@@yogikaadda9664 That's awesome! This Chem Libre page also does a great job with explaining the nomenclature ( chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Smith)/Chapter_17%3A_Benzene_and_Aromatic_Compounds/17.03_Nomenclature_of_Benzene_Derivatives ).
Thanks a lot for your amazing explanation it's helping me since I was in highschool and I'm still watching your videos, if I faced any problem in Chemistry or Maths I start looking for ur help. God bless you 🙏😇❣️
Thank you But u did not mentioned which has the highest priority when naming the parent chain How to know which one to choose nitrobenzene or benzoic acid ...as parent chain?
Aromatic nomenclature? More like automatic know more, greater! Thanks for making all of these wonderful videos and sharing your knowledge with all of us on RUclips!
I get confused when he pronounces words that ends with "-yl" and "-ol" or "-o". Are there any indications that he is saying, for example, phenyl and not phenol? or Acetyl and not aceto? or Nitro and not nitryl? :')
wouldn't the last example be 5-bromo-2-chloronitrobenzene , because wouldn't the NO2 with benzene ring make it the parent name and therefore start at NO2, not Cl?
Halogens and nitro group have the equivalent priority. So you only need to number it in a way that gives the substituents the lowest numbers. Whatever's #1 is the parent name.
I have a question about the last example, how come the NO2 was included when counting despite the fact that it's a parent compound on it's own (i.e Nitro Benzene, as earlier stated) just like the OH and the COOH were in the two questions preceeding it? Does this mean that if an Aniline (NH2) is given in a similar question it would also be counted, making the answer to be something like 4-bromo-1-chloro-2-aniline benzene? Cos you said that once a parent compound is identified, it's automatically number 1, but you didn't do so for that last example, it was as though you took the parent compound to be just Benzene.
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No shit talks, no extra points. The video is straight to point and super easy to understand. Thanks a lot. ❤
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Your 17 minute video is better than my professor's 1 hour and 20 minute one.
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PROFESSOR? WAIT YOUR SUPPOSED TO LEARN THIS IN COLLEGE? IM LEARNING THIS IN HIGHSCHOOL
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ruclips.net/video/fByvvHXoJGQ/видео.html
All benzene derivatives in less than 5 minutes....🔥
More than 50 compounds 👍👍👍🔥
@@yogikaadda9664 That's awesome! This Chem Libre page also does a great job with explaining the nomenclature ( chem.libretexts.org/Bookshelves/Organic_Chemistry/Map%3A_Organic_Chemistry_(Smith)/Chapter_17%3A_Benzene_and_Aromatic_Compounds/17.03_Nomenclature_of_Benzene_Derivatives ).
Great practice my exam is tuesday and this was not only good practice but helped me identify mistakes I could or did make thank you so much!
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Thanks a lot for your amazing explanation it's helping me since I was in highschool and I'm still watching your videos, if I faced any problem in Chemistry or Maths I start looking for ur help. God bless you 🙏😇❣️
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Thank you
But u did not mentioned which has the highest priority when naming the parent chain
How to know which one to choose nitrobenzene or benzoic acid ...as parent chain?
I think the one with C is more likely to be parent chain...
Benzoic acid
Omg this is really helpful not gonna lie, very useful video. Thank you very much
U'RE THE LOML ORG CHEM TUTOR !!!
Thank you sir for this wonderful video... Now I'm understood everything very clearly ❤️🙏
Aromatic nomenclature? More like automatic know more, greater! Thanks for making all of these wonderful videos and sharing your knowledge with all of us on RUclips!
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Excellent and clear explanation
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I get confused when he pronounces words that ends with "-yl" and "-ol" or "-o". Are there any indications that he is saying, for example, phenyl and not phenol? or Acetyl and not aceto? or Nitro and not nitryl? :')
thank you lord of chemistry
Solving these questions in class 12 from India
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wouldn't the last example be 5-bromo-2-chloronitrobenzene , because wouldn't the NO2 with benzene ring make it the parent name and therefore start at NO2, not Cl?
