Please correct answer and don't use hand raiting [10] Annulene has a reactivity similar to normal alkenes. Explain the behavior of this molecule.Classify whether it is aromatic, non-aromatic, or antiaromatic.

[10]Annulene, often represented as [10]annulene, is a fascinating molecule in organic chemistry due…

Answered: [10] Annulene has a reactivity similar…

Introductory Chemistry For Today

8th Edition

ISBN:9781285644561

Author:Seager

Publisher:Seager

Chapter12: Unsaturated Hydrocarbons

Section: Chapter Questions

Problem 12.77E

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1.Discuss how aromaticity is affected in large ring compounds. 2. Discuss the aromaticity of heterocyclic compounds. 3. Discuss the aromaticity of polynuclear hydrocarbons
What are aromatic hydrocarbons? Benzene exhibits resonance. Explain. What are the bond angles in benzene? Give a detailed description of the bonding in benzene. The electrons in benzene are delocalized, while the electrons in simple alkenes and alkynes are localized. Explain the difference.
Classify each of the following compounds as a normal alkane or a branched alkane: a. b. c. d. e. f.
Which one of these molecules are aromatic?
In general, which of the following statements correctly describes the reactivity of alkenes? Select one: A. An alkene is an electron-rich molecule and therefore can react as a nucleophile. B. Alkenes are generally unreactive compared alkanes. C. Alkenes react as electrophiles, whereas alkanes react as nucleophiles. D. Unlike alkynes, alkenes fail to undergo electrophilic addition reactions. Which of the following statements on bond-breaking (cleaving) or bond-forming is correct? Select one: A. In homolytic bond breaking, a bond is broken respectively by the movement of a pair of electrons in the same direction to one of the products. B. In heterolytic bond-forming, electrons flow from a nucleophile to an electrophile. C. Electron flow in homolytic bond breaking is shown by a double-headed arrow from the bond to a nucleophile. D. A double-headed arrow indicates the movement of an electron pair during homolytic bond breaking.
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a. The following compounds have the same molecular formula as benzene. How many monobrominated products could each form? 1. HC‚CC‚CCH2CH3 2. CH2“CHC‚CCH“CH2 b. How many dibrominated products could each of the preceding compounds form? (Do not include stereoisomers.) c. How many dibrominated products could each of the compounds form if stereoisomers are included?
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Explain why benzene can not undergo electrophilic addition reaction, but can only do electrophilic substitution reaction?

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[10] Annulene has a reactivity similar to normal alkenes. Explain the behavior of this molecule. Classify whether it is aromatic, non-aromatic, or antiaromatic.