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
- Highlight each glycosidic bond in the molecule below. Then answer the questions in the table under the drawing area. HO- HO- -0 OH OH HO NG HO- HO- OH OH OH OH NG OHarrow_forward€ + Suppose the molecule in the drawing area below were reacted with H₂ over a platinum catalyst. Edit the molecule to show what would happen to it. That is, turn it into the product of the reaction. Also, write the name of the product molecule under the drawing area. Name: ☐ H C=0 X H- OH HO- H HO- -H CH₂OH ×arrow_forwardDraw the Haworth projection of the disaccharide made by joining D-glucose and D-mannose with a ẞ(1-4) glycosidic bond. If the disaccharide has more than one anomer, you can draw any of them. Click and drag to start drawing a structure. Xarrow_forward
- Epoxides can be opened in aqueous acid or aqueous base to produce diols (molecules with two OH groups). In this question, you'll explore the mechanism of epoxide opening in aqueous acid. 2nd attempt Be sure to show all four bonds at stereocenters using hash and wedge lines. 0 0 Draw curved arrows to show how the epoxide reacts with hydronium ion. 100 +1: 1st attempt Feedback Be sure to show all four bonds at stereocenters using hash and wedge lines. See Periodic Table See Hint H A 5 F F Hr See Periodic Table See Hintarrow_forward03 Question (1 point) For the reaction below, draw both of the major organic products. Be sure to consider stereochemistry. > 1. CH₂CH₂MgBr 2. H₂O 3rd attempt Draw all four bonds at chiral centers. Draw all stereoisomers formed. Draw the structures here. e 130 AN H See Periodic Table See Hint P C Brarrow_forwardYou may wish to address the following issues in your response if they are pertinent to the reaction(s) you propose to employ:1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Please make it in detail and draw it out too in what step what happens. Thank you for helping me!arrow_forward
- 1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Everything in detail and draw out and write it.arrow_forwardCalculating the pH at equivalence of a titration 3/5 Izabella A chemist titrates 120.0 mL of a 0.7191M dimethylamine ((CH3)2NH) solution with 0.5501 M HBr solution at 25 °C. Calculate the pH at equivalence. The pk of dimethylamine is 3.27. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of HBr solution added. pH = ☐ ✓ 18 Ar Boarrow_forwardAlcohols can be synthesized using an acid-catalyzed hydration of an alkene. An alkene is combined with aqueous acid (e.. sulfuric acid in water). The reaction mechanism typically involves a carbocation intermediate. > 3rd attempt 3343 10 8 Draw arrows to show the reaction between the alkene and hydronium ion. that 2nd attempt Feedback 1st attempt تعمال Ju See Periodic Table See Hint F D Ju See Periodic Table See Hintarrow_forward
- Draw the simplified curved arrow mechanism for the reaction of acetone and CHgLi to give the major product. 4th attempt Π Draw the simplified curved arrow mechanism T 3rd attempt Feedback Ju See Periodic Table See Hint H -H H -I H F See Periodic Table See Hintarrow_forwardSelect the correct reagent to accomplish the first step of this reaction. Then draw a mechanism on the Grignard reagent using curved arrow notation to show how it is converted to the final product. 4th attempt Part 1 (0.5 point) Select the correct reagent to accomplish the first step of this reaction. Choose one: OA Mg in ethanol (EtOH) OB. 2 Li in THF O C. Li in THF D. Mg in THF O E Mg in H2O Part 2 (0.5 point) Br Part 1 Bri Mg CH B CH, 1 Draw intermediate here, but no arrows. © TE See Periodic Table See Hint See Hint ין Harrow_forwardSelect the product for the following reaction. HO HO PCC OH ○ OH O HO ○ HO HO HOarrow_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