Chapter 4: Q.10. (page 128)
Question: Give the IUPAC name for each of the five constitutional isomers of molecular formula in Problem 4.3.
Short Answer
Answer
- Hexane
- 2-methylpentane
- 3-methylpentane
- 2,2-dimethylbutane
- 2,3-dimethylbutane
Chapter 4: Q.10. (page 128)
Question: Give the IUPAC name for each of the five constitutional isomers of molecular formula in Problem 4.3.
Answer
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion: Rank the following alkanes in order of increasing boiling point.
Question: For each compound drawn below:
a. Draw representations for the cis and trans isomers using a hexagon for the six membered ring, and wedges and dashed wedges for substituents.
b. Draw the two possible chair conformations for the cis isomer. Which conformation, if either, is more stable?
c. Draw the two possible chair conformations for the trans isomer. Which conformation, if either, is more stable?
d. Which isomer, cis or trans, is more stable and why?
Question: Convert each of the following structures into its more stable chair form. One structure represents menthol and one represents isomenthol. Menthol, the more stable isomer, is used in lip balms and mouthwash. Which structure corresponds to menthol?
Question: Consider the tricyclic structure B.
(a) Label each substituent on the rings as axial or equatorial.
(b) Draw B using chair conformations for each six-membered ring.
(c) Label the atoms on the ring fusions (the carbons that join each set of two rings together) as cis or trans to each other.
B
Question: Draw a chair conformation of cyclohexane with one group and one role="math" localid="1648542173942" group that fits each description.
What do you think about this solution?
We value your feedback to improve our textbook solutions.