What is the structure of the unknown organic compound based on the information listed below?
![Mass Spectrum (not shown): [M]-223 (100%) m/z IR Spectrum (not shown): 3060, 2985, 2850, 2750, 1745, 1600, 1550, 1495, 1350 c](http://img.homeworklib.com/images/571a7582-1c90-491c-bc92-7c320cf3b3f7.png?x-oss-process=image/resize,w_560)
Homework Answers
Add Answer to:
What is the structure of the unknown organic compound based on the information listed below?
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. F...
Spectroscopy Unknown
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For iH NMR Spectra, the integral is given in number of hydrogens (th) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Submit your answer for Quiz 8 at: http://go.osu.edu/CH2550QUIZ Mass Spectrum (not shown): [M-223...
Mass Spectrum (not shown): [M] 259 (100%) m/z IR Spectrum (not shown): 3060, 2985, 1600, 1550,...
Mass Spectrum (not shown): [M] 259 (100%) m/z IR Spectrum (not shown): 3060, 2985, 1600, 1550, 1501, 1350 cm1 (all listed are strong (s) unless otherwise indicated) H NMR Spectrum (400 MHz, CDCls, 25 'C) d (J 8Hz) d (J8 Hz) d (J-2 Hz) t (J 2 Hz) PPM 2H 2H 2H 1H 6H C NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCl,, 25 c) CH) I(CH) (CH) (2 x C) (CH) 60 20 PPM
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 1...
Spectroscopy Unknown. The spectra and data provided were
obtained from a pure organic molecule. For 1 H NMR Spectra, the
integral is given in number of hydrogens (#H) or as a relative
ratio. Important coupling constants (J-values) are listed next to
the peaks for some examples. For some spectra, an inset (grey box)
is also given showing a “zoom-in” on an important part of the
spectrum.
Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985,...
draw the structure for the spectroscopy and show steps and label each part Mass Spectrum (not...
draw the structure for the spectroscopy and show steps
and label each part
Mass Spectrum (not shown): [M] = 302 (75%), 304 (100%), 306 (25%) m/z (all listed are strong (s) unless otherwise IR Spectrum (not shown): 3090, 2985, 2850, 2750, 1715, 1610, 1500 cm indicated) 'H NMR Spectrum (400 MHz, CDCI, 25 °C) t(J = 2 Hz) t(J= 2 Hz) +(J= 2 Hz) 2H 6H 3H 1H 1H 1H PPM HC NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI,...
Predict the structure × Mass Spectrum (not shown): [M] = 193 (100%)m/z IR Spectrum (not shown):...
Predict the structure
×
Mass Spectrum (not shown): [M] = 193 (100%)m/z IR Spectrum (not shown): 3300 (m), 3200 (m) 3060, 2985, 1725, 1600, 1495 cm otherwise indicated) (all listed are strong (s) unless 'H NMR Spectrum (400 MHz, CDCI, 25 °C) d (J-8 Hz) d (J-2 Hz) dd (J-8,2 Hz) m PPM HH 2H 3 NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI, 25 °C) H 6H (C) (C) (C) (CH) (C) (2xCH) i 180 ' 140 ' 120...
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 1H...
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 1H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum Submit your answer for Quiz 3 at: https://uglabs.cbc.osu.edu/cgi-test/organic/spec-quiz.pl Mass Spectrum (not shown): [M-206 (100%) m/z...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224 (25%) m/z IR Spectrum (not...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224
(25%) m/z
IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed
are strong (s) unless otherwise indicated)
Please explain how you determine the organic compound for the
info given. Please check your compound with Chemdraw to verify your
answer before posting your answer (if you have Chemdraw).
Thanks!
NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
Please draw the unknown molecule presented in the specs, Thanks!!! Mass Spectrum (not shown): [M] = 169 (100%) m/z IR S...
Please draw the unknown molecule presented in the specs,
Thanks!!!
Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985, 2250 (m), 1745 cm1 (all listed are strong (s) unless otherwise indicated) H NMR Spectrum (400 MHz, CDC I3, 25 °C) 5 3 PPM 2H 2H 2H 6H 3H C NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI3, 25 °C) (CH2) (C) (CH3) (CH2) (CH3) (C) (C) (CH2) 180 160 80 140 120 100 PPM 60...
Could someone find the structure of this molecule? I'm having alot of trouble. And could you...
Could someone find the structure of this molecule? I'm having
alot of trouble. And could you explain how you found it? If its
just structure, thats okay.
Spectroscopy Unknown Pre-Quiz 5 5 points - Tuesday Lecture (due by 11:59 pm EST 3/16/2020) Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (-values) are listed...
Propose a structure that is consistent with the spectral data below. (The spectra and data provided...
Propose a structure that is consistent with the spectral data below. (The spectra and data provided were obtained from a pure organic molecule. For 'H NMR spectra, the integral is given in number of hydrogens (#H) or as a relative ratio.) Mass Spectrum (not shown): [M] = 162 m/z (100%) IR Spectrum (not shown): 3022, 2980, 1685, 1600, 1510 cm (all listed are strong (s) unless otherwise indicated) 'H NMR Spectrum (300 MHz, DMSO, 25 °C) dd (J= 2 Hz)...
Spectroscopy Unknown
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For iH NMR Spectra, the integral is given in number of hydrogens (th) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Submit your answer for Quiz 8 at: http://go.osu.edu/CH2550QUIZ Mass Spectrum (not shown): [M-223...
