I love the way you go over details! Thank you so much

omg your teaching style is amazing! thank you

This was very simple and clear. Thank you

your handwriting is supreme.

@NOMVUYOELIZABETHNomadolo

7 жыл бұрын

I was just thing the same thing...lol mine is like the total opposite of that

You explain everything so clearly! Super helpful video, thank you!

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Your voice is so motivating lol thank u!

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I've just understood everything! Thank you.

This tutorial is great! Thanks for it.

Amazing explanation, thank you so much.

Great lesson! Congrats! Keep on keeping on!

@koudirkoudir3942

5 жыл бұрын

Can you ask with you ?

mam your way of teaching is very helpful to understand thank you so much :)

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Mam you have good voice, loved your way of teaching

I have an exam in 3 days time and you just simplified this topic for me 😭😁... Thank you so much

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Thank you for clear explanation

Any other videos by the same teacher? Thanks!

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Aldehydes and ketones undergo a variety of reactions that lead to many different products. The most common reactions are nucleophilic addition reactions, which lead to the formation of alcohols, alkenes, diols, cyanohydrins (RCH(OH)C&tbond;N), and imines R 2C&dbond;NR), to mention a few representative examples.

Wow! Pretty nice, I like it. Thanks

thank you , it is very helpful to me

Best video

Miss please do exercise solutions on this chapter

thank you ... sorry but i have a quick question : in the last example you reacted ketone with ( CH3Li ) not with (CH3MgLi ) my question is does it the same i mean it doesn't matter if i react ketone with grignard or with alkyl-Li ? :)

Nice video

Wow,I have never enjoyed mechanism of reactions like l did in this one today🔥🔥 Bsc industrial chemistry ( University of Embu-Kenya.)

Can u setback again in this teaching profession.I need ur guidance. I got a clarified explanation about them n need some more can u plzz

Thank you for explain

what happened to the hydrogen in example 3 ? at 5:52

Thank you very much!

@shersinghyadav1217

5 жыл бұрын

Keep , it. Up

Thank you somuch

Acyl chlorides do react with NaBH4! They undergo 2 succesive reactions with NaBH4. (Source: Organic Chemistry P.Y Bruice 7th edition)

good one

LIFE SAVER

thanks a lot!!

Thank you so much!! T_T

Is CH3Li (last example) considered as a hydride reagent. Does it work like LiAlH4? Thank you by the way! Very clear

@kumudtyagi1518

7 жыл бұрын

Samuel Swanzy no. it works just like grignard's reagent. the oh- obtained from hydroysis will combine with lithium.

Thank you!!

So good teach mam

Thank you.

Good

great!

In the minute 9:56 you obtain OH? Or is H2O

Will not there be rearrangement in the second example and the hydroxide will attach to the benzene ring?

@Imubozuu

7 жыл бұрын

There is no carbocation formation thus there won't be rearrangement. -in any case it would remove the aromaticity of the benzene making it less stable -hypothetically speaking

thanks for this useful video

What will happen if I react 1 degree alkyl halide with LiAlH4 and NaBH4 separately?

@sabinacharya5235

7 жыл бұрын

Apoorv Tyagi if u treat that then reaction padkinxa

I now Understand

super

any good LEAVING groups **

Thank you but aldehydes react with griganard to get primary alcohols .ketones react with griganard to get

@Dennis-io1ku

9 жыл бұрын

Karri Nagesu the only grignard to get a primary alkohol is with formaldehyd, if you use another aldehyd youll get a secondary alk. and if you use a keton youll get a tertriary alk.

ah your persian thank you for the vid

dddownsu yehhhhh buddy :P We now know more than anyone else O:) the last reaction :P

Thanks alot! I am surely going to ace my chemistry 4 paper :) Psstt : anyone here for edexcel gce chemistry unit 4? :P

@kaizoniumnh2405

6 жыл бұрын

so how was it? did u ace it? :)

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So clear ....thank you .