You're correct
Yep
no, because naming IUPAC rules want the smaller numbers so 1,2,4 is more preferable than 1,2,5
Halogens have more priority than nitro, in fact NO2 have the least priority put of all groups.
Halogens and nitro group have the equivalent priority. So you only need to number it in a way that gives the substituents the lowest numbers. Whatever's #1 is the parent name.
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Best explaination . Time saving.
I have a question about the last example, how come the NO2 was included when counting despite the fact that it's a parent compound on it's own (i.e Nitro Benzene, as earlier stated) just like the OH and the COOH were in the two questions preceeding it? Does this mean that if an Aniline (NH2) is given in a similar question it would also be counted, making the answer to be something like 4-bromo-1-chloro-2-aniline benzene? Cos you said that once a parent compound is identified, it's automatically number 1, but you didn't do so for that last example, it was as though you took the parent compound to be just Benzene.
I think it's because benzene-NH2 has a common name (aniline) while benzene-NO2 don't (nitro*benzene*)
@@tomusuki so is this the reason he didnot choose benzyl chloride as a parent chain?
Benzene is the only type of ring I can afford
16:48 I thought since the parent name will be nitrobenzene then nitro should lead the numbering 😅 just like in alkyne.
samee i am still confused about it
😅
I to did the same
Awesome.. it's important & pretty explaining
Whenever I him saying "let's try ine more example"❤❤❤❤❤
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😀
ruclips.net/video/fByvvHXoJGQ/видео.html
All benzene derivatives in less than 5 minutes....🔥
More than 50 compounds 👍👍👍🔥
You’re the best man
It was so helpfull..thank you 😘
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Better living through chemistry.
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Thank you once again.
May God bless you.
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try a video regarding how to make condensed formula for benzene derivatives that has cl attached to it
yeah I learn a lot
Under electronic microscope can we se cyclic ring based organic compounds why for what where when to be used applied
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Love from 🇮🇳
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Save my semester!
Thanks sir
Why don't you list down the priority of the substitute for naming🙁🙁🙁
thank you very much😍💙
Thankyou for an amazing video
Thanks so much sir..
Can anyone tell me the difference between phenyl and benzene when to use phenyl and benzene????????
phenyl has one less hydrogen so its basically a benzene that is NOT the parent chain bonded to a longer carbon chain
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I ❤ this video
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Thank you very much!
Is that last example wrong? I'm confused. Doesn't the parent (nitro) become the -1 carbon and not the chloro? Shouldn't it be 1, 2, 5 still?
u should rlly focus on what he was explaining
When the benzene ring named as a branch if attatched to an alkyl group?
Amazing 👍😘😘
Thank you so much!
Thanks
Thank you so Much 😊❤️❤️
Thank you so much 🤍
How to name a chemical the Benzene which 6 Hydrogen atoms are replaced by F, Cl, Br, NO2, OCH3 and CH=CH2 in clockwise direction?
2-Bromo-3-Chloro-4-Fluoro-1-Nitro-5-Vinyl-Anisol
Thanks 🥰
Thanks you sir
Ch3 is benzaldehyde
Thank you so much
Thank you so much 🥰
Can I get the link to watch Isomerism, functional group, IUPAC Nomenclature and naming of Alkanes,Alkenes, Alkynes, and other compounds
I'm lost for words 🙉 just wow
Benzene or benzamide more reactive?
amazing video
Thanks a lot 🙏
If there is another subscribe button I would've subscribed a hundered times and send it to my teacher
Hi, why didnt you use a parent name in the last example?
explain in detail tell us why its anisole how did the name come about
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Organic Chemistry is such a headache.....
it is😢
Cannot wait for this class to be over
I would have agreed but inorganic is worse
Yahh!😩
It is, but I'll take this over biochemistry any day lol.
Thank you 🥺
Good 👍
Is it only 17 min video or it is longer if you are a member?
what happens OCH3 and CH3 comes in the same benzene ring? what will be the patent name? toluene or anisole?
I thought we no the lowest possible no to the alkanes while the halogens and nitro are not given the lowest no.