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Concept explainers
(a)
Interpretation:
The given ketone has to be named using
Concept Introduction:
For naming a ketone in IUPAC nomenclature, the suffix “-one” is added to the parent
IUPAC rules for naming a ketone:
The longest parent carbon chain is identified that includes the carbonyl group.
The parent chain name is changed by replacing the suffix “-e” with “-one”.
Numbering is done in a way that the carbonyl group gets the least numbering. The position of the carbonyl group is indicated in the name.
The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
Cyclic
ketones are named by adding the suffix “-one” to the name of the carbon ring. The substituents are numbered so that it gets the least numbering starting from the carbonyl group that is given the number 1.
(b)
Interpretation:
The given ketone has to be named using IUPAC nomenclature.
Concept Introduction:
For naming a ketone in IUPAC nomenclature, the suffix “-one” is added to the parent alkane name.
IUPAC rules for naming a ketone:
The longest parent carbon chain is identified that includes the carbonyl group.
The parent chain name is changed by replacing the suffix “-e” with “-one”.
Numbering is done in a way that the carbonyl group gets the least numbering. The position of the carbonyl group is indicated in the name.
The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
Cyclic ketones are named by adding the suffix “-one” to the name of the carbon ring. The substituents are numbered so that it gets the least numbering starting from the carbonyl group that is given the number 1.
(c)
Interpretation:
The given ketone has to be named using IUPAC nomenclature.
Concept Introduction:
For naming a ketone in IUPAC nomenclature, the suffix “-one” is added to the parent alkane name.
IUPAC rules for naming a ketone:
The longest parent carbon chain is identified that includes the carbonyl group.
The parent chain name is changed by replacing the suffix “-e” with “-one”.
Numbering is done in a way that the carbonyl group gets the least numbering. The position of the carbonyl group is indicated in the name.
The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
Cyclic ketones are named by adding the suffix “-one” to the name of the carbon ring. The substituents are numbered so that it gets the least numbering starting from the carbonyl group that is given the number 1.
(d)
Interpretation:
The given ketone has to be named using IUPAC nomenclature.
Concept Introduction:
For naming a ketone in IUPAC nomenclature, the suffix “-one” is added to the parent alkane name.
IUPAC rules for naming a ketone:
The longest parent carbon chain is identified that includes the carbonyl group.
The parent chain name is changed by replacing the suffix “-e” with “-one”.
Numbering is done in a way that the carbonyl group gets the least numbering. The position of the carbonyl group is indicated in the name.
The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
Cyclic ketones are named by adding the suffix “-one” to the name of the carbon ring. The substituents are numbered so that it gets the least numbering starting from the carbonyl group that is given the number 1.
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Chapter 15 Solutions
General, Organic, and Biological Chemistry
- Predict the major organic product(s), if any, of the following reactions. Assume all reagents are in excess unless otherwise indicated.arrow_forwardHow many signals would you expect to find in the 1 H NMR spectrum of each given compound? Part 1 of 2 2 Part 2 of 2 HO 5 ☑ Х IIIIII***** §arrow_forwardA carbonyl compound has a molecular ion with a m/z of 86. The mass spectra of this compound also has a base peak with a m/z of 57. Draw the correct structure of this molecule. Drawingarrow_forward
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- Write the systematic name of each organic molecule: structure name show work. don't give Ai generated solutionarrow_forwardShow work with explanation needed. Don't give Ai generated solutionarrow_forwardA Elschboard Part of SpeechT-D Alt Leaming App app.aktiv.com Curved arrows are used to illustrate the flow of electrons. Using the provided resonance structures, draw the curved electron- pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps. Include all lone pairs and formal charges in the structures. Problem 45 of 10 I Select to Add Arrows N Please selarrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
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