
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Question
Chapter 15.5, Problem 11CC
Interpretation Introduction
Interpretation:
The reason for the existence of one extra signal to the right of 3000
Concept Introduction:
IR spectral studies: It is a spectroscopic technique which is used to determine the
Wavenumber: It is defined as the number of waves in one centimeter. The wavenumber indicates the location of each signal with respect to the functional group in the molecule and its unit is
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
In the synthesis of benzotriazole, adding NaNO2 heats the solution. State the reason.
Indicate the products obtained by treating benzotriazole with dimethyl sulfate or methyl iodide in a basic medium.
Indicate some general procedures to obtain pyrazoles.
Chapter 15 Solutions
Organic Chemistry, Binder Ready Version
Ch. 15.3 - Prob. 1CCCh. 15.3 - Prob. 2CCCh. 15.3 - Prob. 3CCCh. 15.3 - Prob. 4CCCh. 15.4 - Prob. 5CCCh. 15.4 - Prob. 6CCCh. 15.4 - Prob. 7CCCh. 15.5 - Prob. 8CCCh. 15.5 - Prob. 9CCCh. 15.5 - Prob. 10CC
Ch. 15.5 - Prob. 11CCCh. 15.6 - Prob. 1LTSCh. 15.6 - Prob. 12PTSCh. 15.6 - Prob. 13ATSCh. 15.7 - Prob. 2LTSCh. 15.7 - Prob. 14PTSCh. 15.7 - Prob. 15ATSCh. 15.7 - Prob. 16ATSCh. 15.7 - Prob. 17ATSCh. 15.7 - Prob. 18ATSCh. 15.9 - Prob. 19CCCh. 15.9 - Prob. 20CCCh. 15.10 - Prob. 3LTSCh. 15.10 - Prob. 21PTSCh. 15.10 - Prob. 22ATSCh. 15.11 - Prob. 23CCCh. 15.11 - Prob. 24CCCh. 15.12 - Prob. 25CCCh. 15.12 - Prob. 26CCCh. 15.12 - Prob. 27CCCh. 15.12 - Prob. 28CCCh. 15.13 - Prob. 29CCCh. 15.13 - Prob. 30CCCh. 15.16 - Prob. 4LTSCh. 15.16 - Prob. 31PTSCh. 15.16 - Prob. 32PTSCh. 15.16 - Prob. 33ATSCh. 15.16 - Prob. 34ATSCh. 15.16 - Prob. 35ATSCh. 15.16 - Prob. 36ATSCh. 15.16 - Prob. 37ATSCh. 15 - Prob. 38PPCh. 15 - Prob. 39PPCh. 15 - Prob. 40PPCh. 15 - Prob. 41PPCh. 15 - Prob. 42PPCh. 15 - Prob. 43PPCh. 15 - Prob. 44PPCh. 15 - Prob. 45PPCh. 15 - Prob. 46PPCh. 15 - Prob. 47PPCh. 15 - Prob. 48PPCh. 15 - Prob. 49PPCh. 15 - Prob. 50PPCh. 15 - Prob. 51PPCh. 15 - Prob. 52PPCh. 15 - Prob. 53PPCh. 15 - Prob. 54PPCh. 15 - Prob. 55PPCh. 15 - Prob. 56PPCh. 15 - Prob. 57PPCh. 15 - Prob. 58PPCh. 15 - Prob. 59PPCh. 15 - Prob. 60PPCh. 15 - Prob. 61IPCh. 15 - Prob. 62IPCh. 15 - Prob. 63IPCh. 15 - Prob. 64IPCh. 15 - Prob. 65IPCh. 15 - Prob. 66IPCh. 15 - Prob. 67IPCh. 15 - Prob. 68IPCh. 15 - Prob. 69IP
Knowledge Booster
Similar questions
- Indicate the differences between the spectra of 1-methyl-benzimidazole and benzimidazole.arrow_forwardProvide reasons as to why appropriate sampling is important in relation to food?arrow_forwardWhat is the significance of selecting a "representative" sample for chemical analysis, and how does this practice ensure accurate and reliable results with respect to chemical analyses?arrow_forward
- Identify and provide an explanation of the differences between homogeneous and heterogeneous sampling in the context of sampling methods.arrow_forwardГ C-RSA CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0.0 b.092 0.797 1.088 1.813 C-RSA CHROMATOPAC CH=1 Report No. =13 ** CALCULATION REPORT ** DATA=1: @CHRM1.000 11/03/05 08:09:52 CH PKNO TIME 1 2 0.797 3 1.088 4 1.813 AREA 1508566 4625442 2180060 HEIGHT 207739 701206 V 287554 V MK IDNO CONC NAME 18.1447 55.6339 26.2213 TOTAL 8314067 1196500 100 C-R8A CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0. 0 087 337. 0.841 1.150 C-R8A CHROMATOPAC CH=1 Report No. =14 DATA=1: @CHRM1.000 11/03/05 08:12:40 ** CALCULATION REPORT ** CH PKNO TIME AREA 1 3 0.841 1099933 41.15 4039778 HEIGHT MK IDNO 170372 649997¯¯¯ CONC NAME 21.4007 78.5993 TOTAL 5139711 820369 100 3 C-R8A CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0.100 0:652 5.856 3 1.165 C-RSA CHROMATOPAC CH-1 Report No. =15 DATA=1: @CHRM1.000 11/03/05 08:15:26 ** CALCULATION REPORT ** CH PKNO TIME AREA HEIGHT MK IDNO CONC NAME 1 3 3 0.856 4 1.165 TOTAL 1253386 4838738 175481 708024 V 20.5739 79.4261 6092124…arrow_forwardDraw the product of the reaction shown below. Ignore small byproducts that would evaporate please.arrow_forward
- Relative Abundance 20- Problems 501 (b) The infrared spectrum has a medium-intensity peak at about 1650 cm. There is also a C-H out-of-plane bending peak near 880 cm. 100- 80- 56 41 69 M(84) LL 15 20 25 30 35 55 60 65 70 75 80 85 90 m/zarrow_forwardPolyethylene furanoate is a polymer made from plant-based sources; it is used for packaging. Identify the monomer(s) used in the production of this polymer using a condensation process.arrow_forwardPhenol 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_forward
- 12 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_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