ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
7th Edition
ISBN: 9781319399849
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 3, Problem 3D.1E
Interpretation Introduction
Interpretation:
Whether all molecules of gas strike walls of their container with same force or not has to be explained.
Concept Introduction:
Kinetic model of gas explains effusion behavior of gases and accounts for
(1) Gas has bunch of molecules in endless random motion.
(2) The gas molecules are considered as extremely small points.
(3) Molecules continuously move in single directions until they collide.
(4) Molecules don’t interact with one another until they collide.
(5) All collisions are considered as elastic.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
5) Oxaloacetic Acid is an important intermediate in the biosynthesis of citric acid. Synthesize oxaloacetic acid
using a mixed Claisen Condensation reaction with two different esters and a sodium ethoxide base. Give your
answer as a scheme
Hint 1: Your final acid product is producing using a decarboxylation reaction.
Hint 2: Look up the structure of oxalic acid.
HO
all
OH
oxaloacetic acid
20. The Brusselator. This hypothetical system was first proposed by a group work-
ing in Brussels [see Prigogine and Lefever (1968)] in connection with spatially
nonuniform chemical patterns. Because certain steps involve trimolecular reac
tions, it is not a model of any real chemical system but rather a prototype that
has been studied extensively. The reaction steps are
A-X.
B+X-Y+D.
2X+ Y-3X,
X-E.
305
It is assumed that concentrations of A, B, D, and E are kept artificially con
stant so that only X and Y vary with time.
(a) Show that if all rate constants are chosen appropriately, the equations de
scribing a Brusselator are:
dt
A-(B+ 1)x + x²y,
dy
=Bx-x²y.
di
Problem 3. Provide a mechanism for the following transformation:
H₂SO A
Me.
Me
Me
Me
Me
Chapter 3 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
Ch. 3 - Prob. 3A.1ASTCh. 3 - Prob. 3A.1BSTCh. 3 - Prob. 3A.2ASTCh. 3 - Prob. 3A.2BSTCh. 3 - Prob. 3A.3ASTCh. 3 - Prob. 3A.3BSTCh. 3 - Prob. 3A.1ECh. 3 - Prob. 3A.2ECh. 3 - Prob. 3A.3ECh. 3 - Prob. 3A.4E
Ch. 3 - Prob. 3A.5ECh. 3 - Prob. 3A.6ECh. 3 - Prob. 3A.7ECh. 3 - Prob. 3A.8ECh. 3 - Prob. 3A.9ECh. 3 - Prob. 3A.10ECh. 3 - Prob. 3B.1ASTCh. 3 - Prob. 3B.1BSTCh. 3 - Prob. 3B.2ASTCh. 3 - Prob. 3B.2BSTCh. 3 - Prob. 3B.3ASTCh. 3 - Prob. 3B.3BSTCh. 3 - Prob. 3B.4ASTCh. 3 - Prob. 3B.4BSTCh. 3 - Prob. 3B.5ASTCh. 3 - Prob. 3B.5BSTCh. 3 - Prob. 3B.6ASTCh. 3 - Prob. 3B.6BSTCh. 3 - Prob. 3B.7ASTCh. 3 - Prob. 3B.7BSTCh. 3 - Prob. 3B.8ASTCh. 3 - Prob. 3B.8BSTCh. 