
Concept explainers
(a)
Interpretation:
IUPAC name for the given compound has to be assigned.
Concept Introduction:
For naming an acid anhydride, it can be structurally viewed in a way that contains two carbonyl groups that is joined by a single oxygen atom. This can also be said as two acyl group joined by a single oxygen atom.
Rules to obtain IUPAC name and common name for an acid anhydride:
- IUPAC name and common name for Symmetric anhydride is obtained by replacing the acid present in the name of parent
carboxylic acid with the word anhydride. - IUPAC name and common name for mixed anhydride is obtained by using the names of the parent carboxylic acids arranged in alphabetical order that is followed by the word anhydride.
(b)
Interpretation:
IUPAC name for the given compound has to be assigned.
Concept Introduction:
For naming an acid chloride, it can be structurally viewed in a way that contains one acyl group with a chlorine atom bonded to the carbonyl group
Rules to obtain IUPAC name and common name for an acid chloride:
- IUPAC name for acid chloride can be obtained from the parent carboxylic acid name. In the parent carboxylic acid name, the ending “-oic acid” is replaced by “-oyl chloride”.
- Common name for acid chloride can be obtained from the parent carboxylic acid name. In the parent carboxylic acid name, the ending “-ic acid” is replaced by “-yl chloride”.
(c)
Interpretation:
IUPAC name for the given compound has to be assigned.
Concept Introduction:
For naming an acid chloride, it can be structurally viewed in a way that contains one acyl group with a chlorine atom bonded to the carbonyl group
Rules to obtain IUPAC name and common name for an acid chloride:
- IUPAC name for acid chloride can be obtained from the parent carboxylic acid name. In the parent carboxylic acid name, the ending “-oic acid” is replaced by “-oyl chloride”.
- Common name for acid chloride can be obtained from the parent carboxylic acid name. In the parent carboxylic acid name, the ending “-ic acid” is replaced by “-yl chloride”.
(d)
Interpretation:
IUPAC name for the given compound has to be assigned.
Concept Introduction:
For naming an acid anhydride, it can be structurally viewed in a way that contains two carbonyl groups that is joined by a single oxygen atom. This can also be said as two acyl group joined by a single oxygen atom.
Rules to obtain IUPAC name and common name for an acid anhydride:
- IUPAC name and common name for Symmetric anhydride is obtained by replacing the acid present in the name of parent carboxylic acid with the word anhydride.
- IUPAC name and common name for mixed anhydride is obtained by using the names of the parent carboxylic acids arranged in alphabetical order that is followed by the word anhydride.

Want to see the full answer?
Check out a sample textbook solution
Chapter 16 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- Beer’s Law is A = εbc, where A is absorbance, ε is the molar absorptivity (which is specific to the compound and wavelength in the measurement), and c is concentration. The absorbance of a 2.31 × 10-5 M solution of a compound is 0.822 at a wavelength of 266 nm in a 1.00-cm cell. Calculate the molar absorptivity at 266 nm.arrow_forwardHow to calculate % of unknown solution using line of best fit y=0.1227x + 0.0292 (y=2.244)arrow_forwardGiven a 1,3-dicarbonyl compound, state the (condensed) formula of the compound obtaineda) if I add hydroxylamine (NH2OH) to give an isooxazole.b) if I add thiosemicarbazide (NH2-CO-NH-NH2) to give an isothiazole.arrow_forward
- Complete the following acid-base reactions and predict the direction of equilibrium for each. Justify your prediction by citing pK values for the acid and conjugate acid in each equilibrium. (a) (b) NHs (c) O₂N NH NH OH H₁PO₁arrow_forward23.34 Show how to convert each starting material into isobutylamine in good yield. ཅ ནད ཀྱི (b) Br OEt (c) (d) (e) (f) Harrow_forwardPlease help me Please use https://app.molview.com/ to draw this. I tried, but I couldn't figure out how to do it.arrow_forward
- Propose a synthesis of 1-butanamine from the following: (a) a chloroalkane of three carbons (b) a chloroalkane of four carbonsarrow_forwardSelect the stronger base from each pair of compounds. (a) H₂CNH₂ or EtzN (b) CI or NH2 NH2 (c) .Q or EtzN (d) or (e) N or (f) H or Harrow_forward4. Provide a clear arrow-pushing mechanism for each of the following reactions. Do not skip proton transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted without ambiguity. a. 2. 1. LDA 3. H3O+ HOarrow_forward
- b. H3C CH3 H3O+ ✓ H OHarrow_forward2. Provide reagents/conditions to accomplish the following syntheses. More than one step is required in some cases. a. CH3arrow_forwardIdentify and provide an explanation that distinguishes a qualitative and quantitative chemical analysis. Provide examples.arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning


