Solutions Manual for Organic Chemistry
Solutions Manual for Organic Chemistry
10th Edition
ISBN: 9781259636387
Author: Carey Dr., Francis A
Publisher: McGraw-Hill Education
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 11, Problem 26P

Write structural formulas for each of the following:

3,4-Octadiene

( E , E )-3,5-Octadiene

( Z , Z )-1,3-Cyclooctadiene

( Z , Z )-1,4-Cyclooctadiene

( E , E )-1,5-Cyclooctadiene

5-Allyl-1,3-cyclopentadiene ( 2 E , 4 Z , 6 E )-2,4,6-Octatriene

t r a n s -1,2-Divinylcyclopropane

2,4-Dimethyl-1,3-pentadiene

Expert Solution & Answer
Check Mark
Interpretation Introduction

Interpretation:

The structural formula of the given compounds is to be written.

Concept introduction:

When writing the structural formula of any compound, first the functional group from the suffix of the given name is identified.

The longest carbon chain containing the functional group is located.

The carbon atoms of the chain are numbered in a way that the functional group is at lowest numbered carbon atom.

Substituents are attached to the parent chain according to their positions given in the name.

In alkenes, the Z isomers have the higher ranked substituents on the same side of the double bond, and in E isomers, higher ranked substituents are on the opposite sides of the double bond.

Answer to Problem 26P

Solution:

a)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  1

b)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  2

c)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  3

d)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  4

e)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  5

f)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  6

g)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  7

h)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  8

i)

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  9

Explanation of Solution

a) The given compound is 3,4 octadiene.

The parent name contains the word “octa” in it, which means that the longest carbon chain contains eight carbon atoms. The suffix added to octa is -diene, which means that there are two double bonds present in the parent chain. The numbers 3 and 4 indicate the positions of the double bonds in the parent chain.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  10

b) The given compound is (E,E)3,5 octadiene.

The parent name contains the word “octa” in it, which means that the longest carbon chain contains eight carbon atoms. The suffix added to octa is -diene, which means that there are two double bonds present in the parent chain. The numbers 3 and 5 indicate the positions of the double bonds in the parent chain. Both the double bonds have E configuration. The higher priority groups must be on the opposite sides of the double bond.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  11

c) The given compound is (Z,Z)1,3 cyclooctadiene.

The parent name contains the word “cycloocta” in it, which means that the parent carbon chain contains eight carbon atoms in a cyclic form. The suffix added is -diene, which means that there are two double bonds present in the parent chain. The numbers 1 and 3 indicate the positions of the double bonds in the parent chain. Both the double bonds have Z configuration. The higher priority groups must be on the same sides of the double bond.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  12

d) The given compound is (Z,Z)1,4 cyclooctadiene.

The parent name contains the word “cycloocta” in it, which means that the parent carbon chain contains eight carbon atoms in a cyclic form. The suffix added is -diene, which means that there are two double bonds present in the parent chain. The numbers 1 and 4 indicate the positions of the double bonds in the parent chain. Both the double bonds have Z configuration. The higher priority groups must be on the same sides of the double bond.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  13

e) The given compound is (E,E)1,5 cyclooctadiene.

The parent name contains the word “cycloocta” in it, which means that the parent carbon chain contains eight carbon atoms in a cyclic form. The suffix added is -diene, which means that there are two double bonds present in the parent chain. The numbers 1 and 5 indicate the positions of the double bonds in the parent chain. Both the double bonds have E configuration. The higher priority groups must be on the opposite sides of the double bond.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  14

f) The given compound is (Z,Z)1,4 octatriene.

The parent name contains the word “octa” in it, which means that the longest carbon chain contains eight carbon atoms. The suffix added to octa is -triene, which means that there are three double bonds present in the parent chain. The numbers 2, 4, 6 indicate the positions of the double bonds in the parent chain. The double bonds between C2-C3 and between C6-C7 have E configuration. The double bond between C4-C5 has Z configuration.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  15

g) The given compound is 5allyl1,3cyclopentadiene.

The parent name contains the word “cyclopenta” in it, which means that the parent carbon chain contains five carbon atoms in a cyclic form. The suffix added is -diene, which means that there are two double bonds present in the parent chain. The numbers 1 and 3 indicate the positions of the double bonds in the parent chain. There is an allyl group attached to the C5 carbon atom.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  16

h) The given compound is trans1,2divinylcyclopropane.

