Concept explainers
(a)
Interpretation:
The structure of nitrogen-containing compound that is obtained when the given amide undergoes acidic hydrolysis has to be drawn.
Concept Introduction:
Amides are derivatives of
Acidic hydrolysis of amides gives the product as carboxylic acid and
Basic hydrolysis of amides gives the product as carboxylic acid salt and amine. Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.
(b)
Interpretation:
The structure of nitrogen-containing compound that is obtained when the given amide undergoes acidic hydrolysis has to be drawn.
Concept Introduction:
Amides are derivatives of carboxylic acid. Amides are not much reactive as of carboxylic acids. They are also stable relatively in aqueous solution. But under strenuous conditions amides undergo hydrolysis. The conditions are presence of acid, base or enzymes.
Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt. Amine salt is obtained because in acidic conditions the amine is converted into amine salt.
Basic hydrolysis of amides gives the product as carboxylic acid salt and amine. Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.
(c)
Interpretation:
The structure of nitrogen-containing compound that is obtained when the given amide undergoes acidic hydrolysis has to be drawn.
Concept Introduction:
Amides are derivatives of carboxylic acid. Amides are not much reactive as of carboxylic acids. They are also stable relatively in aqueous solution. But under strenuous conditions amides undergo hydrolysis. The conditions are presence of acid, base or enzymes.
Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt. Amine salt is obtained because in acidic conditions the amine is converted into amine salt.
Basic hydrolysis of amides gives the product as carboxylic acid salt and amine. Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.
(d)
Interpretation:
The structure of nitrogen-containing compound that is obtained when the given amide undergoes acidic hydrolysis has to be drawn.
Concept Introduction:
Amides are derivatives of carboxylic acid. Amides are not much reactive as of carboxylic acids. They are also stable relatively in aqueous solution. But under strenuous conditions amides undergo hydrolysis. The conditions are presence of acid, base or enzymes.
Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt. Amine salt is obtained because in acidic conditions the amine is converted into amine salt.
Basic hydrolysis of amides gives the product as carboxylic acid salt and amine. Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.
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Chapter 6 Solutions
EBK ORGANIC AND BIOLOGICAL CHEMISTRY
- The kinetics of a gas phase reaction of the form A → Products results in a rate constant of 0.00781 M/min. For this reaction, the initial concentration of A is 0.501 M. How many minutes will it take for the concentration of A to reach 0.144 Marrow_forwardWhat is the rate for the second order reaction A → Products when [A] = 0.256 M? (k = 0.761 M⁻¹s⁻¹)arrow_forwardFor reaction N2(g) + O2(g) --> 2NO(g) Write the rate of the reaction in terms of change of NO.arrow_forward
- What is the name of the major product formed during the reaction between benzoyl chloride and phenol? benzyl ester O phenyl benzoate ○ cyclopentanoate ○ benzyl phenoate ○ benzenecarboxylic acidarrow_forwardProvide the proper IUPAC or common name for the following compound. Dashes, commas, and spaces must be used correctly.arrow_forwardProvide the proper IUPAC name (only) for the following compound. Dashes, commas, and spaces must be used correctly. HO. OHarrow_forward
- Question 2 0/1 pts Provide the proper IUPAC name only for the following compound. Dashes, commas, and spaces must be used correctly. HO CH 3 1-methyl-1-cyclohexanecarboxylic acidarrow_forwardPlease assign all the carbons for C-NMR and hydrogen for H-NMR. Please if I can get that less than hourarrow_forwardAssign these peaks spectrum ( H-NMR and C-NMR)arrow_forward
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
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