I appologise for the previous answer.
After analysing the whole question the answer will be an equilibrium product. ( complete explanation willonly be worth explaning if someone is really willing to get into the depth of NMR Aand IR however i would love to if i know questioner level of understanding)
DBE = 5.
what i am sure about that the given answer is the most
probable or some data is missing in the question or the question is
incomplete.
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 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,...
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...
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 (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] = 159 (100%) m/2 IR Spectrum (not shown): 3031, 2981,...
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.
Unknown number: 1039 Callam/Paul Chemistry 2540 Spectroscopy Unknown - 25 points Information: Each spectra below...
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.
Unknown number: 2111 Callam/Paul Chemistry 2540 Spectroscopy Unknown - 25 points Information: Each spectra below...
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 cm otherwise indicated) (all listed are strong (s) unless H NMR Spectrum (400 MHz, CDCl3, 25 °C) d (J 8 Hz) d (J 2 Hz) quin dd(J 8, 2 Hz) 2 PPM 1H 1H 1H1H 1H 2H 3H 3H 13C NMR Spectrum (with DEPT), proton-decoupled...
provide the skeletal structure and the name of it.
nformation: Each spectra below was obtained from a pure compound. for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm1 1H NMR Spectra, the integral is given in number of hydrogens (8H) 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...
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)...
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,...
Draw the skeletal structure of the unknown compound
Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is...