(a)
Interpretation:
The IUPAC name of the given amide is to be stated.
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 IUPAC name of the given amide is to be stated.
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 IUPAC name of the given amide is to be stated.
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.
(d)
Interpretation:
The IUPAC name of the given amide is to be stated.
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
Chemistry for Today: General, Organic, and Biochemistry
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- Synthadotin is a promising anticancer drug in clinical trials. (see attachment) Question: Classify any amine or amide as 1°, 2°, or 3°.arrow_forwardUse the structure of aniline provided and draw the condensedformula for each of the following amines.a. N-Methylaniline c. N-Ethylanilineb. N,N-Dimethylaniline d. N-Isopropylanilinearrow_forwardDraw a structural formula for each amine and amine derivative. Q.) Benzylaminearrow_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_forwardDraw condensed and skeletal structures for each of the following amines:a. 2-methyl-N-propyl-1-propanamine b. N-ethylethanamine c. 5-methyl-1-hexanamine d. methyldipropylamine e. N,N-dimethyl-3-pentanamine f. cyclohexylethylmethylaminearrow_forwardKindly give all the NEW IUPAC NAME and COMMON NAME of Roman Numeral I A, B, C. DRAW the STRUCTURES of the following on Roman Numeral II A, B, C, D Roman Numeral 3 give the reaction of the given amidesarrow_forward
- What acyl chloride and amine are required to synthesize the following amides?a. N-ethylbutanamide b. N,N-dimethylbenzamidearrow_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_forwardwhy Acetanilide at room temperature is less soluble?arrow_forward
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