Naming Carboxylic Acids - IUPAC Nomenclature - Organic Chemistry 

Final Exams and Video Playlists: www.video-tutor.net/

Fast and acurate explanation including a lot of examples. Love it.

Ur so good I been struggling in these chapter. U just explain it briefly with In less than 16 min thank you. A big hug from Ethiopia 🇪🇹🇪🇹💚💛❤️

your videos have saved me from failing numerous times, thank you for your heard work! Much appreciated.

youre kind of amazing.. thank you so much

AMAZINGLY clear explanations that help me feel less like an idiot - thank you so much for your help!

The best explanation ever💌💌 love from Pakistan 🇵🇰 A big thank you..💖

How much I love you bro ! much love from Ethiopia

I love you💗🫶🥹 your videos are always so helpful, thank you!!

thanks so much oh my goodness. Science deploma is tmro and I've watched so many of ur vids to brush up on stuff we learend, plus learned some tips from you too. Ur a life saver, thanks so much

Oxo is for the ketone substituent and formyl is for the aldheyde substituent....right ???

Your explanations are The best . Thanks a lot for uploading this video

I was able to understand so much after this video! very great and to the point!

thank you so much for the video its the best one out there i was really confused with this chapter im feeling more confident now thanks to your videos

God bless you God will prosper you and your family😭😭🙏🏼🙏🏼🙏🏼❤❤❤

Out here saving lives

7:39 why didn't you begin numbering at the carbon that is within the carboxylic acid group??

Nice interface. My eyes are not get tired faster

Very good explanation 👌love from India ❤️

Not sure if the correction has been addressed, but @6:08, shouldn't the name of the compound be 4-amino-7-ethoxy formyl octanoic acid?

Amazing video. You are my savior

Was there any video made about this topic prior to this?

From Somalia thanks teacher

thank you sir;it was really helpful.

Thank you very much. Your videos are really helpful

is it wrong to have space between cyclohexane and carboxylic acid at 6:48?

Could you help me figure out what you would call a certain plant phenol from magnolia called Honokiol or, ((3’,5-di-(2-propenyl)-1,1’-biphenyl-2,2’-diol); (hypothetical) converted to phenolate salt using sodium carbonate, then neutralized pH with hcl? would there be a side reaction induced by the CO2 gas released from the hcl/sodium carbonate neutralization significant enough to convert it to carboxylic acid salt? Just wondering idk if I have this right but trying to learn.

Thank youu for your efforts👍🏻

very helpful for self-study

it was really helpful .thank you

Thanks for existing mate.

Like for real thnks🥰,,,understood evrythng basically

i genuinely love you💌💌💌💌💌💌

Thank you once again.

6:06 aldehyd substitution oxo ????

Nice

Thankyou very much sir

in last example 2_methyl 3 ethyl is not possible????

Why the dislikes?

I love this man

love your videos

Thank you so much

You are my saviour

Why in the three example named as (E)-2- butanoic not as 4-methyl butanoic acid or as trans!?

It helped alot

Great thank you sir

Thank you.

6:35 why is it not called cyclohexanoic acid?

does the E and Z the same with trans and cis

8:51 Is there supposed to be a capital letter and space there?

12:08 please I don’t understand how methyl got to the naming, cuz I can only see ethyl as a substituent, but methyl is not a substituent there??

2 degree name (carboxylic acid) will use if carboxylic acid is directly attached with cyclic compound.(oic acid will not use)

awesome video

How to name compounds with three carboxylic acid groups attached to a carbon chain?

You are the best

thank you so much ❤️❤️❤️❤️❤️❤️❤️

Why don't we name it cyclohexyl methanoic acid ? Since it looks like a substituent 6:45

1:38, what if, in the end of carbon 5 has a CH3?

I quite not understand the last compound you name, shouldn't you indicate the positions of the carboxylic acid , I think it should be hexane-1,6-dioic acid right

U R great.

thank you

Quick q , when do we remove the 'e' when naming for example pentane to pentan?

3:20 i can't understand it

I named the last one as using xy i.e ethoxy, methoxy Why is it ethyl and methyl

What am i suppose to do when there are more that one double or triple bond??? Anyooone?

I really hope someone can answer this: How can we name it if the carboxylic group is not on the end of the longest chain like when it is placed in the middle?

What if there are only 3 carbons?

Love you man

thanks sir

9:29 ETHERRRRRRR

I'm here in 2023 really thank you 💓

Ofika ekhaya Kobe kuhlatshiwe JG......uyastakula

Why do we use E and Z instead of cis and trans ? Please reply anyone

thanks!

6:08 but my teacher said when aldhyde act as lower priority the suffix is "Formyl" While oxo only apply on ketone. Can anyone explain?

Thanx alot 💙🤍

i love your other videos but this is hard.i cant understand

thanks :)

can benzoic acid be also named as benzene carboxylic acid? Why is it so?

6:48 why isn't it cyclohexanoic acid?

please upload a video about Carboxylic Acid and nitriles

My brain hurts haha I hate chemistry with a passion but of course I have to take it for nursing

i love you

How can butanoic acid form there are only 2 carbons

dont aldehydes use formyl instead of oxo????

Ethoxy should be numbered first then amino, right??

Why is Bio so difficult

Audio can be improved

Why cant cyclohexane caboxylic be called cyclohexanoic acid?

عسل عسل ماشاء الله 😔💜

oxo is the substituent name for ketones, not aldehydes, it;s supposed to be methanoyl?

correction at 1:42 possibly? (E-3) Pentoic Acid. I was taught to drop the (e) and add(oic)

❤️❤️❤️

0:21 Carboxylic acid can’t be called CO2H because there is no bonding between O-atom.

Not helping

5: 11 wrong❌ structure...