3 - Prob. 3B.1ECh. 3 - Prob. 3B.2ECh. 3 - Prob. 3B.5ECh. 3 - Prob. 3B.6ECh. 3 - Prob. 3B.9ECh. 3 - Prob. 3B.10ECh. 3 - Prob. 3B.11ECh. 3 - Prob. 3B.12ECh. 3 - Prob. 3B.13ECh. 3 - Prob. 3B.14ECh. 3 - Prob. 3B.15ECh. 3 - Prob. 3B.16ECh. 3 - Prob. 3B.17ECh. 3 - Prob. 3B.18ECh. 3 - Prob. 3B.19ECh. 3 - Prob. 3B.20ECh. 3 - Prob. 3B.21ECh. 3 - Prob. 3B.22ECh. 3 - Prob. 3B.23ECh. 3 - Prob. 3B.24ECh. 3 - Prob. 3B.25ECh. 3 - Prob. 3B.26ECh. 3 - Prob. 3B.27ECh. 3 - Prob. 3B.28ECh. 3 - Prob. 3B.29ECh. 3 - Prob. 3B.30ECh. 3 - Prob. 3B.31ECh. 3 - Prob. 3B.32ECh. 3 - Prob. 3B.33ECh. 3 - Prob. 3B.34ECh. 3 - Prob. 3B.35ECh. 3 - Prob. 3B.36ECh. 3 - Prob. 3B.37ECh. 3 - Prob. 3B.38ECh. 3 - Prob. 3B.39ECh. 3 - Prob. 3B.40ECh. 3 - Prob. 3B.41ECh. 3 - Prob. 3B.42ECh. 3 - Prob. 3C.1ASTCh. 3 - Prob. 3C.1BSTCh. 3 - Prob. 3C.2ASTCh. 3 - Prob. 3C.2BSTCh. 3 - Prob. 3C.3ASTCh. 3 - Prob. 3C.3BSTCh. 3 - Prob. 3C.1ECh. 3 - Prob. 3C.2ECh. 3 - Prob. 3C.3ECh. 3 - Prob. 3C.4ECh. 3 - Prob. 3C.5ECh. 3 - Prob. 3C.6ECh. 3 - Prob. 3C.7ECh. 3 - Prob. 3C.8ECh. 3 - Prob. 3C.9ECh. 3 - Prob. 3C.10ECh. 3 - Prob. 3C.11ECh. 3 - Prob. 3C.12ECh. 3 - Prob. 3C.13ECh. 3 - Prob. 3C.14ECh. 3 - Prob. 3C.15ECh. 3 - Prob. 3C.16ECh. 3 - Prob. 3D.1ASTCh. 3 - Prob. 3D.1BSTCh. 3 - Prob. 3D.2ASTCh. 3 - Prob. 3D.2BSTCh. 3 - Prob. 3D.1ECh. 3 - Prob. 3D.2ECh. 3 - Prob. 3D.3ECh. 3 - Prob. 3D.4ECh. 3 - Prob. 3D.5ECh. 3 - Prob. 3D.6ECh. 3 - Prob. 3D.7ECh. 3 - Prob. 3D.8ECh. 3 - Prob. 3D.9ECh. 3 - Prob. 3D.10ECh. 3 - Prob. 3D.11ECh. 3 - Prob. 3D.12ECh. 3 - Prob. 3D.13ECh. 3 - Prob. 3D.14ECh. 3 - Prob. 3D.15ECh. 3 - Prob. 3D.16ECh. 3 - Prob. 3D.17ECh. 3 - Prob. 3D.18ECh. 3 - Prob. 3E.1ASTCh. 3 - Prob. 3E.1BSTCh. 3 - Prob. 3E.1ECh. 3 - Prob. 3E.2ECh. 3 - Prob. 3E.3ECh. 3 - Prob. 3E.4ECh. 3 - Prob. 3E.5ECh. 3 - Prob. 3E.6ECh. 3 - Prob. 3E.7ECh. 3 - Prob. 3E.8ECh. 3 - Prob. 3E.9ECh. 3 - Prob. 3E.10ECh. 3 - Prob. 3E.13ECh. 3 - Prob. 3E.14ECh. 3 - Prob. 3F.1ASTCh. 3 - Prob. 3F.1BSTCh. 3 - Prob. 3F.2ASTCh. 3 - Prob. 3F.2BSTCh. 3 - Prob. 3F.3ASTCh. 3 - Prob. 3F.3BSTCh. 3 - Prob. 3F.1ECh. 3 - Prob. 3F.2ECh. 3 - Prob. 3F.3ECh. 3 - Prob. 3F.4ECh. 3 - Prob. 3F.5ECh. 3 - Prob. 3F.6ECh. 3 - Prob. 3F.7ECh. 3 - Prob. 3F.8ECh. 3 - Prob. 3F.9ECh. 3 - Prob. 3F.10ECh. 3 - Prob. 3F.11ECh. 3 - Prob. 3F.12ECh. 3 - Prob. 3F.13ECh. 3 - Prob. 3F.14ECh. 3 - Prob. 3F.15ECh. 3 - Prob. 3F.16ECh. 3 - Prob. 3F.17ECh. 3 - Prob. 3F.18ECh. 3 - Prob. 3F.19ECh. 3 - Prob. 3F.20ECh. 3 - Prob. 3F.21ECh. 3 - Prob. 3F.22ECh. 3 - Prob. 3G.1ECh. 3 - Prob. 3G.2ECh. 3 - Prob. 3G.3ECh. 3 - Prob. 3G.4ECh. 3 - Prob. 3G.5ECh. 3 - Prob. 3G.6ECh. 3 - Prob. 3G.7ECh. 3 - Prob. 3G.8ECh. 3 - Prob. 3G.9ECh. 3 - Prob. 3G.10ECh. 3 - Prob. 3G.11ECh. 3 - Prob. 3G.12ECh. 3 - Prob. 3G.13ECh. 3 - Prob. 3G.14ECh. 3 - Prob. 3G.15ECh. 3 - Prob. 3G.16ECh. 3 - Prob. 3G.17ECh. 3 - Prob. 3G.18ECh. 3 - Prob. 3H.1ASTCh. 3 - Prob. 3H.1BSTCh. 3 - Prob. 3H.2ASTCh. 3 - Prob. 3H.2BSTCh. 