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 14.143EP
IUPAC name for the given compound is methylthioethane and common name is ethyl 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 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 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 methylthioethane.
The IUPAC name of the given thioether is methylthioethane.
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 an ethyl 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 methyl 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 14.143EP
IUPAC name for the given compound is 2-methylthiopropane and common name is isopropyl 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 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 methylthio as it contains only one carbon atom. The point of attachment in the propane for methylthio 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-methylthiopropane.
The IUPAC name of the given thioether is 2-methylthiopropane.
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 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 isopropyl methyl 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 14.143EP
IUPAC name for the given compound is methylthiocyclohexane and common name is cyclohexyl 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 six carbon cyclic chain that is saturated. Hence, the base name is cyclohexane.
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 methylthiocyclohexane.
The IUPAC name of the given thioether is methylthiocyclohexane.
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 cyclohexyl 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 cyclohexyl 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 14.143EP
IUPAC name for the given compound is 3-(methylthio)-1-propene and common name is allyl 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 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 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 3-(methylthio)-1-propene.
The IUPAC name of the given thioether is 3-(methylthio)-1-propene.
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 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 methyl sulfide.
IUPAC name and common name for the given thioether is assigned.
Want to see more full solutions like this?
Chapter 14 Solutions
General, Organic, and Biological Chemistry
- What are Clathrin coated vesicles and what is their function?arrow_forwardHow is a protein destined for the Endoplasmic Reticulum (ER), imported into the ER? Be concise.arrow_forwardFind out about the organisations and the movements aimed at the conservation of our natural resources. Eg Chipko movement and Greenpeace. Make a project report on such an organisation.arrow_forward
- What are biofertilizers and mention the significancearrow_forwardPCBs and River Otters: Otters in Washington State’s Green-Duwamish River have high levels of polychlorinated biphenyls (PCBs) in their livers. PCBs can bind to the estrogen receptors in animals and disrupt the endocrine system of these otters. The PCBs seem to increase the estrogen to androgen ratio, skewing the ratio toward too much estrogen. How would increased estrogen affect the river otter population? Based on your reading of the materials in this unit, what factors can affect fertility in humans? Explain how each of the factors affecting human fertility that you described can disrupt the human endocrine system to affect reproduction.arrow_forwardOther than oil and alcohol, are there other liquids you could compare to water (that are liquid at room temperature)? How is water unique compared to these other liquids? What follow-up experiment would you like to do, and how would you relate it to your life?arrow_forward
- Selection of Traits What adaptations do scavengers have for locating and feeding on prey? What adaptations do predators have for capturing and consuming prey?arrow_forwardCompetition Between Species What natural processes limit populations from growing too large? What are some resources organisms can compete over in their natural habitat?arrow_forwardSpecies Interactions Explain how predators, prey and scavengers interact. Explain whether predators and scavengers are necessary or beneficial for an ecosystem.arrow_forward
- magine that you are conducting research on fruit type and seed dispersal. You submitted a paper to a peer-reviewed journal that addresses the factors that impact fruit type and seed dispersal mechanisms in plants of Central America. The editor of the journal communicates that your paper may be published if you make ‘minor revisions’ to the document. Describe two characteristics that you would expect in seeds that are dispersed by the wind. Contrast this with what you would expect for seeds that are gathered, buried or eaten by animals, and explain why they are different. (Editor’s note: Providing this information in your discussion will help readers to consider the significance of the research).arrow_forwardWhat is the difference between Uniporters, Symporters and Antiporters? Which of these are examples of active transport?arrow_forwardWhat are coupled transporters?arrow_forward
- Biology Today and Tomorrow without Physiology (Mi...BiologyISBN:9781305117396Author:Cecie Starr, Christine Evers, Lisa StarrPublisher:Cengage Learning
- Anatomy & PhysiologyBiologyISBN:9781938168130Author:Kelly A. Young, James A. Wise, Peter DeSaix, Dean H. Kruse, Brandon Poe, Eddie Johnson, Jody E. Johnson, Oksana Korol, J. Gordon Betts, Mark WomblePublisher:OpenStax CollegeHuman Heredity: Principles and Issues (MindTap Co...BiologyISBN:9781305251052Author:Michael CummingsPublisher:Cengage Learning