ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
9th Edition
ISBN: 9780137249442
Author: Wade
Publisher: INTER PEAR
bartleby

Concept explainers

Question
100%
Book Icon
Chapter 7, Problem 7.40SP

(a)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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.

(a)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of 3-methylpent-1-ene is shown in Figure 1.

Explanation of Solution

The given compound is 3-methylpent-1-ene. The root name pent-1-ene signifies five carbon atoms in a chain with alkene group present on first carbon of a longest hydrocarbon chain. The number 3 indicates that methyl group is present on C3. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  1

Figure 1

(b)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of cis-3-methyl-3-hexene is shown in Figure 2.

Explanation of Solution

The given compound is cis-3-methyl-3-hexene. The root name 3-hexene signifies six carbon atoms in a chain with alkene group present on third carbon of a longest hydrocarbon chain. The number 3 indicates that methyl group is present on C3 in cis configuration. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  2

Figure 2

(c)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of 3,4-dibromobut-1-ene is shown in Figure 3.

Explanation of Solution

The given compound is 3,4-dibromobut-1-ene. The root name but-1-ene signifies four carbon atoms in a chain with alkene group present on first carbon of a longest hydrocarbon chain. The number 3,4-dibromo indicates that bromine atoms are present on C3 and C4 respectively. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  3

Figure 3

(d)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of 1,3-cyclohexadiene is shown in Figure 4.

Explanation of Solution

The given compound is 1,3-cyclohexadiene. The root name cyclohexadiene signifies six carbon atoms in a ring with alkene group. The number 1,3 indicates that alkene groups are present on first and third carbon of a ring. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  4

Figure 4

(e)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of cycloocta-1,4-diene is shown in Figure 5.

Explanation of Solution

The given compound is cycloocta-1,4-diene. The root name cycloocta signifies eight carbon atoms in a ring. The number 1,4-diene indicates that alkene groups are present on first and fourth carbon of a ring. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  5

Figure 5

(f)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of (Z)-3-methyl-2-octene is shown in Figure 6.

Explanation of Solution

The given compound is (Z)-3-methyl-2-octene. The root name 2-octene signifies eight carbon atoms in a chain with alkene group present on second carbon of a longest hydrocarbon chain. The number (Z)-3-methyl indicates that methyl group is present on C3 in Z configuration. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  6

Figure 6

(g)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: Alkanes are saturated hydrocarbons and their names end by adding suffix –ane to the parent hydrocarbon. Cycloalkanes are cyclic hydrocarbons in which carbons are arranged in the ring. Therefore, they are named by adding prefix cyclo to the name of the hydrocarbon.

(g)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of vinylcyclopropane is shown in Figure 7.

Explanation of Solution

The given compound is vinylcyclopropane. The root name cyclopropane signifies three carbon atoms in a ring. Vinyl group is the functional group having a formula CH=CH2. In vinylcyclopropane, vinyl group is attached to the cyclopropane. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  7

Figure 7

(h)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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.

(h)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of (Z)-2-bromo-2-pentene is shown in Figure 8.

Explanation of Solution

The given compound is (Z)-2-bromo-2-pentene. The root name 2-pentene signifies five carbon atoms in a chain with alkene group present on second carbon of a longest hydrocarbon chain. The number (Z)-2-bromo indicates that bromo group is present on C2 in Z configuration. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  8

Figure 8

(i)

Interpretation Introduction

To determine: The structure for the given compound.

Interpretation: The structure for the given compound is to be drawn.

Concept introduction: 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.

(i)

Expert Solution
Check Mark

Answer to Problem 7.40SP

The structure of (3Z,6E)-1,3,6-octatriene is shown in Figure 9.

Explanation of Solution

The given compound is (3Z,6E)-1,3,6-octatriene. The root name octatriene signifies eight carbon atoms in a chain with alkene group. The number 1,3,6 indicates that the alkene groups are present on first, third and sixth carbon atoms of a longest hydrocarbon chain. The number (3Z,6E) indicates that alkene groups are present on C3 in Z configuration and C6 in E configuration. The structure is shown below.

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS, Chapter 7, Problem 7.40SP , additional homework tip  9

Figure 9

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Please help me with # 4 and 5. Thanks in advance!
A small artisanal cheesemaker is testing the acidity of their milk before it coagulates. During fermentation, bacteria produce lactic acid (K₁ = 1.4 x 104), a weak acid that helps to curdle the milk and develop flavor. The cheesemaker has measured that the developing mixture contains lactic acid at an initial concentration of 0.025 M. Your task is to calculate the pH of this mixture and determine whether it meets the required acidity for proper cheese development. To achieve the best flavor, texture and reduce/control microbial growth, the pH range needs to be between pH 4.6 and 5.0. Assumptions: Lactic acid is a monoprotic acid H H :0:0: H-C-C H :0: O-H Figure 1: Lewis Structure for Lactic Acid For simplicity, you can use the generic formula HA to represent the acid You can assume lactic acid dissociation is in water as milk is mostly water. Temperature is 25°C 1. Write the K, expression for the dissociation of lactic acid in the space provided. Do not forget to include state symbols.…
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :0: :0 H. 0:0 :0: :6: S: :0: Select to Edit Arrows ::0 Select to Edit Arrows H :0: H :CI: Rotation Select to Edit Arrows H. < :0: :0: :0: S:

Chapter 7 Solutions

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS

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
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY