
Concept explainers
a)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Simple sulfides are with no other
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is cyclohexyl isopropyl sulfide.
Explanation of Solution
The sulfide contains a sulfur atom attached to a cyclohexyl group and an isopropyl group.
The IUPAC name of the compound shown is cyclohexyl isopropyl sulfide.
b)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 1, 2-dimethoxy benzene.
Explanation of Solution
The compound contains a benzene ring with two methoxyl groups in ortho relationship.
The IUPAC name of the compound shown is 1, 2-dimethoxy benzene.
c)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
The
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 1, 2-epoxycyclopentane.
Explanation of Solution
The compound given contains a cyclopentane ring with the oxygen atom attached to C1 and C2.
The IUPAC name of the compound shown is 1, 2-epoxycyclopentane.
d)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 2-methyltetrahydrofuran.
Explanation of Solution
The compound has a tetrahydrofuran ring with a methyl group attached on C2.
The IUPAC name of the compound shown is 2-methyltetrahydrofuran.
e)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is cyclopropyl isopropyl ether.
Explanation of Solution
The compound given contains a cyclopropyl and an isopropyl group attached to an oxygen atom.
The IUPAC name of the compound shown is cyclopropyl isopropyl ether.
f)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 2-nitrobenzenethiol.
Explanation of Solution
The compound given contains a benzene ring attached to a thiol group and a nitro groups in 1, 2-relationship.
The IUPAC name of the compound shown is 2-nitrobenzenethiol.
g)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Thioalcohols are named as derivatives of the parent
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 2-(isopropylthio)-3, 4-dimethylhexane.
Explanation of Solution
In the compound shown a sulfur atom is attached to an isopropyl group and a 3, 4-dimethylhexyl group attached through C2.
The IUPAC name of the compound shown is 2-isopropylthio-3, 4-dimethylhexane.
h)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 2, 2-dimethoxypropane.
Explanation of Solution
The compound contains a three carbon straight chain with two methoxy groups attached to C2.
The IUPAC name of the compound shown is 2, 2-dimethoxypropane.
i)
Interpretation:
The IUPAC name of the compound shown is to be given.
Concept introduction:
Simple sulfides are with no other functional groups are named by identifying the two organic substituents and adding the word sulfide. If other functional groups are present, the sulfide part is considered as alkylthio substituent.
To give:
The IUPAC name of the compound shown.

Answer to Problem 39AP
The IUPAC name of the compound shown is 1, 1-(dimethylthio) cyclohexane.
Explanation of Solution
The compound contains a cyclohexane ring with two methylthio groups attached to C1.
The IUPAC name of the compound shown is 1, 1-dimethylthiocyclohexane.
Want to see more full solutions like this?
Chapter 18 Solutions
Student Value Bundle: Organic Chemistry, + OWLv2 with Student Solutions Manual eBook, 4 terms (24 months) Printed Access Card (NEW!!)
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electrons-pushing arrows for the following reaction or mechanistic step(s).arrow_forwardCurved 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. I I I H Select to Add Arrows HCI, CH3CH2OHarrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and the follow the arrows to draw the intermediate and product in this reaction or mechanistic step(s).arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the intermediates and product of the following reaction or mechanistic step(s).arrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and the product in this reaction or mechanistic step(s).arrow_forwardLook at the following pairs of structures carefully to identify them as representing a) completely different compounds, b) compounds that are structural isomers of each other, c) compounds that are geometric isomers of each other, d) conformers of the same compound (part of structure rotated around a single bond) or e) the same structure.arrow_forward
- Given 10.0 g of NaOH, what volume of a 0.100 M solution of H2SO4 would be required to exactly react all the NaOH?arrow_forward3.50 g of Li are combined with 3.50 g of N2. What is the maximum mass of Li3N that can be produced? 6 Li + N2 ---> 2 Li3Narrow_forward3.50 g of Li are combined with 3.50 g of N2. What is the maximum mass of Li3N that can be produced? 6 Li + N2 ---> 2 Li3Narrow_forward
- Concentration Trial1 Concentration of iodide solution (mA) 255.8 Concentration of thiosulfate solution (mM) 47.0 Concentration of hydrogen peroxide solution (mM) 110.1 Temperature of iodide solution ('C) 25.0 Volume of iodide solution (1) used (mL) 10.0 Volume of thiosulfate solution (5:03) used (mL) Volume of DI water used (mL) Volume of hydrogen peroxide solution (H₂O₂) used (mL) 1.0 2.5 7.5 Time (s) 16.9 Dark blue Observations Initial concentration of iodide in reaction (mA) Initial concentration of thiosulfate in reaction (mA) Initial concentration of hydrogen peroxide in reaction (mA) Initial Rate (mA's)arrow_forwardDraw the condensed or line-angle structure for an alkene with the formula C5H10. Note: Avoid selecting cis-/trans- isomers in this exercise. Draw two additional condensed or line-angle structures for alkenes with the formula C5H10. Record the name of the isomers in Data Table 1. Repeat steps for 2 cyclic isomers of C5H10arrow_forwardExplain why the following names of the structures are incorrect. CH2CH3 CH3-C=CH-CH2-CH3 a. 2-ethyl-2-pentene CH3 | CH3-CH-CH2-CH=CH2 b. 2-methyl-4-pentenearrow_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


