Identification of compound by spectral data
IR
3280 cm-1 for N-H stretch
1653 cm-1 for C=C stretch
1H NMR
1.05 ppm (t, 3H) for CH3 next to CH2
1.85 ppm (s, 3H) for CH3 on quaternary alkenic C
2.6 ppm (q, 2H) for CH2 between CH3 and NH
3.08 ppm (s, 2H) for CH2 between NH and alkenic C
4.8 ppm (d, 2H) for terminal alkenic CH2
Structure
Provide a structure for the following compound. C_6 H_13 N; IR: 3280, 1653, 898 cm^-1;^1H NMR...
Provide a structure for the following compound: C6H12O2: IR: 1743 cm-1; 1H NMR spectrum:
Provide a structure for the following compound: C10H13NO2; IR:
3285, 1659, 1246 cm?1; 1H NMR spectrum:
Provide a structure for the following compound:
Provide a stable structure for the following compound: C9H10O3; IR: 2300-3200, 1710, 1600 cm-1; 1H NMR spectrum:
Provide a structure for the following compound: C10H13NO2; IR:
3285, 1659, 1246 cm?1; 1H NMR spectrum:
Provide a structure for the following compound:
Provide a structure for the following compound:
A compound with a molecular formula C5H10O
has the following 1H NMR spectrum. Provide a structure
that is consistent with this spectrum.
3. A compound with a molecular formula CsHioO has the following 'H NMR spectrum. pound with a molecular formula CsHioO has the following H NMR Propose a structure for this compound. PPM
a) Provide the structure that is consistent with the data below. C7H14O2 IR (cm-1): 2950, 1750 1H NMR (d): 2.3 (2H, q), 1.0 (3H, t), 0.9 (9H, s) b) Deduce the identity of the compound from the data provided. C10H14O: IR (cm-1): 3200-3500 (broad), 3050, 2950, 1610 1H NMR(δ): 1.0 (s, 6H), 2.0 (s, 3H), 2.8 (broad s, 1H), 7.3 (d, 2H), 7.6 (d, 2H) c) An unknown compound, C3H5Cl3, gave the following proton NMR...
A compound with a molecular formula C5H11NO has the following 1H NMR spectrum. The IR spectrum shows an absorption at around 3400 cm 1. Which of the following structures is consistent with this spectrum? exchanges with D20 PPM ZI IZ IZ IZ
Need help with number 1. Thanks.
An unknown compound has the molecular formula C_5H_10O_2. Its^1H NMR spectrum is shown below (integral values are shown below each peak). Its IR spectrum shows a strong peak at 1740 cm^-1. Determine its structure and assign all peaks on the NMR spectrum.^1H NMR (300 MHz, in CDCl_3) An unknown compound has the molecular formula C_9H_10O. Its^1H NMR is shown below (integral values are shown next to each peak). Its IR spectrum shows a strong...
On the attached image are 1H NMR, 13C NMR, and IR
spectra of a compound with the formula C4H8O. 1H NMR signal at 1.2
is caused by 3 hydrogens, the sigbal at 2.1 is caused by 3
hydrogens, and the signal at 2.5 is caused by 2 hydrogens. Identify
the compound.
CH 1110 9 8 7 6?4 Problem 6. 'H NMR spectrum of compound HsO Problem 6. 13C NMR spectrum of compound C4HsO 200 180 160 140 120 100 80...
Investigate the following IR Absorption,
13C and 1H
NMR below:
Compound X's IR (BELOW)
Compound X's 13C NMR (BELOW)
Compound X's 1H NMR (BELOW)
1. Investigate the diagnostic IR
Absorption of compound X shown above and
use this to determine the functional groups
present. Use a table that goes (as an
example):
(EXAMPLE ONLY)
Frequency
(cm-1)
Relative Intensity or
Shape
Vibrational
Assignment
2950
Medium
C-H Stretch
1715
Sharp and Strong
C double bond O Stretch
2. Investigate the 1H and...