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 C8.3RE
(a)
Interpretation Introduction
Interpretation :
Structural formula of HCl must be drawn along with partial positive charge and partial negative charge on each atom. Whether HCl is polar or not must also be explained.
Concept Introduction :
Structural formula of a molecule represents the arrangement of atoms.
A molecule is polar if the resultant of all bond moments is non-zero.
A bond with two atoms having different electronegativity exists as a dipole.
(a)
Expert Solution
Answer to Problem C8.3RE
Structural formula of HCl is drawn below.
Explanation of Solution
Cl is more electronegative as compared to hydrogen atom. Thus there is partial positive and partial negative charge on H and Cl atom respectively. The bond moment of HCl is not cancelled due to linear shape of the molecule and thus the molecule is polar.
b)
Interpretation Introduction
Interpretation :
Structural formula of CH4 must be drawn along with partial positive charge and partial negative charge on each atom. Whether CH4 is polar or not must also be explained.
Concept Introduction :
Structural formula of a molecule represents the arrangement of atoms.
A molecule is polar if the resultant of all bond moments is non-zero.
A bond with two atoms having different electronegativity will have bond moment.
b)
Expert Solution
Answer to Problem C8.3RE
Structural formula of CH4 is drawn below.
Explanation of Solution
C is more electronegative as compared to hydrogen atom. Thus there is partial positive and partial negative charge on H and C atom respectively. The four bond moments of CH4 are cancelled due to tetrahedral shape of CH4 methane and thus the molecule is non-polar.
c)
Interpretation Introduction
Interpretation :
Structural formula of H2O must be drawn along with partial positive charge and partial negative charge on each atom. Whether H2O is polar or not must also be explained.
Concept Introduction :
Structural formula of a molecule represents the arrangement of atoms.
A molecule is polar if the resultant of all bond moments is non-zero.
A bond with two atoms having different electronegativity will have bond moment.
c)
Expert Solution
Answer to Problem C8.3RE
Structural formula of H2O is drawn below.
Explanation of Solution
O is more electronegative as compared to hydrogen atom. Thus there is partial positive and partial negative charge on H and O atom respectively. The two bond moments of H2O are not cancelled due to angular shape of H2O molecule and thus the molecule is polar.
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
Which culture produces the most lactic acid? Use the following choices to answer questions. a. E. coli growing ...
Microbiology: An Introduction
Why is petroleum jelly used in the hanging-drop procedure?
Laboratory Experiments in Microbiology (12th Edition) (What's New in Microbiology)
Compare the roles of CO2 and H2O in cellular respiration and photosynthesis.
Campbell Biology (11th Edition)
Why are the top predators in food chains most severely affected by pesticides such as DDT?
Campbell Essential Biology (7th Edition)
16. Explain some of the reasons why the human species has been able to expand in number and distribution to a g...
Campbell Biology: Concepts & Connections (9th Edition)
Community 1 contains 100 individuals distributed among four species: 5A, 5B, 85C, and 5D Community 2 contains 1...
