OWLV2 FOR MASTERTON/HURLEY'S CHEMISTRY:
OWLV2 FOR MASTERTON/HURLEY'S CHEMISTRY:
8th Edition
ISBN: 9781305079304
Author: Hurley
Publisher: IACCENGAGE
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Chapter 23, Problem 10QAP
Interpretation Introduction

Interpretation:

The portion of polymer Lexan chain formed from given monomers needs to be sketched.

Concept introduction:

A polymer is a long chain consists of large number of monomer units. In a polymer, the monomers are linked to each other in a continuous or repetitive manner. These monomer units are linked to each other either through the formation of peptide linkage, glycosidic linkage or by removal of any moiety such as a water molecule. Polyvinyl chloride, Bakelite and polystyrene are some of the examples of polymers.

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It is not unexpected that the methoxyl substituent on a cyclohexane ring prefers to adopt the equatorial conformation. OMe H A G₂ = +0.6 kcal/mol OMe What is unexpected is that the closely related 2-methoxytetrahydropyran prefers the axial conformation: H H OMe OMe A Gp=-0.6 kcal/mol Methoxy: CH3O group Please be specific and clearly write the reason why this is observed. This effect that provides stabilization of the axial OCH 3 group in this molecule is called the anomeric effect. [Recall in the way of example, the staggered conformer of ethane is more stable than eclipsed owing to bonding MO interacting with anti-bonding MO...]
206 Pb 82 Express your answers as integers. Enter your answers separated by a comma. ▸ View Available Hint(s) VAΣ ΜΕ ΑΣΦ Np, N₁ = 82,126 Submit Previous Answers ? protons, neutrons

Chapter 23 Solutions

OWLV2 FOR MASTERTON/HURLEY'S CHEMISTRY:

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