3 - Prob. 3H.3ASTCh. 3 - Prob. 3H.3BSTCh. 3 - Prob. 3H.4ASTCh. 3 - Prob. 3H.4BSTCh. 3 - Prob. 3H.5ASTCh. 3 - Prob. 3H.5BSTCh. 3 - Prob. 3H.1ECh. 3 - Prob. 3H.2ECh. 3 - Prob. 3H.3ECh. 3 - Prob. 3H.4ECh. 3 - Prob. 3H.5ECh. 3 - Prob. 3H.6ECh. 3 - Prob. 3H.7ECh. 3 - Prob. 3H.8ECh. 3 - Prob. 3H.9ECh. 3 - Prob. 3H.10ECh. 3 - Prob. 3H.11ECh. 3 - Prob. 3H.12ECh. 3 - Prob. 3H.13ECh. 3 - Prob. 3H.14ECh. 3 - Prob. 3H.15ECh. 3 - Prob. 3H.16ECh. 3 - Prob. 3H.17ECh. 3 - Prob. 3H.19ECh. 3 - Prob. 3H.20ECh. 3 - Prob. 3H.23ECh. 3 - Prob. 3H.24ECh. 3 - Prob. 3H.25ECh. 3 - Prob. 3H.26ECh. 3 - Prob. 3H.27ECh. 3 - Prob. 3H.28ECh. 3 - Prob. 3H.29ECh. 3 - Prob. 3H.30ECh. 3 - Prob. 3H.31ECh. 3 - Prob. 3H.32ECh. 3 - Prob. 3H.33ECh. 3 - Prob. 3H.34ECh. 3 - Prob. 3H.35ECh. 3 - Prob. 3H.36ECh. 3 - Prob. 3I.1ASTCh. 3 - Prob. 3I.1BSTCh. 3 - Prob. 3I.2ASTCh. 3 - Prob. 3I.2BSTCh. 3 - Prob. 3I.3ASTCh. 3 - Prob. 3I.3BSTCh. 3 - Prob. 3I.4ASTCh. 3 - Prob. 3I.4BSTCh. 3 - Prob. 3I.1ECh. 3 - Prob. 3I.2ECh. 3 - Prob. 3I.3ECh. 3 - Prob. 3I.4ECh. 3 - Prob. 3I.5ECh. 3 - Prob. 3I.6ECh. 3 - Prob. 3I.7ECh. 3 - Prob. 3I.8ECh. 3 - Prob. 3I.11ECh. 3 - Prob. 3I.12ECh. 3 - Prob. 3I.13ECh. 3 - Prob. 3I.14ECh. 3 - Prob. 3I.15ECh. 3 - Prob. 3I.16ECh. 3 - Prob. 3J.1ASTCh. 3 - Prob. 3J.1BSTCh. 3 - Prob. 3J.2ASTCh. 3 - Prob. 3J.2BSTCh. 3 - Prob. 3J.3ASTCh. 3 - Prob. 3J.3BSTCh. 3 - Prob. 3J.1ECh. 3 - Prob. 3J.2ECh. 3 - Prob. 3J.3ECh. 3 - Prob. 3J.4ECh. 3 - Prob. 3J.5ECh. 3 - Prob. 3J.6ECh. 3 - Prob. 3J.7ECh. 3 - Prob. 3J.8ECh. 3 - Prob. 3J.9ECh. 3 - Prob. 3J.10ECh. 3 - Prob. 3J.11ECh. 3 - Prob. 3J.12ECh. 3 - Prob. 3J.13ECh. 3 - Prob. 3J.14ECh. 3 - Prob. 3J.15ECh. 3 - Prob. 3J.16ECh. 3 - Prob. 3.1ECh. 3 - Prob. 3.2ECh. 3 - Prob. 3.3ECh. 3 - Prob. 3.4ECh. 3 - Prob. 3.5ECh. 3 - Prob. 3.6ECh. 3 - Prob. 3.7ECh. 3 - Prob. 3.8ECh. 3 - Prob. 3.9ECh. 3 - Prob. 3.10ECh. 3 - Prob. 3.11ECh. 3 - Prob. 3.12ECh. 3 - Prob. 3.13ECh. 3 - Prob. 3.15ECh. 3 - Prob. 3.18ECh. 3 - Prob. 3.19ECh. 3 - Prob. 3.23ECh. 3 - Prob. 3.24ECh. 3 - Prob. 3.25ECh. 3 - Prob. 3.26ECh. 3 - Prob. 3.27ECh. 3 - Prob. 3.29ECh. 3 - Prob. 3.31ECh. 3 - Prob. 3.32ECh. 3 - Prob. 3.35ECh. 3 - Prob. 3.36ECh. 3 - Prob. 3.37ECh. 3 - Prob. 3.38ECh. 3 - Prob. 3.40ECh. 3 - Prob. 3.41ECh. 3 - Prob. 3.42ECh. 3 - Prob. 3.45ECh. 3 - Prob. 3.47ECh. 3 - Prob. 3.49ECh. 3 - Prob. 3.50ECh. 3 - Prob. 3.51ECh. 3 - Prob. 3.53ECh. 3 - Prob. 3.54ECh. 3 - Prob. 3.55ECh. 3 - Prob. 3.56ECh. 3 - Prob. 3.57ECh. 3 - Prob. 3.58ECh. 3 - Prob. 3.59ECh. 3 - Prob. 3.60ECh. 3 - Prob. 3.61ECh. 3 - Prob. 3.62ECh. 3 - Prob. 3.63ECh. 3 - Prob. 3.64ECh. 3 - Prob. 3.65ECh. 3 - Prob. 3.66ECh. 3 - Prob. 3.67ECh. 3 - Prob. 3.68E
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
