(a)
Interpretation:
The products formed when the following amide is treated with H2O and H2SO4 should be determined:
Concept Introduction:
(b)
Interpretation:
The products formed when the following amide is treated with H2O and H2SO4 should be determined:
Concept Introduction:
Functional groups are the groups of atoms or atoms which are bonded with parent carbon chain in the organic molecule and are responsible for the physical and chemical properties of the compound. In organic chemistry, there are different functional groups such as carboxylic acid, alcohol, ester, or amide.
Amines are the organic compounds with general chemical formula of R-NH2 or R-NH-R whereas carboxylic acids are the organic molecules with R-COOH as general chemical formula.
(c)
Interpretation:
The products formed when the following amide is treated with H2O and H2SO4 should be determined:
Concept Introduction:
Functional groups are the groups of atoms or atoms which are bonded with parent carbon chain in the organic molecule and are responsible for the physical and chemical properties of the compound. In organic chemistry, there are different functional groups such as carboxylic acid, alcohol, ester, or amide.
Amines are the organic compounds with general chemical formula of R-NH2 or R-NH-R whereas carboxylic acids are the organic molecules with R-COOH as general chemical formula.
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EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
- Fenfluramine and phentermine are two components of fen–phen, an appetite suppressant withdrawn from the market in 1997 after it was shown to damage the heart valves in some patients. What products are formed when fenfluramine and phentermine are each treated with acetic acid (CH3CO2H)?arrow_forwardV. Classify each amine as 1', 2 or 3'. Give the IUPAC name for each amine. CH3 a. CH3CHCH,CH2NHCH3 b. CH3-C-CH,NH2 ČH3 ČH3arrow_forwardMatch the description to one of the compounds E– H. a. a compound that contains a 1 ° amine and a 1 ° amide b. a compound that contains a 1 ° amine and a 2 ° amide c. a compound that contains a 2 ° amine and a 3 ° amide d. a compound that contains a 3 ° amine and a 3 ° amidearrow_forward
- VI. What ammonium salt is formed when each amine is treated with HCI? Draw the structure of the resulting salt. a. -NH2 b. -CH,NHCH3arrow_forwardWhat ammonium salt is formed when each amine is treated with HCl? Draw the structure of the resulting salt.arrow_forwardWhat products are formed when each amide is hydrolyzed with water and HCl?arrow_forward
- Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. What functional group Erythronolide B does contain? a. b. H₂CH₂C C. H₂C 1 H₂C 2 3 4 O Amide d. Amine OH Erythronolide B Ketone Aldehyde a CH₂ b C d CH₂ OH JCH₂ 'OH OHarrow_forwardGive an acceptable name for each amide.arrow_forwardWhat are the products of the reaction between acetyl chloride and diethylamine? HCl and N,N-diethylacetamide Оа. o b. HCl and diethylamine chloride ос. HCl and N-ethylacetamide d. Diethylacetamide and acidarrow_forward
- What nitro compound, nitrile, and amide are reduced to each compound?arrow_forward9. Label the following reactions as: A. ionization of a carboxylic acid in water B. neutralization of a carboxylic acid with a base C. formation of an ester D. acid-catalyzed hydrolysis of an ester E. ionization of an amine in water F. neutralization of an amine with an acid G. formation of an amide H. hydrolysis of an amide CH3NH₂ + HCI CH3NH3 Cl CH3CH₂CNHCH 3 HOH CH₂COH CH3COH+ NaOH →→→→ CHICOH heat CHICOH CH3COH + CH3NH₂ CH₂COH CH3CH₂COCH₂CH₂CH + HOHH CH3CH₂COH + HOCH₂CH₂CH3 CHO + H₂O - CH3CO heat CHO CH₂CO *Na + HOH CH3NH₂ + H₂0 CH3NH3* + OH- + H3O+ CH3CH₂C + NH2CH3 R-H R-O-H CH3CNHCH3 + HOH R-N- I O CH₂COH CH3COH + HOCH3 CH3COCH3 + HOH сно сосни, O || R-C-R O 11 R-C-O-R Hydrocarbons Alcohols Amines Ketones Esters R-X R-O-R 0=0|0=0|0=0 R-C-H R-C-0-H R-C-N- I Alkyl halides Ethers Aldehydes Carboxylic Acids Amidesarrow_forwardList the products of each amine reaction. H b. CH;-N-CH-CH, + HCN CH3arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning