What would the chemical name be for C13H8Cl3NOHow would you name this organic compound?What is the rationale...
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What would the chemical name be for C13H8Cl3NO
How would you name this organic compound?What is the rationale of the IUPAC name for DDT?What would the name and formula be for Mo+O+Se?Chemical name : MelamineWhat would the name of this organic compound be?What is the chemical name of the compound H2S4O?What is the iupac name for ch3ch2cooag?What is the chemical name of this derivative of aniline?IUPAC Name for the following?What would be the name of this compound?
$begingroup$
Formula
C13H8Cl3NO
SMILES
C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl
I found the diagram on the left in a book and drew the one on the right using
https://pubchem.ncbi.nlm.nih.gov/edit2/index.html
And got the SMILES description from that.
Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.
Is there a automatic naming engine out there?
A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137
organic-chemistry nomenclature molecular-structure
edited 1 hour ago
andselisk
17k655115
asked 2 hours ago
KalleMPKalleMP
389116
$endgroup$
add a comment |
$begingroup$
Formula
C13H8Cl3NO
SMILES
C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl
I found the diagram on the left in a book and drew the one on the right using
https://pubchem.ncbi.nlm.nih.gov/edit2/index.html
And got the SMILES description from that.
Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.
Is there a automatic naming engine out there?
A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137
organic-chemistry nomenclature molecular-structure
edited 1 hour ago
andselisk
17k655115
asked 2 hours ago
KalleMPKalleMP
389116
$endgroup$
1
$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago
1
$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago
2
$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
1 hour ago
3
$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
1 hour ago
add a comment |
$begingroup$
Formula
C13H8Cl3NO
SMILES
C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl
I found the diagram on the left in a book and drew the one on the right using
https://pubchem.ncbi.nlm.nih.gov/edit2/index.html
And got the SMILES description from that.
Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.
Is there a automatic naming engine out there?
A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137
organic-chemistry nomenclature molecular-structure
edited 1 hour ago
andselisk
17k655115
asked 2 hours ago
KalleMPKalleMP
389116
$endgroup$
Formula
C13H8Cl3NO
SMILES
C1=C(C(=CC(=C1)Cl)Cl)N(C(C2=CC=CC=C2)=O)Cl
I found the diagram on the left in a book and drew the one on the right using
https://pubchem.ncbi.nlm.nih.gov/edit2/index.html
And got the SMILES description from that.
Any clues as to what might be an IUPAC name and the formal way to write it out? Have I have even drawn it correctly? I could not do it exactly because the two rings kept connecting if I followed the same orientation. I don't know enough about double ring compounds to even hazard a guess.
Is there a automatic naming engine out there?
A compound called British Impregnite found in The Scientific method by Louis F. Fieser p.137
organic-chemistry nomenclature molecular-structure
organic-chemistry nomenclature molecular-structure
edited 1 hour ago
andselisk
17k655115
asked 2 hours ago
KalleMPKalleMP
389116
edited 1 hour ago
andselisk
17k655115
asked 2 hours ago
KalleMPKalleMP
389116
edited 1 hour ago
andselisk
17k655115
edited 1 hour ago
andselisk
17k655115
edited 1 hour ago
andselisk
17k655115
17k655115
asked 2 hours ago
KalleMPKalleMP
389116
asked 2 hours ago
KalleMPKalleMP
389116
asked 2 hours ago
KalleMPKalleMP
389116
389116
1
$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago
1
$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago
2
$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
1 hour ago
3
$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
1 hour ago
add a comment |
1
$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago
1
$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago
2
$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
1 hour ago
3
$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
1 hour ago
1
1
$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago
$begingroup$
Try Chemspider chemspider.com
$endgroup$
– Waylander
2 hours ago
1
1
$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago
$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago
2
2
$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
1 hour ago
$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
1 hour ago
3
3
$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
1 hour ago
$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
1 hour ago
add a comment |
2 Answers
2
active
oldest
votes
$begingroup$
Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.
Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide
edited 1 hour ago
Loong♦
33.3k883172
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
$endgroup$
add a comment |
$begingroup$
There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:
Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.
References
- Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.
answered 1 hour ago
andseliskandselisk
17k655115
$endgroup$
add a comment |
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2 Answers
2
active
oldest
votes
2 Answers
2
active
oldest
votes
active
oldest
votes
active
oldest
votes
$begingroup$
Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.
Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide
edited 1 hour ago
Loong♦
33.3k883172
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
$endgroup$
add a comment |
$begingroup$
Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.
Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide
edited 1 hour ago
Loong♦
33.3k883172
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
$endgroup$
add a comment |
$begingroup$
Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.
Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide
edited 1 hour ago
Loong♦
33.3k883172
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
$endgroup$
Well, let's reconstruct that starting from the very right side, where it says a $ce{C_6H_5}$. The ring and the $ce{CO}$ group would be a benzaldehyde if it had an $ce{H}$ instead of an $ce{N}$, right? Or a benzoic acid if it was $ce{OH}$ instead of $ce{N}$. So what would it be if it had an $ce{NH_2}$-group? It would be a benzamide. If the $ce{N}$ is substituted with for example a chloride we call that N-chlorobenzamide. And now we have another $ce{N}$-centered ligand, the second phenyl ring. The ring has three positions, the one where it's connected to the rest of the molecule would be 1, so that makes a 2,4-dichlorophenyl.
Summarizing we get N-chloro-N-(2,4-dichlorophenyl)benzamide
edited 1 hour ago
Loong♦
33.3k883172
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
edited 1 hour ago
Loong♦
33.3k883172
edited 1 hour ago
Loong♦
33.3k883172
edited 1 hour ago
Loong♦
33.3k883172
33.3k883172
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
answered 2 hours ago
JustanotherchemistJustanotherchemist
1,894620
1,894620
add a comment |
add a comment |
$begingroup$
There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:
Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.
References
- Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.
answered 1 hour ago
andseliskandselisk
17k655115
$endgroup$
add a comment |
$begingroup$
There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:
Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.
References
- Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.
answered 1 hour ago
andseliskandselisk
17k655115
$endgroup$
add a comment |
$begingroup$
There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:
Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.
References
- Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.
answered 1 hour ago
andseliskandselisk
17k655115
$endgroup$
There is a paper [1] reporting a structural investigation of aromatic N-chloroamides.
They investigated polymorphs of similar compound they refer to as N-chloro-N-phenylbenzamide:
Chlorinated product, I suspect, is indeed is going to be named N‐chloro‐N‐(2,4‐dichlorophenyl)benzamide, as the first answer suggested.
References
- Naumov, P.; Topcu, Y.; Eckert-Maksić, M.; Glasovac, Z.; Pavošević, F.; Kochunnoonny, M.; Hara, H. Photoinduced Rearrangement of Aromatic N-Chloroamides to Chloroaromatic Amides in the Solid State: Inverted $Π_ce{N}–Σ_ce{N}$ Occupational Stability of Amidyl Radicals. The Journal of Physical Chemistry A 2011, 115 (26), 7834–7848. https://doi.org/10.1021/jp203771c.
answered 1 hour ago
andseliskandselisk
17k655115
answered 1 hour ago
andseliskandselisk
17k655115
answered 1 hour ago
andseliskandselisk
17k655115
answered 1 hour ago
andseliskandselisk
17k655115
17k655115
add a comment |
add a comment |
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1
$begingroup$
Try Chemspider chemspider.com
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– Waylander
2 hours ago
1
$begingroup$
Chemdoodle thinks it is [N-Chloro(2,4-dichlorophenyl)amino]phenylformaldehyde but there is probably a less systematic version as well.
$endgroup$
– matt_black
2 hours ago
2
$begingroup$
@matt_black Wow, that's like most complicated, but very much not systematic name I've seen.
$endgroup$
– Mithoron
1 hour ago
3
$begingroup$
@matt_black That's Chemdoodle being Chemdoodle, I think:)
$endgroup$
– andselisk
1 hour ago