ACHIEVE/CHEMICAL PRINCIPLES ACCESS 2TERM
7th Edition
ISBN: 9781319403959
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Question
Chapter 3, Problem 3I.4E
Interpretation Introduction
Interpretation:
Difference between homogeneous and heterogeneous alloys and pure metals has to be determined.
Concept Introduction:
Alloys are formed from combination of metal with other elements. It retains the properties of metal but affects their crystalline structure. Examples of alloys are stainless steel, brass, bronze, and white gold.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Molecule
Inductive Effects
Resonance Effects
Overall Electron-Density
×
NO2
○ donating
O donating
O withdrawing
O withdrawing
O electron-rich
electron-deficient
no inductive effects
O no resonance effects
O similar to benzene
E
[
CI
O donating
withdrawing
O no inductive effects
Explanation
Check
○ donating
withdrawing
no resonance effects
electron-rich
electron-deficient
O similar to benzene
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Acces
Understanding how substituents activate
Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic
aromatic substitution.
Explanation
HN
NH2
Check
X
(Choose one)
(Choose one)
(Choose one)
(Choose one)
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center A
Identifying electron-donating and electron-withdrawing effects on benzene
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Inductive Effects
Resonance Effects
Overall Electron-Density
Molecule
CF3
O donating
O donating
O withdrawing
O withdrawing
O no inductive effects
O no resonance effects
electron-rich
electron-deficient
O similar to benzene
CH3
O donating
O withdrawing
O no inductive effects
O donating
O withdrawing
Ono resonance effects
O electron-rich
O electron-deficient
O similar to benzene
Explanation
Check
Х
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center
Chapter 3 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 2TERM
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
Similar questions
- * Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forwardDraw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forwardPlease help me with the following questions for chemistry.arrow_forward
- + C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forward→ Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forward
- For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Introductory Chemistry: A FoundationChemistryISBN:9781285199030Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781285199030
Author:Steven S. Zumdahl, Donald J. DeCoste
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
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning