mechanism
Ananya Sharma on Instagram: "Day 20 – SN1 Reaction Today we talk about the two-step substitution where the leaving group leaves first, forming a carbocation, and then the nucleophile attacks. More stable carbocation = faster SN1 🔥 [ SN1 reaction, unimolecular nucleophilic substitution, carbocation intermediate, two-step mechanism, leaving group, rate-determining step, polar protic solvent, tertiary halides, reaction mechanism, nucleophile, substitution reaction, stability trend, reaction kineti
1:21
Ananya Sharma on Instagram: "Day 20 – SN1 Reaction Today we talk about the two-step substitution where the leaving group leaves first, forming a carbocation, and then the nucleophile attacks. More stable carbocation = faster SN1 🔥 [ SN1 reaction, unimolecular nucleophilic substitution, carbocation intermediate, two-step mechanism, leaving group, rate-determining step, polar protic solvent, tertiary halides, reaction mechanism, nucleophile, substitution reaction, stability trend, reaction kineti
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E1 eliminations start the same way as the SN1 reaction, with the leaving group departing to form a carbocation. However instead of acting as a nucleophile the solvent acts as a weak base and an alkene is formed. Given that SN1 and E1 compete heat is added to drive the reaction towards elimination instead of substitution. #organicchemistry #ochem #organicchemistrytutor #STEM #premed
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