Chemistry: The Molecular Science
5th Edition
ISBN: 9781285199047
Author: John W. Moore, Conrad L. Stanitski
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 8, Problem 7QRT
Interpretation Introduction
Interpretation:
Boyle’s law should be explained on the basis of kinetic-molecular theory.
Concept Introduction:
Kinetic-molecular theory of gases:
Properties of gases are different from solids and liquids. When pressure is applied to gases, they are easily compressed to smaller volume and they have low densities. These properties can be explained by a theory called kinetic-molecular theory.
The four assumptions of this theory are given below:
- Gases are made up of particles like atoms or molecules which randomly move and there will be no attractive forces between them.
- Comparing the space occupied by the gas particles and the space between particles, the former is much smaller than the latter.
- The average kinetic energy of gas particles and the Kelvin temperature is proportional.
- There is an elastic collision between gas particles or with the wall of their container and thus no energy is lost during collision and total kinetic energy of the particles is constant.
Boyle’s law:
At fixed temperature and number of molecules, the volume of a fixed amount of gas is inversely proportional to the pressure exerted by the gas.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
None
What is the mechanism by which the 1,4 product is created? Please draw it by hand with arrows and stuff.
What is the relationship between A and B?
H3C
A
Br
Cl
H3C
B
Br
relationship
(check all that apply)
O same molecule
O enantiomer
O diastereomer
structural isomer
O stereoisomer
isomer
O need more information to decide
O same molecule
☐ enantiomer
Br
Br
Br
CH3
Br
CI
CH3
O diastereomer
☐ structural isomer
☐ stereoisomer
isomer
O need more information to decide
O same molecule
O enantiomer
Odiastereomer
structural isomer
O stereoisomer
☐ isomer
O need more information to decide
Chapter 8 Solutions
Chemistry: The Molecular Science
Ch. 8.1 - Prob. 8.1PSPCh. 8.1 - Prob. 8.1ECh. 8.1 - Prob. 8.2ECh. 8.2 - Prob. 8.3CECh. 8.2 - Prob. 8.4CECh. 8.3 - Prob. 8.6CECh. 8.3 - Prob. 8.2PSPCh. 8.3 - Prob. 8.3PSPCh. 8.3 - Prob. 8.4PSPCh. 8.3 - Prob. 8.7CE
Ch. 8.4 - Prob. 8.5PSPCh. 8.4 - Prob. 8.8CECh. 8.4 - Prob. 8.9CECh. 8.4 - Prob. 8.6PSPCh. 8.4 - Prob. 8.10CECh. 8.5 - Prob. 8.7PSPCh. 8.5 - Prob. 8.8PSPCh. 8.5 - Prob. 8.11ECh. 8.6 - Prob. 8.9PSPCh. 8.6 - Prob. 8.12CECh. 8.6 - Prob. 8.13ECh. 8.6 - Prob. 8.10PSPCh. 8.6 - Prob. 8.11PSPCh. 8.7 - Prob. 8.12PSPCh. 8.7 - Prob. 8.14ECh. 8.7 - Prob. 8.16CECh. 8.7 - Prob. 8.17ECh. 8.8 - Prob. 8.13PSPCh. 8.8 - Prob. 8.18ECh. 8.8 - Look up the van der Waals constants, b, for H2,...Ch. 8.11 - List as many natural sources of CO2 as you can,...Ch. 8.11 - Prob. 8.21ECh. 8.11 - Prob. 8.22CECh. 8.11 - Prob. 8.23CECh. 8.11 - Prob. 8.24CECh. 8.12 - Make these conversions for atmospheric...Ch. 8.12 - Prob. 8.25ECh. 8 - In a typical automobile engine, a gasoline...Ch. 8 - Prob. 1QRTCh. 8 - Prob. 2QRTCh. 8 - Prob. 3QRTCh. 8 - Prob. 4QRTCh. 8 - Prob. 5QRTCh. 8 - Prob. 6QRTCh. 8 - Prob. 7QRTCh. 8 - Prob. 8QRTCh. 8 - Prob. 9QRTCh. 8 - Prob. 10QRTCh. 8 - Prob. 11QRTCh. 8 - Prob. 12QRTCh. 8 - Prob. 13QRTCh. 8 - Prob. 14QRTCh. 8 - Prob. 15QRTCh. 8 - Prob. 16QRTCh. 8 - Prob. 17QRTCh. 8 - Prob. 18QRTCh. 8 - Some butane, the fuel used in backyard grills, is...Ch. 8 - Prob. 20QRTCh. 