Chemistry: The Molecular Nature of Matter and Change - Standalone book
Chemistry: The Molecular Nature of Matter and Change - Standalone book
7th Edition
ISBN: 9780073511177
Author: Martin Silberberg Dr., Patricia Amateis Professor
Publisher: McGraw-Hill Education
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Chapter 11, Problem 11.57P

(a)

Interpretation Introduction

Interpretation:

The number of possible different compounds that are formed by changing only the cis-trans arrangements around the double bonds in linoleic acid is to be determined.

Concept introduction:

The cis and trans forms are the types of geometrical or configurational isomers. The cis form indicates that the same functional groups are present on the same side of the carbon-carbon double bond. The trans form indicates that the same functional groups are present on the opposite side of the carbon-carbon double bond. Both isomers have the same formula but a different arrangement of functional groups around the carbon atom.

(b)

Interpretation Introduction

Interpretation:

The different compounds that are possible with three double bonds are to be determined.

Concept introduction:

The isomers are the molecules that have the same molecular formula but a different arrangement of atoms. They do not necessarily have similar properties. The phenomenon by which isomers exist is known as isomerism.

The formula to calculate the numbers of possible isomers is as follows:

  Number of possible isomers=2n        (1)

Here, n is the number of double bonds.

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Chapter 11 Solutions

Chemistry: The Molecular Nature of Matter and Change - Standalone book

Ch. 11 - Prob. 11.3PCh. 11 - Prob. 11.4PCh. 11 - Prob. 11.5PCh. 11 - Give the number and type of hybrid orbital that...Ch. 11 - What is the hybridization of nitrogen in each of...Ch. 11 - What is the hybridization of carbon in each of the...Ch. 11 - Prob. 11.9PCh. 11 - Prob. 11.10PCh. 11 - Prob. 11.11PCh. 11 - Prob. 11.12PCh. 11 - Phosphine (PH3) reacts with borane (BH3) as...Ch. 11 - The illustrations below depict differences in...Ch. 11 - Use partial orbital diagrams to show how the...Ch. 11 - Use partial orbital diagrams to show how the...Ch. 11 - Prob. 11.17PCh. 11 - Prob. 11.18PCh. 11 - Methyl isocyanate, , is an intermediate in the...Ch. 11 - Are these statements true or false? Correct any...Ch. 11 - Prob. 11.21PCh. 11 - Identify the hybrid orbitals used by the central...Ch. 11 - Prob. 11.23PCh. 11 - Identify the hybrid orbitals used by the central...Ch. 11 - Prob. 11.25PCh. 11 - Prob. 11.26PCh. 11 - Certain atomic orbitals on two atoms were combined...Ch. 11 - Prob. 11.28PCh. 11 - Antibonding MOs always have at least one node. Can...Ch. 11 - Prob. 11.30PCh. 11 - Prob. 11.31PCh. 11 - The molecular orbitals depicted are derived from...Ch. 11 - The molecular orbitals depicted below are derived...Ch. 11 - Prob. 11.34PCh. 11 - Use an MO diagram and the bond order you obtain...Ch. 11 - Prob. 11.36PCh. 11 - Prob. 11.37PCh. 11 - Prob. 11.38PCh. 11 - Prob. 11.39PCh. 11 - Epinephrine (or adrenaline; below) is a naturally...Ch. 11 - Prob. 11.41PCh. 11 - Isoniazid (below) is an antibacterial agent that...Ch. 11 - Prob. 11.43PCh. 11 - Prob. 11.44PCh. 11 - Prob. 11.45PCh. 11 - Prob. 11.46PCh. 11 - Tryptophan is one of the amino acids found in...Ch. 11 - Prob. 11.48PCh. 11 - Prob. 11.49PCh. 11 - Prob. 11.50PCh. 11 - Prob. 11.51PCh. 11 - Prob. 11.52PCh. 11 - Sulfur forms oxides, oxoanions, and halides. What...Ch. 11 - Prob. 11.54PCh. 11 - Use an MO diagram to find the bond order and...Ch. 11 - Acetylsalicylic acid (aspirin), the most widely...Ch. 11 - Prob. 11.57P
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