Living By Chemistry: First Edition Textbook
1st Edition
ISBN: 9781559539418
Author: Angelica Stacy
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Question
Chapter U4.14, Problem 1E
Interpretation Introduction
Interpretation:
Whether two different solutions with different volumes can have same concentrations or not needs to be explained.
Concept introduction:
Concentration of a solution is expressed in different units. It can be g/ L of solute. It can be moles of solute per liter of solution. When concentration is taken in terms of mol/L, it is known as molarity.
Expert Solution & Answer
Answer to Problem 1E
If amounts of solute are different then two different solutions can have same concentrations.
Explanation of Solution
Let’s consider one solution has 1 mol solute and volume is 1 L. Another solution has 2 mol solute and volume is 2 L.
For 1st solution molarity is 1/1=1.
For 2nd solution molarity is 2/2=1.
Thus, for both the solution the molarity is 1.
Thus, the ratio of number of moles and volume should be same for two solutions to have same concentartion.
Chapter U4 Solutions
Living By Chemistry: First Edition Textbook
Ch. U4.1 - Prob. 1TAICh. U4.1 - Prob. 1ECh. U4.1 - Prob. 2ECh. U4.1 - Prob. 3ECh. U4.1 - Prob. 4ECh. U4.1 - Prob. 5ECh. U4.1 - Prob. 6ECh. U4.2 - Prob. 1TAICh. U4.2 - Prob. 1ECh. U4.2 - Prob. 2E
Ch. U4.2 - Prob. 3ECh. U4.2 - Prob. 4ECh. U4.2 - Prob. 5ECh. U4.3 - Prob. 1TAICh. U4.3 - Prob. 1ECh. U4.3 - Prob. 2ECh. U4.3 - Prob. 3ECh. U4.3 - Prob. 4ECh. U4.3 - Prob. 6ECh. U4.4 - Prob. 1TAICh. U4.4 - Prob. 1ECh. U4.4 - Prob. 2ECh. U4.4 - Prob. 3ECh. U4.4 - Prob. 4ECh. U4.4 - Prob. 5ECh. U4.4 - Prob. 6ECh. U4.4 - Prob. 7ECh. U4.5 - Prob. 1TAICh. U4.5 - Prob. 1ECh. U4.5 - Prob. 2ECh. U4.5 - Prob. 3ECh. U4.5 - Prob. 4ECh. U4.6 - Prob. 1TAICh. U4.6 - Prob. 1ECh. U4.6 - Prob. 2ECh. U4.6 - Prob. 3ECh. U4.6 - Prob. 5ECh. U4.6 - Prob. 6ECh. U4.6 - Prob. 7ECh. U4.7 - Prob. 1TAICh. U4.7 - Prob. 1ECh. U4.7 - Prob. 2ECh. U4.7 - Prob. 4ECh. U4.7 - Prob. 5ECh. U4.8 - Prob. 1TAICh. U4.8 - Prob. 1ECh. U4.8 - Prob. 2ECh. U4.8 - Prob. 4ECh. U4.8 - Prob. 5ECh. U4.8 - Prob. 6ECh. U4.8 - Prob. 7ECh. U4.8 - Prob. 8ECh. U4.8 - Prob. 9ECh. U4.8 - Prob. 10ECh. U4.8 - Prob. 11ECh. U4.9 - Prob. 1TAICh. U4.9 - Prob. 1ECh. U4.9 - Prob. 2ECh. U4.9 - Prob. 3ECh. U4.9 - Prob. 4ECh. U4.9 - Prob. 5ECh. U4.9 - Prob. 6ECh. U4.9 - Prob. 7ECh. U4.9 - Prob. 8ECh. U4.10 - Prob. 1TAICh. U4.10 - Prob. 1ECh. U4.10 - Prob. 2ECh. U4.10 - Prob. 3ECh. U4.10 - Prob. 4ECh. U4.10 - Prob. 5ECh. U4.10 - Prob. 6ECh. U4.10 - Prob. 7ECh. U4.10 - Prob. 8ECh. U4.11 - Prob. 1TAICh. U4.11 - Prob. 1ECh. U4.11 - Prob. 2ECh. U4.11 - Prob. 3ECh. U4.11 - Prob. 4ECh. U4.11 - Prob. 5ECh. U4.11 - Prob. 6ECh. U4.11 - Prob. 