![GENERAL,ORGANIC,+BIO.CHEM.-MINDTAP](https://www.bartleby.com/isbn_cover_images/9781305866966/9781305866966_largeCoverImage.gif)
Concept explainers
(a)
Interpretation:
The IUPAC name of given ether 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 ether:
- ✓ The base name is found from the longest carbon chain present in ether.
- ✓ The suffix –yl has to be changed to –oxy in order to obtain the alkoxy group name. For example, ethyl becomes as ethoxy, methyl becomes as methoxy etc.
- ✓ Alkoxy name has to be placed first with the number (carbon atom to which the alkoxy group is attached) followed by the base name.
(b)
Interpretation:
The IUPAC name of given ether 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 ether:
- ✓ The base name is found from the longest carbon chain present in ether.
- ✓ The suffix –yl has to be changed to –oxy in order to obtain the alkoxy group name. For example, ethyl becomes as ethoxy, methyl becomes as methoxy etc.
- ✓ Alkoxy name has to be placed first with the number (carbon atom to which the alkoxy group is attached) followed by the base name.
(c)
Interpretation:
The IUPAC name of given ether 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 ether:
- ✓ The base name is found from the longest carbon chain present in ether.
- ✓ The suffix –yl has to be changed to –oxy in order to obtain the alkoxy group name. For example, ethyl becomes as ethoxy, methyl becomes as methoxy etc.
- ✓ Alkoxy name has to be placed first with the number (carbon atom to which the alkoxy group is attached) followed by the base name.
(d)
Interpretation:
The IUPAC name of given ether 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 ether:
- ✓ The base name is found from the longest carbon chain present in ether.
- ✓ The suffix –yl has to be changed to –oxy in order to obtain the alkoxy group name. For example, ethyl becomes as ethoxy, methyl becomes as methoxy etc.
- ✓ Alkoxy name has to be placed first with the number (carbon atom to which the alkoxy group is attached) followed by the base name.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 14 Solutions
GENERAL,ORGANIC,+BIO.CHEM.-MINDTAP
- Please correct answer and don't use hand ratingarrow_forwardNonearrow_forwardDraw Newman projects for each of the following molecules with 3 different rotational angles from carbon 2 to carbon 3. Rank your structures from lowest to highest energy. What causes the energy differences? Label the overlap. a. b. Br OH C. Br Brarrow_forward
- Draw the stereoisomers of 3,5-diethylcylopentane. Identify the different relationships between each molecules (diasteromers, enantiomers, meso compounds, etc.)arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardPlease correct answer and don't use hand rating and don't use Ai solutionarrow_forward
- Show work....don't give Ai generated solutionarrow_forwardIs it possible to do the following reduction in one step? If so, add the necessary reagents and catalysts to the reaction arrow. If not, check the box under the drawing area. T G टे 13arrow_forwardPlease correct answer and don't use hand ratingarrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305081079/9781305081079_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285853918/9781285853918_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305960060/9781305960060_smallCoverImage.gif)