ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
6th Edition
ISBN: 9781264382545
Author: SMITH
Publisher: MCG CUSTOM
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Chapter 15, Problem 48P
Interpretation Introduction

(a)

Interpretation: The MOs of cyclooctatetraene as bonding, antibonding, or nonbonding are to be labeled.

Concept introduction: The inscribed polygon method is helpful to predict whether a compound involves completely filled bonding MOs or not. The all bonding MOs, and the HOMOs of an aromatic compound are completely filled. However, the antibonding MOs are completely vacant.

Interpretation Introduction

(b)

Interpretation: The arrangement of electrons in the MOs of cyclooctatetraene is to be stated and an explanation for the not aromatic nature of it is to be stated.

Concept introduction: The inscribed polygon method is helpful to predict whether a compound involves completely filled bonding MOs or not. The all bonding MOs, and the HOMOs of an aromatic compound are completely filled. However, the antibonding MOs are completely vacant.

Interpretation Introduction

(c)

Interpretation: The number of π electrons that dianion of cyclooctatetraene contain is to be predicted.

Concept introduction: The inscribed polygon method is helpful to predict whether a compound involves completely filled bonding MOs or not. The all bonding MOs, and the HOMOs of an aromatic compound are completely filled. However, the antibonding MOs are completely vacant.

Interpretation Introduction

(d)

Interpretation: The arrangement of π electrons of dianion in MOs is to be stated.

Concept introduction: The inscribed polygon method is helpful to predict whether a compound involves completely filled bonding MOs or not. The all bonding MOs, and the HOMOs of an aromatic compound are completely filled. However, the antibonding MOs are completely vacant.

Interpretation Introduction

(e)

Interpretation: The classification of dianion as aromatic, nonaromatic, or antiaromatic is to be stated and its being so is to be explained.

Concept introduction: The inscribed polygon method is helpful to predict whether a compound involves completely filled bonding MOs or not. The bonding MOs, and the (HOMOs) of an aromatic compound are completely filled. However, the antibonding MOs are completely vacant.

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Students have asked these similar questions
59. Bond Strength I. Cyclobutane II. Cyclopentane 60. Optical Rotation I. 70% R, 30% S 11.30% R, 70% S 61. Which of the following is/ are alternant aromatic compounds? A. benzene B. naphthalene C. anthracene D. all of the given choices 62. Which of the following is/ are not aromatic? A. Cyclobutadiene B. Cyclopentadiene C. Cyclohexadiene D. All of the given choices 63. The following can exhibit tautomerism EXCEPT: A. benzaldehyde B. ethanal C. Cyclohexane carbaldehyde D. Cyclohexanone 64. Which of the following substituents exhibits both - inductive effect and - Resonance effect when attached to the benzene ring? A. -OH B. -CI D. -NO2 D.-CH3 65. Alkyl groups if attached to halogen (example: tert-butyl bromide) would exhibit A. negative inductive effect B. positive inductive effect C. negative resonance effect D. positive resonance effect. 9
question 6. Which of the following is anti-aromatic?
How many moles of Bra are required to completely halogenate the alkene?A. One moleB. Two molesC. Three molesD. Four moles What is the expected arrangement of the bromine atoms relative to each other amongthe carbon involved in pi bonding?A. anti-conformationB. syn-conformationC. trans-configurationD. cis-configuration What happens to bromine when it is adjacent to an alkene during a chemical reaction?A. Bromine becomes stable. (? kasi before brown siya/acidic tas naging colorless? Jk ewan)B. Bromine becomes polarized.C. Bromine becomes hybridized.D. Bromine becomes acidic. The relative arrangement of bromine atoms in the product is primarily due to:A. ElectronegativityB. RepulsionC. Hydrogen bondingD. Atomic weightWhat is your observation after the reaction?A. A yellow flame is produced.B. Bromine water decolorizes.C. The alkene becomes denser.D. A brown precipitate forms.

Chapter 15 Solutions

ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS

Ch. 15 - 17.23 Name each compound and state how many lines...Ch. 15 - Prob. 21PCh. 15 - Prob. 22PCh. 15 - 17.27 Give the IUPAC name for each compounds. a....Ch. 15 - 17.28 Draw a structure corresponding to each...Ch. 15 - 17.29 a. Draw the 14 constitutional isomers of...Ch. 15 - Prob. 26PCh. 15 - Prob. 27PCh. 15 - 17.38 How many electrons does C contain? How...Ch. 15 - Prob. 36PCh. 15 - 17.40 Explain the observed rate of reactivity of...Ch. 15 - 17.41 Draw a stepwise mechanism for the following...Ch. 15 - Prob. 39PCh. 15 - 17.43 Draw additional resonance structures for...Ch. 15 - Prob. 41PCh. 15 - Prob. 42PCh. 15 - 17.46 Which compound in each pair is the stronger...Ch. 15 - 17.47 Treatment of indene with forms its...Ch. 15 - Prob. 45PCh. 15 - 17.49 Draw the conjugate bases of pyrrole and...Ch. 15 - 17.50 a. Explain why protonation of pyrrole occurs...Ch. 15 - Prob. 48PCh. 15 - Prob. 49PCh. 15 - 17.53 How many signals does each compound...Ch. 15 - 17.54 Which of the diethylbenzene isomers (ortho,...Ch. 15 - 17.55 Propose a structure consistent with each...Ch. 15 - 17.56 Propose a structure consistent with each...Ch. 15 - 17.57 Thymol (molecular formula ) is the major...Ch. 15 - 17.58 You have a sample of a compound of molecular...Ch. 15 - 17.59 Explain why tetrahydrofuran has a higher...Ch. 15 - 17.60 Rizatriptan (trade name Maxalt) is a...Ch. 15 - 17.61 Zolpidem (trade name Ambien) promotes the...Ch. 15 - 17.62 Answer the following questions about...Ch. 15 - 17.63 Stanozolol is an anabolic steroid that...Ch. 15 - Prob. 61P
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