![EBK GENERAL, ORGANIC, AND BIOLOGICAL CH](https://www.bartleby.com/isbn_cover_images/8220100853180/8220100853180_largeCoverImage.jpg)
Concept explainers
(a)
Interpretation:
Common name of the given compound has to be assigned.
Concept Introduction:
Amides are derivatives of
IUPAC rules for naming an amide:
- The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
- The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.
For amides, IUPAC name and common names are given using the same rules.
(b)
Interpretation:
Common name of the given compound has to be assigned.
Concept Introduction:
Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.
IUPAC rules for naming an amide:
- The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
- The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.
For amides, IUPAC name and common names are given using the same rules.
(c)
Interpretation:
Common name of the given compound has to be assigned.
Concept Introduction:
Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.
IUPAC rules for naming an amide:
- The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
- The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.
For amides, IUPAC name and common names are given using the same rules.
(d)
Interpretation:
Common name of the given compound has to be assigned.
Concept Introduction:
Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.
IUPAC rules for naming an amide:
- The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
- The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.
For amides, IUPAC name and common names are given using the same rules.
![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 17 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- What is the complete name of the following sugar? но он носн он Write out the words alpha and beta. This question is case-sensitive. Capitalize only the configuration designation, D or L, example: beta-D-glucopyranose.arrow_forwardWhich form of aspartic acid in Problem 18.54 is the zwitterion? What is the pI for the zwitterion?arrow_forwardFollowing are Fischer projection for a group of five carbon sugars,all of which are aldopentoses. Identify the pairs that are enantiomers and the pairs that are epimers.(The sugar shown herebare not all of the possible five carbon sugars.)arrow_forward
- Histidine is an amino acid with three titratable groups: an -NH3+ group (pKa = 9.2), a -COOH group (pKa = 1.8), and an imidazole (amine-like) group (pKa = 6.0). The titration curve for histidine is shown below with four points highlighted. (a) Identify which point on the titration curve corresponds to the pKa for each of the titratable groups, and which point corresponds to the pI. Explain your choices. (b) Calculate the value of pI for histidinearrow_forwardDoes trehalose (Problem 20.68) have an acetal grouping? A hemiacetal grouping? Do you expect trehalose to be a reducing or nonreducing sugar? Classify the linkage between the two monosaccharides.arrow_forwardFollowing are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers and the pairs that are epimers. (The sugars shown here are not all of the possible five-carbon sugars.) 1 СНО 2 СНО СНО Н-С—ОН Н-С—ОН Н—С—ОН Н-С—ОН НО —С—Н Н-С—ОН Н- С—ОН НО—С— Н НО—С—Н CH̟OH CH̟OH ČH̟OH в iоchemistry |61 STATE ATION Republic of the Philippines Romblon State University Romblan, Philippines 4 СНО 5 СНО 6 СНО НО—С—Н Н-С—ОН НО -С—Н Н—С—ОН НО -С—Н НО -С—Н H-C–OH Н-С—ОН НО—С—Н CH,OH ČH,OH CH,OHarrow_forward
- Following are Fischer projections for a groupof five-carbon sugars, all of which are aldopentoses. Identify thepairs that are enantiomers and the pairs that are epimers. (Thesugars shown here are not all of the possible five-carbon sugars.)arrow_forwardwhat is the pI for lysine?arrow_forwardDraw the four stereoisomers of threonine as Fischer projections.arrow_forward
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
![Text book image](https://www.bartleby.com/isbn_cover_images/9780134580999/9780134580999_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781947172517/9781947172517_coverImage_Textbooks.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259398629/9781259398629_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780815344322/9780815344322_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781260159363/9781260159363_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781260231700/9781260231700_smallCoverImage.gif)