EP CHEMISTRY-1-YEAR LICENSE (REALIZE)
12th Edition
ISBN: 9780328928958
Author: WILBRAHAM
Publisher: SAVVAS L
expand_more
expand_more
format_list_bulleted
Question
Chapter 2.1, Problem 11SP
Interpretation Introduction
Interpretation:The property used to separate argon and carbon dioxide gases in the air should be identified.
Concept Introduction:A compound that is made up of two or more chemical components that are not chemically linked with each other is said to be a mixture.
Expert Solution & Answer
Explanation of Solution
A property that is a characteristic of matter and not associated with any change in chemical composition is said to be physical property. The differences in physical properties like phase, boiling point, freezing point, particle size, solubility so on are used to separate mixtures.
The difference in the density and the boiling points of argon and carbon dioxide helps in separating argon and carbon dioxide gases in the air. The density of carbon dioxide is greater than argon so, carbon dioxide would be at the bottom whereas argon would be at the top.
The use of fractional distillation is also helpful in separating air into its constituent gases by using the boiling points of different gases. In this process, the air is cooled to liquefy followed by increasing the temperature so that the gas that reaches its boiling point evaporates and separates.
Chapter 2 Solutions
EP CHEMISTRY-1-YEAR LICENSE (REALIZE)
Ch. 2.1 - Prob. 1LCCh. 2.1 - Prob. 2LCCh. 2.1 - Prob. 3LCCh. 2.1 - Prob. 4LCCh. 2.1 - Prob. 5LCCh. 2.1 - Prob. 6LCCh. 2.1 - Prob. 7LCCh. 2.1 - Prob. 8LCCh. 2.1 - Prob. 9LCCh. 2.1 - Prob. 10SP
Ch. 2.1 - Prob. 11SPCh. 2.2 - Prob. 12LCCh. 2.2 - Prob. 13LCCh. 2.2 - Prob. 14LCCh. 2.2 - Prob. 15LCCh. 2.2 - Prob. 16LCCh. 2.2 - Prob. 17LCCh. 2.2 - Prob. 18LCCh. 2.2 - Prob. 19LCCh. 2.3 - Prob. 20SPCh. 2.3 - Prob. 21SPCh. 2.3 - Prob. 22LCCh. 2.3 - Prob. 23LCCh. 2.3 - Prob. 24LCCh. 2.3 - Prob. 25LCCh. 2.3 - Prob. 26LCCh. 2.3 - Prob. 27LCCh. 2.3 - Prob. 28LCCh. 2.3 - Prob. 29LCCh. 2.3 - Prob. 30LCCh. 2.3 - Prob. 31LCCh. 2.4 - Prob. 32LCCh. 2.4 - Prob. 33LCCh. 2.4 - Prob. 34LCCh. 2.4 - Prob. 35LCCh. 2.4 - Prob. 36LCCh. 2.4 - Prob. 37LCCh. 2.4 - Prob. 38LCCh. 2 - Prob. 39ACh. 2 - Prob. 40ACh. 2 - Prob. 41ACh. 2 - Prob. 42ACh. 2 - Prob. 43ACh. 2 - Prob. 44ACh. 2 - Prob. 45ACh. 2 - Prob. 46ACh. 2 - Prob. 47ACh. 2 - Prob. 48ACh. 2 - Prob. 49ACh. 2 - Prob. 50ACh. 2 - Prob. 51ACh. 2 - Prob. 52ACh. 2 - Prob. 53ACh. 2 - Prob. 54ACh. 2 - Prob. 55ACh. 2 - Prob. 56ACh. 2 - Prob. 57ACh. 2 - Prob. 58ACh. 2 - Prob. 59ACh. 2 - Prob. 60ACh. 2 - Prob. 61ACh. 2 - Prob. 62ACh. 2 - Prob. 63ACh. 2 - Prob. 64ACh. 2 - Prob. 65ACh. 2 - Prob. 66ACh. 2 - Prob. 67ACh. 2 - Prob. 68ACh. 2 - Prob. 69ACh. 2 - Prob. 70ACh. 2 - Prob. 71ACh. 2 - Prob. 72ACh. 2 - Prob. 73ACh. 2 - Prob. 74ACh. 2 - Prob. 75ACh. 2 - Prob. 76ACh. 2 - Prob. 77ACh. 2 - Prob. 78ACh. 2 - Prob. 79ACh. 2 - Prob. 80ACh. 2 - Prob. 81ACh. 2 - Prob. 82ACh. 2 - Prob. 83ACh. 2 - Prob. 84ACh. 2 - Prob. 85ACh. 2 - Prob. 86ACh. 2 - Prob. 87ACh. 2 - Prob. 88ACh. 2 - Prob. 89ACh. 2 - Prob. 90ACh. 2 - Prob. 93ACh. 2 - Prob. 94ACh. 2 - Prob. 95ACh. 2 - Prob. 1STPCh. 2 - Prob. 2STPCh. 2 - Prob. 3STPCh. 2 - Prob. 4STPCh. 2 - Prob. 5STPCh. 2 - Prob. 6STPCh. 2 - Prob. 7STPCh. 2 - Prob. 8STPCh. 2 - Prob. 9STPCh. 2 - Prob. 10STPCh. 2 - Prob. 11STPCh. 2 - Prob. 12STPCh. 2 - Prob. 13STPCh. 2 - Prob. 14STP
Knowledge Booster
Similar questions
- Denote the dipole for the indicated bonds in the following molecules. H3C ✓ CH3 B F-CCl 3 Br-Cl H3C Si(CH3)3 wwwwwww OH НО. HO HO OH vitamin C CH3arrow_forwardFor the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Η 1 D EN Select Draw Templates More C H D N Erasearrow_forwardQ9: Explain why compound I is protonated on O while compound II is protonated on N. NH2 NH2 I IIarrow_forward
- AN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forwardAN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forward(a) What is the hybridization of the carbon in the methyl cation (CH3*) and in the methyl anion (CH3¯)? (b) What is the approximate H-C-H bond angle in the methyl cation and in the methyl anion?arrow_forward
- Q8: Draw the resonance structures for the following molecule. Show the curved arrows (how you derive each resonance structure). Circle the major resonance contributor.arrow_forwardQ4: Draw the Lewis structures for the cyanate ion (OCN) and the fulminate ion (CNO). Draw all possible resonance structures for each. Determine which form for each is the major resonance contributor.arrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. CH3 N CH3 HÖ: H3C CI: ::arrow_forward
- Q3: Draw the Lewis structures for nitromethane (CH3NO2) and methyl nitrite (CH3ONO). Draw at least two resonance forms for each. Determine which form for each is the major resonance contributor.arrow_forwardQ1: Draw a valid Lewis structures for the following molecules. Include appropriate charges and lone pair electrons. If there is more than one Lewis structure available, draw the best structure. NH3 Sulfate Boron tetrahydride. C3H8 (linear isomer) OCN NO3 CH3CN SO2Cl2 CH3OH2*arrow_forwardQ2: Draw all applicable resonance forms for the acetate ion CH3COO. Clearly show all lone pairs, charges, and arrow formalism.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