The parent name contains the word cyclopropane in it, which means that the parent carbon chain contains three carbon atoms in a cyclic form. There are two vinyl groups attached to the cyclopropane. The numbers 1 and 2 indicate the positions of the vinyl groups on the parent chain. These two vinyl groups are trans to each other.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  17

i) The given compound is 2,4dimethyl1,3pentadiene.

The parent name contains the word “penta” in it, which means that the longest carbon chain contains five carbon atoms. The suffix added is -diene, which means that there are two double bonds present in the parent chain. The numbers 1 and 3 indicate the positions of the double bonds in the parent chain. One methyl group is attached to C2 while another methyl group is attached to C4 carbon atom.

The structural formula is as follows:

Solutions Manual for Organic Chemistry, Chapter 11, Problem 26P , additional homework tip  18

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
Show how 5-methyl-1,3-cyclopentadiene rearranges to form 1-methyl-1,3-cyclopentadiene and 2-methyl1,3-cyclopentadiene.
Classify the following dienes and polyenes as isolated, conjugated, cumulated, or some combination of theseclassifications.(a) cycloocta-1,4-diene (b) cycloocta-1,3-diene (c) cyclodeca-1,2-diene(d) cycloocta-1,3,5,7-tetraene (e) cyclohexa-1,3,5-triene (benzene) (f) penta-1,2,4-triene
Classify the following dienes and polyenes as isolated, conjugated, cumulated, or some combination of theseclassifications.(a) cycloocta-1,4-diene (b) cycloocta-1,3-diene (c) cyclodeca-1,2-diene(d) cycloocta-1,3,5,7-tetraene (e) cyclohexa-1,3,5-triene (benzene)

Chapter 11 Solutions

Solutions Manual for Organic Chemistry

Ch. 11.5 - Prob. 11PCh. 11.6 - Prob. 12PCh. 11.8 - Prob. 13PCh. 11.9 - What dienes containing isolated double bonds are...Ch. 11.10 - Prob. 15PCh. 11.10 - Prob. 16PCh. 11.11 - Prob. 17PCh. 11.12 - Dicarbonyl compounds such as quinones are reactive...Ch. 11.12 - 2,3-Di-tert-butyl-1,3-butadiene is extremely...Ch. 11.12 - Methyl acrylate (H2C=CHCO2CH3) reacts with...Ch. 11.13 - Prob. 21PCh. 11.14 - What diene and dienophile could you use to prepare...Ch. 11.14 - Write equations in the synthetic direction for the...Ch. 11.16 - Prob. 24PCh. 11.16 - Prob. 25PCh. 11 - Write structural formulas for each of the...Ch. 11 - Give an acceptable IUPAC name for each of the...Ch. 11 - A certain species of grasshopper secretes an...Ch. 11 - Which of the following are chiral?...Ch. 11 - Describe the molecular geometry expected for...Ch. 11 - Prob. 31PCh. 11 - What compound of molecular formula C6H10 gives...Ch. 11 - Prob. 33PCh. 11 - Prob. 34PCh. 11 - Prob. 35PCh. 11 - Prob. 36PCh. 11 - Identify the more reactive dienophile in each of...Ch. 11 - Prob. 38PCh. 11 - Prob. 39PCh. 11 - Prob. 40PCh. 11 - Prob. 41PCh. 11 - Prob. 42PCh. 11 - Prob. 43PCh. 11 - Prob. 44PCh. 11 - Prob. 45PCh. 11 - Prob. 46PCh. 11 - Show how to prepare each of the following...Ch. 11 - Prob. 48PCh. 11 - Prob. 49PCh. 11 - Prob. 50PCh. 11 - Compound A was converted to compound B by the...Ch. 11 - Suggest reasonable explanations for each of the...Ch. 11 - Prob. 53PCh. 11 - Prob. 54PCh. 11 - Prob. 55DSPCh. 11 - Prob. 56DSPCh. 11 - Prob. 57DSPCh. 11 - Prob. 58DSPCh. 11 - Prob. 59DSP
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
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
How to Design a Total Synthesis; Author: Chemistry Unleashed;https://www.youtube.com/watch?v=9jRfAJJO7mM;License: Standard YouTube License, CC-BY