8 - Suppose you have a sample of CO2 in a gas-tight...Ch. 8 - Prob. 22QRTCh. 8 - Prob. 23QRTCh. 8 - Prob. 24QRTCh. 8 - A sample of gas occupies 754 mL at 22 C and a...Ch. 8 - Prob. 26QRTCh. 8 - Prob. 27QRTCh. 8 - Prob. 28QRTCh. 8 - Prob. 29QRTCh. 8 - Prob. 30QRTCh. 8 - Prob. 31QRTCh. 8 - Prob. 32QRTCh. 8 - Calculate the molar mass of a gas that has a...Ch. 8 - Prob. 34QRTCh. 8 - Prob. 35QRTCh. 8 - Prob. 36QRTCh. 8 - Prob. 37QRTCh. 8 - Prob. 38QRTCh. 8 - Prob. 39QRTCh. 8 - Prob. 40QRTCh. 8 - Prob. 41QRTCh. 8 - Prob. 42QRTCh. 8 - Prob. 43QRTCh. 8 - Prob. 44QRTCh. 8 - Prob. 45QRTCh. 8 - Prob. 46QRTCh. 8 - Prob. 47QRTCh. 8 - Prob. 48QRTCh. 8 - The build-up of excess carbon dioxide in the air...Ch. 8 - Prob. 50QRTCh. 8 - Prob. 51QRTCh. 8 - Prob. 52QRTCh. 8 - Prob. 53QRTCh. 8 - Prob. 54QRTCh. 8 - Prob. 55QRTCh. 8 - Benzene has acute health effects. For example, it...Ch. 8 - The mean fraction by mass of water vapor and cloud...Ch. 8 - Acetylene can be made by reacting calcium carbide...Ch. 8 - Prob. 59QRTCh. 8 - You are given two flasks of equal volume. Flask A...Ch. 8 - Prob. 61QRTCh. 8 - Prob. 62QRTCh. 8 - Prob. 63QRTCh. 8 - Prob. 64QRTCh. 8 - Prob. 65QRTCh. 8 - Prob. 66QRTCh. 8 - Prob. 67QRTCh. 8 - Prob. 68QRTCh. 8 - Prob. 69QRTCh. 8 - Prob. 70QRTCh. 8 - Prob. 71QRTCh. 8 - Prob. 72QRTCh. 8 - Prob. 73QRTCh. 8 - Prob. 74QRTCh. 8 - Prob. 75QRTCh. 8 - Prob. 76QRTCh. 8 - Prob. 77QRTCh. 8 - Prob. 78QRTCh. 8 - Prob. 79QRTCh. 8 - Prob. 80QRTCh. 8 - Prob. 81QRTCh. 8 - Prob. 82QRTCh. 8 - Prob. 83QRTCh. 8 - Prob. 84QRTCh. 8 - Prob. 85QRTCh. 8 - Name a favorable effect of the global increase of...Ch. 8 - Prob. 87QRTCh. 8 - Assume that limestone, CaCO3, is used to remove...Ch. 8 - Prob. 89QRTCh. 8 - Prob. 90QRTCh. 8 - Prob. 91QRTCh. 8 - Prob. 92QRTCh. 8 - Prob. 93QRTCh. 8 - Prob. 94QRTCh. 8 - Prob. 95QRTCh. 8 - Prob. 96QRTCh. 8 - Prob. 97QRTCh. 8 - Prob. 98QRTCh. 8 - Prob. 99QRTCh. 8 - Prob. 100QRTCh. 8 - Prob. 101QRTCh. 8 - Prob. 102QRTCh. 8 - Prob. 103QRTCh. 8 - Prob. 104QRTCh. 8 - Prob. 105QRTCh. 8 - Prob. 106QRTCh. 8 - Prob. 107QRTCh. 8 - Prob. 108QRTCh. 8 - Prob. 109QRTCh. 8 - Consider these four gas samples, all at the same...Ch. 8 - Prob. 111QRTCh. 8 - Prob. 112QRTCh. 8 - Prob. 113QRTCh. 8 - Prob. 114QRTCh. 8 - Prob. 115QRTCh. 8 - Prob. 116QRTCh. 8 - Prob. 117QRTCh. 8 - Prob. 118QRTCh. 8 - Prob. 119QRTCh. 8 - Prob. 120QRTCh. 8 - Prob. 121QRTCh. 8 - Prob. 122QRTCh. 8 - Prob. 123QRTCh. 8 - Prob. 124QRTCh. 8 - Prob. 125QRTCh. 8 - Prob. 126QRTCh. 8 - Prob. 127QRTCh. 8 - Prob. 128QRTCh. 8 - Prob. 129QRTCh. 8 - Prob. 8.ACPCh. 8 - Prob. 8.BCP
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- b. Please complete the zig-zag conformation of the compound (3R,4S)-3,4-dichloro-2,5-dimethylhexane by writing the respective atoms in the boxes. 4arrow_forwardc. Serricornin, the female-produced sex pheromone of the cigarette beetle, has the following structure. OH What is the maximum number of possible stereoisomers? Is this structure a meso compound? d. Please consider the natural product alkaloids shown below. Are these two structures enantiomers, diastereomers or conformers? H HO H H HN HO HN R R с R=H cinchonidine R=ET cinchonine Harrow_forwardNail polish remover containing acetone was spilled in a room 5.23 m × 3.28 m × 2.76 m. Measurements indicated that 2,250 mg of acetone evaporated. Calculate the acetone concentration in micrograms per cubic meter.arrow_forward
