In the given IR spectrum, a strong peak observed in 3200- 3400 cm-1 clearly indicates that the given compound is alcohol. All other peaks are absent like for -NH2 ( 3100 3500 cm-1 medium peak), double bond peak ( 1600-1680cm-1 ), carbonyl peak ( 1715-1750 cm-1 ). So option-3 is correct.
Question 16 2 pts Which of the following compounds corresponds to the IR spectrum shown here?...
Analyze the FTIR Spectrum for the following FTIR Spectrum for starting material: 2-chloro-2-methyl-propane BP: FTIR Common Name: IUPAC Name: MP: MICRONS 2,2 2,3 24 25 26 27 28 29 3 3,5 4 45 5 5,5 7 8 9 10 11 12 13 100 14_15 16 17 18 19 21 22 200 7 05 90 % 80 7 10.1 T 70 A N 80 0.28 50 03 40 -0.44 N30 c E 20 -0.5 0.6 -07 E08 F1.0 10 4500 4400...
5. One of the following compounds is responsible for the IR spectrum shown. Label the peaks and choose the structure of the responsible compound. 1 TT NoC=0 ou C=0 O-H rsp. c-H Heath Hon da aroa 3,5 4 45 Wavelength (mm) 5 55 6 7 8 9 10 11 12 13 14 15 16 3500 MOO 2500 2000 1800 1800 wavenumber icm) 1400 1200 1000
Can someone help me analyze the important peaks? The molecule is 2-bromocyclohexanone Common Name: BP: FTIR IUPAC Name: MP: 22 23 24 25 2.6 2.7 2.8 2.93 100 3.5 4.5 5.5 MICRONS G 10 11 12 13 14 15 16 17 18 19 21 23 25 90 4.05 % 80 -0.1 70 IN -0.28 BO 50 MOZ-uz- 40 S O -0.3 R B -0.4 C -0.5 -0.6 -0.7 F0.8 1.0 30 20 10 0 4500 4400 4200 4000 3800 3600...
(6 pts)9a. Which of the following compounds is consistent with the following IR spectrum? Clearly show your work to support your choice. Include all signals that discussed in lecture videos. کے NH NHCH NH NH NICHE CH Lo "CHO II IN IV CH, b. Which of the following compounds is consistent with the following IR spectrum? Clearly show your work to support your choice. Include all signals that discussed in lecture videos. m هه wavenumber OH = لہ 'H ځ...
Analyze the IR and HNMR for 4-Hydroxy-4-phenyl-butan-2-one BP: FTIR Common Name: 4-Hydroxy-4-phenyl-butan-2-one JUPAC Name: MP: MICRONS 2,2 2,3 2,4 2,5 2,6 2,7 2,02.03 3.5 5,5 G 7 8 9 10 11 12 13 14 15 16 17 18 19 21 23 25 100 LILL+0.0 90 4.05 * 80 -0.1 A 70 80 * Z0-EECZOW M 50 40 -0.2 S 0 -0.3 R B A -0.4N C -0.6 E -0.6 -0.7 F0.8 +1.0 N 30 E 20 10 d 4500 4400...
synthesize of 3,3-dimethyl-1,2-epoxybutan Identify the relevant peaks in the FTIR spectrum and record the position and associated functional group for each in the FTIR table below: Identify all of the peaks in the NMR spectrum and record the chemical shift, the splitting, and the number of hydrogens for each peak in the NMR table below: Do the FTIR and NMR spectra you measured and recorded in the tables above confirm that you synthesized the assigned target compound? Explain BP: FTIR...