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MW is 98
1HNMR: 1.7 quintet, 1.8 quintet, 2.3 triplet
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- An antihistamine shows sharp peaks at Raman shifts of v 488, 725,875, 925, and 1350 cm-1. At what wavelengths in nanometers would the Stokes and anti-Stokes lines for the antihistamine appear if the source were (a) a helium-neon Laser (632.8 nm)? (b) an argon-ion laser (488.0 nm)?Myriam 1718 1. 4000 3000 1600 1200 800 V (cm¹) 100 Mass Spectrum 43 119 80 60 JIK M+* 40 176 20 161 C12 H16 O 40 80 200 280 120 160 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) expansion 188 IR Spectrum (liquid film) % of base peak DEPT CH₂ CH₂ CH proton decoupled L 200 ¹H NMR Spectrum (200 MHz, CDCI, solution) J 1 9 10 I 8 2000 160 the 1 7 6 240 120 130 130 125 ppm 125 ppm L 5 expansion 1 80 1 4 solvent Problem 99 UV Spectrum max 262 nm (log₁0 € 2.5) solvent methanol 40 t I 3 1 2 4 08 (ppm) TMS 1 0 8 (ppm) 1 1 205Transmittance (%) 100% 75% 50% 25% 0% 4000 3500 3000 OH 2500 2000 Spectrum 3B 1750 حسيمة 1500 Wavenumber (cm-¹) 1250 .OH 1000 OH 750 500
- C5H100. ICRONS 23 23 24 2s 24 27 4 24 NEAT 00 4400 4200 4000 3800 3600 3400 2400 2200 WAVENUMBERs NICOLET 20SX FT-IR Note: The relative pintegration for the proton NMR is a follows: the triplet at 2.4 ppm (2H), the singlet at 2.12 ppm (3H), the multiplet at 1.6 ppm (2H), and the triplet at 0.91 ppm (3H).3296 IR Spectrum (quid film) ....... wwwddd 4000 100 80 60 40F 8 -28 20 40 proton decoupled 10 13C NMR Spectrum (100 MHz, CDC, solution) 2H - 3000 ¹H NMR Spectrum (400 MHz, CDC, solution) 55 200 2.5 9 80 82 2114 8 2000 M = 83 120 V (cm-¹) 2H L 160 expansion 1600 1200 C₂H₂N 160 200 240 280 m/e DEPT CH, I CH₂ 1 CH 1 2.0 I 7 1H 6 L 120 Mass Spectrum 2H 1.5 800 5 solvent I 80 exchanges with DO 4 2H L 3 No significant UV absorption above 220 nm ||| L 40 2 113 08 (ppm) 1 1 TMS 0 8 (ppm) IR: List bands and possible/probable structural units responsible Band (cm³) Possible stretches/functional groups MS: Molecular Formula 13C NMR: 1 2 3 4 5 6 ¹H NMR: 1 Chem. Shift (8) Type of C (sp, sp2², carbonyl, etc.) 2 Chem. Shift (8) Multiplicity (singlet, doublet, etc.) IHD(DU)= 3 4 5 6 If you need more space, add any additional signal info here: (Show calculation) of attached c # of attached H's # of identical C's in signal Probable Type of H (methyl, aromatic, etc.) # of identical H's in signalUnknown 3 9 200 4000 8 7 6 3000 5 180 160 140 120 100 4 2000 80 1500 wavenumber (1/cm) 60 2 40 1 20 0 0 ¹H NMR data 0 (ppm) multiplicity integration 0.86 t 3 1.50 2.02 6.71 7.24 my 1000 13C NMR data (ppm) 13.7 19.0 37.9 176.4 500 sextet t S S 2 2 1 1
- 13C NMR Analysis of Aspirin Chemical Shift (Observed ppm) Assignment(s) (A'-J') Expected Chemical Shift Range (ppm) B' D' E' JOH Acetylsalicylic Acid (Aspirin) 169 & 170 152 125 135 (4 peaks) - 122 20 160 140 120 100 Figure 14.13 125.7-MHz 13C-NMR spectrum of aspirin in CDCl3. solvent 80 60 40 20 ppmMolecular Formula: C10H14 8 LOD TRANSMITTANCE1% D 4000 STRUCTURE: mult. t 2.72 q 6.90 S d t ppm 1.18 7.11 7.53 3000 H 6 4 1 2 1 5 2000 SPECTRUM 5 4 PPM HAVENUMBERI-L 1500 3 1000 50043 184 IR Spectrum (Iquid film) 4000 3000 100 80 60 40 20 40 13C NMR Spectrum (100.0 MHz, CDCI, solution) 9 80 DEPT CH₂ CH₂4 CHA proton decoupled 200 ¹H NMR Spectrum (400 MHz CDCI, solution) expansion 7.5 7.3 ppm 8 P 10 SAMSUNG Galaxy A53 5G 2000 1600 V (cm) 105 M+- 134 120 160 m/e 160 09b0f2ca-eac1-4... 1200 T L 120 2.8 2.7 ppm 7 6 ww 800 Mass Spectrum C10H14 200 240 280 T 1 5 solvent " 80 expansions 1.8 1.7 ppm 1 4 3:54 م 0 *1 470 صفحة Problem 96 UV Spectrum max 260 nm (log10=2.5) PE 40 1.45 1.35 ppm 3 2 Problem 97 08 (ppm) expansion 1.05 0.95 TMS I 0 8 (ppm) 1 202 تمشح بـ 100 جيجابايت تخزين على OneDrive cloud لمدة 6 أشهر 185.
- MASS % of Base Peak IR 100 5045 % Transmittance 100 T 50 4000 1540 ¹H NMR 300 MHz t 557 5.0 Hz 60 alla illle 677 69 1140 4.5 70 4.0 13C/DEPT NMR 75.5 MHz 3000 130 120 110 100 الد الله da 110 113 100 110 mm 817 Hz 500 90 80 m/z Wavenumber (cm-¹) 3.5 ми линия 80 90 480 Hz 957 3.0 70 2000 440 2.5 Hz 1450 2.0 -1126 120 1000 60 50 40 30 1287 130 1.5 ppm 20 ppmSketch the appearance of the 1H-NMR spectrum of diethyl ether using J = 6.97 Hz in a spectrometer operating ati) 400 MHz. ii) 650 MHz.Establish the difference between the multiplicity of a signal and the integral (integration) of the signal in spectroscopy of 1H-NMR.