Can I get a table for the 1H-NMR with a labeled diagram of chemical shift , multiplet structure, integration, assignmentbased on the 1H-NMR data below Spectra (Infrared in KBr, 'H-NMR in DMSO-d6, 400 MHz)LODD4000300020001500000T500HAVENUMB ERI -||3088662667701438661142a179374D69115935030545714114911258474512297355131819105239712Б4OH28086716716B1200671046476867928256014806212684195679648642885147564117379916585607026636214466611618481678480B6CITRANSMETTANCEIX! 141210642HSP-41-134ppmChemical ShiftIntegrationMultiplet13.431S7.811d7.561d7.5517.451t00

Answered: Image /qna-images/answer/3aae469e-f28a-4486-8ae2-fb303fe7a5ad.jpg

Spectra (Infrared in KBr, 'H-NMR in DMSO-d6, 400 MHz) LOD D 4000 3000 2000 1500 1000 500 HAVENUMB ERI -l 3088 66 2667 70 1438 66 1142 81 793 74 3054 57 1411 49 1125 84 745 12 Þ691 2973 55 1593 50 1318 19 1052 39 712 Б4 C- OH 2008 2825 67 1671 6B 1200 67 1046 47 606 79 60 1480 62 1268 41 956 79 648 64 2885 2663 88 1475 64 1173 79 916 58 560 70 62 1446 66 1161 84 816 70 480 86 CI TRANSMITTANCEI

Spectra (Infrared in KBr, 'H-NMR in DMSO-d6, 400 MHz) LOD D 4000 3000 2000 1500 1000 500 HAVENUMB ERI -l 3088 66 2667 70 1438 66 1142 81 793 74 3054 57 1411 49 1125 84 745 12 Þ691 2973 55 1593 50 1318 19 1052 39 712 Б4 C- OH 2008 2825 67 1671 6B 1200 67 1046 47 606 79 60 1480 62 1268 41 956 79 648 64 2885 2663 88 1475 64 1173 79 916 58 560 70 62 1446 66 1161 84 816 70 480 86 CI TRANSMITTANCEI

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working
THIS CAN NOT BE HAND - DRAWN Illustrate using a computer program the molecule from the molecular formula and interpret each of the following 1H NMR spectra. The integration for each peak is given above the peak. All spectra were taken from http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/direct_frame_top.cgi.
predict the shift for the carbon indicated by the arrows please. USE NMR SPECTRUM TABLE please.
FOR EACH SPECTRUM BELOW, • IDENTIFY (ASSIGN) THE MOLECULAR ION PEAK AND THE MOLECULAR WT OF THE COMPOUND. ( KEEP IN MIND THAT SOMETIMES THE MOLECULAR ION MAY NOT BE PRESENT, ESPECIALLY FOR LARGE AND BRANCHED CHAIN MOLECULES WITH NO RINGS SINCE THEY CAN FORM STABLE CATION FRAGMENTS) • IDENTIFY THE BASE PEAK AND DRAW STRUCTURE FOR IT ( ASSIGNING THE PEAKS).) • ASSIGN STRUCTURES FOR OTHER PROMINENT FRAGMENTS IF POSSIBLE • BASED ON THIS, SUGGEST A STRUCTURE FOR THE COMPOUND THAT IS CONSISTENT WITH THE DEGREE OF UNSATURATION OF THE COMPOUND INDICATE THE BONDS THAT FRAGMENT, RESULTING IN THE OBSERVED MASS SPECTRAL FRAGMENTS
FOR EACH SPECTRUM BELOW, • IDENTIFY (ASSIGN) THE MOLECULAR ION PEAK AND THE MOLECULAR WT OF THE COMPOUND. ( KEEP IN MIND THAT SOMETIMES THE MOLECULAR ION MAY NOT BE PRESENT, ESPECIALLY FOR LARGE AND BRANCHED CHAIN MOLECULES WITH NO RINGS SINCE THEY CAN FORM STABLE CATION FRAGMENTS) • IDENTIFY THE BASE PEAK AND DRAW STRUCTURE FOR IT ( ASSIGNING THE PEAKS).) • ASSIGN STRUCTURES FOR OTHER PROMINENT FRAGMENTS IF POSSIBLE • BASED ON THIS, SUGGEST A STRUCTURE FOR THE COMPOUND THAT IS CONSISTENT WITH THE DEGREE OF UNSATURATION OF THE COMPOUND INDICATE THE BONDS THAT FRAGMENT, RESULTING IN THE OBSERVED MASS SPECTRAL FRAGMENTS
Please help, am using old tests to study for MCAT and i need help with this question! Which compounds (from the picture attached) corresponds to the 4H NMR in the image attached. Annotate the spectra with any and all relevant signals that demonstrate the relationship and support your answer choice.Explain the meaning behind your annotations and how they correspond to the structure you choose. thanks in advance
Do not give handwriting solution.
A.) How many signals are seen for the CNMR spectrum of the unknowns C6H14O? B.) Explain the chemical shifts of the signals seen based upon the location of the carbons that are relative to deshielding group if any are seen in the compound (unknown is C6H14O)? For question A. I believe it is 4 signals. For question B. I know that none of the signals are in the deshielding are of the chart but are all located in the shielded region but i am unsure of how to determine the chemical shifts of the given signal. If possible an in-depth explanation would be greatly appreciated in order to understand this better.
Identify all proton environments and predict the chemical shift, multiplicity, coupling constants, observed integration, and number of hydrogens for each environment.
1.11