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

This organic chemistry video tutorial explains how to name esters. It discusses the iupac nomenclature of esters including the common names as well and the rules that go with it. It contains plenty of examples and practice problems including esters with branches and complex substituents plus esters with other functional groups such as alcohols, alkyl halides ketones, and amines. It shows you how to tell which group has more priority and how to count the number of carbon atoms to determine what the parent name of each portion should be. The examples in this video also include benzene rings, diesters, and halides.
Organic Chemistry - Basic Introduction: • Organic Chemistry - Ba...
Organic Chemistry PDF Worksheets: www.video-tuto...
Organic Chemistry Exam 1 Playlist: bit.ly/3kJnNXU
Organic Chemistry 1 Exam 2 Playlist: bit.ly/3PKEApB
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How To Draw Lewis Structures: • Organic Chemistry - Ho...
Functional Groups Review: • Functional Groups
How To Calculate Formal Charge: • How To Calculate The F...
Valence Bond Theory: • Valence Bond Theory & ...
Hybridization of Atomic Orbitals: • Hybridization of Atomi...
Bond Length & Bond Strength: • Bond Strength and Bond...
Resonance Structures: • Resonance Structures
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Acids and Bases - Introduction: • Acids and Bases - Basi...
pKa Values of Acids: • pKa Values of Acids - ...
Constitutional Isomers: • Constitutional Isomers
IUPAC Nomenclature of Alkanes: • IUPAC Nomenclature of ...
Naming Cycloalkanes: • Naming Cycloalkanes Wi...
Naming Bicyclic Compounds: • Naming Bicyclic Compounds
Boiling Point of Organic Compounds: • Boiling Point of Organ...
Newman Projections: • Newman Projections
Chair Conformations: • Chair Conformation and...
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Organic Chemistry Exam 1 Review: • Organic Chemistry Exam...
Organic Chemistry Exam 1 Questions: • Organic Chemistry Exam...
Stereochemistry R/S Configuration: • Stereochemistry - R S ...
Optical Activity & Specific Rotation: • Optical Activity - Spe...
SN1, SN2, E1, E2 Reaction Mechanisms: • SN2 SN1 E1 E2 Reaction...
SN2 Reaction Mechanisms: • SN2 Reaction Mechanisms
SN1 Reaction Mechanisms: • SN1 Reaction Mechanism
SN1, SN2, E1, E2 - Practice Test: • SN1 SN2 E1 E2 Reaction...
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Naming Alkenes - E/Z System: • Naming Alkenes Using E...
Index of Hydrogen Deficiency: • Degree of Unsaturation...
Alkene Reactions Review: • Alkene Reactions
Alkyne Reactions Review: • Alkyne Reactions
Organic Chemistry Exam 2 Review: • Organic Chemistry 1 Ex...
Organic Chemistry Exam 2 Questions: • Organic Chemistry 1 Ex...
Alcohol Reactions: • Alcohol Reactions - HB...
Free Radical Reactions: • Free Radical Reactions
Organic Chemistry Reactions Summary: • Organic Chemistry Reac...
_______________________________________________________________________________________________
Organic Chemistry 1 Final Exam Review: • Organic Chemistry 1 Fi...
Organic Chemistry 2 Final Exam Review: • Organic Chemistry 2 Fi...

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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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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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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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[@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.

[@aldrichibia8302]

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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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[@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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U explain better than my teacher :)

[@AngeliaMeow]

I have a question about the one at 4:30 -- Why is it Butyl Propanoate and not Propyl Butanoate? Is it because the longer chain's name has to go first?

[@AngeliaMeow]

Also: Can 14:15 also be named Methyl isobutanoate?

[@JuliaNazneen-ve8ig]

Exactly that's what I was thinking it doesnt follow the pattern of the other examples.

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how you can know where to devid the molecular to part that contain ester group and ather doesn't contain .

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[@iZenZation]

15:30 would it not be ethyl-3-methyl butanoate? Would need to separate the ethyl and the number 3 with a hyphen , no?

[@arjunasok952]

In the naming of 3-methy butyl ethanoate,according to numbering possibility is 2 -methyl in the right handside?

[@abhishekgupta-fy9ic]

I think so bro...

[@aspirantsam633]

No, FG gets the priority and the carbon just after oxygen is counted the first.

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[@Helado123]

Finally i understood esters 😂

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[@hipsterrific4886]

it's kinda confusing me, does rules of parent chain doesn't apply in Esthers?

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[@harshaverma53]

Shouldn't the compound called phenyl benzoate be phenyl benzene carboxylate? Btw please keep posting it helps me so much. xxx

[@soumyapachpor5544]

how to do if carboxylic group and ester come in same compound
please help

[@JAYasSYNCOP]

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

[@suroop7339]

Yaa I got the answer.. Helped a lot