4.Which of the following species are aromatic or anti-aromatic (assuming n-systems are fully planar)?Circle those that are aromaticPut an X through those that are anti-aromaticDo nothing to the structure otherwise5.Which of the following compounds will have the larger Amax ?Briefly explain in terms of MO theory and photon energy & basic wave property equations.6.For the allyl anion below,A)Draw the second resonance structure and show the arrow-pushing needed to get to that structure.B)Draw the Valence Bond Theory Orbital Overlap Diagram of the resonance hybridC)Make an Aufbau diagram of the relative energies of the n molecular orbitals, distribute the electrons of the p orbitals to the MO's, and label theMO's as r, mb, and ri (molecular orbital theory)D)Sketch the shapes of the 3 molecular orbitals in part C.

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Answered: Which of the following species are…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter18: Aromaticity

Section: Chapter Questions

Problem 15E

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Circle any of the following which you think are aromatic systems. For the ones that are aromatic systems, give the "n" (Huckel number.) It's possible tk have more than one. Thank you!
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Without counting hydrogens, determine which one of the following CANNOT be the unknownmolecule with molecular formula C7H8NOBr , and explain your reasoning.
Be sure to answer all parts. Hydrocarbon A possesses a significant dipole, even though it is composed of only C-C and C-H bonds. Part 1 out of 2 Complete a resonance structure of the above molecule so that the positive pole is on the left and the negative pole is on the right. Hint edit structure ... Solutic 2 attempts left Check my work Next part Guided So
Q4. Draw the orbitals of thiophene to show that is aromatic.
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13. Aniline and nitrobenzene are two substituted benzene compounds that contain nitrogen atoms. A) Use resonance structures to identify all carbon atoms that are electron rich on aniline. Mark the appropriate carbons in the figure below with a d-. NH₂ nitrobenzene aniline Note: this is benzene B) Use resonance structures to identify all carbon atoms that are electron deficient on nitrobenzene. Mark the appropriate carbons in the figure below with a dª.
Hi. I have trouble to answer this question. Help to label each compound B-E as an isomer or resonance structure of compound A.. could you explain to me in details how it be especially for each isomer , please indicate what bonds differ from compound A.. Thak you for your help.

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Which of the following species are aromatic or anti-aromatic (assuming n-systems are fully planar)? Circle those that are aromatic Put an X through those that are anti-aromatic Do nothing to the structure otherwise