Chemistry 2012 Student Edition (hard Cover) Grade 11
12th Edition
ISBN: 9780132525763
Author: Prentice Hall
Publisher: Prentice Hall
expand_more
expand_more
format_list_bulleted
Question
Chapter 24.3, Problem 19LC
Interpretation Introduction
Interpretation: The
Concept introduction: Peptide bonds are referred to as amide bonds. Amide bonds are covalent
Expert Solution & Answer
Answer to Problem 19LC
In amide bonds, a carboxyl functional group and an amino group are bonded to one another.
Explanation of Solution
The formation of an amide bond or a peptide bond takes place when the amino group of one acid combines with the carboxyl group of another acid. A water molecule will be produced as a byproduct, and an amide bond will be formed.
Conclusion
In amide bonds, a carboxyl functional group and an amino group are bonded to one another.
Chapter 24 Solutions
Chemistry 2012 Student Edition (hard Cover) Grade 11
Ch. 24.1 - Prob. 1LCCh. 24.1 - Prob. 2LCCh. 24.1 - Prob. 3LCCh. 24.1 - Prob. 4LCCh. 24.1 - Prob. 5LCCh. 24.1 - Prob. 6LCCh. 24.1 - Prob. 7LCCh. 24.2 - Prob. 8LCCh. 24.2 - Prob. 9LCCh. 24.2 - Prob. 10LC
Ch. 24.2 - Prob. 11LCCh. 24.2 - Prob. 12LCCh. 24.2 - Prob. 13LCCh. 24.2 - Prob. 14LCCh. 24.2 - Prob. 15LCCh. 24.3 - Prob. 16LCCh. 24.3 - Prob. 17LCCh. 24.3 - Prob. 18LCCh. 24.3 - Prob. 19LCCh. 24.3 - Prob. 20LCCh. 24.3 - Prob. 21LCCh. 24.4 - Prob. 22LCCh. 24.4 - Prob. 23LCCh. 24.4 - Prob. 24LCCh. 24.4 - Prob. 25LCCh. 24.4 - Prob. 26LCCh. 24.4 - Prob. 27LCCh. 24.4 - Prob. 28LCCh. 24.5 - Prob. 29LCCh. 24.5 - Prob. 30LCCh. 24.5 - Prob. 31LCCh. 24.5 - Prob. 32LCCh. 24.5 - Prob. 33LCCh. 24.6 - Prob. 35LCCh. 24.6 - Prob. 36LCCh. 24.6 - Prob. 37LCCh. 24.6 - Prob. 38LCCh. 24.6 - Prob. 39LCCh. 24.6 - Prob. 40LCCh. 24 - Prob. 41ACh. 24 - Prob. 42ACh. 24 - Prob. 43ACh. 24 - Prob. 44ACh. 24 - Prob. 45ACh. 24 - Prob. 46ACh. 24 - Prob. 47ACh. 24 - Prob. 48ACh. 24 - Prob. 49ACh. 24 - Prob. 50ACh. 24 - Prob. 51ACh. 24 - Prob. 52ACh. 24 - Prob. 53ACh. 24 - Prob. 54ACh. 24 - Prob. 55ACh. 24 - Prob. 56ACh. 24 - Prob. 57ACh. 24 - Prob. 58ACh. 24 - Prob. 59ACh. 24 - Prob. 60ACh. 24 - Prob. 61ACh. 24 - Prob. 62ACh. 24 - Prob. 63ACh. 24 - Prob. 64ACh. 24 - Prob. 65ACh. 24 - Prob. 66ACh. 24 - Prob. 67ACh. 24 - Prob. 68ACh. 24 - Prob. 69ACh. 24 - Prob. 70ACh. 24 - Prob. 71ACh. 24 - Prob. 72ACh. 24 - Prob. 73ACh. 24 - Prob. 74ACh. 24 - Prob. 75ACh. 24 - Prob. 76ACh. 24 - Prob. 77ACh. 24 - Prob. 78ACh. 24 - Prob. 79ACh. 24 - Prob. 80ACh. 24 - Prob. 81ACh. 24 - Prob. 82ACh. 24 - Prob. 83ACh. 24 - Prob. 84ACh. 24 - Prob. 85ACh. 24 - Prob. 86ACh. 24 - Prob. 87ACh. 24 - Prob. 88ACh. 24 - Prob. 89ACh. 24 - Prob. 90ACh. 24 - Prob. 91ACh. 24 - Prob. 92ACh. 24 - Prob. 93ACh. 24 - Prob. 94ACh. 24 - Prob. 95ACh. 24 - Prob. 96ACh. 24 - Prob. 97ACh. 24 - Prob. 98ACh. 24 - Prob. 99ACh. 24 - Prob. 100ACh. 24 - Prob. 101ACh. 24 - Prob. 102ACh. 24 - Prob. 103ACh. 24 - Prob. 104ACh. 24 - Prob. 105ACh. 24 - Prob. 106ACh. 24 - Prob. 107ACh. 24 - Prob. 108ACh. 24 - Prob. 109ACh. 24 - Prob. 110ACh. 24 - Prob. 111ACh. 24 - Prob. 112ACh. 24 - Prob. 113ACh. 24 - Prob. 115ACh. 24 - Prob. 116ACh. 24 - Prob. 117ACh. 24 - Prob. 118ACh. 24 - Prob. 119ACh. 24 - Prob. 120ACh. 24 - Prob. 121ACh. 24 - Prob. 122ACh. 24 - Prob. 123ACh. 24 - Prob. 124ACh. 24 - Prob. 125ACh. 24 - Prob. 126ACh. 24 - Prob. 127ACh. 24 - Prob. 128ACh. 24 - Prob. 129ACh. 24 - Prob. 130ACh. 24 - Prob. 131ACh. 24 - Prob. 132ACh. 24 - Prob. 133ACh. 24 - Prob. 1STPCh. 24 - Prob. 2STPCh. 24 - Prob. 3STPCh. 24 - Prob. 4STPCh. 24 - Prob. 5STPCh. 24 - Prob. 6STPCh. 24 - Prob. 7STPCh. 24 - Prob. 8STPCh. 24 - Prob. 9STPCh. 24 - Prob. 10STPCh. 24 - Prob. 11STPCh. 24 - Prob. 12STPCh. 24 - Prob. 13STPCh. 24 - 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 LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples 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 EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary 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