For each of the species below, identify any cyclic conjugated system, then: A. Determine the number of electrons in a system of cyclic conjugation (zero if no cyclic conjugation). B. Specify whether the species is "a"-aromatic, "aa"-anti-aromatic, or "na"-non-aromatic (neither aromatic nor anti-aromatic). (Presume rings to be planar unless structure obviously prevents planarity. If there is more than one conjugated ring, count electrons in the largest.) 1. A.Electrons in a cyclic conjugated system. B.The compound is (a, aa, or na) 2. A.Electrons in a cyclic conjugated system. B.The compound is (a, aa, or na) Submit Answer Retry Entire Group 9 more group attempts remaining Show Hint Cengage Learning Cengage Technical Support F4 DII F5 F6 $ % 5 6 R T Y об г 7 U PrtScn F8 8 Previous Next Email Instructor Save Home End PgUp PgDn F9 F10 F11 F12 ( 9 P ว Ins Ba

For each of the species below, identify any cyclic conjugated system, then: A. Determine the number of electrons in a system of cyclic conjugation (zero if no cyclic conjugation). B. Specify whether the species is "a"-aromatic, "aa"-anti-aromatic, or "na"-non-aromatic (neither aromatic nor anti-aromatic). (Presume rings to be planar unless structure obviously prevents planarity. If there is more than one conjugated ring, count electrons in the largest.) 1. A.Electrons in a cyclic conjugated system. B.The compound is (a, aa, or na) 2. A.Electrons in a cyclic conjugated system. B.The compound is (a, aa, or na) Submit Answer Retry Entire Group 9 more group attempts remaining Show Hint Cengage Learning Cengage Technical Support F4 DII F5 F6 $ % 5 6 R T Y об г 7 U PrtScn F8 8 Previous Next Email Instructor Save Home End PgUp PgDn F9 F10 F11 F12 ( 9 P ว Ins Ba

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter18: Aromaticity

Section: Chapter Questions

Problem 6CTQ

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Either the reactant (X) or the major organic product is missing from the equation below. Draw the missing compound. H3C CH3 Pd/C X + H2 CH;CHCHCHCH3 ČH3 • You do not have to consider stereochemistry. • In the case of a missing reactant, there may be more than one answer. If so, draw all possible reactants, • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.
I need help figuring out the number of electrons in a cyclic conjugated system and determining if the compound is aromatic, anti-aromatic, or neither.
I keep getting this question wrong but I’m doing everything correctly.
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A. Determine the number of electrons in a system of cyclic conjugation (zero if no cyclic conjugation). B. Specify whether the species is "a"-aromatic, "aa"-anti-aromatic, or "na"-non- aromatic (neither aromatic nor anti-aromatic). (Presume rings to be planar unless structure obviously prevents planarity. If there is more than one conjugated ring, count electrons in the largest.) 1. A.Electrons in a cyclic conjugated system. B. The compound is (a, aa, or na) o A.Electrons in a cyclic conjugated system. B.The compound is (a, aa, or na) 2. Previous Next
A. Determine the number of electrons in a system of cyclic conjugation (zero if no cyclic conjugation).B. Specify whether the species is "a"-aromatic, "aa"-anti-aromatic, or "na"-non-aromatic (neither aromatic nor anti-aromatic).(Presume rings to be planar unless structure obviously prevents planarity. If there is more than one conjugated ring, count electrons in the largest.)
Could you please explain how to get the answer? Thank you
please help
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Draw a molecular orbital diagram for the pi system of tetrazole (including the piacemen oi iis pi electrons) and provide an analysis of its aromaticity using Hückel's rule denoting whether tetrazole is in fact aromatic, antiaromatic, or nonaromatic. H N° Tetrazole b. Provide a picture of the Highest occupied Molecular Orbital (HOMO) and the Lowest Unnocupied Molecular Orbital (LUMO) of tetrazole depicting the phases of thep orbitals, the bonding, antibonding, and non-bonding interactions.