Acylation (Acid Chloride Reactions)

[@husseinbaker1819]

Sir you are a great teacher i love you (no homo) great techer

[@cactus8911]

don't wanna change the like count bruh.

[@Hxtice]

I’m honestly so grateful for this you have no idea, you explained everything so clearly and concisely. Literally wish you were my chem teacher! Thank you so much

[@nusulax3952]

Thankyou for the efforts you put into these videos, they are very helpful!

[@harrydonna90677]

LITERAL LEGEND, I was really struggling with this and you helped me so much!! thank you x

[@BoomShax123]

Thank you very much for this video! So so so helpful

[@alfonsobaladi1878]

So helpful!

[@AlleryChemistry]

Heh. Cheers! Please share vids. The more people that use them the better! 😉

[@cactus8911]

My God you're a lifesaver.

[@alinalfc]

Thank you so much for this video!

[@zobiaahmad889]

Absolutely stunning

[@mobap1554]

Does OCR need to know the four acyl chloride reactions as mechanisms too? Or do we just need to simply know the reactions themselves, e.g to make a RCOOH from Acyl Chlorides, you need cold water.

[@briannahawkins1364]

better than my actual lecturer cheers

[@abdulemalik8848]

Thank you.

[@AlleryChemistry]

You're welcome!

[@jeevg7890]

Thanks for this video btw you’re the best.

[@shaanveersamra954]

I thought with the amide reaction the hydrogen ion forms an ammonium ion which then reacts with chlorine forming ammonium chloride as opposed to hydrogen chloride

[@rt-viz954]

what happnes is you form HCl as he showed, but what he didnt show is you do this reacion with excess NH3. So what happens is the HCl reacts excess NH3, which forms ammonium cloride. (NH4+ Cl-)

[@jeevg7890]

Would you need to show the second ammonia molecule accepting the hydrogen with ammonia?

[@eesha5906]

Love your videos thank you! Quick question, shouldn’t the delta negative Cl & O atoms mean that they are open to attack from electrophiles too? Please please reply :(

[@salmanqureshi3361]

For AQA will we need to be able to name the products of each mechanism and write the overall equation? Just wondering. Great video by the way as usual- I have learnt a lot from your videos :)

[@andrewbegbey1407]

Great video though, really useful sum up.

[@AlleryChemistry]

You're welcome!

[@pranjaljoshi5661]

better than my coaching teacher

[@catalyzt7162]

Thank you

[@Letik3x]

We don’t need to know the mechanics for these now do we ?

[@rumaisachaudhry1360]

Will i lose marks if i use a double headed arrow? For the arrow removing the single electron from O

[@saycute7281]

Thanks

[@saraahmed632]

hello for the ocr a exam board do we not need to know anything for any of the mechanisms

[@charlesdale2600]

Won't the Cl- take the hydrogen of the newly connected H2O molecule? (after the double bond drops down kicking out the Cl) that why H-Cl is also a product. You have to show arrows showing where the hydrogen went.

[@jeevg7890]

Thought HCL wasn’t produced with NH3 thought it was NH4cl?

[@vedika6260]

Great!!

[@daalhead1098]

I feel like the N-substitued amide should be called an N-substituted ester or an R-substituted amide

[@musichighlight3852]

There is something that I am a bit confused about, what is the difference between acyl and carbonyl group ?

[@omarf4210]

A carbonyl group is a Carbon double bonded with Oxygen. An Acyl group is a halogen attached to that carbonyl functional group

[@RaviKumar-zg6eo]

Sir please explain mesalamine react with propionic anhydride...

[@sabinfatima6877]

So helpful

[@AlleryChemistry]

Glad it was helpful!

[@jeevg7890]

Is a primary amine more reactive than ammonia because of the positive inductive effect of the CH3 group or am I talking about something else?

[@jeevg7890]

Kerboodle book gets it the wrong way round?

[@منصورپوپل-ف9ي]

can you make wather acid colaraid

[@joebloor1413]

Legend

[@mohsaj7652]

Sir looks like Murr from Impractical jokers

[@mafazsyed8365]

Did he throw his pen at 10:43

[@منصورپوپل-ف9ي]

hi