Concept explainers
(a)
Interpretation:
The IUPAC name and common name for the given thioether has to be assigned.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of
Root word represents the longest continuous carbon skeleton of the organic molecule.
IUPAC rules for naming thioether:
- ✓ The base name is found from the longest carbon chain present in thioether.
- ✓ The suffix –thio has to be added in order to obtain the alkylthio group name. For example, ethyl becomes as ethylthio, methyl becomes as methylthio etc.
- ✓ Alkylthio name has to be placed first with the number (carbon atom to which the alkykthio group is attached) followed by the base name.
Rules for assigning common names to thioether:
For obtaining common name for thioether, two rules are applicable, one for symmetrical ethers and one for unsymmetrical ethers.
- ✓ For unsymmetrical thioethers, the two hydrocarbon groups that is attached to the oxygen atom is arranged in an alphabetical order and the word sulfide is added. The words are separated by a space. These names have three words with space between them.
- ✓ For symmetrical ethers, prefix di- is used. Then the word sulfide is added with a space between the two words. These names have two words with space between them.
(a)

Answer to Problem 3.144EP
IUPAC name for the given compound is ethylthioethane and common name is diethyl sulfide.
Explanation of Solution
Given structure of compound is shown below,
First step is to identify the longest carbon chain. In this case it is a two carbon chain. Hence, the base name is ethane.
Next step is to identify the alkylthio group. In the given thioether, the alkylthio group is found to be ethylthio as it contains two carbon atoms.
Alkylthio name is placed before the base name with the appropriate number that gives information about to which carbon atom the alkylthio group is attached. This gives the IUPAC name as ethylthioethane.
The IUPAC name of the given thioether is ethylthioethane.
To obtain common name the two hydrocarbon groups that are attached to the sulfur atom is named first. In the given structure, two ethyl groups are present. Therefore, prefix di- is added to the alkyl group followed by the word sulfide. Common name for the given thioether is diethyl sulfide.
IUPAC name and common name for the given thioether is assigned.
(b)
Interpretation:
The IUPAC name and common name for the given thioether has to be assigned.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
Root word represents the longest continuous carbon skeleton of the organic molecule.
IUPAC rules for naming thioether:
- ✓ The base name is found from the longest carbon chain present in thioether.
- ✓ The suffix –thio has to be added in order to obtain the alkylthio group name. For example, ethyl becomes as ethylthio, methyl becomes as methylthio etc.
- ✓ Alkylthio name has to be placed first with the number (carbon atom to which the alkykthio group is attached) followed by the base name.
Rules for assigning common names to thioether:
For obtaining common name for thioether, two rules are applicable, one for symmetrical ethers and one for unsymmetrical ethers.
- ✓ For unsymmetrical thioethers, the two hydrocarbon groups that is attached to the oxygen atom is arranged in an alphabetical order and the word sulfide is added. The words are separated by a space. These names have three words with space between them.
- ✓ For symmetrical ethers, prefix di- is used. Then the word sulfide is added with a space between the two words. These names have two words with space between them.
(b)

Answer to Problem 3.144EP
IUPAC name for the given compound is 2-ethylthiopropane and common name is ethyl isopropyl sulfide.
Explanation of Solution
Given structure of compound is shown below,
First step is to identify the longest carbon chain. In this case it is a three carbon chain. Hence, the base name is propane.
Next step is to identify the alkylthio group. In the given thioether, the alkylthio group is found to be ethylthio as it contains two carbon atoms. The point of attachment in the propane for ethylthio group is in the second carbon atom.
Alkylthio name is placed before the base name with the appropriate number that gives information about to which carbon atom the alkylthio group is attached. This gives the IUPAC name as 2-ethylthiopropane.
The IUPAC name of the given thioether is 2-ethylthiopropane.
To obtain common name the two hydrocarbon groups that are attached to the sulfur atom is named first. In the given structure, an ethyl and an isopropyl group is present. Arranging them in the alphabetical order and adding the word sulfide after them gives the common name for the given thioether. Common name for the given thioether is ethyl isopropyl sulfide.
