Chemistry: The Molecular Nature of Matter and Change
Chemistry: The Molecular Nature of Matter and Change
8th Edition
ISBN: 9781259631757
Author: Martin Silberberg Dr., Patricia Amateis Professor
Publisher: McGraw-Hill Education
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Chapter 15, Problem 15.25P

(a)

Interpretation Introduction

Interpretation:

The structure of 3-bromohexane has to be drawn and the optical activity has to be determined.

Concept Introduction:

The structure of the compound is given by its systematic name.

To give the structure from the name of the compound, the root name has to be identified.  The root name indicates the number of carbon atoms present in the longest chain.

Then the functional group (suffix) has to be identified.  It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.

The prefix of the name indicates the branched groups and their positions on the carbon chain.

The name of the compound is in the form

Prefix + Root + Suffix

The isomers which are mirror images of each other and are non-superimposable are said to be optical isomers and the isomerism is said to be optical isomerism.  The optical isomers are also called as enantiomers.  The optical isomers which rotates the plane-polarized light are optically active.

The optical isomers are asymmetric and plane of symmetry will be absent.  An organic molecule is said to be chiral when it is bonded to four different groups and is asymmetric.  The carbon atom bonded to four different groups is said to be chiral carbon or asymmetric carbon.  An organic compound is said to be optically active when it contains at least one chiral center.

(b)

Interpretation Introduction

Interpretation:

The structure of 3-chloro-3-methylpentane has to be drawn and the optical activity has to be determined.

Concept Introduction:

The structure of the compound is given by its systematic name.

To give the structure from the name of the compound, the root name has to be identified.  The root name indicates the number of carbon atoms present in the longest chain.

Then the functional group (suffix) has to be identified.  It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.

The prefix of the name indicates the branched groups and their positions on the carbon chain.

The name of the compound is in the form

Prefix + Root + Suffix

The isomers which are mirror images of each other and are non-superimposable are said to be optical isomers and the isomerism is said to be optical isomerism.  The optical isomers are also called as enantiomers.  The optical isomers which rotates the plane-polarized light are optically active.

The optical isomers are asymmetric and plane of symmetry will be absent.  An organic molecule is said to be chiral when it is bonded to four different groups and is asymmetric.  The carbon atom bonded to four different groups is said to be chiral carbon or asymmetric carbon.  An organic compound is said to be optically active when it contains at least one chiral center.

(c)

Interpretation Introduction

Interpretation:

The structure of 1,2-dibromo-2-methylbutane has to be drawn and the optical activity has to be determined.

Concept Introduction:

The structure of the compound is given by its systematic name.

To give the structure from the name of the compound, the root name has to be identified.  The root name indicates the number of carbon atoms present in the longest chain.

Then the functional group (suffix) has to be identified.  It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.

The prefix of the name indicates the branched groups and their positions on the carbon chain.

The name of the compound is in the form

Prefix + Root + Suffix

The isomers which are mirror images of each other and are non-superimposable are said to be optical isomers and the isomerism is said to be optical isomerism.  The optical isomers are also called as enantiomers.  The optical isomers which rotates the plane-polarized light are optically active.

The optical isomers are asymmetric and plane of symmetry will be absent.  An organic molecule is said to be chiral when it is bonded to four different groups and is asymmetric.  The carbon atom bonded to four different groups is said to be chiral carbon or asymmetric carbon.  An organic compound is said to be optically active when it contains at least one chiral center.

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6. Consider the following exothermic reaction below. 2Cu2+(aq) +41 (aq)2Cul(s) + 12(aq) a. If Cul is added, there will be a shift left/shift right/no shift (circle one). b. If Cu2+ is added, there will be a shift left/shift right/no shift (circle one). c. If a solution of AgNO3 is added, there will be a shift left/shift right/no shift (circle one). d. If the solvent hexane (C6H14) is added, there will be a shift left/shift right/no shift (circle one). Hint: one of the reaction species is more soluble in hexane than in water. e. If the reaction is cooled, there will be a shift left/shift right/no shift (circle one). f. Which of the changes above will change the equilibrium constant, K?

