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what is the H NMR, C NMR, and IR of cyclopentaol?
This first picture is of...
What is the H NMR, C NMR, and IR of cyclohexanol? The first picture is thr...
What is the H NMR, C NMR, and IR of cyclohexanol? The first picture
is thr NMR of cyclohexanol and the second is an example of the
format. Thank you!
... ow.o.o.. . .ooooolt over boet erot COBIOL.owerowerol MW= 82.1 UK-B Cyclonexanol -- SUNIU. II.P - 91.3 l. 'H NMR (DMSO-d6, 500 MHz) 8 = 9.42 (s, 1H), 8.48 (m, 1H), 8.34 (dd, J= 7.5, 2.5 Hz,1H), 8.0 (d, J= 7.5 Hz, 1H), 7.92 (d, J= 6.0 Hz, 2H), 7.85...
analyze this NMR & IR S23 CDC13 QE-300 240 UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz....
analyze this NMR & IR
S23 CDC13 QE-300 240 UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
A compound, C,H100, shows an IR peak at 1690 cm. Its 'H NMR spectrum has peaks...
A compound, C,H100, shows an IR peak at 1690 cm. Its 'H NMR spectrum has peaks at delta 7.9 (2H, multiplet), 7.6-7.4 (3H, multiplet), 2.95 (2H, quartet, J = 7 Hz), 1.25 (3H, triplet, J= 7 Hz). Draw its structure in the window below. . You do not have to consider stereochemistry. ChemDoodle A compound, C3H100, exhibits IR absorption at 1730 cm-1. Its carbon NMR shifts and substitution, determined by DEPT, are given below. 13C NMR: 822.6 (3), 23.6 (1),...
For the last picture: The values for the NMR are 7.59, 7.58, 7.57, 7.57, 7.55, 7.55,...
For the last picture: The values for the NMR are 7.59,
7.58, 7.57, 7.57, 7.55, 7.55, 7.55, 7.53, 7.25 (cdcl3), 7.01, 7.01,
7.00, 6.99, 6.98, 6.98, 6.97, 6.97, 6.96, 6.95. (from left to
right). Also the values found for the IR and NMR are listed in the
first picture. I need help figuring out their functional groups and
why (preferably an explanation if you don't mind). Also I need help
analyzing the TLC and find it's value.
I added the...
(a) From the spectral data ( H, C NMR, IR, MS) you were given, identify the...
(a) From the spectral data ( H, C NMR, IR, MS) you were given,
identify the structure of your product. Explain why you chose your
particular product based on the spectroscopic data.
(b) Fully assign the 1H NMR spectrum of your product (i.e.
determine which peaks in the 1H NMR correspond to which hydrogens
in the product). You will not receive full marks for determination
of the unknown unless you assign the 1H NMR spectrum
completely.
(c) Now work backwards...
Given the C-NMR, H-HNMR and IR spectrum, what is this compound? It has a melting point...
Given the C-NMR, H-HNMR and IR
spectrum, what is this compound? It has a melting point of 134
degrees celsius and is in deuterated chloroform
solvent.
#40-B C NMR 0.5 abundance 18010 170.0 1600 150.0 140.0 130.0 1200 110.0 100.0 90.0 80.0 70.0 60.0 50.0 40.0 30.0 20.0 173.1580 147.4781 140.9673 129.7718 118.2608 9ISSILL 77.1310 76.7103 18.8397 X: parts per Million : 13C CD bundance 7.0 8.0 X: parts per Million: 1H 7.3613 7.3270 7. 98 7.2766 6.2053 6.1962 6.1824...
What is the H NMR, C NMR, and IR of cyclohexanol? The first picture
is thr NMR of cyclohexanol and the second is an example of the
format. Thank you!
... ow.o.o.. . .ooooolt over boet erot COBIOL.owerowerol MW= 82.1 UK-B Cyclonexanol -- SUNIU. II.P - 91.3 l. 'H NMR (DMSO-d6, 500 MHz) 8 = 9.42 (s, 1H), 8.48 (m, 1H), 8.34 (dd, J= 7.5, 2.5 Hz,1H), 8.0 (d, J= 7.5 Hz, 1H), 7.92 (d, J= 6.0 Hz, 2H), 7.85...
analyze this NMR & IR
S23 CDC13 QE-300 240 UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
A compound, C,H100, shows an IR peak at 1690 cm. Its 'H NMR spectrum has peaks at delta 7.9 (2H, multiplet), 7.6-7.4 (3H, multiplet), 2.95 (2H, quartet, J = 7 Hz), 1.25 (3H, triplet, J= 7 Hz). Draw its structure in the window below. . You do not have to consider stereochemistry. ChemDoodle A compound, C3H100, exhibits IR absorption at 1730 cm-1. Its carbon NMR shifts and substitution, determined by DEPT, are given below. 13C NMR: 822.6 (3), 23.6 (1),...
For the last picture: The values for the NMR are 7.59,
7.58, 7.57, 7.57, 7.55, 7.55, 7.55, 7.53, 7.25 (cdcl3), 7.01, 7.01,
7.00, 6.99, 6.98, 6.98, 6.97, 6.97, 6.96, 6.95. (from left to
right). Also the values found for the IR and NMR are listed in the
first picture. I need help figuring out their functional groups and
why (preferably an explanation if you don't mind). Also I need help
analyzing the TLC and find it's value.
I added the...
(a) From the spectral data ( H, C NMR, IR, MS) you were given,
identify the structure of your product. Explain why you chose your
particular product based on the spectroscopic data.
(b) Fully assign the 1H NMR spectrum of your product (i.e.
determine which peaks in the 1H NMR correspond to which hydrogens
in the product). You will not receive full marks for determination
of the unknown unless you assign the 1H NMR spectrum
completely.
(c) Now work backwards...
Given the C-NMR, H-HNMR and IR
spectrum, what is this compound? It has a melting point of 134
degrees celsius and is in deuterated chloroform
solvent.
#40-B C NMR 0.5 abundance 18010 170.0 1600 150.0 140.0 130.0 1200 110.0 100.0 90.0 80.0 70.0 60.0 50.0 40.0 30.0 20.0 173.1580 147.4781 140.9673 129.7718 118.2608 9ISSILL 77.1310 76.7103 18.8397 X: parts per Million : 13C CD bundance 7.0 8.0 X: parts per Million: 1H 7.3613 7.3270 7. 98 7.2766 6.2053 6.1962 6.1824...
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