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can you also upload for inorganic chem

can u make more videos like this dealing with recent IIT NEET exams

Great video!

Thank you🫂🫂

thanks

That was amazing tnx❤❤❤

well explained, thank u

This video was way better than the ones I just saw. Thanks

thank you so much man

Thank you❤❤

ur explanation is amazing. what a gem, thank you so much

thank you for so many examples

The best

why can't you touch the hydrogens in the benzene ring and replace them with a chlorine?

Thank you so much.That was amazing🙏😆❤

helped a lot, thank you so much

thanks sir was searching for it for like past 30 min

wow, great practiced subscribed!

thank you 😢

Thank you so much sir

Keep it up, I really appreciate the effort you've made to make this content it's been really grateful

I am very grateful for your videos. I am a Turkish Chemistry student in Turkiye, but I was having difficulty while studying for my organic chemistry 1 course and biochemistry course because I could not find enough resources, but thanks to your detailed explanations, I understand very well.

thank you sir!😊

Thank you. Very simple explanation

pls upload a pdf of thiss

How is OH a weak nucleophile?

Thank you so much fr

THANK YOU

You are such a life saver. Thank you for doing this.

Thanks so much, so well explained, I'm so happy

why is the sucrose glycosidic bond alpha and beta whilst the lactose one isnt ? ik it sounds dumb but im new to this.

super helpful video!! Thank you !!

Thanks for this amazing explanation, I am so glad I stumbled on this channel❤❤

Thanks 😊

Great video

Sorry i dont understand on 11.10, where the chirality, like its attached to 2 methyl groups, its the same

Thank you so much!!! Just what I needed

More explanation for low iq students in Ghana

At 25:00 I dont understand what you said about chiral centres. Can you please explain?

Hi there! Could you please explain why tertiary alkyl would react with a primary alcohol to form an ether via SN1? Because I though that primary alcohols are more likely to undergo a nucleophilic subsitution reaction via SN2 pathway as with SN1 the steric hindrance around the tertiary carbon in the alkyl halide makes it less favorable for SN1 to occur? Thank you :)

Thank you so much!

At 23:05, ring contraction should occur. A major product is not a six membered ring but a five membered ring.

Thank you sir🙏

amazing video! quick question how do we find the number of the bond coupling of J?

The tutorial really help, thanks ❤

Thank you so much ! You dont know how much i needed this right now May god bless you

why is NaSH strong nuc but KO isnt

The second example is confusing. I think, there should be 5 chiral centers.

On the very first one, why would you not hydride shift from the carbon on the left since it would form a more stable product ?

Thank you for explaining and labeling Non Bonding MO and Anti Bonding MO. I finally get it!!!