Naming Esters - IUPAC Nomenclature, Branches, Substituents, & Benzene Rings - Organic Chemistry

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Our instructor literally copied all the givens here with the same sequence and made it an activity for us in naming esters. I am so happy I found this vlog 😂😂

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[@hlohi3550]

Thank you very much.
Carboxylic acid, Sulphonic acid and acid anhydride have higher priority than ester. So please make a video on that one when ester is a prefix (when these above mentioned functional groups are present). It will be very helpful.

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I just wanted to revise the naming of esters and it was a good quick revision
Really helped me

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this video really helped me to understand esters nomenclature, thank you so so much for this video! ❤️🇵🇭

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Thank you so much,it became easier for naming esters now❤️

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[@fullsun6335]

I think we can name 14:05 as methyl isobutanoate(I) or methyl isobutyrate (C).
edit: thank u sm for this! your lecture videos literally help me during exam szns

[@zangwoo]

No isobutanoate would be a common name here we are doing iupac nomenclature

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[@sharvina249]

Thank you very much for this video. I thought I won't be able to name the esters but you made it possible. Thank you very much!!

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[@myrau.ibrahim2771]

Well then, I assume I'll perfect my quiz tomorrow for naming esters. Thanks a lot.

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These videos explain esters so well

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Thanks so much I can't even imagine how l passed the ester naming

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[@ameyabelamkar4209]

Good video. Can you do one on just amides?

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Single handedly took down my doubts.

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[@jonathanvallejo1368]

16:30
i think is 2-methyl butyl ethanoate NOT 3-methyl butyl ethanoate
because when naming a long hydrocarbon chain we need to start from the side where the first substituent is found the closest.
Keep up the good work Sir..... and please reply if im wrong

[@rwayle]

The butyl chain is numbered as carbon 1 being the one attached to the oxygen.

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@@rwayle Thanks! Cause I've also wondered that

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[@Been_az]

Finally i understood esters 😂

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Bro at 21:12 ketonic group takes precedence over halogen in the prefix naming

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[@yvetteimsand5989]

For example 11, why wouldn’t we number the group without oxygen from right to left to but the methyl group on a lower number (2) instead of putting it on 3?

[@nabiha5772]

if you're talking about 15:25 then I've got the same problem

[@martinsimbeye9119]

the exact reason i came to the comment section

[@OreoWaffles44]

because the ester takes priority? you number the carbons going away from the ester. thus 3rd carbon and not the 2nd.

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5:58 this compound forms coox which is oyl halide.

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