IUPAC name and common name for the given thioether is assigned.
(c)
Interpretation:
The IUPAC name and common name for the given thioether has to be assigned.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
Root word represents the longest continuous carbon skeleton of the organic molecule.
IUPAC rules for naming thioether:
- ✓ The base name is found from the longest carbon chain present in thioether.
- ✓ The suffix –thio has to be added in order to obtain the alkylthio group name. For example, ethyl becomes as ethylthio, methyl becomes as methylthio etc.
- ✓ Alkylthio name has to be placed first with the number (carbon atom to which the alkykthio group is attached) followed by the base name.
Rules for assigning common names to thioether:
For obtaining common name for thioether, two rules are applicable, one for symmetrical ethers and one for unsymmetrical ethers.
- ✓ For unsymmetrical thioethers, the two hydrocarbon groups that is attached to the oxygen atom is arranged in an alphabetical order and the word sulfide is added. The words are separated by a space. These names have three words with space between them.
- ✓ For symmetrical ethers, prefix di- is used. Then the word sulfide is added with a space between the two words. These names have two words with space between them.
(c)

Answer to Problem 3.144EP
IUPAC name for the given compound is methylthiocyclopentane and common name is cyclopentyl methyl sulfide.
Explanation of Solution
Given structure of compound is shown below,
First step is to identify the longest carbon chain. In this case it is a five carbon cyclic chain that is saturated. Hence, the base name is cyclopentane.
Next step is to identify the alkylthio group. In the given thioether, the alkylthio group is found to be methylthio as it contains only one carbon atom.
Alkylthio name is placed before the base name with the appropriate number that gives information about to which carbon atom the alkylthio group is attached. This gives the IUPAC name as methylthiocyclopentane.
The IUPAC name of the given thioether is methylthiocyclopentane.
To obtain common name the two hydrocarbon groups that are attached to the sulfur atom is named first. In the given structure, a methyl and a cyclopentyl group is present. Arranging them in the alphabetical order and adding the word sulfide after them gives the common name for the given thioether. Common name for the given thioether is cyclopentyl methyl sulfide.
IUPAC name and common name for the given thioether is assigned.
(d)
Interpretation:
The IUPAC name and common name for the given thioether has to be assigned.
Concept Introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the root name.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
Root word represents the longest continuous carbon skeleton of the organic molecule.
IUPAC rules for naming thioether:
- ✓ The base name is found from the longest carbon chain present in thioether.
- ✓ The suffix –thio has to be added in order to obtain the alkylthio group name. For example, ethyl becomes as ethylthio, methyl becomes as methylthio etc.
- ✓ Alkylthio name has to be placed first with the number (carbon atom to which the alkykthio group is attached) followed by the base name.
Rules for assigning common names to thioether:
For obtaining common name for thioether, two rules are applicable, one for symmetrical ethers and one for unsymmetrical ethers.
- ✓ For unsymmetrical thioethers, the two hydrocarbon groups that is attached to the oxygen atom is arranged in an alphabetical order and the word sulfide is added. The words are separated by a space. These names have three words with space between them.
- ✓ For symmetrical ethers, prefix di- is used. Then the word sulfide is added with a space between the two words. These names have two words with space between them.
(d)

Answer to Problem 3.144EP
IUPAC name for the given compound is 3-(ethylthio)-1-propene and common name is allyl ethyl sulfide.
Explanation of Solution
Given structure of compound is shown below,
First step is to identify the longest carbon chain. In this case it is a three carbon chain with a double bond. Hence, the base name is propene.
Next step is to identify the alkylthio group. In the given thioether, the alkylthio group is found to be ethylthio as it contains two carbon atoms.
Alkylthio name is placed before the base name with the appropriate number that gives information about to which carbon atom the alkylthio group is attached. This gives the IUPAC name as 3-(ethylthio)-1-propene.
