Input interpretation
![p-menth-4(8)-ene | aromatic atom count](../image_source/6d2c63f61d6d3d19ca6cebbf4724a697.png)
p-menth-4(8)-ene | aromatic atom count
Result
![0 atoms](../image_source/c2509487e51766e102e48ff0e063e9f2.png)
0 atoms
Aromatic atoms in place
![Begin by drawing the structure diagram for p-menth-4(8)-ene and selecting those atoms capable of forming aromatic bonds. These include carbon, nitrogen, oxygen, phosphorus, sulfur, arsenic, boron and selenium: Eliminate any atoms not in a ring: Eliminate any atoms with more than 3 neighbors, as these will be sp^3 hybridized and will not have an available \!\(\*StyleBox[](../image_source/46c37177528b884fa3273f8ac3b2516b.png)
Begin by drawing the structure diagram for p-menth-4(8)-ene and selecting those atoms capable of forming aromatic bonds. These include carbon, nitrogen, oxygen, phosphorus, sulfur, arsenic, boron and selenium: Eliminate any atoms not in a ring: Eliminate any atoms with more than 3 neighbors, as these will be sp^3 hybridized and will not have an available \!\(\*StyleBox["p", FontSlant->"Italic"]\) orbital for aromaticity (hydrogens shown in this step for clarity): There are no aromatic elements in p-menth-4(8)-ene, so it is not aromatic: Answer: | |
Quantitative molecular descriptors
![longest chain length | 7 atoms longest straight chain length | 3 atoms longest aliphatic chain length | 3 atoms aromatic atom count | 0 atoms H-bond acceptor count | 0 atoms H-bond donor count | 0 atoms](../image_source/d3a9baaf932bc019e198f7156c950335.png)
longest chain length | 7 atoms longest straight chain length | 3 atoms longest aliphatic chain length | 3 atoms aromatic atom count | 0 atoms H-bond acceptor count | 0 atoms H-bond donor count | 0 atoms