Given the molecular formula C4H10O. with this molecular formula it can be either Alcohol or Ether.
but an Alcohol must contain a broad and strong peak (Hydrogen bonded -OH) at 3500-3300 cm-1 which is not present in both the spectra.
And with Ether a characteristic stretching vibration of 1150-1060 cm-1 (moderate to strong peak) must be present which is not present in spectra.
In first spectrum characteristic strong stretching vibration peaks at 1715 cm-1 which indicates a Ketone functional group and moderate stretching vibration peak at 2991 cm-1 indicates -CH stretching (SP3 Carbon) and peaks containing C-C(O)-C bending vibrations present in between 1300-1100cm-1 . so with this information and with the given molecular formula in the question the compound is 2-Butanone C4H8O, not C4H10O.
CH3-CH2-CO-CH3
In the second spectra at 1731 cm-1 a sharp stretching vibration peak indicates an Aldehyde functional group and moderate stretching vibrations at 2976 cm-1 indicates -CH stretching vibrations (SP3 Carbon) and at 2827 cm-1 whic corresponds to aldehyde-CH stretching vibration, so with this information and with the given molecular formula in the question the compound is Butyraldehyde or Butanal with molecular formula C4H8O, not C4H10O.
CH3-CH2-CH2-CHO.
The question is complete. that is all that was given ALL INFORMATION IS POSTED 3. The...
3. The following IR spectra are of two different compounds both with the molecular formula of C4H80. Identify the two compounds and interpret the significant signals in the IR spectra. TENSRETTENCEIN 2991 V 71715 THOSETTANTEI 2976 1731 NU
3. The following IR spectra are of two different compounds both with the molecular formula of Hofmistake) Identify the two compounds and interpret the significant signals in the IR spectra. 1731
The molecular formulas IR and 1H NMR spectra of different organic compounds are shown below. the 1 H NMR all run that 300 MHz in CDCl3. identify the compound by interpreting both the spectrum. All piece must be assigned for the appropriate functional groups (IR) and protons (NMR) to earn full credit. The molecular formulas IR and 1H NMR spectra of different organic compounds are shown below. the 1 H NMR all run that 300 MHz in CDCl3. identify the...
NMR OChem 2 question. Answers are not posted. From the following spectra, determine the structure of the unknown compound. Be sure to list out the number signals, chemicals shift, integration values and splitting for each signal, and identify any major functional groups in the IR spectrum and a molecular ion peak for any mass spectrum. 1001 2-1-S 3. 102030405060708090100 m/z 93-1-4 AguPA ago naaaaawe“
wolned Spectra Problems it all together": mbined Spectra Problems The Combin friends, the moment has come... During the past two semesters, we have talked about infrared spectros- y (IR), 'H-NMR spectroscopy, "C-NMR spectroscopy, and Mass spec- trometry (MS). We've also talked about using information gathered from the mass spectrum to generate a molecular formula and the index of hydro- gen deficiency which helps us determine information about our compound when there isn't any available. The moment has come in which...
Compound 3: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 3 and the table is given below. Determine the molecular formula of 3 from the MS given below. . relative abundance m/z 152 100 153 9.7 154 4.5 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 'H- and 13C-NMR spectra...
bined Spectra Problems All Together": within mbined Spectra Problems friends, the moment has come... pre puring the past two semesters, we have talked about infrared spectros- (IR), 'H-NMR spectroscopy, "C-NMR spectroscopy, and Mass spec trometry (MS). We've also talked about using information gathered from the mass spectrum to generate a molecular formula and the index of hydro- gen deficiency which helps us determine information about our compound when there isn't any available. The moment has come in which we piece...
DIRECTIONS: You must complete the entire assignment. 1. Given the 'H NMR spectrum below and a molecular formula of CH, 0, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1600-1650 cm (multiple peaks) (5 pts.) 3H, 3H,t 2H, d 2H, d 2H,9 PPM 2. Given the 'H NMR spectrum below and a molecular formula of C.H.O. provide a structure. Note you must assign all of the signals in...
identify compounds A-E based on the information in order to receive full credit: given. Please note that you must show all of your reasoning Compound A had the molecular formula CtHa Its proton NMR is shown below. Reaction of A bromosuccinimide, and subsequent workup, produced with N- one product, compound B. but one was Compound C had the molecular formula CaH,o2: Its proton NMR consisted of only two signals extremely downfield (around 10ppm). Also, its IR included a very strong...
Hints for identifying compounds in multiple-choice problems (problems 1:5); 1. Closely compare the given compounds. Determine which piece of information (molecular weight from MS, number of peaks in the NMR, presence of a special functional group in the IR, etc) would be the easiest for distinguishing between the given compounds. You might not need to use all types of given spectra to find your correct compound! 2. Based on your answer from step 1, consult the appropriate spectrum first. For...