Homework Answers
Add Answer to:
Draw the organic structure that is represented by the
following spectra:
R Spectrum Mass Spectrum absorption...
Draw the organic structure that is represented by the following spectra: R Spectrum 1600 1200 800...
Draw the organic structure that is represented by the
following spectra:
R Spectrum 1600 1200 800 00 Mass Specthumos C10Hyss 40 0 12 160 200 20 280 200 250 300 3C NMR Spectrum 200 160 120 80 (ppm) H NMR Spectrum 10 (ppm) Problem 65 Loc 2112 of 3148 74%
Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
Problem 19 IR Spectrum 2000 1600 1200 800 100 Mass Spectrum No significant UV absorption above...
Problem 19 IR Spectrum 2000 1600 1200 800 100 Mass Spectrum No significant UV absorption above 220 nm 40 M+ 147149 40 80 120 160 200 240 280 m/e 3C NMR Spectrum (100 MHE, CDC, solution) proton decoupled 200 160 120 40 0 8(ppm) H NMR Spectrum 22 ppm 8 5 2 δ(ppm)
Deduce the structure based on the information below: Concepts: organic spectroscopy, organic chemistry - Problem 53...
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
- Problem 53 IR Spectrum (liquid film) 4000 3000 1600 1200 . 800 2000 V (cm Mass Spectrum % of baso peak No significant UV absorption above 220 nm 115 M+ 146 40 80 200 240 120 160 m/e 280 13C NMR Spectrum (50.0 MHz, CDC, solution) solvent proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum (200 MHZ, CDCI, solution) TMS LIIIIIIIIIIIIIIIII...
Label the spectra and propose a structure for the compound. Compound 6 1 1755 IR Spectrum...
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...
Label the spectra and propose a structure for the compound. Compound 2 R Spectrum Bedie 3400...
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 4 IR Spectrum hould 4000...
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...
Label the spectra and propose a structure for the compound. Compound 5 IR Spectrum Olquid fim...
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)
Deduce the structure based on the information below: Concepts: organic spectroscopy, organic chemistry Problem 52 IR...
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
Problem 52 IR Spectrum (Tiquid film) t760 U 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum TTTTTTTTTT % of base peak No significant UV absorption above 220 mm 87 M+* = 146 (<1%) LLLLLLLLLLLL 40 80 120 160 m/e 200 240 280 13C NMR Spectrum (20.0 MHz, CDCI, solution) solvent proton decoupled www pornowww 200 160 120 80 40 0 8 (ppm) 1H NMR...
Label the spectra and propose a structure for the compound. Compound IR Spectrum Olquid fim 1740...
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)
Draw the organic structure that is represented by the
following spectra:
R Spectrum 1600 1200 800 00 Mass Specthumos C10Hyss 40 0 12 160 200 20 280 200 250 300 3C NMR Spectrum 200 160 120 80 (ppm) H NMR Spectrum 10 (ppm) Problem 65 Loc 2112 of 3148 74%
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
Problem 19 IR Spectrum 2000 1600 1200 800 100 Mass Spectrum No significant UV absorption above 220 nm 40 M+ 147149 40 80 120 160 200 240 280 m/e 3C NMR Spectrum (100 MHE, CDC, solution) proton decoupled 200 160 120 40 0 8(ppm) H NMR Spectrum 22 ppm 8 5 2 δ(ppm)
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
- Problem 53 IR Spectrum (liquid film) 4000 3000 1600 1200 . 800 2000 V (cm Mass Spectrum % of baso peak No significant UV absorption above 220 nm 115 M+ 146 40 80 200 240 120 160 m/e 280 13C NMR Spectrum (50.0 MHz, CDC, solution) solvent proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum (200 MHZ, CDCI, solution) TMS LIIIIIIIIIIIIIIIII...
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...
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 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...
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)
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
Problem 52 IR Spectrum (Tiquid film) t760 U 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum TTTTTTTTTT % of base peak No significant UV absorption above 220 mm 87 M+* = 146 (<1%) LLLLLLLLLLLL 40 80 120 160 m/e 200 240 280 13C NMR Spectrum (20.0 MHz, CDCI, solution) solvent proton decoupled www pornowww 200 160 120 80 40 0 8 (ppm) 1H NMR...
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)
Most questions answered within 3 hours.
-
Calculate the approximate number of residues of Rubisco, which
is involved in carbon fixation in plants,...
asked 27 minutes ago -
Other decisions about scientific claims can have a much broader
impact.ENERGYarrow-10x10.png, environment, health, security - all...
asked 1 hour ago -
I need to write a research paper and work cited about this
topic: The United States...
asked 1 hour ago -
Hello! I was wondering if I could have some help?
If the vapor pressure of carvone...
asked 2 hours ago -
An economist wants to estimate the mean per capita income (in
thousands of dollars) for a...
asked 2 hours ago -
What would be the input/output characteristic of a circuit
obtained by putting two of your 2's-complementers...
asked 2 hours ago -
In Drosophila, the transition from the syncytial blastoderm
stage to the cellular blastoderm stage is a...
asked 2 hours ago -
Project management question:
Name 3 different types of resources (hint: humans are one
type)
asked 3 hours ago -
Consider the following reaction: C 2H 2( g) + 2H 2( g) C 2H 6(
g)...
asked 3 hours ago -
Consider a 1.0 L buffer containing 0.092 mol L-1 HCOOH and 0.100
mol L-1 HCOO-. What...
asked 3 hours ago -
Koch Realty has owned a vacant land with a FMV of
$775,000 and an adjusted basis...
asked 3 hours ago -
It is estimated 29% of all adults in United States invest in
stocks and that 85%...
asked 3 hours ago