(a)
Interpretation:
The structure of the benzamide is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by
Rules for writing IUPAC name from the structural formula are:
• First, identify the longest carbon chain.
• The next step is to identify the groups attached to the longest chain.
• Identify the position, location, and a number of the substituents bonded to the carbon chain.
• Use prefix di, tri, tetra if the same type of substituents is present.
• Name the substituents in alphabetical order.
(b)
Interpretation:
The structure of the
Concept introduction:
The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of the organic compound is correctly interpreted from the name.
Rules for writing IUPAC name from the structural formula are:
• First, identify the longest carbon chain.
• The next step is to identify the groups attached to the longest chain.
• Identify the position, location, and a number of the substituents bonded to the carbon chain.
• Use prefix di, tri, tetra if the same type of substituents is present.
• Name the substituents in alphabetical order.
(c)
Interpretation:
The structure of the
Concept introduction:
The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of the organic compound is correctly interpreted from the name.
Rules for writing IUPAC name from the structural formula are:
• First, identify the longest carbon chain.
• The next step is to identify the groups attached to the longest chain.
• Identify the position, location, and a number of the substituents bonded to the carbon chain.
• Use prefix di, tri, tetra if the same type of substituents is present.
• Name the substituents in alphabetical order.
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Chapter 16 Solutions
Bundle: Chemistry For Today: General, Organic, And Biochemistry, 9th + Owlv2 With Mindtap Reader, 1 Term (6 Months) Printed Access Card
- Which of the following compounds is WILL NOT form an amide in a reaction with a carboxylic acid derivative? a. secondary amine b. primary amine c. tertiary amine d. ammoniaarrow_forwardPre-Lab Study Questions 1. What is the functional group in amines? In amides? 2. What products are formed when amides are hydrolyzed? 3. Draw the condensed structural formulas for each of the following amines and amides: a. 1-propanamine b. 2-methyl-3-hexamine c. N-methylpentamide d. N,N-dimethylbenzamide 139arrow_forwardBy functional group interconversion, which of the following compounds is not a good starting material for the synthesis of primary amine. A. Alkylhalide B. Alcohol C. Aldehyde D. Acetonitrilearrow_forward
- Draw the structural formula for each of the following amines: a. diisopropylamine b. p-ethylaniline c. 2-methylcyclopentanamine d. N-methyl-3-ethylanilinearrow_forwardWhich of the following is a suitable name for the ester CH3CH2CH2CH2CO2CH2CH2CH2CH3 Select one: a. pentyl butanoate b. nonanoate c. butyl pentanoate d. pentanebutanate Amides have Select one: a. an -OR group bonded to the carbonyl C atom b. an -NH2, -NHR, or NR2 group bonded to the carbonyl C atom c. an -OH group bonded to the carbonyl C atomarrow_forwardN-p-hydroxyphenylethanamide is commonly known as a. acetaminophen b. acetamide c. acetanilide d. formamide High molar mass amines have __________ odor. a.strong ammoniacal b.fruity c.fishy d.obnoxious Trimethyl amine has _________ odor. a.obnoxious b.fishy c. ammoniacal d. fruityarrow_forward
- The following are central stimulants: Select one or more: A. Barbiturates. B. Morphine. C. Benzodiazepines. D. Cocaine. E. Amphetamines.arrow_forwardCyclic amides are called which of the following? a. lactams b. lactanes c. lactones d. lactinesarrow_forwardC. Amides 1. Amidation a. Acetic acid + ammoniaarrow_forward
- In general, amines are nucleophilic due to: Select one: a. Existence of negative charge in amine group b. Amines are more electronegative than other functional groups C. Lone pairs in the amine group available for donation d. None of the abovearrow_forward10. Under certain conditions interacts with sodium nitrite: A. Resorcinol B. Nicotinic acid C. Butadion D. Morphine hydrochloride E. Benzoic acidarrow_forwardA. Use the structure of aniline provided and draw the complete structural formula for each of the following: N-Methylaniline N,N-Dimethylaniline 3-Octanamine 4-Chloro-5-iodo-1-nonanamine N-Isopropylanilinearrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
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