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is 1,1-bis(3,4-dimethylphenyl)ethane a member of aromatics?

Input interpretation

1, 1-bis(3, 4-dimethylphenyl)ethane | is aromatic
1, 1-bis(3, 4-dimethylphenyl)ethane | is aromatic

Result

True
True

Aromatic atoms in place

Begin by drawing the structure diagram for 1, 1-bis(3, 4-dimethylphenyl)ethane 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:  For every highlighted atom, find the number of electrons available for aromaticity: • Atoms with a single cyclic π-bond contribute one electron.  Now examine the ring systems in 1, 1-bis(3, 4-dimethylphenyl)ethane. The first ring has 6 delocalized π electrons. Since this can be written as 4 n + 2 with n = 1 this ring is aromatic according to Hückel's rule:  The next ring has 6 delocalized π electrons. Since this can be written as 4 n + 2 with n = 1 this ring is aromatic according to Hückel's rule:  Highlight all aromatic atoms and bonds in 1, 1-bis(3, 4-dimethylphenyl)ethane: Answer: |   |
Begin by drawing the structure diagram for 1, 1-bis(3, 4-dimethylphenyl)ethane 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: For every highlighted atom, find the number of electrons available for aromaticity: • Atoms with a single cyclic π-bond contribute one electron. Now examine the ring systems in 1, 1-bis(3, 4-dimethylphenyl)ethane. The first ring has 6 delocalized π electrons. Since this can be written as 4 n + 2 with n = 1 this ring is aromatic according to Hückel's rule: The next ring has 6 delocalized π electrons. Since this can be written as 4 n + 2 with n = 1 this ring is aromatic according to Hückel's rule: Highlight all aromatic atoms and bonds in 1, 1-bis(3, 4-dimethylphenyl)ethane: Answer: | |