ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
6th Edition
ISBN: 9781264382545
Author: SMITH
Publisher: MCG CUSTOM
Question
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Chapter 3, Problem 56P
Interpretation Introduction

(a)

Interpretation: The product of the reaction of acebutolol with HCl is to be drawn.

Concept introduction: The most basic amine group present in a molecule react with HCl to form the corresponding hydrochloride salt.

Interpretation Introduction

(b)

Interpretation: The solubility of acebutolol and its hydrochloride salt in water is to be discussed.

Concept introduction: The solubility of a compound depends on its interactions with the solvent molecule.

Interpretation Introduction

(c)

Interpretation: The reason as to why acebutolol is marketed as a hydrochloride salt rather than a neutral molecule is to be stated.

Concept introduction: The drug having more solubility is marketed for its maximum utilization.

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(f) SO: Best Lewis Structure 3 e group geometry:_ shape/molecular geometry:, (g) CF2CF2 Best Lewis Structure polarity: e group arrangement:_ shape/molecular geometry: (h) (NH4)2SO4 Best Lewis Structure polarity: e group arrangement: shape/molecular geometry: polarity: Sketch (with angles): Sketch (with angles): Sketch (with angles):
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Chapter 3 Solutions

ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS

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