The IUPAC name of the given thioether is 3-(ethylthio)-1-propene.
To obtain common name the two hydrocarbon groups that are attached to the sulfur atom is named first. In the given structure, an ethyl and an allyl group is present. Arranging them in the alphabetical order and adding the word sulfide after them gives the common name for the given thioether. Common name for the given thioether is allyl ethyl sulfide.
IUPAC name and common name for the given thioether is assigned.
Want to see more full solutions like this?
Chapter 3 Solutions
EBK ORGANIC AND BIOLOGICAL CHEMISTRY
- Synthesis of 1-metilbenzotriazole from 1,2-diaminobenceno.arrow_forwardSynthesis of 1-metilbenzotriazole.arrow_forwardIndicate the formula of the compound, that is the result of the N- alquilación (nucleofílic substitution), in which an additional lateral chain was formed (NH-CH2-COOMe). F3C. CF3 NH NH2 Br о OMe K2CO3, DABCO, DMFarrow_forward
- Identify the mechanism through which the following reaction will proceed and draw the major product. Part 1 of 2 Br KOH EtOH Through which mechanism will the reaction proceed? Select the single best answer. E1 E2 neither Part: 1/2 Part 2 of 2 Draw the major product formed as a result of the reaction. Click and drag to start drawing a structure. Xarrow_forwardWhat is single-point calibration? Provide an example.arrow_forwardDraw the major product formed via an E1 pathway.arrow_forward
- Part 9 of 9 Consider the products for the reaction. Identify the major and minor products. HO Cl The E stereoisomer is the major product and the Z stereoisomer is the minor product ▼ S major product minor productarrow_forwardConsider the reactants below. Answer the following questions about the reaction mechanism and products. HO Clarrow_forwardjulietteyep@gmail.com X YSCU Grades for Juliette L Turner: Orc X 199 A ALEKS - Juliette Turner - Modul X A ALEKS - Juliette Turner - Modul x G butane newman projection - Gox + www-awa.aleks.com/alekscgi/x/Isl.exe/10_u-IgNslkr7j8P3jH-IBxzaplnN4HsoQggFsejpgqKoyrQrB2dKVAN-BcZvcye0LYa6eXZ8d4vVr8Nc1GZqko5mtw-d1MkNcNzzwZsLf2Tu9_V817y?10Bw7QYjlb il Scribbr citation APA SCU email Student Portal | Main Ryker-Learning WCU-PHARM D MySCU YSCU Canvas- SCU Module 4: Homework (Ch 9-10) Question 28 of 30 (1 point) | Question Attempt: 1 of Unlimited H₂SO heat OH The mechanism of this reaction involves two carbocation intermediates, A and B. Part 1 of 2 KHSO 4 rearrangement A heat B H₂O 2 OH Draw the structure of A. Check Search #t m Save For Later Juliet Submit Assignm 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forward
- The electrons flow from the electron-rich atoms of the nucleophile to the electrons poor atoms of the alkyl halide. Identify the electron rich in the nucleophile. Enter the element symbol only, do not include any changes.arrow_forwardHello, I am doing a court case analysis in my Analytical Chemistry course. The case is about a dog napping and my role is prosecution of the defendant. I am tasked in the Area of Expertise in Neutron Activation and Isotopic Analysis. Attached is the following case study reading of my area of expertise! The landscaping stone was not particularly distinctive in its decoration but matched both the color and pattern of the Fluential’s landscaping stone as well as the stone in the back of the recovered vehicle. Further analysis of the stone was done using a technique called instrumental neutron activation analysis. (Proceed to Neutron Activation data) Photo Notes: Landscaping stone recovered in vehicle. Stone at Fluential’s home is similar inappearance. Finally, the white paint on the brick was analyzed using stable isotope analysis. The brick recovered at the scene had smeared white paint on it. A couple of pieces of brick in the back of the car had white paint on them. They…arrow_forwardCite the stability criteria of an enamine..arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning





