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 U2, Problem 17STP
Interpretation Introduction
Interpretation:
The condition that illustrates the statement “Like dissolves like” needs to be identified.
Concept introduction:
This concept is based on the polarity of solute and solvent molecules. The polar molecule of solvent can only dissolve in polar solvent and non-polar can only dissolve in non-polar solvent.
Expert Solution & Answer
Answer to Problem 17STP
(B) Iodine, I2, is more soluble in oil than water.
Explanation of Solution
Reason for correct option:
The statement “Like Dissolves Like” means polar solute molecule dissolves in polar solvent and non polar molecule of solute dissolves in non-polar solvent.
Polar solvent are hydrophilic in nature means they like water or can dissolve in water
Here, Iodine is a non-polar molecule so it dissolves more in non-polar solvent like oil.
Conclusion
Reasons for incorrect options:
(A) Iodine,I2, is more soluble in water than KI .(Incorrect).
The water is polar in nature thus, iodine will not dissolve in water. Iodine can react with KI to form KI3 which is soluble in water. Thus, iodine can dissolve in KI more than water.
(C) Vinegar, CH3COOH3 is more soluble oil than in water. (Incorrect)
Vinegar or acetic acid is polar in nature so it dissolves in water. Vinegar or acetic acid is polar in nature so it dissolves in water and not in oil.
(D) Sodium chloride, NaCl is more soluble in oil than in water. (Incorrect)
Salts form ionic bonds which are polar in nature. All salts are soluble in water because water is a polar solvent. So, NaCl is more soluble in water than oil.
Chapter U2 Solutions
Living by Chemistry
Ch. U2.28 - Prob. 1TAICh. U2.28 - Prob. 1ECh. U2.28 - Prob. 2ECh. U2.28 - Prob. 3ECh. U2.28 - Prob. 4ECh. U2.28 - Prob. 7ECh. U2.28 - Prob. 8ECh. U2.29 - Prob. 1TAICh. U2.29 - Prob. 1ECh. U2.29 - Prob. 2E
Ch. U2.29 - Prob. 3ECh. U2.29 - Prob. 4ECh. U2.29 - Prob. 5ECh. U2.29 - Prob. 6ECh. U2.29 - Prob. 7ECh. U2.30 - Prob. 1TAICh. U2.30 - Prob. 1ECh. U2.30 - Prob. 2ECh. U2.30 - Prob. 3ECh. U2.30 - Prob. 4ECh. U2.30 - Prob. 5ECh. U2.31 - Prob. 1TAICh. U2.31 - Prob. 1ECh. U2.31 - Prob. 2ECh. U2.31 - Prob. 3ECh. U2.31 - Prob. 4ECh. U2.31 - Prob. 5ECh. U2.31 - Prob. 6ECh. U2.31 - Prob. 7ECh. U2.31 - Prob. 8ECh. U2.32 - Prob. 1TAICh. U2.32 - Prob. 1ECh. U2.32 - Prob. 2ECh. U2.32 - Prob. 3ECh. U2.32 - Prob. 4ECh. U2.32 - Prob. 5ECh. U2.32 - Prob. 6ECh. U2.32 - Prob. 7ECh. U2.32 - Prob. 8ECh. U2.32 - Prob. 9ECh. U2.33 - Prob. 1TAICh. U2.33 - Prob. 1ECh. U2.33 - Prob. 2ECh. U2.33 - Prob. 3ECh. U2.33 - Prob. 4ECh. U2.33 - Prob. 5ECh. U2.33 - Prob. 6ECh. U2.33 - Prob. 7ECh. U2.33 - Prob. 8ECh. U2.33 - Prob. 9ECh. U2.33 - Prob. 10ECh. U2.33 - Prob. 11ECh. U2.34 - Prob. 1TAICh. U2.34 - Prob. 1ECh. U2.34 - Prob. 2ECh. U2.34 - Prob. 3ECh. U2.34 - Prob. 4ECh. U2.34 - Prob. 5ECh. U2.35 - Prob. 1TAICh. U2.35 - Prob. 1ECh. U2.35 - Prob. 2ECh. U2.35 - Prob. 3ECh. U2.35 - Prob. 4ECh. U2.35 - Prob. 5ECh. U2.35 - Prob. 6ECh. U2.36 - Prob. 1TAICh. U2.36 - Prob. 1ECh. U2.36 - Prob. 2ECh. U2.36 - Prob. 3ECh. U2.36 - Prob. 4ECh. U2.36 - Prob. 5ECh. U2.36 - Prob. 6ECh. U2.36 - Prob. 7ECh. U2.37 - Prob. 1TAICh. U2.37 - Prob. 1ECh. U2.37 - Prob. 