Living by Chemistry
2nd Edition
ISBN: 9781464142314
Author: Angelica M. Stacy
Publisher: W. H. Freeman
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter U1.17, Problem 9E
Interpretation Introduction
Interpretation:
The colors of the flame for the given compounds are to be predicted and explained.
Concept introduction:
Different compounds produce different colors in a flame test. Flame test is done by heating a small sample of a compound in a flame such as a Bunsen burner. The color of the flame determines which atom is present in the compound.
Expert Solution & Answer
Answer to Problem 9E
The following table shows the colors of flame produced by given compounds.
| Compounds | Flame color |
| Na2CO3 | Yellow - orange |
| Ba(OH)2 | Green |
| KOH | Pink - lilac |
| K2CO3 | Pink - lilac |
| BaO | Green |
Explanation of Solution
Given information:
Following compounds are given:
| Na2CO3 |
| Ba(OH)2 |
| KOH |
| K2CO3 |
| BaO |
Each metal atom is associated with a specific flame color. A flame test can be used to confirm the presence of a particular atom in a compound. Color patterns with a flame test indicate the presence of a specific metal atom in a compound. Non -metal part of the compound does not give any color.
- Na2CO3 - All sodium compounds burn with yellow - orange flame. Sodium carbonate is also a sodium compound. So it will burn with a yellow - orange flame.
- Ba(OH)2 - All barium compounds burn with greenflame. Barium hydroxide is also a barium compound. So it will burn with a green flame.
- KOH - All potassium compounds burn with pink - lilacflame. Potassium hydroxide is also a potassium compound. So it will burn with a pink - lilac flame.
- K2CO3 - All potassium compounds burn with pink - lilacflame. Potassium hydroxide is also a potassium compound. So it will burn with a pink - lilac flame.
- BaO - All barium compounds burn with greenflame. Barium oxide is a barium compound. So it will burn with a green flame.
Conclusion
Color patterns with a flame test indicate the presence of a specific metal atom in a compound.
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
Raw Oysters and Antacids: A Deadly Mix? The highly acidic environment of the stomach kills most bacteria before...
Microbiology with Diseases by Body System (5th Edition)
1. Which is a function of the skeletal system? (a) support, (b) hematopoietic site, (c) storage, (d) providing ...
Anatomy & Physiology (6th Edition)
Flask A contains yeast cells in glucose-minimal salts broth incubated at 30C with aeration. Flask B contains ye...
Microbiology: An Introduction
27. Consider the reaction.
Express the rate of the reaction in terms of the change in concentration of each of...
Chemistry: Structure and Properties (2nd Edition)
16. A 200 g mass attached to a horizontal spring oscillates at a frequency of 2.0 Hz. At , the mass is at and ...
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
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)
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
- The rate coefficient of the gas-phase reaction 2 NO2 + O3 → N2O5 + O2 is 2.0x104 mol–1 dm3 s–1 at 300 K. Indicate whether the order of the reaction is 0, 1, or 2.arrow_forward8. Draw all the resonance forms for each of the following molecules or ions, and indicate the major contributor in each case, or if they are equivalent. (4.5 pts) (a) PH2 سمةarrow_forward3. Assign absolute configuration (Rors) to each chirality center. a. H Nitz C. он b. 0 H-C. C H 7 C. ་-4 917-417 refs H 1つ ८ ડુ d. Но f. -2- 01 Ho -OH 2HNarrow_forward
- How many signals do you expect in the H NMR spectrum for this molecule? Br Br Write the answer below. Also, in each of the drawing areas below is a copy of the molecule, with Hs shown. In each copy, one of the H atoms is colored red. Highlight in red all other H atoms that would contribute to the same signal as the H already highlighted red. Note for advanced students: In this question, any multiplet is counted as one signal. Number of signals in the 'H NMR spectrum. For the molecule in the top drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in top molecule For the molecule in the bottom drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in bottom moleculearrow_forwardIn the drawing area below, draw the major products of this organic reaction: 1. NaOH ? 2. CH3Br If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. No reaction. Click and drag to start drawing a structure. ☐ : A คarrow_forwardPredict the major products of the following organic reaction: NC Δ ? Some important Notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to draw bonds carefully to show important geometric relationships between substituents. Note: if your answer contains a complicated ring structure, you must use one of the molecular fragment stamps (available in the menu at right) to enter the ring structure. You can add any substituents using the pencil tool in the usual way. Click and drag to start drawing a structure. Х аarrow_forward
- Predict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. + ☑ OH 1. TsCl, py .... 文 P 2. t-BuO K Click and drag to start drawing a structure.arrow_forwardConsider this organic reaction: ( Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significant rate, check the box under the drawing area instead. Click and drag to start drawing a structure. Х : а ค 1arrow_forwardIn the drawing area below, draw the major products of this organic reaction: If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. 1. NaH 2. CH3Br ? Click and drag to start drawing a structure. No reaction. : ☐ Narrow_forward
- + Predict the major product of the following reaction. : ☐ + ☑ ค OH H₂SO4 Click and drag to start drawing a structure.arrow_forwardConsider this organic reaction: ... OH CI Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significant rate, check the box under the drawing area instead. ☐ No Reaction. Click and drag to start drawing a structure. : аarrow_forwardConsider the following reactants: Br Would elimination take place at a significant rate between these reactants? Note for advanced students: by significant, we mean that the rate of elimination would be greater than the rate of competing substitution reactions. yes O no If you said elimination would take place, draw the major products in the upper drawing area. If you said elimination would take place, also draw the complete mechanism for one of the major products in the lower drawing area. If there is more than one major product, you may draw the mechanism that leads to any of them. Major 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
Quantum Mechanics - Part 1: Crash Course Physics #43; Author: CrashCourse;https://www.youtube.com/watch?v=7kb1VT0J3DE;License: Standard YouTube License, CC-BY