Is that any relation between hukel role and the position on the aromatic molecule? * Yes, the position number is equal to the (n) in the hukel role No, there is no relation between them. Hukel role correlated to the aromaticity only and no reference mention this relation For benzene, naphthalene and anthracene, yes there is such relation but for other we don't now

Is that any relation between hukel role and the position on the aromatic molecule? * Yes, the position number is equal to the (n) in the hukel role No, there is no relation between them. Hukel role correlated to the aromaticity only and no reference mention this relation For benzene, naphthalene and anthracene, yes there is such relation but for other we don't now

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter15: Benzene And Aromaticity

Section15.SE: Something Extra

Problem 53AP: Consider the aromatic anions below and their linear counterparts. Draw all of the resonance forms...

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For the following molecule classify it is as aromatic, antiaromatic, or nonaromatic, and identify the best supporting explanation. O aromatic cylic conjugated system with Hückel's number of TT electrons O antiaromatic; It only has 4 11 bonds O nonaromatic; there is not a continuous system of TT electrons due to the NH O antiaromatic; the compound has 4n TT electrons O aromatic; there is a porbital on every atom in the rings 4
Give answe of both question just with small explanation Asaap Thanks
Which one of the following statements from Chapter 8 and 18 is FALSE? O For a compound to be classified as aromatic, it must have an odd number of pairs of r-electrons and must be fully conjugated, cyclic and planar. O Inclusion of heteroatoms as part of the conjugated ring system renders the molecule to be considered non-aromatic. O Benzene is a six-membered ring where the r-electrons are equally shared across all six carbons in the ring and thus it possesses 36 kcal/mol of resonance stabilization energy. O All EAS reactions follow the same three mechanistic steps: (1) generate the electrophile, (2) capture the electrophile to give a carbocation intermediate, and (3) loss of a proton to regain aromaticity.
Consider the aromatic anions below and their linear counterparts. Draw all of the resonance forms for each. What patterns emerge?
Is the following compound aromatic or not? choose the correct answer (with motive) from the options given O A It has 8 TT electrons and satisfy Huckel's rule therefore it is aromatic O B. It is aromatic with electrons 10 m electrons and satisfy Huckel's rule OC It is not aromatic because the total number of electrons and does not satisfy Huckel's rule O D.It has 6 T electrons, therefore it does not satisfiy Huckel's rule
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Is the following molecule/compound aromatic or not aromatic? Choose the correct answer (and motive) from options provided ( ZI O It has 10 T aelectrons, therefore aromatic It has 6 m electrons and satisfy Hückel's rule, therefore aromatic O is not aromatic because it has 10 m electrons and does not satisfy Huckel's rule for aromatic compounds O It has 8 mr electrons, and therefore aromatic
is this molecule aromatic ，anti aromoatic，or non aromatic？？
Is the following compound aromatic or not? Choose the correct answer (with motive ) from the options given