Master Organic Chemistry 2 with Every Reaction You Need to Know!

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Are you ready to master Organic Chemistry 2? 🌟 In this ultimate guide, we cover all the crucial reactions you need to know to excel in your course and ace your exams. From fundamental mechanisms to advanced concepts, we've got you covered. 🧪📘
What You'll Learn:
✅ Diels-Alder Reactions: Dive into the cycloaddition reaction that forms six-membered rings, a cornerstone in organic synthesis.
✅ Ketones and Aldehydes: Explore nucleophilic addition reactions and understand their reactivity and applications.
✅ Carboxylic Acid Derivatives: Learn about acyl substitution mechanisms and the transformations of esters, amides, and anhydrides.
✅ Organometallic Chemistry: Get to grips with Suzuki coupling, Grignard reagents, and their role in forming carbon-carbon bonds.
✅ Electrophilic Aromatic Substitution: Uncover the principles behind halogenation, nitration, sulfonation, and Friedel-Crafts reactions.
✅ And More! Including reduction and oxidation reactions, protecting groups, and complex synthetic pathways.
Whether you're a student preparing for exams or a chemistry enthusiast aiming to deepen your understanding, this video is packed with valuable insights and practical knowledge. Hit play now and take your Organic Chemistry 2 skills to the next level! 🚀🔬
Don’t forget to like, comment, and subscribe for more in-depth chemistry tutorials! If you have any questions, feel free to drop them in the comments below, and I'll be sure to help.
#OrganicChemistry #ChemistryTutorial #OrganicChem2 #DielsAlder #GrignardReagents #SuzukiCoupling #EAS #CarboxylicAcids #Ketones #Aldehydes #scienceeducation
Chapters:
0:00 Conjugated Dienes
1:59 Diels-Alder and Pericyclic Reactions
8:26 Benzene and Benzylic Reactions
11:57 Electrophilic Aromatic Substitution Reactions
15:00 Reactions of Ketones and Aldehydes
18:19 Carboxylic Acid Reactions
19:52 Acid Chloride Reactions
22:34 Anyhydride Reactions
25:35 Esters and Amides
28:18 Enols and Enolates
35:11 Preparation of Amines
38:09 Reactions of Aryl Diazonium Salts
40:00 Organometallic Chemistry

Опубликовано:

4 авг 2024

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Комментарии : 12

@rojaslab Месяц назад

If you enjoyed this video, don't forget to give it a thumbs up, subscribe for more educational content, and hit the notification bell to stay updated! Have questions or specific topics you'd like me to cover? Drop them below, and let's keep the chemistry conversation going! #ScienceCommunity #LearningTogether #OrganicChemistry

@Oxyten Месяц назад

This video is amazing! As a chemist, I can say there are a lot of things, that chemists should know, compared in one video, and I've never seen videos like that before. Good Job!

@rojaslab Месяц назад

This is the nicest comment I’ve ever received! Thank you 🙏🏽 You made my day!

@tamarabutterworth4461 Месяц назад

Omg! This is so helpful! I will probably watch this 20 times over the next few weeks 😂

@rojaslab Месяц назад

Woohoo! Good luck. You’ve got this! 💪🏾

@maxfrost2360 Месяц назад

I kinda get that you have time constraints but this is more like an excercise rather than a video for learning the reactions. If i know how sigmatropic rearrangements and diels alder behave under light und heat in regards to orbitals then the rest is pretty much refreshing stuff that i forgot some time ago. Anyway thx for your service

@rojaslab Месяц назад

Oh I totally agree! In fact, that was on purpose. I have individual videos that actually do the teaching of each of these topics. This video is to help review. If you’ve ever taken organic chemistry 2, then you know there’s a LOT of reactions to keep track of. This video is meant to help that, not be an introduction to new material!

@maxfrost2360 Месяц назад

Thanks for clarifying! One thing that i‘d like to add is that the formation of the enolate with LDA/NaH is also dependent on the temperature. You can get the thermodynamically favoured product with LDA -78C then heat it at room temp to form the thermodynamic product and subsequently trap it at -78C to react it further. This might be a question on peoples exams.

@rojaslab Месяц назад

@@maxfrost2360 You got it, Max! Absolutely crushing it!

@DOCB-op1qc 8 дней назад

34:46 is there a rule that's states when beta alkylation of a alkene would happen? why isnt it the alpha position??

@DOCB-op1qc 8 дней назад

is it just the major product due to steric hindrance?

@rojaslab 6 дней назад

This is a phenomenal question! I actually have a video about 1,2 and 1,4 cojugate addition reactions. Also known as Michael Additions. The full explanation is here: ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-QUfvvJz7-Lg.htmlsi=pqGkk6Kocx7D7z4p&t=496 Thanks for asking!