Propose a structure for an acyclic alkane having the following spectrum. The results of the DEPT spectra are given following the signals. Include a condensed structure to provide your answer.
Propose a structure for an acyclic alkane having the following spectrum. The results of the DEPT spectra are given following the signals. Include a condensed structure to provide your answer.
Use a condensed structure to provide your answer. Propose a structure for an acyclic alkane having the following spectrum. The results of the DEPT spectra are given following the signals.4-6.jpg4-5.jpg
Use a condensed structure to provide your answer. Propose a structure for an acyclic alkane having the following spectrum. The results of the DEPT spectra are given following the signals.I need the answer for the 2nd spectrum.4-5.jpg
5. Use a condensed structure to provide your answer. Propose a structure for an acyclic alkane having the following spectrum. The results of the DEPT spectra are given following the signals. IU 8 C,H2 CH₃ CH3
Label the spectra and propose a structure for the compound. Compound 3 IR Spectrum quid 4000 3000 2000 V (cm 1000 ) 1200 800 of base peak more Cg H100 280 40 80 120 160 200 240 C NMR Spectrum 50. 0 00, DEPT Chi sont on GGL 200 160120 120 80 40 0 5 (ppm) TH NMR Spectrum (200 M . CDCI, solution 10 9 8 7 6 5 4 3 2 i 8 (ppm)
Label the spectra and propose a structure for the compound. Compound IR Spectrum Olquid fim 1740 4000 3000 2000 1800 1200 800 100 Mass Spectrum yood M = 150/152 (15) CH40, CI 240 280 40 80 120 160 mle 200 13C NMR Spectrum (500 MG, COO, solo DEPT CH CH.CH selvon proton decoupled 200 160 120 80 40 0 (ppm) 'H NMR Spectrum (200 ML. COCI, solution) 10 9 8 7 6 5 4 3 2 1 (ppm)
Label the spectra and propose a structure for the compound. Compound 5 IR Spectrum Olquid fim 1740 4000 3000 20 ,1600 1200 300 100% Mass Spectrum M = 150/152 (15) CH,40, CI 240 280 40 80 120 160 200 13C NMR Spectrum (500 M , CDC, son DEPT CH CH CH selvon proton decoupled 200 160 120 80 40 0 8 (ppm) 'H NMR Spectrum (200 MH. COCI, solution 10 9 8 7 6 5 4 3 2 (ppm)
Label the spectra and propose a structure for the compound. Compound 4 IR Spectrum hould 4000 3000 17000 2000 2000 V (cm 1600 ) 1200 800 Mass Spectrum TTTTTTTT Sofhose pas No significant UV absorption above 220 mm M 100 CHOO 0 120 180 200 200 200 13C NMR Spectrum (1000 MHCOCI, solution DEPT CHICK CH proton decoupled 200 160 120 80 40 0 (ppm) "H NMR Spectrum (400 MHE. CDC, solution 10 9 8 7 6 5 4 3...
Analzye the following spectra, and propose a structure for each. The bottom set of 3 spectra are DEPT spectra, top: CH only, middle: CH, CH3 up, CH2 down, bottom: normal BB decoupled spectrum. Explain your assignments . Analyze means determine integrals, draw splitting trees, determine carbon type (C, vs CH vs CH2 vs CH3 and structural environment. Use ChemDraw to check your proposed structure (include output), Problem C 7.5 7.0 .5 6.05.55.0 4.5 4.03.5 3.0 2.5 ppm 31 ppm 140...
Label the spectra and propose a structure for the compound. Compound 2 R Spectrum Bedie 3400 1720 4000 3000 2004 1600 vomi) 1200 800 183 Mass Spectrum Softbase de UV Spectrum . mar 253 nm 109,96 26) mas 250 nm 109,2.7) 2 mar 284 m 109,0 2.5) M -220N) CH2O 280 40 80 120 160 200 240 13C NMR Spectrum (100 . CDC, DEPT CH Chicht protondeco 200 160 120 80 400 (ppm) 'H NVR Spectrum (400MCDO, Exchanges wayo Exchanges...
Label the spectra and propose a structure for the compound. Compound 6 1 1755 IR Spectrum quid fim 1120 4000 3000 2000 V (cm 16001200800 ) Mass Spectrum So base peak M" 158 (<1%) No significant UV absorption above 220 nm C₂ H₂ 403 280 40 80 120 160 200 240 13C NMR Spectrum 150.0 MHz, CDCI, solution) DEPT Chut Chitch! proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum 2200 MHZ. CDC, solution) 150 10...