OCR A 6.1.3 Carboxylic Acids and Esters REVISION

[@kimdengjames6604]

Thank you sir. Much love from South Sudan. Stay blessed..🙏

[@AlleryChemistry]

You're welcome!

[@raphaeljohnny7227]

Thank you so much for your hard work sir

[@AlleryChemistry]

It's my pleasure

[@atchek6304]

What’s the difference between nucleophilic addition -elimination and nucleophilic substitution sir? I thought they were the same

[@martynaborisenkova8723]

Your videos are great! After watching I understand it perfectly. Thank you!

[@AlleryChemistry]

Glad you like them!

[@A_-.328]

Thanks for the video sir, but the last slide is wrong, the reaction is not reversible as its split into the carboxylate ion and not the carboxylic acid

[@bassamanvermohideen7994]

Can you please split this video into parts like you have done with previous videos.

[@morti5733]

fax

[@lucasandu5591]

25:00 how is the base hydrolysis of the ester reversible?

[@morti5733]

its not

[@khan99ish]

Do we need to know how to draw the addition-elimination reactions of acyl chlorides for OCR A?

[@tahmidchoudhury1013]

Hey Chris, can you do these PowerPoint revision walkthroughs for AQA A-level topics like you did for AS? Really enjoy your videos - Thanks!

[@AlleryChemistry]

There will be another poll soon to decide which exam board to do next. Stay tuned.

[@pokeninjaful]

9:06 Isn't an acyl group just -CO- not -COCl-

[@martynaborisenkova8723]

no its cocl the cl group makes it an acyl chloride

[@seselimbu6011]

CO is carbonyl group