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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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.
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.
Organic Chemistry Explain your solution in a step by step fashion. Explain everything clearly and do not leave out any major or minor steps or details. Provide a thoughtful explanation to the question. In other words, provide your reasoning for why you picked your answer. Why are the molecules enantiomers? etc
12) What is the major difference between an antiaromatic and aromatic compound? A) The structure must be cyclic for aromatic but not antiaromatic compounds? B) Antiaromatic compounds have at least one sp3 hybridized atom in the ring C) Antiaromatic compounds can assume a chair-like structure while aromatic compounds are nearly flat D) Aromatic compounds cannot have a charged atom in the structure E) Only aromatic compounds follow Huckle's rule.
Describe bromination of aromatic compounds. How do aromatic compounds undergo bromination reactions? What is the green way of brominating aromatic compounds?
Which of the following compounds is NOT an aromatic molecule? S. IZ
One test for the presence of alkenes is to add a small amount of bromine, which is a red-brown liquid, and look for the disappearance of the red-brown color. This test does not work for detecting the presence of an aromatic hydrocarbon. Explain.
1. The acid-catalyzed elimination of an alcohol is an equilibrium reaction and requires special reac- tion conditions to favour the formation of the alkene product. What chemical principle controls the amount of alkene product that is produced? Provide two laboratory techniques that can be used to obtain good alkene yields in alcohol elimination reactions.
Which of the following a chemist would call a resonance stabilized carbocation? A) B) C) D) H3N CI O A O B
How many monochloro substitution products are produced when the alkanes below are chlorinated? Consider constitutional isomers only, ignore stereoisomers. a) b) The number of monochloro substitution products is 4 The number of monochloro substitution products is 3 X.
The rate law for addition of Br2 to an alkenes is first order in Br2 and first order in the alkene. Does this information suggest that the mechanism of addition of Br2 to an alkene proceeds in the same matter as for addition of HBr? Explain.

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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.