2ECh. U2.37 - Prob. 3ECh. U2.37 - Prob. 4ECh. U2.37 - Prob. 5ECh. U2.37 - Prob. 6ECh. U2.37 - Prob. 7ECh. U2.37 - Prob. 8ECh. U2.37 - Prob. 9ECh. U2.38 - Prob. 1TAICh. U2.38 - Prob. 1ECh. U2.38 - Prob. 2ECh. U2.38 - Prob. 3ECh. U2.38 - Prob. 4ECh. U2.38 - Prob. 5ECh. U2.38 - Prob. 6ECh. U2.38 - Prob. 7ECh. U2.39 - Prob. 1TAICh. U2.39 - Prob. 1ECh. U2.39 - Prob. 2ECh. U2.39 - Prob. 3ECh. U2.39 - Prob. 4ECh. U2.39 - Prob. 5ECh. U2.39 - Prob. 6ECh. U2.39 - Prob. 7ECh. U2.40 - Prob. 1TAICh. U2.40 - Prob. 1ECh. U2.40 - Prob. 2ECh. U2.40 - Prob. 3ECh. U2.40 - Prob. 4ECh. U2.40 - Prob. 5ECh. U2.41 - Prob. 1TAICh. U2.41 - Prob. 1ECh. U2.41 - Prob. 2ECh. U2.41 - Prob. 3ECh. U2.41 - Prob. 4ECh. U2.41 - Prob. 5ECh. U2.41 - Prob. 6ECh. U2.41 - Prob. 7ECh. U2.41 - Prob. 8ECh. U2.42 - Prob. 1TAICh. U2.42 - Prob. 1ECh. U2.42 - Prob. 2ECh. U2.42 - Prob. 4ECh. U2.42 - Prob. 5ECh. U2.42 - Prob. 6ECh. U2.43 - Prob. 1TAICh. U2.43 - Prob. 1ECh. U2.43 - Prob. 2ECh. U2.43 - Prob. 3ECh. U2.43 - Prob. 4ECh. U2.43 - Prob. 6ECh. U2.43 - Prob. 7ECh. U2.44 - Prob. 1TAICh. U2.44 - Prob. 1ECh. U2.44 - Prob. 2ECh. U2.44 - Prob. 3ECh. U2.44 - Prob. 4ECh. U2.44 - Prob. 5ECh. U2.44 - Prob. 6ECh. U2.44 - Prob. 7ECh. U2.44 - Prob. 8ECh. U2.44 - Prob. 9ECh. U2.45 - Prob. 1TAICh. U2.45 - Prob. 1ECh. U2.45 - Prob. 2ECh. U2.45 - Prob. 3ECh. U2.45 - Prob. 4ECh. U2.45 - Prob. 5ECh. U2.45 - Prob. 6ECh. U2.45 - Prob. 7ECh. U2.46 - Prob. 1TAICh. U2.46 - Prob. 1ECh. U2.46 - Prob. 2ECh. U2.46 - Prob. 3ECh. U2.46 - Prob. 4ECh. U2.46 - Prob. 5ECh. U2.46 - Prob. 6ECh. U2.46 - Prob. 7ECh. U2.46 - Prob. 8ECh. U2.46 - Prob. 9ECh. U2.47 - Prob. 1TAICh. U2.47 - Prob. 1ECh. U2.47 - Prob. 2ECh. U2.47 - Prob. 3ECh. U2.47 - Prob. 4ECh. U2.47 - Prob. 5ECh. U2.47 - Prob. 6ECh. U2.47 - Prob. 7ECh. U2.47 - Prob. 8ECh. U2.47 - Prob. 9ECh. U2.48 - Prob. 1TAICh. U2.48 - Prob. 1ECh. U2.48 - Prob. 2ECh. U2.48 - Prob. 3ECh. U2.48 - Prob. 4ECh. U2.48 - Prob. 6ECh. U2 - Prob. C6.1RECh. U2 - Prob. C6.2RECh. U2 - Prob. C6.3RECh. U2 - Prob. C6.4RECh. U2 - Prob. C6.5RECh. U2 - Prob. C7.1RECh. U2 - Prob. C7.2RECh. U2 - Prob. C7.3RECh. U2 - Prob. C7.4RECh. U2 - Prob. C7.5RECh. U2 - Prob. C8.1RECh. U2 - Prob. C8.2RECh. U2 - Prob. C8.3RECh. U2 - Prob. C8.4RECh. U2 - Prob. C8.5RECh. U2 - Prob. C8.6RECh. U2 - Prob. C9.1ECh. U2 - Prob. C9.2ECh. U2 - Prob. C9.3ECh. U2 - Prob. C9.4ECh. U2 - Prob. C9.5ECh. U2 - Prob. 1RECh. U2 - Prob. 2RECh. U2 - Prob. 3RECh. U2 - Prob. 4RECh. U2 - Prob. 5RECh. U2 - Prob. 6RECh. U2 - Prob. 7RECh. U2 - Prob. 8RECh. U2 - Prob. 1STPCh. U2 - Prob. 2STPCh. U2 - Prob. 3STPCh. U2 - Prob. 4STPCh. U2 - Prob. 5STPCh. U2 - Prob. 6STPCh. U2 - Prob. 7STPCh. U2 - Prob. 8STPCh. U2 - Prob. 9STPCh. U2 - Prob. 10STPCh. U2 - Prob. 11STPCh. U2 - Prob. 12STPCh. U2 - Prob. 13STPCh. U2 - Prob. 14STPCh. U2 - Prob. 15STPCh. U2 - Prob. 16STPCh. U2 - Prob. 17STPCh. U2 - Prob. 18STPCh. U2 - Prob. 19STPCh. U2 - Prob. 20STP
Additional Science Textbook Solutions
Find more solutions based on key concepts
15. A woman with severe discoloration of her tooth enamel has four children with a man who has normal tooth ena...
Genetic Analysis: An Integrated Approach (3rd Edition)
How Would the experiments result charge if oxygen (O2) were induced in the spark chamber?