Mass Spectrum (not shown): [M] 259 (100%) m/z IR Spectrum (not shown): 3060, 2985, 1600, 1550, 1501, 1350 cm1 (all listed are strong (s) unless otherwise indicated) H NMR Spectrum (400 MHz, CDCls, 25 'C) d (J 8Hz) d (J8 Hz) d (J-2 Hz) t (J 2 Hz) PPM 2H 2H 2H 1H 6H C NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCl,, 25 c) CH) I(CH) (CH) (2 x C) (CH) 60 20 PPM
Spectroscopy Unknown. The spectra and data provided were
obtained from a pure organic molecule. For 1 H NMR Spectra, the
integral is given in number of hydrogens (#H) or as a relative
ratio. Important coupling constants (J-values) are listed next to
the peaks for some examples. For some spectra, an inset (grey box)
is also given showing a “zoom-in” on an important part of the
spectrum.
Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985,...
draw the structure for the spectroscopy and show steps
and label each part
Mass Spectrum (not shown): [M] = 302 (75%), 304 (100%), 306 (25%) m/z (all listed are strong (s) unless otherwise IR Spectrum (not shown): 3090, 2985, 2850, 2750, 1715, 1610, 1500 cm indicated) 'H NMR Spectrum (400 MHz, CDCI, 25 °C) t(J = 2 Hz) t(J= 2 Hz) +(J= 2 Hz) 2H 6H 3H 1H 1H 1H PPM HC NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI,...
Predict the structure
×
Mass Spectrum (not shown): [M] = 193 (100%)m/z IR Spectrum (not shown): 3300 (m), 3200 (m) 3060, 2985, 1725, 1600, 1495 cm otherwise indicated) (all listed are strong (s) unless 'H NMR Spectrum (400 MHz, CDCI, 25 °C) d (J-8 Hz) d (J-2 Hz) dd (J-8,2 Hz) m PPM HH 2H 3 NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI, 25 °C) H 6H (C) (C) (C) (CH) (C) (2xCH) i 180 ' 140 ' 120...
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 1H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum Submit your answer for Quiz 3 at: https://uglabs.cbc.osu.edu/cgi-test/organic/spec-quiz.pl Mass Spectrum (not shown): [M-206 (100%) m/z...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224
(25%) m/z
IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed
are strong (s) unless otherwise indicated)
Please explain how you determine the organic compound for the
info given. Please check your compound with Chemdraw to verify your
answer before posting your answer (if you have Chemdraw).
Thanks!
NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
Please draw the unknown molecule presented in the specs,
Thanks!!!
Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985, 2250 (m), 1745 cm1 (all listed are strong (s) unless otherwise indicated) H NMR Spectrum (400 MHz, CDC I3, 25 °C) 5 3 PPM 2H 2H 2H 6H 3H C NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI3, 25 °C) (CH2) (C) (CH3) (CH2) (CH3) (C) (C) (CH2) 180 160 80 140 120 100 PPM 60...
Could someone find the structure of this molecule? I'm having
alot of trouble. And could you explain how you found it? If its
just structure, thats okay.
Spectroscopy Unknown Pre-Quiz 5 5 points - Tuesday Lecture (due by 11:59 pm EST 3/16/2020) Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (-values) are listed...
Propose a structure that is consistent with the spectral data below. (The spectra and data provided were obtained from a pure organic molecule. For 'H NMR spectra, the integral is given in number of hydrogens (#H) or as a relative ratio.) Mass Spectrum (not shown): [M] = 162 m/z (100%) IR Spectrum (not shown): 3022, 2980, 1685, 1600, 1510 cm (all listed are strong (s) unless otherwise indicated) 'H NMR Spectrum (300 MHz, DMSO, 25 °C) dd (J= 2 Hz)...
Most questions answered within 3 hours.
-
Write a program to score the paper-rock-scissor game. Each of
two users types in either P,R...
asked 8 minutes ago -
Calculate the equillibrium constent K for a redox reaction that
has E°cell = -.98 V at...
asked 21 minutes ago -
A concave spherical mirror has a radius of curvature of
magnitude 19.6 cm.
(a) Find the...
asked 22 minutes ago -
3. draw a diagram of the magnetic field:
a. around a long straight wire with a...
asked 21 minutes ago -
If you titrated 30.0 mL of 0.1 M HCl with 0.1 M NaOH, indicate
the approximate...
asked 29 minutes ago -
NADH passes electrons into the electron transport chain. List
the carriers that would receive the electrons,...
asked 38 minutes ago -
A cylindrical cable with a resistivity of 1.6x10-8 Ω·m and cross
sectional area of 3x10-5 m^2...
asked 37 minutes ago -
True or False.
A consumer with convex preferences who is indifferent between
the bundles (5,2) and...
asked 41 minutes ago -
A diamond's index of refraction for red light, 656 nm, is 2.410,
while that for blue...
asked 54 minutes ago -
Compare HPLC, SPE, and GC. Identify the differences, the
advantages, and the weaknesses of each method.
asked 55 minutes ago -
Characteristic x-rays emitted by potassium have a wavelength of
0.374 nm. What is the energy of...
asked 58 minutes ago -
there is a function to create two random numbers between 1 and
25 and a function...
asked 1 hour ago