(a)
Interpretation:
Correct IUPAC name for the given ketone has to be assigned.
Concept Introduction:
For naming a ketone in
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:
Correct IUPAC name for the given ketone has to be assigned.
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:
Correct IUPAC name for the given ketone has to be assigned.
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:
Correct IUPAC name for the given ketone has to be assigned.
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
- Which of the following compounds is a dihydroxy alcohol? a. 2-propanol b. 1,2-ethanediol c. 1,2,3-propanetriol d. ethanol e. both 1,2-ethanediol and 1,2,3-propanetriolarrow_forward1. Which of the following structural features is possessed by aldehydes but not ketones? a. At least one hydroxyl group is bonded to the carbonyl carbon atom. b. At least one hydrogen atom is bonded to the carbonyl carbon atom. c. The carbonyl carbon atom is bonded to two other carbon atoms. d. The carbonyl carbon atom is part of a ring structure. 2. What is the IUPAC name of the following compound in the attached photo? a. 3-chloro-4-nitrobenzoic acid b. 2-chloro-4-carboxynitrobenzene c. 2-nitro-5-carboxychlorobenzene d. 2-chloro-1-nitro-4-benzoic acid 3. Which of the following is the correct bond-line structure for CH3C≡C(CH2)2CH(CH3)2? a. Structure I b. Structure II c. Structure III d. Structure IVarrow_forwardWrite a condensed structural formula for each of the following alcohols. a. 2-Methyl-1-propanol b. 4-Methyl-2-pentanol c. 2-Phenyl-2-propanol d. 2-Methycyclobutanolarrow_forward
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- 9. Assign an IUPAC name to each of the following compounds. 2. a. CH3-C-O-C-CH2-CH, b. CH3-CH2-CH-CH-C-CI L. C. CH3-CH-CH-C-Cl ČH3 CH3 d. CH3-CH-C-0-C-H Draw the structures of the esters formed by reacting the following substances 1 molecule methanol and 1 molecule phosphoric acid 2 molecules methanol and 1 molecule phosphoric acid 1 molecule methanol and 1 molecule nitric acid 1 molecule ethylene glycol and 2 molecules of nitric acid 0. A. В. C, D.arrow_forwardWhat is the IUPAC name for the following compound? O A. 2-isopropyl-3-pentyne O B. 4-isopropyl-2-pentyne OC 4,5-dimethyl-2-hexyne O D.2,3-dimethyl-4-hexynearrow_forwardwhich of the following alcohols can be oxidized to form ketone as a product? a.) 1-butanol, b.) 2-butanol, c.) tert-butanol, d.) both b and carrow_forward
- Draw a structural formula for each of the following aldehydes. a. 3-Methylpentanal b. 2-Ethylhexanal 4-21arrow_forwardMost simple ketones and aldehydes exist mainly as the keto tautomer form. A. True B. Falsearrow_forwardIdentify the IUPAC name of the given structure. A. 2 - methylhexan-5-one B. 5 - methylhexan-2-one C. 2 - heptanone D. 5 - heptanone Identify the IUPAC name of the given structure. A. 4 - bromopentan-3-one B. 1 - bromobutan-2-one C. 2 - bromobutan-one D. None of the abovearrow_forward
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,