Living by Chemistry
2nd Edition
ISBN: 9781464142314
Author: Angelica M. Stacy
Publisher: W. H. Freeman
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter U1.4, Problem 3E
Interpretation Introduction
Interpretation:
The possibility of prediction of volume of an object by just looking it needs to be predicted.
Concept introduction:
Chemistry deals with the different processes which occur in surrounding and directly or indirectly related to each other. Physical properties can be used to explain physical nature of any substance.
Different physical properties of matter are used to explain the nature of matter and its interaction with other substances. For example; volume of a substance represents the amount of space a substance takes up.
Expert Solution & Answer
Answer to Problem 3E
The volume of an object can be just predicted by looking but it is not possible for all the objects. For example, the volume of objects with irregular shape and size cannot be predicted by looking at them.
Explanation of Solution
All the properties of matter can be explained with the help of different physical properties such as mass, volume, density, melting point, boiling point etc.
The volume of an object can be just predicted by looking but it is not possible for the objects with irregular shape and size.
The volume of an object with regular shape and size can be predicted by looking at them and can be further calculated with the help of mass and density.
For example; volume of objects with irregular shape like stone cannot be determined just by looking it but the volume of a cube can be predicted due to its fixed size and shape.
Conclusion
The volume of an object can be just predicted by looking but it is not possible for the objects with irregular shape and size.
Chapter U1 Solutions
Living by Chemistry
Ch. U1.1 - Prob. 1TAICh. U1.1 - Prob. 1ECh. U1.1 - Prob. 2ECh. U1.1 - Prob. 3ECh. U1.1 - Prob. 4ECh. U1.1 - Prob. 5ECh. U1.1 - Prob. 6ECh. U1.1 - Prob. 7ECh. U1.1 - Prob. 8ECh. U1.2 - Prob. 1TAI
Ch. U1.2 - Prob. 1ECh. U1.2 - Prob. 2ECh. U1.2 - Prob. 5ECh. U1.3 - Prob. 1TAICh. U1.3 - Prob. 1ECh. U1.3 - Prob. 2ECh. U1.3 - Prob. 3ECh. U1.3 - Prob. 4ECh. U1.3 - Prob. 5ECh. U1.3 - Prob. 6ECh. U1.4 - Prob. 1TAICh. U1.4 - Prob. 1ECh. U1.4 - Prob. 2ECh. U1.4 - Prob. 3ECh. U1.4 - Prob. 4ECh. U1.4 - Prob. 5ECh. U1.4 - Prob. 6ECh. U1.4 - Prob. 7ECh. U1.4 - Prob. 8ECh. U1.4 - Prob. 9ECh. U1.4 - Prob. 10ECh. U1.4 - Prob. 11ECh. U1.5 - Prob. 1TAICh. U1.5 - Prob. 1ECh. U1.5 - Prob. 2ECh. U1.5 - Prob. 3ECh. U1.5 - Prob. 4ECh. U1.5 - Prob. 5ECh. U1.5 - Prob. 6ECh. U1.5 - Prob. 7ECh. U1.6 - Prob. 1TAICh. U1.6 - Prob. 1ECh. U1.6 - Prob. 2ECh. U1.6 - Prob. 3ECh. U1.6 - Prob. 4ECh. U1.6 - Prob. 5ECh. U1.6 - Prob. 6ECh. U1.7 - Prob. 1TAICh. U1.7 - Prob. 1ECh. U1.7 - Prob. 2ECh. U1.7 - Prob. 3ECh. U1.7 - Prob. 4ECh. U1.7 - Prob. 5ECh. U1.8 - Prob. 1TAICh. U1.8 - Prob. 1ECh. U1.8 - Prob. 2ECh. U1.8 - Prob. 4ECh. U1.8 - Prob. 5ECh. U1.8 - Prob. 6ECh. U1.8 - Prob. 7ECh. U1.9 - Prob. 1TAICh. U1.9 - Prob. 1ECh. U1.9 - Prob. 2ECh. U1.9 - Prob. 5ECh. U1.9 - Prob. 7ECh. U1.10 - Prob. 1TAICh. U1.10 - Prob. 1ECh. U1.10 - Prob. 2ECh. U1.10 - Prob. 3ECh. U1.10 - Prob. 4ECh. U1.10 - Prob. 5ECh. U1.10 - Prob. 6ECh. U1.10 - Prob. 7ECh. U1.10 - Prob. 8ECh. U1.11 - Prob. 1TAICh. U1.11 - Prob. 1ECh. U1.11 - Prob. 2ECh. U1.11 - Prob. 3ECh. U1.11 - Prob. 4ECh. U1.11 - Prob. 5ECh. U1.11 - Prob. 6ECh. U1.11 - Prob. 7ECh. U1.11 - Prob. 9ECh. U1.11 - Prob. 11ECh. U1.11 - Prob. 12ECh. U1.12 - Prob. 1TAICh. U1.12 - Prob. 1ECh. U1.12 - Prob. 2ECh. U1.12 - Prob. 3ECh. U1.12 - Prob. 4ECh. U1.12 - Prob. 5ECh. U1.12 - Prob. 6ECh. U1.12 - Prob. 7ECh. U1.12 - Prob. 8ECh. U1.13 - Prob. 1TAICh. U1.13 - Prob. 1ECh. U1.13 - Prob. 2ECh. U1.13 - Prob. 3ECh. U1.13 - Prob. 4ECh. U1.13 - Prob. 5ECh. U1.13 - Prob. 6ECh. U1.13 - Prob. 7ECh. U1.13 - Prob. 8ECh. U1.13 - Prob. 9ECh. U1.14 - Prob. 1TAICh. U1.14 - Prob. 1ECh. U1.14 - Prob. 2ECh. U1.14 - Prob. 3ECh. U1.14 - Prob. 4ECh. U1.14 - Prob. 5ECh. U1.14 - Prob. 6ECh. U1.14 - Prob. 7ECh. U1.14 - Prob. 8ECh. U1.14 - Prob. 9ECh. U1.14 - Prob. 10ECh. U1.14 - Prob. 11ECh. U1.14 - Prob. 12ECh. U1.14 - Prob. 13ECh. U1.14 - Prob. 14ECh. U1.15 - Prob. 1TAICh. U1.15 - Prob. 1ECh. U1.15 - Prob. 2ECh. U1.15 - Prob. 3ECh. U1.15 - Prob. 4ECh. U1.15 - Prob. 5ECh. U1.15 - Prob. 6ECh. U1.15 - Prob. 7ECh. U1.15 - Prob. 8ECh. U1.15 - Prob. 9ECh. U1.15 - Prob. 10ECh. U1.15 - Prob. 11ECh. U1.15 - Prob. 12ECh. U1.16 - Prob. 1TAICh. U1.16 - Prob. 1ECh. U1.16 - Prob. 2ECh. U1.16 - Prob. 3ECh. U1.16 - Prob. 4ECh. U1.16 - Prob. 5ECh. U1.16 - Prob. 6ECh. U1.17 - Prob. 1TAICh. U1.17 - Prob. 1ECh. U1.17 - Prob. 2ECh. U1.17 - Prob. 3ECh. U1.17 - Prob. 4ECh. U1.17 - Prob. 5ECh. U1.17 - Prob. 6ECh. U1.17 - Prob. 7ECh. U1.17 - Prob. 8ECh. U1.17 - Prob. 9ECh. U1.17 - Prob. 10ECh. U1.17 - Prob. 11ECh. U1.18 - Prob. 1TAICh. U1.18 - Prob. 1ECh. U1.18 - Prob. 2ECh. U1.18 - Prob. 3ECh. U1.18 - Prob. 4ECh. U1.18 - Prob. 5ECh. U1.18 - Prob. 6ECh. U1.18 - Prob. 7ECh. U1.18 - Prob. 8ECh. U1.18 - Prob. 9ECh. U1.18 - Prob. 10ECh. U1.19 - Prob. 1TAICh. U1.19 - Prob. 1ECh. U1.19 - Prob. 2ECh. U1.19 - Prob. 3ECh. U1.19 - Prob. 4ECh. U1.19 - Prob. 5ECh. U1.19 - Prob. 6ECh. U1.19 - Prob. 7ECh. U1.19 - Prob. 8ECh. U1.19 - Prob. 9ECh. U1.19 - Prob. 10ECh. U1.19 - Prob. 11ECh. U1.19 - Prob. 12ECh. U1.19 - Prob. 13ECh. U1.19 - Prob. 14ECh. U1.19 - Prob. 15ECh. U1.19 - Prob. 16ECh. U1.20 - Prob. 1TAICh. U1.20 - Prob. 1ECh. U1.20 - Prob. 2ECh. U1.20 - Prob. 3ECh. U1.20 - Prob. 4ECh. U1.20 - Prob. 5ECh. U1.20 - Prob. 6ECh. U1.20 - Prob. 7ECh. U1.21 - Prob. 1TAICh. U1.21 - Prob. 1ECh. U1.21 - Prob. 2ECh. U1.21 - Prob. 3ECh. U1.21 - Prob. 4ECh. U1.21 - Prob. 5ECh. U1.21 - Prob. 6ECh. U1.21 - Prob. 7ECh. U1.21 - Prob. 8ECh. U1.22 - Prob. 1TAICh. U1.22 - Prob. 1ECh. U1.22 - Prob. 2ECh. U1.22 - Prob. 3ECh. U1.22 - Prob. 4ECh. U1.22 - Prob. 5ECh. U1.22 - Prob. 6ECh. U1.22 - Prob. 7ECh. U1.23 - Prob. 1TAICh. U1.23 - Prob. 1ECh. U1.23 - Prob. 2ECh. U1.23 - Prob. 3ECh. U1.23 - Prob. 4ECh. U1.23 - Prob. 5ECh. U1.24 - Prob. 1TAICh. U1.24 - Prob. 1ECh. U1.24 - Prob. 2ECh. U1.24 - Prob. 3ECh. U1.24 - Prob. 4ECh. U1.24 - Prob. 5ECh. U1.24 - Prob. 6ECh. U1.24 - Prob. 7ECh. U1.24 - Prob. 8ECh. U1.24 - Prob. 9ECh. U1.24 - Prob. 10ECh. U1.24 - Prob. 11ECh. U1.24 - Prob. 12ECh. U1.24 - Prob. 13ECh. U1.25 - Prob. 1TAICh. U1.25 - Prob. 1ECh. U1.25 - Prob. 2ECh. U1.25 - Prob. 3ECh. U1.25 - Prob. 4ECh. U1.25 - Prob. 5ECh. U1.25 - Prob. 6ECh. U1.26 - Prob. 1TAICh. U1.26 - Prob. 1ECh. U1.26 - Prob. 2ECh. U1.26 - Prob. 3ECh. U1.26 - Prob. 4ECh. U1.26 - Prob. 5ECh. U1.26 - Prob. 6ECh. U1.26 - Prob. 7ECh. U1.26 - Prob. 8ECh. U1.26 - Prob. 9ECh. U1.26 - Prob. 10ECh. U1.27 - Prob. 1TAICh. U1.27 - Prob. 1ECh. U1.27 - Prob. 2ECh. U1.27 - Prob. 3ECh. U1.27 - Prob. 4ECh. U1.27 - Prob. 5ECh. U1.27 - Prob. 6ECh. U1.27 - Prob. 7ECh. U1 - Prob. C1.1RECh. U1 - Prob. C1.2RECh. U1 - Prob. C1.3RECh. U1 - Prob. C1.4RECh. U1 - Prob. C1.5RECh. U1 - Prob. C1.6RECh. U1 - Prob. C2.1RECh. U1 - Prob. C2.2RECh. U1 - Prob. C2.3RECh. U1 - Prob. C2.4RECh. U1 - Prob. C3.1RECh. U1 - Prob. C3.2RECh. U1 - Prob. C3.3RECh. U1 - Prob. C3.4RECh. U1 - Prob. C4.1RECh. U1 - Prob. C4.2RECh. U1 - Prob. C4.3RECh. U1 - Prob. C4.4RECh. U1 - Prob. C5.1RECh. U1 - Prob. C5.2RECh. U1 - Prob. C5.3RECh. U1 - Prob. C5.4RECh. U1 - Prob. 1RECh. U1 - Prob. 2RECh. U1 - Prob. 3RECh. U1 - Prob. 4RECh. U1 - Prob. 5RECh. U1 - Prob. 6RECh. U1 - Prob. 7RECh. U1 - Prob. 8RECh. U1 - Prob. 9RECh. U1 - Prob. 10RECh. U1 - Prob. 11RECh. U1 - Prob. 12RECh. U1 - Prob. 1STPCh. U1 - Prob. 2STPCh. U1 - Prob. 3STPCh. U1 - Prob. 4STPCh. U1 - Prob. 5STPCh. U1 - Prob. 6STPCh. U1 - Prob. 7STPCh. U1 - Prob. 8STPCh. U1 - Prob. 9STPCh. U1 - Prob. 10STPCh. U1 - Prob. 11STPCh. U1 - Prob. 12STPCh. U1 - Prob. 13STPCh. U1 - Prob. 14STPCh. U1 - Prob. 15STPCh. U1 - Prob. 16STPCh. U1 - Prob. 17STPCh. U1 - Prob. 18STPCh. U1 - Prob. 19STPCh. U1 - Prob. 20STPCh. U1 - Prob. 21STPCh. U1 - Prob. 22STP
Additional Science Textbook Solutions
Find more solutions based on key concepts
All of the following processes are involved in the carbon cycle except: a. photosynthesis b. cell respiration c...
Human Biology: Concepts and Current Issues (8th Edition)
The glycine cleavage system is a group of four enzymes that together catalyze the following reaction: glycine+T...
Organic Chemistry (8th Edition)
What are the minimum and maximum ages of the island of Kauai? Minimum age: ______million yr Maximum age: ______...
Applications and Investigations in Earth Science (9th Edition)
Why was Whler astonished to find he had made urea?
Campbell Biology (11th Edition)
Which culture uses NAD+? Use the following choices to answer questions. a. E. coli growing in glucose broth at ...
Microbiology: An Introduction
51. I A tennis player hits a ball 2.0 m above the ground. The ball leaves his racquet with a speed of 20.0 m/s ...
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
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
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles 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 Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY