Question
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Chapter 26, Problem 91IAE
Interpretation Introduction

(a)

Interpretation:

The names of functional groups present in ephedrine should be determined.

Concept introduction:

Functional groups are atom or groups of atoms which are responsible for special chemical or physical properties of the molecule. IUPAC purposed a complete list of different functional groups with their prefix and suffix which can be used in the naming of the molecule. Some of the atoms can act as functional group such as −Cl, -F, -Br etc whereas some of them are groups of atoms like −NH2, -NO2, -OH etc.

Interpretation Introduction

(b)

Interpretation:

Identify the hybridization of numbered C atoms and N atom in ephedrine.

Concept introduction:

Hybridization is the process of mixing of atomic orbitals to form same energy and same shape hybrid orbitals which form covalent bond with overlapping of atomic orbitals of other atoms. The number of chemical bonds formed by the atom always determines type of hybridization. Sigma bonds could only form by hybrid orbitals whereas pi bonds are always formed by overlapping of un-hybrid orbitals hence hybridization is not part of pi bond formation.

Interpretation Introduction

(c)

Interpretation:

Identify the chiral C atoms in ephedrine.

Concept introduction:

A chiral carbon atom is the carbon atom which is bonded with four different atoms or group of atoms. The presence of chiral carbon atom makes that molecule optically active so it can rotate the plane polarized light either clockwise or anti-clockwise. Such molecules are called as optically active molecule and two different configuration of same molecule are called as enantiomers. They are non-superimposable mirror images of each other.

Interpretation Introduction

(d)

Interpretation:

Calculate the pKb value for ephedrine with the help of given information.

Concept introduction:

Ephedrine is a weak base which is mainly used as a center nervous system stimulant. Since it acts as a weak base therefore it gives OH- ions in its aqueous solution.

C10H15ON(aq) + H2O(l)     C10H15ONH+(aq) + OH-(aq)

The base dissociation constant Kb for this reaction can be written as:

Kb=[C10H15ONH+(aq)] [OH-(aq)][C10H15ON(aq) ]

The relation between Kb and pKb is:

pKb= - log [Kb]

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Chapter 26 Solutions

General Chemistry: Principles and Modern Applications - With Solutions Manual and Modified MasteringChemistry Code

Ch. 26 - Prob. 11ECh. 26 - Prob. 12ECh. 26 - Identify the chiral carbon atoms, ¡f any, in the...Ch. 26 - Prob. 14ECh. 26 - Identify the chiral carbon atoms, ¡f any, in the...Ch. 26 - Prob. 16ECh. 26 - Prob. 17ECh. 26 - Prob. 18ECh. 26 - Prob. 19ECh. 26 - By name or formula, give one example of each of...Ch. 26 - Prob. 21ECh. 26 - Prob. 22ECh. 26 - Prob. 23ECh. 26 - Prob. 24ECh. 26 - Prob. 25ECh. 26 - Prob. 26ECh. 26 - Prob. 27ECh. 26 - Prob. 28ECh. 26 - Prob. 29ECh. 26 - Prob. 30ECh. 26 - Prob. 31ECh. 26 - Prob. 32ECh. 26 - Prob. 33ECh. 26 - Prob. 34ECh. 26 - Does each of the following names convey sufficient...Ch. 26 - Prob. 36ECh. 26 - Prob. 37ECh. 26 - Supply condensed structural formulas for the...Ch. 26 - Prob. 39ECh. 26 - Prob. 40ECh. 26 - Classify the carbon atoms in, a. methylbutane, and...Ch. 26 - Classity the carbon atoms in a....Ch. 26 - Prob. 43ECh. 26 - Draw Newman projections for the staggered and...Ch. 26 - Draw the most stable conformation for the molecule...Ch. 26 - Prob. 46ECh. 26 - Prob. 47ECh. 26 - Prob. 48ECh. 26 - Prob. 49ECh. 26 - Prob. 50ECh. 26 - Prob. 51ECh. 26 - Prob. 52ECh. 26 - Prob. 53ECh. 26 - Prob. 54ECh. 26 - Prob. 55ECh. 26 - Prob. 56ECh. 26 - Draw suitable structural formulas to show that...Ch. 26 - Which of the following pairs of molecules are...Ch. 26 - Prob. 59ECh. 26 - Prob. 60ECh. 26 - Name the following molecules with the appropriate...Ch. 26 - Name the following molecules with the appropriate...Ch. 26 - Name the following molecules with the appropriate...Ch. 26 - Prob. 64ECh. 26 - Draw the structure for each of the following. a....Ch. 26 - Prob. 66ECh. 26 - Prob. 67ECh. 26 - Prob. 68ECh. 26 - Prob. 69ECh. 26 - Prob. 70ECh. 26 - Prob. 71ECh. 26 - Prob. 72ECh. 26 - Prob. 73ECh. 26 - Prob. 74ECh. 26 - Supply condensed or structural formulas for the...Ch. 26 - Prob. 76IAECh. 26 - Prob. 77IAECh. 26 - Prob. 78IAECh. 26 - Prob. 79IAECh. 26 - Prob. 80IAECh. 26 - Combustion of a 0.1908 g sample of a compound gave...Ch. 26 - Prob. 82IAECh. 26 - In the monochiorination of hydrocarbons, a...Ch. 26 - A particular colorless organic liquid is known to...Ch. 26 - Prob. 85IAECh. 26 - Give the systematic names, including any...Ch. 26 - Prob. 87IAECh. 26 - Prob. 88IAECh. 26 - Levomethadyl acetate (shown below) is used in the...Ch. 26 - Thiamphenicol (shown below) is an antibacterial...Ch. 26 - Prob. 91IAECh. 26 - Prob. 92IAECh. 26 - Prob. 93IAECh. 26 - Prob. 94IAECh. 26 - Prob. 95IAECh. 26 - For each of the following molecules (a) draw the...Ch. 26 - Prob. 97FPCh. 26 - Prob. 98SAECh. 26 - Explain the important distinctions between each...Ch. 26 - Describe the characteristics of each of the...Ch. 26 - The compound isoheptane is best represented by the...Ch. 26 - Prob. 102SAECh. 26 - Prob. 103SAECh. 26 - Prob. 104SAECh. 26 - Assign configurations, R or S, to the chiral...Ch. 26 - Consider the following pairs of structures In each...Ch. 26 - Prob. 107SAECh. 26 - Prob. 108SAECh. 26 - Prob. 109SAECh. 26 - Prob. 110SAECh. 26 - Prob. 111SAE
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