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can someone provide me with the peaks and data from the IR spectrums in a table
1) table
2) table
and also explain both of them to me?
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- Calculate the index of hydrogen deficiency of this compound Q.)Pyridine, C5H5N1 Can one distinguish between the Markovnikov and anti-Markovnikov complement products I and II byinfrared spectroscopy? How about nuclear magnetic resonance? Justify your answersImine compounds usually show stretching bands in the IR in the range of 1690-1649cm-1 and aromatic amines show a C-N stretch at 1340-1265cm-1. A related compound, N-benzylideneaniline, does not show tautomerism and has a C-N stretch at 1678cm-1 while H2SB-1(2-(2-hydroxybenzylideneamino)phenol ) shows a C-N stretch of 1590 cm-1. Given this information, does H2SB-1 show some C-N single bond character.
- Please fully annotate this IR spectrum in the picture below, no need to annotate the fingerprint region (400-1500 cm-1). Thank you so much!!Determine the structure of the following compound using the spectral data shown below. You must show your reasoning for full credit. Molecular formula: C7H5FO IR: 1705cm-1 (aromatic aldehyde) Broadband de-coupled: 116, 132, 133, 169 and 191. DEPT-90: 116, 132 and 191. DEPT-135 negative: None. DEPT-135 positive: 116, 132 and 191These are the characteristics of the IR spectrum, what type of molecule is formed? can you show the drawing. Wavenumber cm -1 Bond Vibration Shape Intensity Functional group or description 3348, 3423 N-H Stretch Sharp Strong Primary amine 3042-3074 =C-H Stretch Sharp Medium Aromatic 1511 N-H Bending Sharp Strong Amine 1236 C-O Stretch Sharp Strong Ether 827 =C-H Bending Sharp Strong Aromatic
- I need help with questions please show on charts, please information Functional group- primary amine Derivatives - Benzamide unknown compound C3H9N 1: Label identifiable absorption above 1400 cm-1, sp2 carbon stretch foralkenes and aromatic, sp3 carbon-hydrogen stretch, sp2 carbon-hydrogenstretch, carbon hydrogen stretches of aldehyde, O-H stretch for alcohols, andcarboxylic acid, C=O stretches, N-H for amines.2- 1HNMR: Draw the structure neatly on the spectrum with each of the hydrogenclearly labelled. Identify which signal is associated with each type of H asmuch as possible.3- 13CNMR: Draw the structure neatly on the spectrum with each of the carbonclearly labelled. Identify which signal is associated with each type of carbonas much as possibleOrganic Chemistry: IR spectroscopy A student obtains an IR spectrum with an intense, broad absorption at about 3350 cm-1. The student claims that the sample is an alcohol, but the professor says that the absorption is there because the sample is contaminated with water. What peak(s) could be looked for to show that the sample is indeed an alcohol? Which functional groups would make it difficult to use this strategy?Unrounded Rounded ε∗,L/μmolε∗,L/μmol 0.0259825 0.0260 heres data: TZ # Concentration Absorbance at 430 nmnm 1 33.6480 0.931 2 25.2360 0.757 3 16.8420 0.210 4 8.41200 0.137 5 4.20600 0.122
- What is the check digit for the Flamin’ Hot Cheetos with the following UPC: 0 28400 58989Complete the following answer using the data provided here: Molecular formula: C4H8O2 Important IR data (cm-1): 3280 (broad); 2980-2730 (many); 1690; 1254 All 1H NMR data (ppm, splitting, integration): 11.0 ppm (s), 1; 2.57 ppm (m), 1; 1.07 ppm (d), 6 1. Sketch out a 1H NMR spectrum showing peak locations and peak splitting on a ppm scale for the data provided above. Include the data labels above in your spectrum, but do not show integration lines. 2. draw the most proper line bond structure for the data given aboveORGO II NMR please help fill out the chart and label. my unknown is C6H10O.