- You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: xi 1. ☑ 2. H₂O хе i Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. There is no reagent that will make this synthesis work without complications. : ☐ S ☐arrow_forwardPredict the major products of this organic reaction: H OH 1. LiAlH4 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. G C टेarrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new C-C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 CI MgCl ? Will the first product that forms in this reaction create a new CC bond? Yes No MgBr ? Will the first product that forms in this reaction create a new CC bond? Yes No G टेarrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. དྲ。 ✗MgBr ? O CI Will the first product that forms in this reaction create a new C-C bond? Yes No • ? Will the first product that forms in this reaction create a new CC bond? Yes No × : ☐ Xarrow_forwardPredict the major products of this organic reaction: OH NaBH4 H ? CH3OH Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. ☐ : Sarrow_forwardPredict the major products of this organic reaction: 1. LIAIHA 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. X : ☐arrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new C - C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 tu ? ? OH Will the first product that forms in this reaction create a new CC bond? Yes No Will the first product that forms in this reaction create a new CC bond? Yes No C $ ©arrow_forwardAs the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C-C bond as its major product: 1. MgCl ? 2. H₂O* If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new CC bond. G marrow_forwardIncluding activity coefficients, find [Hg22+] in saturated Hg2Br2 in 0.00100 M NH4 Ksp Hg2Br2 = 5.6×10-23.arrow_forward
- give example for the following(by equation) a. Converting a water insoluble compound to a soluble one. b. Diazotization reaction form diazonium salt c. coupling reaction of a diazonium salt d. indacator properties of MO e. Diazotization ( diazonium salt of bromobenzene)arrow_forward2-Propanone and ethyllithium are mixed and subsequently acid hydrolyzed. Draw and name the structures of the products.arrow_forward(Methanesulfinyl)methane is reacted with NaH, and then with acetophenone. Draw and name the structures of the products.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Living By Chemistry: First Edition TextbookChemistryISBN:9781559539418Author:Angelica StacyPublisher:MAC HIGHER
Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Living By Chemistry: First Edition Textbook
Chemistry
ISBN:9781559539418
Author:Angelica Stacy
Publisher:MAC HIGHER
Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
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
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning