please provide detailed explanation of solution for thumbs up 6. Reaction Coordinate Diagrams (10 points) (a)...
label indicated peaksnwjth appropriate functional groups
this is close up of IR values. this is all the informatikn
that is given.
(d) (2 poin with the appropriate functional group. nts) For the IR spectrum illustrated below, label each of the indicated peaks 100 2 At. (e) (1 point) Was the reaction sequence successful (yes or no?) (1) (2 points) Draw the structure of the compound represented by the spectra given above in the box given below. The spectra for this...
if you could also explain how you can determine the answer, I
would really appreciate it!
1. (15 points) Assign the resonances in the spectrum shown. The resonances on the spectrum are labelled A-D. On the lines provided, write the label that corresponds to each of the groups. The multiplicity (s = singlet, d = doublet, etc) and the integrals are given for each resonance. OCH3 + S, 6H H3 C CH₂ H OCH₃ x D s, 3H d, 2H...
1. (15 points) Assign the resonances in the spectrum shown. The resonances on the spectrum are labelled A-D. On the lines provided, write the label that corresponds to cach of the groups. The multiplicity (s - singlet, d-doublet, etc) and the integrals are given for each resonance. OCH, S, 6H нс сня й осн, х 5, 3H 2. (5 points) Below is the 'H NMR spectrum of a compound with molecular formula of C H2O2. The IR spectrum has a...
CHE 230-001 Homework Assignment 9 Due Date: Friday November 8 by midnight. Please keep all responses within the boxes provided. Name: Student ID: 1. (15 points) Assign the resonances in the spectrum shown. The resonances on the spectrum are labelled A-D. On the lines provided, write the label that corresponds to each of the groups. The multiplicity (s = singlet. d = doublet, etc) and the integrals are given for each resonance. OCH, S, 6H H3CCHE HOCHz S, 3H d....
Spr 19 CHEM332 2. Draw a structure of formula CsH,N that is consistent with both the 'H and 1IC NMR spectra given below Clearly label the H's and C's on your structure with letters and assign them to the appropriate peaks on each NMR spectrum. [8 pts 5 4 3 21 Ppm 11 10 97 Peak data for 'H NMR (ppm): 2.55 (sextet, 1H), 1.63 (quintet, 2H), 1.32 (doublet 3H), 1.1 (triplet, 3H). 200 180 160 140120 100 0 40...
(15 points) Assign the resonances in the spectrum shown. The resonances on the spectrum are labelled A D. On the lines provided, write the label that corresponds to each of the groups. The multiplicity (s= singlet, d = doublet, etc) and the integrals are given for each resonance. 1. В осH;- s, 6H Нас CH н ОСнз D S, ЗH C A d, 2H t, 1H T O 11 10 7 5 4 1 ppm (5 points) Below is the...
match compound with graph
9. You have a sample of each of the esters shown below and take a 'H NMR spectrum of each one. You realize after the fact that you forgot to label the samples. Using the spectra you obtained (below), determine which compound is which Ethyl phenylacetate Benzyl propionate a. Compound A 2H S 5H, m 3H, t 2H, q 8 PPM b. Compound B 5H, m 2H, s 3H, t 2H, q 01 5 PPM
1. The IR spectra shown below is for a compound of formula C.H.O (a) Calculate the degree(s) of unsaturation (b) What are the functional groups indicated ? (C)Match the peaks to each of the corresponding functional group. (d) Propose a structure (10 points) 90 % Transmittance 1250 Wernumbers ( 1) 2. The NMR spectra shown is for a compound of formula C.H.O. (a) Calculate the degree(s) of unsaturation (b) What are the functional groups indicated ? (c)Match the peaks to...
Provide the correct structure for your unknown based on the
spectroscopic data provided. Provide the correct name for your
compound. Either the IUPAC name, or a commonly accepted name (i.e.,
ethyl acetate in place of ethyl ethanoate) will be accepted.IR
spectrum: Assign as many peaks as possible. In particular, you
should assign peaks that were important in making your structural
interpretation (i.e. functional group peaks such as OH, C=O, N-H,
etc.).
1H-NMR spectrum: Assign all the peaks in the spectrum...
I kind of know where to start for these but I get so confused
trying to draw the structure and how to read and interpret the
CNMR. Looking at the IR frequencies i think there is a benzene
ring, as well as sp2 and sp3 C-H bonds, there is no O-H or N-H
bonds, as well as no carbon triple bonds to nitrogen or carbon, and
no carbon double bonded to oxygen bonds.I know there has to be 8
hydrogens...