- Please help me answer number 1. 1. If your graphs revealed a mathematical relationship between specific heat and atomic mass, write down an equation for the relationship. I also don't understand, is the equation from the line regression the one that I'm suppose use to show the relationship? If so could you work it all the way out?arrow_forwardDescribe the principle of resonance and give a set of Lewis Structures to illustrate your explanation.arrow_forwardDon't used hand raitingarrow_forward
- It is not unexpected that the methoxyl substituent on a cyclohexane ring prefers to adopt the equatorial conformation. OMe H A G₂ = +0.6 kcal/mol OMe What is unexpected is that the closely related 2-methoxytetrahydropyran prefers the axial conformation: H H OMe OMe A Gp=-0.6 kcal/mol Methoxy: CH3O group Please be specific and clearly write the reason why this is observed. This effect that provides stabilization of the axial OCH 3 group in this molecule is called the anomeric effect. [Recall in the way of example, the staggered conformer of ethane is more stable than eclipsed owing to bonding MO interacting with anti-bonding MO...]arrow_forward206 Pb 82 Express your answers as integers. Enter your answers separated by a comma. ▸ View Available Hint(s) VAΣ ΜΕ ΑΣΦ Np, N₁ = 82,126 Submit Previous Answers ? protons, neutronsarrow_forwardPlease draw the inverted chair forms of the products for the two equilibrium reactions shown below. Circle the equilibrium reaction that would have a AG = 0, i.e., the relative energy of the reactant (to the left of the equilibrium arrows) equals the relative energy of the product? [No requirement to show or do calculations.] CH3 CH3 HH CH3 1 -CH3arrow_forward
- 5. Please consider the Newman projection of tartaric acid drawn below as an eclipsed conformer (1). Please draw the most stable conformer and two intermediate energy conformers noting that staggered conformers are lower in energy than eclipsed forms even if the staggered conformers have gauche relationships between groups. [Draw the substituents H and OH on the front carbons and H, OH and CO₂H on the back carbons based on staggered forms. -CO₂H is larger than -OH.] OH COH ICOOH COOH COOH 1 2 COOH COOH 3 4 Staggered Staggered Staggered (most stable) Indicate the number of each conformer above (1, 2, 3 and 4) that corresponds to the relative energies below. Ref=0 Rotation 6. (60 points) a. Are compounds 1 and 2 below enantiomers, diastereomers or identical? OH OH HO HO LOH HO HO OH 2 OH OH b. Please complete the zig-zag conformation of the compound (3R,4S)-3,4-dichloro-2,5-dimethylhexane by writing the respective atoms in the boxes. 3.arrow_forwardThe plutonium isotope with 144 neutrons Enter the chemical symbol of the isotope.arrow_forwardThe mass ratio of sodium to fluorine in sodium fluoride is 1.21:1. A sample of sodium fluoride produced 26.1 gg of sodium upon decomposition. How much fluorine was formed?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningLiving By Chemistry: First Edition TextbookChemistryISBN:9781559539418Author:Angelica StacyPublisher:MAC HIGHERChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Living By Chemistry: First Edition Textbook
Chemistry
ISBN:9781559539418
Author:Angelica Stacy
Publisher:MAC HIGHER
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning