IR data showed that compound contains 1) disubstituted benzene 2) Ester group (1720 ir value) 3) Alkyl group (2950 ir value)
so from this three information we only predict propose structure
not conform one
propose two different potential structures for each of your unknowns 2. Propose two different potential structures...
which of the above 8 terpenes does the IR spectrum
belongs to ?
determine the peaks that belongs to the terpene.
attached are reference table for finding peaks .
U right scandidate terpenes narrone Citral litronellol p-upmene Myreene geraniol linenene Menthone Transance 4000 101 - Wed Oct 15 703 322019 GMT-0001 3500 3000 2964.0B 304704 3D08.40 2919.65 205448 2500 2000 1715.80 1645.25 1622 07 159331 1576 51 1495 54 1449.04 1376.494 133870 126369 115592 109716 980 65 955.96 914 BBB...
1. Using the IR correlation table on the second image,
indicate how you could distanguish between the following pairs of
compounds by using infrared spectroscopy. Give two specific
absence/appearance of wavrnumbers for each compound:
2. For this experiment, what is the purpose of adding acetone?
Predict what would happen if you omitted the acetone in the
experimental procedure.
3. Draw four different resonance structures of the
triphenylmethyl cation.
*IR correlation table
PRE-LAB QUESTIONS 1. Using the IR correlation table on...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) 30 Unsat. Index = (2C+2-H-X+NY2 = 200 25 e = 2.00 ppm, 4.90 f = 1.27 ppm, 20 720 Compound 18a: C,H,O, singlet, 2H triplet, 3H 127 15 d = 2.66 ppm, a = 7.21 ppm, b = 7.18 ppm, doublet, 2H doublet, 2H C = 4.90...