Acylation (Acid Chloride Reactions)

A real energetic bunch of reactions. Luckily you are safe with this video. It shows what an acid chloride and acid anhydride is and show the advantages and disadvantages of using them in industry. The video also shows the mechanisms with 4 different nucleophiles.

[@husseinbaker1819]

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

[@cactus8911]

don't wanna change the like count bruh.

[@harrydonna90677]

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

[@nusulax3952]

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

[@alinalfc]

Thank you so much for this video!

[@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

[@zobiaahmad889]

Absolutely stunning

[@jeevg7890]

Thanks for this video btw you’re the best.

[@BoomShax123]

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

[@cactus8911]

My God you're a lifesaver.

[@alfonsobaladi1878]

So helpful!

[@AlleryChemistry]

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

[@catalyzt7162]

Thank you

[@vedika6260]

Great!!

[@briannahawkins1364]

better than my actual lecturer cheers

[@joebloor1413]

Legend

[@saraahmed632]

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

[@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 :)

[@rumaisachaudhry1360]

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

[@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.

[@jeevg7890]

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

[@saycute7281]

Thanks

[@abdulemalik8848]

Thank you.

[@AlleryChemistry]

You're welcome!

[@andrewbegbey1407]

Great video though, really useful sum up.

[@AlleryChemistry]

You're welcome!

[@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-)

[@pranjaljoshi5661]

better than my coaching teacher

[@user-pp1lr1bs6e]

can you make wather acid colaraid

[@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?

[@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...

[@jeevg7890]

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

[@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.

[@Letik3x]

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

[@daalhead1098]

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

[@mohsaj7652]

Sir looks like Murr from Impractical jokers

[@mafazsyed8365]

Did he throw his pen at 10:43

[@user-pp1lr1bs6e]

hi