Campbell Biology in Focus (2nd 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
- Answer F pleasearrow_forward4. Refer to the data below to answer the following questions: The octapeptide saralasin is a specific antagonist of angiotensin II. A derivative of saralasin is used therapeutically as an antihypertensive. Amino acid analysis of saralasin show the presence of the following amino acids: Ala, Arg, His, Pro, Sar, Tyr, Val, Val A.Sar is the abbreviation for sarcosine, N-methyl aminoethanoic acid. Draw the structure of sarcosine. B. N-Terminal analysis by the Edman method shows saralasin contains sarcosine at the N-terminus. Partial hydrolysis of saralasin with dilute hydrochloric acid yields the following fragments: Tyr-Val-His Sar-Arg-Val His-Pro-Ala Val-Tyr-Val Arg-Val-Tyr What is the structure of saralasin?arrow_forwardWhat is the structure of the DNA backbone?arrow_forward
- PLEASE PLEASE PLEASE use hand drawn structures when possarrow_forward. M 1- MATCH each of the following terms to a structure from the list below. There is only one correct structure for each term and structures may be used more than once. Place the letter of the structure in the blank to the left of the corresponding term. A. Sanger dideoxy method C. Watson-Crick B. GAUCGUAAA D. translation E. HOH2C OH OH G. transcription I. AUGGCUGAG 0 K. OPOH2C 0- OH N- H NH2 F. -OPOH2C 0- OH OH H. Maxam-Gilbert method J. replication N L. HOH2C a. b. C. d. e. f. g. B M. AGATCGCTC a pyrimidine nucleoside RNA base sequence with guanine at the 3' end. DNA base sequence with cytosine at the 3' end. a purine nucleoside DNA sequencing method for the human genome 2'-deoxyadenosine 5'-phosphate process by which mRNA directs protein synthesis OH NH2arrow_forwardPlease use hand drawn structures when neededarrow_forward
- B. Classify the following amino acid. Atoms other than carbon and hydrogen are labeled. a. acidic b. basic C. neutral C. Consider the following image. Which level of protein structure is shown here? a. primary b. secondary c. tertiary d. quaternary D. Consider the following image. H RH H HR H R HR HR RH Which level of protein structure is shown in the box? a. primary b. secondary R c. tertiary d. quaternary コー Rarrow_forwardBriefly answer three from the followings: a. What are the four structures of the protein? b. Why is the side chain (R) attached to the alpha carbon in the amino acids is important for the function? c. What are the types of amino acids? And how is it depend on the (R) structure? d. Write a reaction to prepare an amino acid. prodarrow_forwardAnswe Answer A and B pleasearrow_forward
- 3. Refer to the data below to answer the following questions: Isoelectric point Amino Acid Arginine 10.76 Glutamic Acid 3.22 Tryptophan 5.89 A. Define isoelectric point. B. The most basic amino acid is C. The most acidic amino acid is sidizo zoarrow_forward3. A gas mixture contains 50 mol% H2 and 50 mol% He. 1.00-L samples of this gas mixture are mixed with variable volumes of O2 (at 0 °C and 1 atm). A spark is introduced to allow the mixture to undergo complete combustion. The final volume is measured at 0 °C and 1 atm. Which graph best depicts the final volume as a function of the volume of added O2? (A) 2.00 1.75 Final Volume, L 1.50 1.25 1.00 0.75 0.50 0.25 0.00 0.00 0.25 0.50 2.00 (B) 1.75 1.50 Final Volume, L 1.25 1.00 0.75 0.50- 0.25 0.00 0.75 1.00 0.00 0.25 Volume O₂ added, L 2 0.50 0.75 1.00 Volume O₂ added, L 2 2.00 2.00 (C) (D) 1.75 1.75 1.50 1.50 Final Volume, L 1.25 1.00 0.75 0.50 Final Volume, L 1.25 1.00 0.75 0.50 0.25 0.25 0.00 0.00 0.00 0.25 0.50 0.75 1.00 0.00 0.25 Volume O₂ added, L 0.50 0.75 1.00 Volume O₂ added, L 2arrow_forwardLeucine is an essential amino acid with the systematic name 2-amino-3-methylpentanoic acid. It has pai 2.36 and pKa2 = 9.60. H2N-C(R)H-COOH and R is -CH2-CH(CH3)2 A. Draw the condensed structure for leucine, and label all chirality centers with an asterisk. B. How many possible stereoisomers of leucine are there? C. Draw a Fischer projection of L-leucine and label the chirality center(s) as R or S. D. What is the p/ of leucine? E. Draw the structure of the predominant form of leucine at 10.00. F. Draw the structure of the predominant form of leucine at pH = 1.50. G. Leucine is described as an essential amino acid. What does this mean? H. Show the alkyl halide you would use to prepare leucine by the amidomalonate method. =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
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License