Biology: Life on Earth with Physiology (11th Edition)
Why are the top predators in food chains most severely affected by pesticides such as DDT?
Campbell Essential Biology with Physiology (5th Edition)
Modified True/False 9. A giant bacterium that is large enough to be seen without a microscope is Selenomonas.
Microbiology with Diseases by Body System (5th 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)
1. Which is a function of the skeletal system? (a) support, (b) hematopoietic site, (c) storage, (d) providing ...
Anatomy & Physiology (6th 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
- Phenol is the starting material for the synthesis of 2,3,4,5,6-pentachlorophenol, known al-ternatively as pentachlorophenol, or more simply as penta. At one time, penta was widely used as a wood preservative for decks, siding, and outdoor wood furniture. Draw the structural formula for pentachlorophenol and describe its synthesis from phenol.arrow_forward12 Mass Spectrometry (d) This unknown contains oxygen, but it does not show any significant infrared absorption peaks above 3000 cm . 59 100- BO 40 Relative Abundance M(102) - 15 20 25 30 35 40 45 50 5 60 65 70 75 80 85 90 95 100 105 mizarrow_forwardDraw a Haworth projection of a common cyclic form of this monosaccharide: H HO H HO H HO H H -OH CH2OH Click and drag to start drawing a structure. Х : Darrow_forward
- : Draw the structure of valylasparagine, a dipeptide made from valine and asparagine, as it would appear at physiological pH. Click and drag to start drawing a structure. P Darrow_forwardDraw the Haworth projection of α-L-mannose. You will find helpful information in the ALEKS Data resource. Click and drag to start drawing a structure. : ཊི Х Darrow_forwardDraw the structure of serine at pH 6.8. Click and drag to start drawing a structure. : d كarrow_forward
- Take a look at this molecule, and then answer the questions in the table below it. CH2OH H H H OH OH OH CH2OH H H H H OH H H OH H OH Is this a reducing sugar? yes α β ロ→ロ no ☑ yes Does this molecule contain a glycosidic bond? If you said this molecule does contain a glycosidic bond, write the symbol describing it. O no 0+0 If you said this molecule does contain a glycosidic bond, write the common names (including anomer and enantiomer labels) of the molecules that would be released if that bond were hydrolyzed. If there's more than one molecule, separate each name with a comma. ☐arrow_forwardAnswer the questions in the table below about this molecule: H₂N-CH₂ -C—NH–CH–C—NH–CH—COO- CH3 CH CH3 What kind of molecule is this? 0= CH2 C If you said the molecule is a peptide, write a description of it using 3-letter codes separated ☐ by dashes. polysaccharide peptide amino acid phospolipid none of the above Хarrow_forwardDraw a Haworth projection of a common cyclic form of this monosaccharide: CH₂OH C=O HO H H -OH H OH CH₂OH Click and drag to start drawing a structure. : ☐ Х S '☐arrow_forward
- Nucleophilic Aromatic Substitution 22.30 Predict all possible products formed from the following nucleophilic substitution reactions. (a) (b) 9 1. NaOH 2. HCI, H₂O CI NH₁(!) +NaNH, -33°C 1. NaOH 2. HCl, H₂Oarrow_forwardSyntheses 22.35 Show how to convert toluene to these compounds. (a) -CH,Br (b) Br- -CH3 22.36 Show how to prepare each compound from 1-phenyl-1-propanone. 1-Phenyl-1-propanone ہتی. Br. (b) Br (racemic) 22.37 Show how to convert ethyl benzene to (a) 2,5-dichlorobenzoic acid and (b) 2,4-dichlorobenzoic acid. 22.38 Show reagents and conditions to bring about the following conversions. (a) 9 NH2 8 CO₂H NH2 CO₂Et (d) NO2 NH2 S NH₂ NO2 CHS CHarrow_forwardive the major organic product(s) of each of the following reactions or sequences of reactions. Show all rant stereochemistry. [10 only] A. B. NaN3 1. LiAlH4, ether Br 2. H₂O CH3 HNO3 H₂/Pt H₂SO ethanol C. 0 0 CH3CC1 NaOH NHCCH AICI H₂O . NH₂ CH3CH2 N CH2CH3 + HCI CH₂CH 3 1. LIAIH, THE 2. H₂Oarrow_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
Solutions: Crash Course Chemistry #27; Author: Crash Course;https://www.youtube.com/watch?v=9h2f1Bjr0p4;License: Standard YouTube License, CC-BY