Concept explainers
(a)
Interpretation:
The molarity of
Concept introduction:
Henry’s law gives the quantitative relationship between the pressure of the gas and its solubility. It states that the amount of gas dissolved in a liquid is proportional to the partial pressure of the gas. Higher the partial pressure of the gas, more will be its solubility and vice-versa.
The formula to calculate the solubility of gases according to Henry’s law is as follows:
Here,
Molarity is defined as the number of moles of solute that are dissolved in one litre of solution. It is represented by
(a)
Answer to Problem 13.162P
The molarity of
Explanation of Solution
The pressure of the nitrogen gas is calculated as follows:
Substitute
The solubility is equal to the molarity so the molarity of nitrogen gas in the blood is
The molarity of
(b)
Interpretation:
The molarity of
Concept introduction:
The formula to calculate the solubility of gases according to Henry’s law is as follows:
The formula to calculate the pressure at any height is as follows:
Here
The conversion factor to convert
The conversion factor to convert inches to
The conversion factor to convert
(b)
Answer to Problem 13.162P
The molarity of
Explanation of Solution
Substitute
The total pressure is calculated as follows:
Substitute
The pressure of the nitrogen gas is calculated as follows:
Substitute
The solubility is equal to the molarity so the molarity of nitrogen is
The molarity of
(c)
Interpretation:
The volume of
Concept introduction:
The formula of an ideal gas equation is as follows:
Here,
(c)
Answer to Problem 13.162P
The volume of
Explanation of Solution
Rearrange equation (4) to calculate the volume of gas as follows:
The formula to calculate the number of moles is as follows:
Substitute
Substitute
The volume of
Want to see more full solutions like this?
Chapter 13 Solutions
Student Solutions Manual For Silberberg Chemistry: The Molecular Nature Of Matter And Change With Advanced Topics
- Shown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. C H H C H :Ö: Click and drag to start drawing a structure.arrow_forwardShown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. C H H C. H H H H Click and drag to start drawing a structure. Xarrow_forwardA new brand of lotion is causing skin rush unlike the old brand of the same lotion. With the aid of well labelled diagram describe an experiment that could be done to isolate the pigment that cause the skin rusharrow_forward
- Don't used hand raitingarrow_forwardDon't used hand raitingarrow_forwardRelative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 100 HS-NJ-0547 80 60 31 20 S1 84 M+ absent 10 30 40 50 60 70 80 90 100 100- MS2016-05353CM 80- 60 40 20 135 137 S2 164 166 0-m 25 50 75 100 125 150 m/z 60 100 MS-NJ-09-43 40 20 20 80 45 S3 25 50 75 100 125 150 175 m/zarrow_forward
- Don't used hand raiting and don't used Ai solutionarrow_forwardPredicting the pro Predict the major products of this organic reaction. Explanation Check m ☐ + 5 1.03 Click and drag t drawing a stru 2. (CH₂)₂S 3 2 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardstarting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... X Explanation Check C टे Br T Add/Remove step ☐ Br Br © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacarrow_forward
- Don't used hand raitingarrow_forwardRelative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 100 HS-NJ-0547 80 60 31 20 S1 84 M+ absent 10 30 40 50 60 70 80 90 100 100- MS2016-05353CM 80- 60 40 20 135 137 S2 164 166 0-m 25 50 75 100 125 150 m/z 60 100 MS-NJ-09-43 40 20 20 80 45 S3 25 50 75 100 125 150 175 m/zarrow_forwardPart II. Given two isomers: 2-methylpentane (A) and 2,2-dimethyl butane (B) answer the following: (a) match structures of isomers given their mass spectra below (spectra A and spectra B) (b) Draw the fragments given the following prominent peaks from each spectrum: Spectra A m/2 =43 and 1/2-57 spectra B m/2 = 43 (c) why is 1/2=57 peak in spectrum A more intense compared to the same peak in spectrum B. Relative abundance Relative abundance 100 A 50 29 29 0 10 -0 -0 100 B 50 720 30 41 43 57 71 4-0 40 50 60 70 m/z 43 57 8-0 m/z = 86 M 90 100 71 m/z = 86 M -O 0 10 20 30 40 50 60 70 80 -88 m/z 90 100arrow_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