Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 3.4, Problem 12P
Interpretation Introduction

a) 3,4-Dimethylnonane

Interpretation:

The structure of the following organic compounds are to be proposed.

Concept introduction:

The IUPAC name of the following organic compounds are to be followed while drawing the structure of these compounds.

Interpretation Introduction

b) 3-Ethyl-4,4-dimethylheptane

Interpretation:

The structure of the following organic compounds are to be proposed.

Concept introduction:

The IUPAC name of the following organic compounds are to be followed while drawing the structure of these compounds.

Interpretation Introduction

c) 2, 2-Dimethyl-4-propyloctane

Interpretation:

The structure of the following organic compounds are to be proposed.

Concept introduction:

The IUPAC name of the following organic compounds are to be followed while drawing the structure of these compounds.

Interpretation Introduction

d) 2,2,4-trimethylpentane

Interpretation:

The structure of the following organic compounds are to be proposed.

Concept introduction:

The IUPAC name of the following organic compounds are to be followed while drawing the structure of these compounds.

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Students have asked these similar questions
(b) Draw structures corresponding to the following IUPAC names. (a) 3,4-Dimethylnonane (c) 2,2-Dimethyl-4-propyloctane (d) 2,2,4-Trimethylpentane (b) 3-Ethyl-4,4-dimethylheptane
Draw structures corresponding to the following IUPAC names: (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile
(B) Draw a structural diagram for each of the following organic compounds:  (a) 2-ethyl-4-methyl-2-pentanol   (b) 1,2-ethandiol  (c) 1,3-dimethylbenzene

Chapter 3 Solutions

Organic Chemistry

Ch. 3.4 - Give IUPAC names for the following compounds:Ch. 3.4 - Prob. 12PCh. 3.4 - Name the eight 5-carbon alkyl groups you drew in...Ch. 3.4 - Give the IUPAC name for the following hydrocarbon,...Ch. 3.7 - Make a graph of potential energy versus angle of...Ch. 3.7 - Sight along the C2-C1 bond of 2-methylpropane...Ch. 3.7 - Sight along the C2-C3 bond of 2,3-dimethylbutane,...Ch. 3.7 - Draw a Newman projection along the C2-C3 bond of...Ch. 3.SE - Prob. 19VCCh. 3.SE - Prob. 20VCCh. 3.SE - Draw a Newman projection along the C2-C3 bond of...Ch. 3.SE - Prob. 22APCh. 3.SE - Prob. 23APCh. 3.SE - Propose structures for the following: (a) A...Ch. 3.SE - Prob. 25APCh. 3.SE - Draw the structures of the following molecules:...Ch. 3.SE - Draw structures that meet the following...Ch. 3.SE - Prob. 28APCh. 3.SE - In each of the following sets, which structures...Ch. 3.SE - There are seven constitutional isomers with the...Ch. 3.SE - Prob. 31APCh. 3.SE - Draw compounds that contain the following: (a) A...Ch. 3.SE - Prob. 33APCh. 3.SE - Draw and name all monochloro derivatives of...Ch. 3.SE - Draw structures for the following: (a)...Ch. 3.SE - Prob. 36APCh. 3.SE - Draw a compound that: (a) Has nine primary...Ch. 3.SE - Give IUPAC names for the following compounds:Ch. 3.SE - Name the five isomers of C6H14.Ch. 3.SE - Explain why each of the following names is...Ch. 3.SE - Prob. 41APCh. 3.SE - Consider 2-methylbutane (isopentane). Sighting...Ch. 3.SE - What are the relative energies of the three...Ch. 3.SE - Construct a qualitative potential-energy diagram...Ch. 3.SE - Prob. 45APCh. 3.SE - Draw the most stable conformation of pentane,...Ch. 3.SE - Draw the most stable conformation of...Ch. 3.SE - Prob. 48APCh. 3.SE - Prob. 49APCh. 3.SE - Formaldehyde, H2C=O, is known to all biologists...Ch. 3.SE - Prob. 51APCh. 3.SE - Increased substitution around a bond leads to...Ch. 3.SE - Prob. 53APCh. 3.SE - In the next chapter we'll look at...Ch. 3.SE - We’ll see in the next chapter that there are two...
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