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You can remember this as the PAD-PEAD(protonation,elimination,addition,deprotonation) mechanism.

@senorsuraj8428

4 ай бұрын

Thank you so much! This made it so much easier to remember

I wonder why my O chem professor never covered this? This is all over the MCAT and DAT thanks man!

@Michelle-rv9ns

5 жыл бұрын

Hey, is there a great mcat practice book you recommend? I'm taking it next year

@ArielStar

5 жыл бұрын

@@Michelle-rv9ns Kaplan is pretty solid

@123magicT

5 жыл бұрын

my ochem professor covering it and it goes hands in hand with my MCAT studying!!!

@Jack-ky6ds

Жыл бұрын

The Villian studying ochem??? Incredible

@AYUSHV602

7 ай бұрын

we have in 12the class😂😂

JEE peeps take note, this question came in Mains 2021.

@dhruvmishra415

Жыл бұрын

Thanks bhai

@DeveshBhatt-vo6wl

9 ай бұрын

Thanks buddy❤

Can someone please help me? If I were to get the cyclic acetal structure formed after I did the protection group reaction, what would KMnO4 do to the cyclic acetal? Will it break it to for two carboxylic acids or not react with the cyclic acetal group?

hi do you mind putting your carbohydrate video back up ? I was watching it and now it says its deleted.

Hey your vids for algebra got me a 100% on a test thank you！

5:43 why didn't you use the water to deprotonate turning it into h3o+, is this feasible in this type of reaction?

It was really nice... Love from India ❤

5:21 why do we need to form the carbonyl again, why can't we just react it with CH3-OH and the OH2 leaves?

wow thanks for the video

Ma'am u r great ❤❤

It's there a protecting group site?

Hi, Please can you tell the programm do you use for drawing the molecules and chemistry reactions .. thank you so much in advance

@AdityaSharma-qb5qp

Жыл бұрын

bruh that stuff could be literally done on mspaint

9:37 could the acid remove the alcohol, leaving water, instead of remove the protecting group?

@limmuquan4796

2 жыл бұрын

You would get an unstable primary carbocation, so I don't think that would happen

Thank you once again.

At 6:00 didn't you form a ketal and not an acetal since you started with a ketone?

@taylorteehungpiao4814

3 жыл бұрын

Conventionally, all acetals and ketals are called as acetals right now

@doomedfleur12974

Жыл бұрын

@@taylorteehungpiao4814 dude thank you

Good man

Youhave all my support ...you are the best☺

lol the same question from 7:24 came in my test

Thank you!!!

Nice

Good video

Why is acetone not good at protecting a 1,3-diol but is good at protecting a 1,2-diol?

@rutilantly4572

Жыл бұрын

Idk man

@rutilantly4572

Жыл бұрын

It is what it is I guess

Protecting group 7:23

At 1:40, isn't it Ketal instead of Acetal? bc your staring product is a cyclic ketone?

@isaacreasmochia3240

4 жыл бұрын

It is a Ketal. May be he thought the structure was an aldehyde

🥰

To be honest, you were only saying what you were drawing, nothing was really explained to my understanding. I prefer other of your videos to this.

still useful but you were really better than this. too fast!!!