@@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 🙏😇❣️
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 UA-cam!
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?
Chill bro😅 its not the end of this world . Gradually u will understand it. The tutor is also a human with no exceptional abilities so if he can then why we cant
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.
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? :')
@@mawddahll1911 are you sure? I read in a book the priority order is -COOH, -SO3H, -CHO, -CN, ......-R, -NO2, -X. So halogen is the last priority based on the book. But based on the link given above you are right.😅 I am confused now
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All benzene derivatives in less than 5 minutes....🔥
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@@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 ).
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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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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 UA-cam!
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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
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Chill bro😅 its not the end of this world . Gradually u will understand it. The tutor is also a human with no exceptional abilities so if he can then why we cant
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ua-cam.com/video/fByvvHXoJGQ/v-deo.html
All benzene derivatives in less than 5 minutes....🔥
More than 50 compounds 👍👍👍🔥
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Hey, at 9:28 can we say meta-dimethylbenzene? Or does it only work when we say xylene? 😊
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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.
May God bless you.
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والله انك فنان
thank you very teachable easy to gets
Thankyou for an amazing video
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?
I'm lost for words 🙉 just wow
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try a video regarding how to make condensed formula for benzene derivatives that has cl attached to it
You are the best
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
Thank you so much 🥰
I ❤ this video
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? :')
Under electronic microscope can we se cyclic ring based organic compounds why for what where when to be used applied
Thank you so much!
Thanks a lot 🙏
Thanks sir
Thanks 🥰
Can I get the link to watch Isomerism, functional group, IUPAC Nomenclature and naming of Alkanes,Alkenes, Alkynes, and other compounds
Thank you so much
Thank you 🥺
Thanks you sir
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
amazing video
Thanks
Good 👍
Benzene is the only type of ring I can afford
Ch3 is benzaldehyde
Question: At 11:09 can I name it 2-bromo-1-methylbenzene ? thank you
@Usama thank you :)
1-brome-2-methylbenzene the priority to the halogen
@@mawddahll1911 are you sure? I read in a book the priority order is -COOH, -SO3H, -CHO, -CN, ......-R, -NO2, -X. So halogen is the last priority based on the book.
But based on the link given above you are right.😅 I am confused now
Hi, why didnt you use a parent name in the last example?
Meeeeddddd u too good abeg
Is it only 17 min video or it is longer if you are a member?
for the last example, can I name it with 4-bromo-2-nitrochlorobenzene?
Exactly what came to my mind
Thanks a lot :)
based on what was he choosing the parent chain ?
explain in detail tell us why its anisole how did the name come about
Benzene or benzamide more reactive?