2. READ THE DIRECTIONS TO EACH QUESTION CAREFULLY - not following the directions means you get the question wrong!3. FORMAT YOUR ANSWERS AS DIRECTED - formatting your answers incorrect means you get the question wrong!4. Below are the IR regions and NMR chemical shifts table for use with the spectroscopy problems:¹H NMR12 11 10 9RO=COH RO=CHCO87ppm6OHH C=C-H5NHH-C-XH-C-O-OHX = F, Cl, Br(i.e. electronegative atom)3-NH-2H-C-NH-C-SC=C-HH-C-C=CHC1H-C-C=O-CH-CH3-CH₂-04000IDsmall rangerange of valuesbroad peak=C-HN-H3250-3300broad with spikes-33003500-O-Hbroad-3300-3400-0-H CENN-HHH2730-2820-C-HusuallyCOCO strong=CH3000- 2 peaks3100 I2850-2960HO<-C-O-Hbroad-30003000-CEN↓2200-CICHB22002500wavenumber, cm-12000HCCCNH1600-166016800000000OR173017101600NR₂165015001000 Match a structure with the correct IR spectrum. You will, of course, notice that there are more structures than spectra, sosome structures are not represented. Simply fill in the blank with the product number (i.e. 1, 2, 3, etc.).Transmitance1.00.80.60.40.20.0100Transmittance %T100Transmittance %T80A04000E40003500300030009000LOHProduct 1Product 4www.250020002000wavenumber cm-120001500Wavenumbers (cm-1)wavenumber cm-11500OHProduct 2Product 5vy1500VM1000amm10001000HO.500500Product 6500Product 3OHPart a Answer:Part b Answer:Part c Answer:

here we are required to find the IR spectra which matches correctly with the given compound

Match a structure with the correct IR spectrum. You will, of course, notice that there are more structures than spectra, so some structures are not represented. Simply fill in the blank with the product number (i.e. 1, 2, 3, etc.). 0.8 100 sur A 4000 E 3500 3000 Product 1 Product 4 2500 2000 OH 2000 vavenumber cm 1 2000 1500 Wavenumbers (cm-1) wavenumber cm'l {1}1 1500 Product 2 Product 5 M 1500 1000 1000 1000 HO Product 6 m 500 500 Product 3 100 OH Part a Answer: Part b Answer: Part c Answer:

Match a structure with the correct IR spectrum. You will, of course, notice that there are more structures than spectra, so some structures are not represented. Simply fill in the blank with the product number (i.e. 1, 2, 3, etc.). 0.8 100 sur A 4000 E 3500 3000 Product 1 Product 4 2500 2000 OH 2000 vavenumber cm 1 2000 1500 Wavenumbers (cm-1) wavenumber cm'l {1}1 1500 Product 2 Product 5 M 1500 1000 1000 1000 HO Product 6 m 500 500 Product 3 100 OH Part a Answer: Part b Answer: Part c Answer:

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

What are the structures? Please help
Use the drop-down selection boxes to rank the IR absorptions of the coloured bonds in terms of decreasing wavenumbers, from highest to lowest. C H. CEN b H CH₂ -CECIH
Molecular Formula: C₁1H15O₂N ¹H spectrum 160 2H, d J = 7.5 Hz 13C spectrum 140 2H, d J = 7.5 Hz 120 100 5 PPM 80 PPM 60 1H, quintet J = 7 Hz 3 1 6H. triplet J = 7 Hz 4H, quintet J = 7 Hz 40 20
ADUDULCE The following MS spectrum is for a compound which contains one oxygen atom (as well as C and H, of course, but no other atoms). Propose a structure which is consistent with this MS; also identify the species responsible for each peak whose numerical m/z is given (remember resonance!). d a n с e dp 100 80 60 40 20 0 0 20 31 40 60 m/z 77 80 91 % (M+1) /M = 7.93 100 107 108 120
Which of the following will show exactly two peaks in its normal broadband proton decoupled 13C NMR?
Give detailed Solution with explanation needed...don't give Handwritten answer. don't copy answer anywhere. Don't use Ai for answering this
Which C-H bonds are responsible for the following peaks/signals? C6H1202 s are Peak A = Peak B= Peak C= Enter 12 if a H is not labeled that created the peak/signal. this peak disappears with the addition of D20 By PPM
Which molecule matches this mass spectrum
Figures below give a molecular formula, an infrared spectrum,and a 1H NMR spectrum for an unknown compound.What is the structure of the compound? Explain briefly.
Identify likely groups and identify likely signals on the IR. (ex. OH, NH, C=C, C-H sp3, aromatic etc)
Determine the structures of these spectrums (each has an unsaturation of 5)
Typo: The chemical formula is missing an oxygen. It should read as: C10H1202. Choose the correct structure of the compound with the following data. Formula: C10H120 100 - 50 4000 3000 2000 1500 1000 500 Wavenumber (3) (2) (5) múltiplet (2) 9 8 6 4 PPM II Ph - C-о-сH,CH-CH3 || Ph-c-CH2 -0-CH2CH3 || Ph -C- CH2CH2-0- CH3 A) B) Structure A O Structure B Structure C O=U O=U O=U Transmittance