Concept explainers
Locate the isoprene units in each compound.
a. c.
b. d.
(a)
Interpretation: The isoprene units in the given compound are to be located.
Concept introduction: An isoprene unit possesses following properties.
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
Answer to Problem 30.11P
The isoprene units in the given terpene (geraniol) are located as,
Explanation of Solution
Terpenes are composed of repeating five-carbon units. These units are called isoprene units.
Figure 1
An isoprene unit possesses following properties.
➢ It involves one branched carbon and
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
The isoprene units in the given terpene (geraniol) are located as,
Figure 2
The isoprene units in the given terpene (geraniol) are located in Figure 2.
(b)
Interpretation: The isoprene units in the given compound are to be located.
Concept introduction: An isoprene unit possesses following properties.
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
Answer to Problem 30.11P
The isoprene units in the given terpene (vitamin A) are located as,
Explanation of Solution
Terpenes are composed of repeating five-carbon units. These units are called isoprene units.
Figure 1
An isoprene unit possesses following properties.
➢ It involves one branched carbon and
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
The isoprene units in the given terpene (vitamin A) are located as,
Figure 3
The isoprene units in the given terpene (vitamin A) are located in Figure 3.
(c)
Interpretation: The isoprene units in the given compound are to be located.
Concept introduction: An isoprene unit possesses following properties.
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
Answer to Problem 30.11P
The isoprene units in the given terpene (grandisol) are located as,
Explanation of Solution
Terpenes are composed of repeating five-carbon units. These units are called isoprene units.
Figure 1
An isoprene unit possesses following properties.
➢ It involves one branched carbon and
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
The isoprene units in the given terpene (grandisol) are located as,
Figure 4
The isoprene units in the given terpene (grandisol) are located in Figure 4.
(d)
Interpretation: The isoprene units in the given compound are to be located.
Concept introduction: An isoprene unit possesses following properties.
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
Answer to Problem 30.11P
The isoprene units in the given terpene (camphor) are located as,
Explanation of Solution
Terpenes are composed of repeating five-carbon units. These units are called isoprene units.
Figure 1
An isoprene unit possesses following properties.
➢ It involves one branched carbon and
➢ It may either consist of
➢ It is always connected by one or more
➢ Each isoprene unit is consist of
➢ While locating an isoprene unit, the presence of heteroatoms is ignored.
The isoprene units in the given terpene (camphor) are located as,
Figure 5
The isoprene units in the given terpene (camphor) are located in Figure 5.
Want to see more full solutions like this?
Chapter 30 Solutions
Organic Chemistry-Package(Custom)
- Draw all stereoisomers formed when each alkene is treated with mCPBA.arrow_forwardDraw the organic products formed when each compound is treated with H2, Pd-C. Indicate the three-dimensional structure of all stereoisomers formed.arrow_forwardDraw the products formed when each alkene is treated with BH3 followed by H2O2,HO−. Include the stereochemistry at all stereogenic centers.arrow_forward
- Give the IUPAC name for each compound, including the R, S designation for each stereogenic center. In a. b. C.arrow_forwardGiven that syn addition of H2 occurs from both sides of a trigonal planar double bond, draw all stereoisomers formed when each compound is treated with H2.arrow_forwardClassify each substituent as electron donating or electron withdrawing.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning