Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 7, Problem 7.43SP

(a)

Interpretation Introduction

To determine: The correct name for the given compound.

Interpretation: The correct name for the given compound is to be stated.

Concept introduction: The IUPAC nomenclature of organic compound is a method used for naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alkenes and alkynes are unsaturated hydrocarbons and are named by identifying the longest chain of carbon atoms that contain double or triple bond, their names end by adding suffix –ene and –yne to the parent hydrocarbon.

(b)

Interpretation Introduction

To determine: The correct name for the given compound.

Interpretation: The correct name for the given compound is to be stated.

Concept introduction: The IUPAC nomenclature of organic compound is a method used for naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alkenes and alkynes are unsaturated hydrocarbons and are named by identifying the longest chain of carbon atoms that contain double or triple bond, their names end by adding suffix –ene and –yne to the parent hydrocarbon.

(c)

Interpretation Introduction

To determine: The correct name for the given compound.

Interpretation: The correct name for the given compound is to be stated.

Concept introduction: The IUPAC nomenclature of organic compound is a method used for naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alkenes and alkynes are unsaturated hydrocarbons and are named by identifying the longest chain of carbon atoms that contain double or triple bond, their names end by adding suffix –ene and –yne to the parent hydrocarbon.

(d)

Interpretation Introduction

To determine: The correct name for the given compound.

Interpretation: The correct name for the given compound is to be stated.

Concept introduction: The IUPAC nomenclature of organic compound is a method used for naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alkenes and alkynes are unsaturated hydrocarbons and are named by identifying the longest chain of carbon atoms that contain double or triple bond, their names end by adding suffix –ene and –yne to the parent hydrocarbon.

(e)

Interpretation Introduction

To determine: The correct name for the given compound.

Interpretation: The correct name for the given compound is to be stated.

Concept introduction: The IUPAC nomenclature of organic compound is a method used for naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alkenes and alkynes are unsaturated hydrocarbons and are named by identifying the longest chain of carbon atoms that contain double or triple bond, their names end by adding suffix –ene and –yne to the parent hydrocarbon.

(f)

Interpretation Introduction

To determine: The correct name for the given compound.

Interpretation: The correct name for the given compound is to be stated.

Concept introduction: The IUPAC nomenclature of organic compound is a method used for naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alkenes and alkynes are unsaturated hydrocarbons and are named by identifying the longest chain of carbon atoms that contain double or triple bond, their names end by adding suffix –ene and –yne to the parent hydrocarbon.

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Chapter 7 Solutions

Organic Chemistry (9th Edition)

Ch. 7.8B - Use the data in Table7-2 to predict the energy...Ch. 7.8C - Prob. 7.13PCh. 7.8E - Explain why each of the following alkenes is...Ch. 7.8F - Prob. 7.15PCh. 7.10 - Prob. 7.16PCh. 7.10A - SN1 substitution and E1 elimination frequently...Ch. 7.10C - Prob. 7.18PCh. 7.10C - Prob. 7.19PCh. 7.10C - Prob. 7.20PCh. 7.11 - Prob. 7.21PCh. 7.11 - Prob. 7.22PCh. 7.12 - Prob. 7.23PCh. 7.12 - Prob. 7.24PCh. 7.13 - Prob. 7.25PCh. 7.14B - Prob. 7.26PCh. 7.14B - Make models of the blowing compounds, and predict...Ch. 7.15 - Prob. 7.28PCh. 7.15 - Prob. 7.29PCh. 7.15 - Prob. 7.30PCh. 7.15 - Prob. 7.31PCh. 7.16 - Predict the major and minor elimination products...Ch. 7.17B - Predict the products and mechanisms of the...Ch. 7.18 - Propose mechanisms for the following reactions.Ch. 7.18 - Prob. 7.35PCh. 7.19B - The dehydrogenation of butane to trans-but-2-ene...Ch. 7.19B - Prob. 7.37PCh. 7.19B - Prob. 7.38PCh. 7.19B - Prob. 7.39PCh. 7 - Prob. 7.40SPCh. 7 - Prob. 7.41SPCh. 7 - Prob. 7.42SPCh. 7 - Prob. 7.43SPCh. 7 - Prob. 7.44SPCh. 7 - Prob. 7.45SPCh. 7 - Prob. 7.46SPCh. 7 - The energy difference between cis- and...Ch. 7 - Prob. 7.48SPCh. 7 - Prob. 7.49SPCh. 7 - Prob. 7.50SPCh. 7 - What halides would undergo E2 dehydrohalogenation...Ch. 7 - Prob. 7.52SPCh. 7 - Prob. 7.53SPCh. 7 - Write a balanced equation for each reaction,...Ch. 7 - Prob. 7.55SPCh. 7 - Using cyclohexane as your starting material, show...Ch. 7 - Show how you would prepare cyclopentene from each...Ch. 7 - Prob. 7.58SPCh. 7 - E1 eliminations of alkyl halides are rarely useful...Ch. 7 - Prob. 7.60SPCh. 7 - Propose mechanisms for the following reactions....Ch. 7 - Prob. 7.62SPCh. 7 - Prob. 7.63SPCh. 7 - Prob. 7.64SPCh. 7 - Prob. 7.65SPCh. 7 - Prob. 7.66SPCh. 7 - Prob. 7.67SPCh. 7 - Prob. 7.68SPCh. 7 - Prob. 7.69SPCh. 7 - Explain the dramatic difference in rotational...Ch. 7 - One of the following dichloronorbornanes undergoes...Ch. 7 - A graduate student wanted to make...Ch. 7 - Prob. 7.73SPCh. 7 - Prob. 7.74SPCh. 7 - Prob. 7.75SPCh. 7 - Prob. 7.76SP
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