7ECh. U4.11 - Prob. 8ECh. U4.12 - Prob. 1TAICh. U4.12 - Prob. 1ECh. U4.12 - Prob. 2ECh. U4.12 - Prob. 3ECh. U4.12 - Prob. 4ECh. U4.13 - Prob. 1TAICh. U4.13 - Prob. 1ECh. U4.13 - Prob. 2ECh. U4.13 - Prob. 3ECh. U4.13 - Prob. 4ECh. U4.13 - Prob. 5ECh. U4.13 - Prob. 6ECh. U4.13 - Prob. 7ECh. U4.13 - Prob. 8ECh. U4.13 - Prob. 9ECh. U4.13 - Prob. 10ECh. U4.14 - Prob. 1TAICh. U4.14 - Prob. 1ECh. U4.14 - Prob. 2ECh. U4.14 - Prob. 3ECh. U4.14 - Prob. 4ECh. U4.14 - Prob. 5ECh. U4.14 - Prob. 6ECh. U4.14 - Prob. 7ECh. U4.14 - Prob. 8ECh. U4.14 - Prob. 9ECh. U4.15 - Prob. 1TAICh. U4.15 - Prob. 1ECh. U4.15 - Prob. 2ECh. U4.15 - Prob. 3ECh. U4.15 - Prob. 4ECh. U4.15 - Prob. 5ECh. U4.15 - Prob. 6ECh. U4.15 - Prob. 7ECh. U4.15 - Prob. 8ECh. U4.16 - Prob. 1TAICh. U4.16 - Prob. 1ECh. U4.16 - Prob. 2ECh. U4.16 - Prob. 3ECh. U4.16 - Prob. 4ECh. U4.16 - Prob. 5ECh. U4.16 - Prob. 6ECh. U4.16 - Prob. 7ECh. U4.17 - Prob. 1TAICh. U4.17 - Prob. 1ECh. U4.17 - Prob. 2ECh. U4.17 - Prob. 3ECh. U4.17 - Prob. 5ECh. U4.17 - Prob. 6ECh. U4.17 - Prob. 7ECh. U4.18 - Prob. 1TAICh. U4.18 - Prob. 1ECh. U4.18 - Prob. 2ECh. U4.18 - Prob. 3ECh. U4.18 - Prob. 4ECh. U4.18 - Prob. 5ECh. U4.18 - Prob. 6ECh. U4.18 - Prob. 7ECh. U4.18 - Prob. 8ECh. U4.19 - Prob. 1TAICh. U4.19 - Prob. 1ECh. U4.19 - Prob. 2ECh. U4.19 - Prob. 3ECh. U4.19 - Prob. 4ECh. U4.19 - Prob. 6ECh. U4.19 - Prob. 7ECh. U4.19 - Prob. 8ECh. U4.20 - Prob. 1TAICh. U4.20 - Prob. 1ECh. U4.20 - Prob. 2ECh. U4.20 - Prob. 3ECh. U4.20 - Prob. 4ECh. U4.20 - Prob. 5ECh. U4.20 - Prob. 6ECh. U4.20 - Prob. 7ECh. U4.20 - Prob. 8ECh. U4.21 - Prob. 1TAICh. U4.21 - Prob. 1ECh. U4.21 - Prob. 2ECh. U4.21 - Prob. 4ECh. U4.21 - Prob. 5ECh. U4.21 - Prob. 6ECh. U4.21 - Prob. 7ECh. U4.21 - Prob. 8ECh. U4.22 - Prob. 1TAICh. U4.22 - Prob. 1ECh. U4.22 - Prob. 2ECh. U4.22 - Prob. 3ECh. U4.22 - Prob. 4ECh. U4.22 - Prob. 5ECh. U4.22 - Prob. 6ECh. U4.23 - Prob. 1ECh. U4.23 - Prob. 2ECh. U4.23 - Prob. 3ECh. U4.23 - Prob. 4ECh. U4.23 - Prob. 5ECh. U4.23 - Prob. 6ECh. U4.23 - Prob. 7ECh. U4.24 - Prob. 1ECh. U4.24 - Prob. 2ECh. U4.24 - Prob. 3ECh. U4.24 - Prob. 5ECh. U4.24 - Prob. 6ECh. U4.25 - Prob. 1TAICh. U4.25 - Prob. 1ECh. U4.25 - Prob. 2ECh. U4.25 - Prob. 3ECh. U4.25 - Prob. 4ECh. U4.26 - Prob. 1TAICh. U4.26 - Prob. 1ECh. U4.26 - Prob. 2ECh. U4.26 - Prob. 4ECh. U4.26 - Prob. 5ECh. U4.26 - Prob. 6ECh. U4 - Prob. SI3RECh. U4 - Prob. SI4RECh. U4 - Prob. SII1RECh. U4 - Prob. SII2RECh. U4 - Prob. SII3RECh. U4 - Prob. SII5RECh. U4 - Prob. SII6RECh. U4 - Prob. SIII1RECh. U4 - Prob. SIII2RECh. U4 - Prob. SIII3RECh. U4 - Prob. SIII4RECh. U4 - Prob. SIII5RECh. U4 - Prob. SIII6RECh. U4 - Prob. SIII7RECh. U4 - Prob. SIII8RECh. U4 - Prob. SIV1RECh. U4 - Prob. SIV2RECh. U4 - Prob. SIV3RECh. U4 - Prob. SIV4RECh. U4 - Prob. SV1RECh. U4 - Prob. SV2RECh. U4 - Prob. SV3RECh. U4 - Prob. 1RECh. U4 - Prob. 4RECh. U4 - Prob. 5RECh. U4 - Prob. 6RECh. U4 - Prob. 7RECh. U4 - Prob. 8RECh. U4 - Prob. 9RECh. U4 - Prob. 10RECh. U4 - Prob. 11RECh. U4 - Prob. 12RE
