
To find:
a) The combination of an acid and an
b) The combination of an acid and an amine pair, which produces a ring closest to the amine end of the tube.
c) Which two of the six possible combinations produce rings in the same position, assuming the measurements can be made to the nearest centimeter?

Answer to Problem 10.129QA
Solution:
a) Acetic acid (
b) Hydrochloric acid (
c) No two of the six possible combinations produce the rings in the same position.
Explanation of Solution
1) Concept:
We are given two acids and three amines. We calculate molar mass of each acid and amine. Then using Graham’s law of effusion, we can calculate the ratio of the rate of effusion between any two of the six possible combinations. If the rates of effusion calculated for a combination are the same, then they will travel equal distance from two ends and will meet at the center of the tube.
2) Formula:
where
3) Given:
The molar mass of each molecule is calculated using the periodic table given in book.
Molecule | Molar mass |
4) Calculations:
a) The combination of an acid and an amine which gives a white ring halfway between the two ends:
The combination of an acid and an amine gives a white ring halfway between the two ends. This indicates that both the acid and the amine travel equal distance in the same time. Therefore, the rate of effusion of the acid and rate of effusion of the amine is the same.
Squaring both sides of the rightmost equality yields
This indicates that the molar mass of the acid and the amine should be the same or very close. From the given list of acids and amines, the molar mass of acetic acid (
b) The combination of an acid and an amine that will produce a ring closest to the amine end of the tube:
The result shows a ring closest to the amine end of the tube. This indicates that the amine travels a smaller distance while the acid travels a larger distance in the tube. Therefore, the rate of effusion of the acid is more than the rate of effusion of the amine. This also means that the molar mass of the amine should be greater than that of the acid. From this, we can write the equation
Squaring both sides of the rightmost equality yields
This shows that molar mass of the amine should be larger than the molar mass of the acid. From the given list of acid and amines, we select an acid and an amine such that the molar mass of the amine is greater than that of the acid. Therefore, hydrochloric acid (
c) Calculations for the two of the six possible combinations that produce rings in the same position is as follows:
The six possible combinations and their effusion rates are listed as
Combination | Molar mass (g/mol) | Ratio |
No two values in the ratio for
Conclusion:
Using Graham’s law of effusion, the rate of effusion can be calculated. The higher the molar mass, the slower will be the effusion rates and vice versa.
Want to see more full solutions like this?
Chapter 10 Solutions
Chemistry: An Atoms-Focused Approach (Second Edition)
- Would the following organic synthesis occur in one step? Add any missing products, required catalysts, inorganic reagents, and other important conditions. Please include a detailed explanation and drawings showing how the reaction may occur in one step.arrow_forward(a) Sketch the 'H NMR of the following chemical including the approximate chemical shifts, the multiplicity (splitting) of all signals and the integration (b) How many signals would you expect in the 13C NMR? CH3arrow_forwardDraw the Show the major and minor product(s) for the following reaction mechanisms for both reactions and show all resonance structures for any Explain why the major product is favoured? intermediates H-Brarrow_forward
- 3. Draw ALL THE POSSBILE PRODUCTS AND THE MECHANISMS WITH ALL RESONANCE STRUCTURES. Explain using the resonance structures why the major product(s) are formed over the minor product(s). H₂SO4, HONO CHarrow_forward7. Provide the product(s), starting material(s) and/or condition(s) required for the No mechanisms required. below reaction HO + H-I CI FO Br2, FeBr3 O I-Oarrow_forward6. Design the most efficient synthesis of the following product starting from phenot Provide the reaction conditions for each step (more than one step is required) and explain the selectivity of each reaction. NO MECHANISMS ARE REQUIRED. OH step(s) CIarrow_forward
- What is the skeletal structure of the product of the following organic reaction?arrow_forwardIf a reaction occurs, what would be the major products? Please include a detailed explanation as well as a drawing showing how the reaction occurs and what the final product is.arrow_forwardWhat is the major organic product of the following nucleophilic acyl substitution reaction of an acid chloride below?arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





