Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
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Question
Chapter 3, Problem 3.48P
Interpretation Introduction
(a)
Interpretation: The product of the reaction of acebutolol with HCl is to be drawn.
Concept introduction: The most basic
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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Students have asked these similar questions
Many drugs are sold as their hydrochloride salts (R2NH2+ Cl−), formed by reaction of an amine (R2NH) with HCl.
a. Draw the product (a hydrochloride salt) formed by reaction of acebutolol with HCl. Acebutolol is a β blocker used to treat high blood pressure.
b. Discuss the solubility of acebutolol and its hydrochloride salt in water.
c. Offer a reason as to why the drug is marketed as a hydrochloride salt rather than a neutral amine.
Many drugs are sold as their hydrochloride salts (R2NH2+ Cl−), formed by reaction of an amine (R2NH) with HCl.
a.Draw the product (a hydrochloride salt) formed by reaction of acebutolol with HCl. Acebutolol is a β blocker used to treat high blood pressure.
b. Discuss the solubility of acebutolol and its hydrochloride salt in water. c.Offer a reason as to why the drug is marketed as a hydrochloride salt rather than a neutral amine.
17. During alkalosis of a protein, shown below, salt bridges are broken, resulting in
denaturation. Which choice shows the products of alkalosis?
Н
alkalosis
H-N
NO salt bridge
Он
Н
Н
H-N
H-N-
Но.
Н
d.
a.
Н
Н
H-N
b.
Н
Н
e.
H-N-
но
Н
c.
IIZ:
Chapter 3 Solutions
Organic Chemistry-Package(Custom)
Ch. 3 - Prob. 3.1PCh. 3 - Prob. 3.2PCh. 3 - Draw the structure of a compound fitting each...Ch. 3 - Draw structures that fit each description and name...Ch. 3 - What types of intermolecular forces are present in...Ch. 3 - Prob. 3.6PCh. 3 - Explain why the boiling point of propanamide, is...Ch. 3 - Predict which compound in each pair has the higher...Ch. 3 - Prob. 3.9PCh. 3 - Prob. 3.10P
Ch. 3 - a Label the hydrophobic and hydrophilic portions...Ch. 3 - Prob. 3.12PCh. 3 - Prob. 3.13PCh. 3 - Prob. 3.14PCh. 3 - Prob. 3.15PCh. 3 - Nonactin and valinomycin each contain only two...Ch. 3 - Prob. 3.17PCh. 3 - Problem 3.26 Label the electrophilic and...Ch. 3 - Problem 3.27 Considering only electron density,...Ch. 3 - The fact that sweet-tasting carbohydrates like...Ch. 3 - 3.29
Identify the functional groups in the...Ch. 3 - Prob. 3.22PCh. 3 - 3.32 Identify the functional groups in each...Ch. 3 - Draw the seven constitutional isomers having...Ch. 3 - 3.33 Identify each functional group located in the...Ch. 3 - Draw seven constitutional isomers with molecular...Ch. 3 - Prob. 3.27PCh. 3 - Prob. 3.28PCh. 3 - Prob. 3.29PCh. 3 - Intramolecular force of attraction are often...Ch. 3 - 3.40 (a) Draw four compounds with molecular...Ch. 3 - Prob. 3.32PCh. 3 - Explain why CH3CH2NHCH3 has higher boiling point...Ch. 3 - Prob. 3.34PCh. 3 - Prob. 3.35PCh. 3 - Explain the observed trend in the melting points...Ch. 3 - Prob. 3.37PCh. 3 - Prob. 3.38PCh. 3 - Prob. 3.39PCh. 3 - 3.48 Explain why diethylether and have similar...Ch. 3 - Prob. 3.41PCh. 3 - 3.50 Predict the solubility of each of the...Ch. 3 - Prob. 3.43PCh. 3 - Prob. 3.44PCh. 3 - THC is the active component in marijuana, and...Ch. 3 - Prob. 3.46PCh. 3 - Prob. 3.47PCh. 3 - Prob. 3.48PCh. 3 - Label the electrophilic and nucleophilic sites in...Ch. 3 - By using only electron density arguments,...Ch. 3 - Prob. 3.51PCh. 3 - Prob. 3.52PCh. 3 - Prob. 3.53PCh. 3 - Prob. 3.54PCh. 3 - Prob. 3.55PCh. 3 - Recall from section 1.10B that there is restricted...
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