Additional Science Textbook Solutions
Find more solutions based on key concepts
One isomer of methamphetamine is the addictive illegal drug known as crank. Another isomer is a medicine for si...
Campbell Essential Biology (7th Edition)
WHAT IF? Rabies, a viral disease in mammals, is not currently found in the British Isles. If you were in charg...
Campbell Biology (11th Edition)
10.71 Identify each of the following as an acid or a base: (10.1)
H2SO4
RbOH
Ca(OH)2
HI
...
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Based on your answers to Questions 2 and 3, which part of the Atlantic basin appears to have opened first?
Applications and Investigations in Earth Science (9th Edition)
Draw the mechanism for the hydroxide ion-catalyzed cleavage of fructose-l.6-bisphosphate.
Organic Chemistry (8th Edition)
8. A human maintaining a vegan diet (containing no animal products) would be a:
a. producer
b. primary consume...
Human Biology: Concepts and Current Issues (8th Edition)
Knowledge Booster
Similar questions
- Using reaction free energy to predict equilibrium composition Consider the following equilibrium: 2NOCI (g) 2NO (g) + Cl2 (g) AGº =41. kJ Now suppose a reaction vessel is filled with 4.50 atm of nitrosyl chloride (NOCI) and 6.38 atm of chlorine (C12) at 212. °C. Answer the following questions about this system: ? rise Under these conditions, will the pressure of NOCI tend to rise or fall? x10 fall Is it possible to reverse this tendency by adding NO? In other words, if you said the pressure of NOCI will tend to rise, can that be changed to a tendency to fall by adding NO? Similarly, if you said the pressure of NOCI will tend to fall, can that be changed to a tendency to rise by adding NO? yes no If you said the tendency can be reversed in the second question, calculate the minimum pressure of NO needed to reverse it. Round your answer to 2 significant digits. 0.035 atm ✓ G 00. 18 Ararrow_forwardHighlight 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_forward
- Draw 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_forwardEpoxides 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_forward
- You 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_forward1) 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_forward
- Alcohols 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_forwardDraw 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_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