
Concept explainers
Locate the isoprene units in each compound.
a. b.

(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 18P
The isoprene units in the given terpene (
Explanation of Solution
The given compound (
Figure 1
Terpenes are composed of repeating five-carbon units. These units are called isoprene units.
Figure 2
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 (
Figure 3
The isoprene units in the given compound (

(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 18P
The isoprene units in the given terpene (humulene) are located as,
Explanation of Solution
The given compound (humulene) is a terpene. Its structure is in ball-and stick form. It is converted into skeletal structure by replacing black ball with
Figure 4
Terpenes are composed of repeating five-carbon units. These units are called isoprene units.
Figure 2
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 (humulene) are located as,
Figure 5
The isoprene units in the given compound (humulene) are located in Figure 5.
Want to see more full solutions like this?
Chapter 29 Solutions
ORGANIC CHEMISTRY (LOOSELEAF)
- Hi, I need your help with the drawing, please. I have attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forwardHi, I need your help i dont know which one to draw please. I’ve attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forward5. Write the formation reaction of the following complex compounds from the following reactants: 6. AgNO₃ + K₂CrO₂ + NH₄OH → 7. HgNO₃ + excess KI → 8. Al(NO₃)₃ + excess NaOH →arrow_forward
- Indicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. CO₂C2H5 + CH3-NH-NH,arrow_forwardDraw the major product of this reaction N-(cyclohex-1-en-1-yl)-1-(pyrrolidino) reacts with CH2=CHCHO, heat, H3O+arrow_forwardDraw the starting material that would be needed to make this product through an intramolecular Dieckmann reactionarrow_forward
- Draw the major product of this reaction. Nitropropane reacts + pent-3-en-2-one reacts with NaOCH2CH3, CH3CHOHarrow_forwardIndicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. OC2H5 + CoHs-NH-NH,arrow_forwardExplain how substitutions at the 5-position of barbituric acid increase the compound's lipophilicity.arrow_forward
- Explain how substitutions at the 5-position of phenobarbital increase the compound's lipophilicity.arrow_forwardName an interesting derivative of barbituric acid, describing its structure.arrow_forwardBriefly describe the synthesis mechanism of barbituric acid from the condensation of urea with a β-diketone.arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

