
(a)
Interpretation:
Chemical equation for the conversion of given
Concept Introduction:
The name of the carboxylic acid itself implies that it is acidic. Addition of carboxylic acid to water results in ionization. Hydrogen ion transfer occurs from carboxylic acid to water and hydronium ion is formed. Carboxylate ion is also formed due to the loss of hydrogen ion from carboxylic acid.
Carboxylate ion is the negative ion which is formed when one or more acidic protons are lost from carboxylic acid. Similar to carboxylic acid it reacts with strong base to form carboxylic acid salt and water.
Carboxylic acid salts when treated with a strong acid produces carboxylic acid as the product.
Carboxylic acid forms carboxylic acid salt by reacting with a strong base. The general reaction scheme for the formation of carboxylic acid salt is given as shown below,
The reverse of the above reaction is conversion of carboxylic acid salt to carboxylic acid. This is accomplished by using strong acid. The scheme is shown below,
From the above chemical equation it is found that the carboxylic acid salt reacts with strong acid to form carboxylic acid.
(a)

Explanation of Solution
Given carboxylic acid salt is calcium propanoate. The structure of calcium propanoate can be given as shown below,
Carboxylic acid sat is converted to carboxylic acid by reaction with strong acid. In the problem statement it is given that the strong acid is
Chemical equation for the conversion of given carboxylic acid salt to carboxylic acid using hydrochloric acid is written.
(b)
Interpretation:
Chemical equation for the conversion of given carboxylic acid salt to its parent carboxylic acid using
Concept Introduction:
The name of the carboxylic acid itself implies that it is acidic. Addition of carboxylic acid to water results in ionization. Hydrogen ion transfer occurs from carboxylic acid to water and hydronium ion is formed. Carboxylate ion is also formed due to the loss of hydrogen ion from carboxylic acid.
Carboxylate ion is the negative ion which is formed when one or more acidic protons are lost from carboxylic acid. Similar to carboxylic acid it reacts with strong base to form carboxylic acid salt and water.
Carboxylic acid salts when treated with a strong acid produces carboxylic acid as the product.
Carboxylic acid forms carboxylic acid salt by reacting with a strong base. The general reaction scheme for the formation of carboxylic acid salt is given as shown below,
The reverse of the above reaction is conversion of carboxylic acid salt to carboxylic acid. This is accomplished by using strong acid. The scheme is shown below,
From the above chemical equation it is found that the carboxylic acid salt reacts with strong acid to form carboxylic acid.
(b)

Explanation of Solution
Given carboxylic acid salt is sodium lactate. The structure of sodium lactate can be given as shown below,
Carboxylic acid sat is converted to carboxylic acid by reaction with strong acid. In the problem statement it is given that the strong acid is
Chemical equation for the conversion of given carboxylic acid salt to carboxylic acid using hydrochloric acid is written.
(c)
Interpretation:
Chemical equation for the conversion of given carboxylic acid salt to its parent carboxylic acid using
Concept Introduction:
The name of the carboxylic acid itself implies that it is acidic. Addition of carboxylic acid to water results in ionization. Hydrogen ion transfer occurs from carboxylic acid to water and hydronium ion is formed. Carboxylate ion is also formed due to the loss of hydrogen ion from carboxylic acid.
Carboxylate ion is the negative ion which is formed when one or more acidic protons are lost from carboxylic acid. Similar to carboxylic acid it reacts with strong base to form carboxylic acid salt and water.
Carboxylic acid salts when treated with a strong acid produces carboxylic acid as the product.
Carboxylic acid forms carboxylic acid salt by reacting with a strong base. The general reaction scheme for the formation of carboxylic acid salt is given as shown below,
The reverse of the above reaction is conversion of carboxylic acid salt to carboxylic acid. This is accomplished by using strong acid. The scheme is shown below,
From the above chemical equation it is found that the carboxylic acid salt reacts with strong acid to form carboxylic acid.
(c)