Chapter 15 Solutions

Chemistry: The Molecular Nature of Matter and Change

Ch. 15.4 - Prob. 15.4BFPCh. 15.4 - Prob. 15.5AFPCh. 15.4 - Prob. 15.5BFPCh. 15.4 - Prob. 15.6AFPCh. 15.4 - Prob. 15.6BFPCh. 15.4 - Prob. 15.7AFPCh. 15.4 - Prob. 15.7BFPCh. 15.6 - Prob. B15.4PCh. 15.6 - Prob. B15.5PCh. 15 - Prob. 15.1PCh. 15 - Prob. 15.2PCh. 15 - Prob. 15.3PCh. 15 - Silicon lies just below carbon in Group 4A(14) and...Ch. 15 - What is the range of oxidation states for carbon?...Ch. 15 - Prob. 15.6PCh. 15 - Prob. 15.7PCh. 15 - Define each type of isomer: (a) constitutional;...Ch. 15 - Prob. 15.9PCh. 15 - Prob. 15.10PCh. 15 - Prob. 15.11PCh. 15 - How does an aromatic hydrocarbon differ from a...Ch. 15 - Prob. 15.13PCh. 15 - Prob. 15.14PCh. 15 - Prob. 15.15PCh. 15 - Prob. 15.16PCh. 15 - Prob. 15.17PCh. 15 - Prob. 15.18PCh. 15 - Prob. 15.19PCh. 15 - Prob. 15.20PCh. 15 - Prob. 15.21PCh. 15 - Prob. 15.22PCh. 15 - Prob. 15.23PCh. 15 - Prob. 15.24PCh. 15 - Draw structures from the following names, and...Ch. 15 - Prob. 15.26PCh. 15 - Prob. 15.27PCh. 15 - Prob. 15.28PCh. 15 - Prob. 15.29PCh. 15 - Prob. 15.30PCh. 15 - Prob. 15.31PCh. 15 - Prob. 15.32PCh. 15 - Prob. 15.33PCh. 15 - Prob. 15.34PCh. 15 - Prob. 15.35PCh. 15 - Prob. 15.36PCh. 15 - Prob. 15.37PCh. 15 - Prob. 15.38PCh. 15 - Prob. 15.39PCh. 15 - Prob. 15.40PCh. 15 - Determine the type of each of the following...Ch. 15 - Prob. 15.42PCh. 15 - Prob. 15.43PCh. 15 - Prob. 15.44PCh. 15 - Prob. 15.45PCh. 15 - Prob. 15.46PCh. 15 - Prob. 15.47PCh. 15 - Prob. 15.48PCh. 15 - Prob. 15.49PCh. 15 - Prob. 15.50PCh. 15 - Prob. 15.51PCh. 15 - Prob. 15.52PCh. 15 - Prob. 15.53PCh. 15 - Prob. 15.54PCh. 15 - Prob. 15.55PCh. 15 - Prob. 15.56PCh. 15 - Prob. 15.57PCh. 15 - Prob. 15.58PCh. 15 - Prob. 15.59PCh. 15 - Prob. 15.60PCh. 15 - Prob. 15.61PCh. 15 - Prob. 15.62PCh. 15 - Prob. 15.63PCh. 15 - Prob. 15.64PCh. 15 - Prob. 15.65PCh. 15 - Prob. 15.66PCh. 15 - Prob. 15.67PCh. 15 - Prob. 15.68PCh. 15 - Prob. 15.69PCh. 15 - Prob. 15.70PCh. 15 - Prob. 15.71PCh. 15 - Prob. 15.72PCh. 15 - Prob. 15.73PCh. 15 - Prob. 15.74PCh. 15 - Prob. 15.75PCh. 15 - Prob. 15.76PCh. 15 - Prob. 15.77PCh. 15 - Prob. 15.78PCh. 15 - Prob. 15.79PCh. 15 - Prob. 15.80PCh. 15 - Prob. 15.81PCh. 15 - Prob. 15.82PCh. 15 - Prob. 15.83PCh. 15 - Prob. 15.84PCh. 15 - Prob. 15.85PCh. 15 - Prob. 15.86PCh. 15 - Prob. 15.87PCh. 15 - What is the key structural difference between...Ch. 15 - Protein shape, function, and amino acid sequence...Ch. 15 - What linkage joins the monomers in each strand of...Ch. 15 - What is base pairing? How does it pertain to DNA...Ch. 15 - RNA base sequence, protein amino acid sequence,...Ch. 15 - Prob. 15.93PCh. 15 - Prob. 15.94PCh. 15 - Draw the structure of each of the following...Ch. 15 - Prob. 15.96PCh. 15 - Write the sequence of the complementary DNA strand...Ch. 15 - Prob. 15.98PCh. 15 - Prob. 15.99PCh. 15 - Prob. 15.100PCh. 15 - Prob. 15.101PCh. 15 - Amino acids have an average molar mass of 100...Ch. 15 - Prob. 15.103PCh. 15 - Prob. 15.104PCh. 15 - Some of the most useful compounds for organic...Ch. 15 - Prob. 15.106PCh. 15 - Prob. 15.107PCh. 15 - Prob. 15.108PCh. 15 - Prob. 15.109PCh. 15 - Prob. 15.110PCh. 15 - Prob. 15.111PCh. 15 - Prob. 15.112PCh. 15 - The polypeptide chain in proteins does not exhibit...Ch. 15 - Prob. 15.114PCh. 15 - Prob. 15.115PCh. 15 - Prob. 15.116PCh. 15 - Prob. 15.117PCh. 15 - Wastewater from a cheese factory has the following...Ch. 15 - Prob. 15.119P
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