Thank you for your help! Question 9 (6 points) Seved Acetanilide: Match the peaks to the...
Question 8 (5 points) Saved Acetanilide: Match the peaks to the appropriate number on the structure. A letter may correspond to more than one number. SH 11 10 1. 1
4. and 5. A compound with the molecular formula C:0H12O; displays the following 'Hand SC NMR data. Propose a structure for this compound and label the peaks in the NMR spectra as to how they correspond to your structure. integration 3 multiplicity - triplet integrations Integration 2 multiplicity Quartet each of these peaks has integration : 2 múltiplicity'- triplet s 2 peaks at 128 ppm TTTTTTTT 200 180 160 140 120 CD-10-063 80 60 40 20 0 100 Apm
1. Match the structure of each of these C2H/6 isomers to the proper '3C NMR spectrum (all students). A. 2-ethylhex-1-ene B. 3,3-dimethylhex-1-ene C. trans-oct-4-ene D. cis-1,2-dimethylcyclohexane E. 2,4,4-trimethylpent-1-ene 200 180 160 140 120 100 80 60 40 20 0 200 180 160 140 120 100 80 60 40 20 0 200 180 160 140 120 100 80 60 40 20 0 200 180 160 140 120 100 80 60 40 20 0 200 180 160 140 120 100 80 60...
Can you help to figure out the formula and the structure ? 50) 4. Determine the structure of the molecule from these spectra, and draw your answer in the box. 100 80 40 20 4000 2000- 3000 1500 1000 400 100 -[ 196 80 196 40 20 200 20 40 60 80 100 120 140 160 180 200 3H,t 2H,m 2H,t 2H,m 3 2 peaks 20 80 100 120 140 160 180 200 3H,t 2H,d 2H,d 2H,m 2H,t 2H,m 8...
step1 illustrate the structure and name the compund step 2 explain notes that help indfity the structure step 3 for CNMR count the number of carbon atoms and identity characteristic peaks. step 4 for HNMR count the number if carbon atoms and indentity characteristics peaks. explain the separation patterns. step 5 for IR indentity characteristic peaks. 200 180 160 140 120 100 80 60 40 20 11 10 98 76543 2 1 0 ppm 100 6o 40 20 10 15...
Determine the structure of the assigned acyl chloride. Find molecular formula, lable peaks and stuctures. Acyl Chloride #1 d-1.303 g/mL 100004-025 M+ 160 80 60 40 M+2 162 20 20 40 60 8100 120 140 160 180 200 m/z Hint: aromatic ring is a thiophene 11 10 5 432 ppm All singlets (6 total signals) Three peaks 200 180 160 140 120 100 60 420 CDS-05-174
step 1 illustrate the structure and name the compound step 2 explain notes that help identify the structure step 3 for CNMR count the number of carbons atoms and identify characterics peaks step 4 for HNMR count the number of carbons atoms and idenitfy characterics peaks Step 5 for IR identify the characterics peaks 200 180 160 40 120 100 40 20 o ppn 11 109 ppm 80 Poren 60 40 C-tH 20 125 50 75 100 25 m/z 200...
You are provided with the molecular formula for each compound. calculate the unsaturation index for each problem. -u2C+2+N-X-H For IR, determine the functional groups present and annotate the absorbances that confirm the functional group (including finger print region absorbances). 2 . For 1H NMR, label each signal (a, b, c,.... starting from the right (0.0 PPM). Draw the structure of the compound in the spectra and annotate. 13C NMR spectra is provided for information. Annotation of the 13C NMR is...
Spectroscopy of C5H10O 1. Correctly label 2 peaks in the IR spectrum with the appropriate functional group. 2. Correctly label 1 peak in the 13C NMR spectrum. 3. Draw some possible structures (isomers) as you analyze the 'H NMR spectrum. 4. Draw your final choice of structure to match the IR. 13C NMR, and H NMR 5. Label the different types of hydrogens on your structure as a, b, c, etc. Label the peaks in the 'H NMR spectrum with...
13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral data. 160 140 120 80 60 40 20 0 200 180 CDS-00-748 100 ppm 2. Propose a structure for the compound CaH;Br, with the following C NMR spectral data. 200 180 160 140 120 80 60 40 100 ppm 20 0 3. Propose a structure for the compound C H2O2, with the following "'C NMR spectral data. 200 180 160 140 120 30600 T...