Explanation of Solution
Given carboxylic acid salt is magnesium succinate. The structure of magnesium succinate can be given as shown below,
Carboxylic acid sat is converted to carboxylic acid by reaction with strong acid. In the problem statement it is given that the strong acid is
Chemical equation for the conversion of given carboxylic acid salt to carboxylic acid using hydrochloric acid is written.
(d)
Interpretation:
Chemical equation for the conversion of given carboxylic acid salt to its parent carboxylic acid using
Concept Introduction:
The name of the carboxylic acid itself implies that it is acidic. Addition of carboxylic acid to water results in ionization. Hydrogen ion transfer occurs from carboxylic acid to water and hydronium ion is formed. Carboxylate ion is also formed due to the loss of hydrogen ion from carboxylic acid.
Carboxylate ion is the negative ion which is formed when one or more acidic protons are lost from carboxylic acid. Similar to carboxylic acid it reacts with strong base to form carboxylic acid salt and water.
Carboxylic acid salts when treated with a strong acid produces carboxylic acid as the product.
Carboxylic acid forms carboxylic acid salt by reacting with a strong base. The general reaction scheme for the formation of carboxylic acid salt is given as shown below,
The reverse of the above reaction is conversion of carboxylic acid salt to carboxylic acid. This is accomplished by using strong acid. The scheme is shown below,
From the above chemical equation it is found that the carboxylic acid salt reacts with strong acid to form carboxylic acid.
(d)

Explanation of Solution
Given carboxylic acid salt is potassium benzoate. The structure of potassium benzoate can be given as shown below,
Carboxylic acid sat is converted to carboxylic acid by reaction with strong acid. In the problem statement it is given that the strong acid is
Chemical equation for the conversion of given carboxylic acid salt to carboxylic acid using hydrochloric acid is written.
Want to see more full solutions like this?
Chapter 16 Solutions
General, Organic, And Biological Chemistry, Hybrid (with Owlv2 Quick Prep For General Chemistry Printed Access Card)
- 18. Arrange the following carbocations in order of decreasing stability. 1 2 A 3124 B 4213 C 2431 D 1234 E 2134 SPL 3 4arrow_forwardAcetic acid is added to DI water at an initial concentration of 10 -6 M (Ka=1.8x10-5) A. Using the "ICE" Method, what would the pH be at equilibrium? State assumptions and show your work. B. Using the simultaneous equations method, what would the pH be at equilibrium? Show your workarrow_forward1. Show that the change in entropy for a fixed amount of ideal gas held at a constant temperature undergoing a volume change is given by the simple equation AS = NkB In Hint: Start with the equation M dS = du + (Œ) dv - Ž (#) an, dU du+av-dN; j=1 Why doesn't the equation for the entropy of an ideal gas depend on the strength of the intermolecular forces for the gas?arrow_forward
- 2. Make an ice cube at 1 bar pressure by freezing an amount of liquid water that is 2 cm x 2 cm x 2 cm in volume. The density of liquid water at 0 °C is 1.000 g cm³ and the density of ice at 0 °C is 0.915 g cm³. Note that this difference in density is the reason your water pipes burst if they freeze and why you shouldn't forget to take your bottle of pop out of the freezer if you put it in there to try and cool it down faster. A. What is the work of expansion upon freezing? B. Is work done on the system or by the system?arrow_forwardI have a excitation/emission spectra of a quinine standard solution here, and I'm having trouble interpreting it. the red line is emission the blue line is excitation. i'm having trouble interpreting properly. just want to know if there is any evidence of raman or rayleigh peaks in the spectra.arrow_forwardGive the major product of the following reaction. excess 1. OH, H₂O 1.OH H CH3CH2CH21 H 2. A.-H₂O Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.arrow_forward
- 2. Use Hess's law to calculate the AH (in kJ) for: rxn CIF(g) + F2(g) → CIF 3 (1) using the following information: 2CIF(g) + O2(g) → Cl₂O(g) + OF 2(g) AH = 167.5 kJ ΔΗ 2F2 (g) + O2(g) → 2 OF 2(g) 2C1F3 (1) + 202(g) → Cl₂O(g) + 3 OF 2(g) о = = -43.5 kJ AH = 394.1kJarrow_forwardci Draw the major product(s) of the following reactions: (3 pts) CH3 HNO3/H2SO4 HNO3/ H2SO4 OCH3 (1 pts)arrow_forwardProvide the product for the reactionarrow_forward
- What is the net ionic equation for the reaction between tin(IV) sulfide and nitric acid?arrow_forwardThe combustion of 28.8 g of NH3 consumes exactly _____ g of O2. 4 NH3 + 7 O2 ----> 4 NO2 + 6 H2Oarrow_forwardWhat is the molecular formula of the bond-line structure shown below OH HO ○ C14H12O2 ○ C16H14O2 ○ C16H12O2 O C14H14O2arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning




