A compound(C10H1202)whose spectrum is shown here was isolated from a reaction mixture containing 2-phenylethanol and acetic acid.

  1. Propose a structure for this compound.
  2. Assign peaks to show which protons give rise to which signals in the spectrum.

Short Answer

Expert verified

a)

Phenethyl acetate

b)

a = δ 7.2-7.3 (multiplet, 5H) , b = δ 4.3 (triplet, 2H) , c = δ 2.9 (triplet, 2H) ,

d = δ 2.0 (singlet, 3H)

Step by step solution

01

Explanation of part (a):

A compound having molecular formula (C10H1202), must have been formed through the reaction of 2-phenylethanol and acetic acid. Alcohol and acid combine to form ester as the product. The reaction is known as esterification reaction and usually takes place in presence of acid catalyst.

Formation of Phenethyl acetate

02

Explanation of part (b):

The chemical shift values depend on the nearby environment and the electronegativities of neighbouring atoms also. If a neighboring atom is more electronegative, then the chemical shift value of a proton which is near to that electronegative atom or adjacent to it will be higher and it will be in a deshielded environment. Benzene protons have a chemical shift value of around 7.2-7.3. Proton-b, which is adjacent to the oxygen atom, will have a high value of chemical shift, that is, 4.3. Proton-d will have a chemical shift value of 2.0 due to shielded environment.

The chemical shift values of protons in phenethyl acetate will be,

a = δ 7.2-7.3 (multiplet, 5H) , b = δ 4.3 (triplet, 2H) , c = δ 2.9 (triplet, 2H) ,

d = δ 2.0 (singlet, 3H)

Different kinds of protons have different chemical shifts in phenethyl acetate

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Most popular questions from this chapter

Determine the ratios of the peak areas in the following spectra. Then use this information, together with the chemical shifts, to pair up the compounds with their spectra. Assign the peaks in each spectrum to the protons they represent in the molecular structure.

Possible structures:

A compound was isolated as a minor constituent in an extract from garden cress. Its spectra are shown here.

  1. Look at each spectrum individually and list the structural characteristics you can determine from that spectrum.
  2. Look at the set of spectra as a group and propose a tentative structure.
  3. Verify that your proposed structure accounts for the major features of each spectrum.

Question:Using a 60-MHz spectrometer, a chemist observes the following absorption: doublet, J = 7 Hz, at 4.00

(a) What would the chemical shift () be in the 500-MHz spectrum?

(b) What would the splitting value J be in the 500-MHz spectrum?

(c) How many hertz from the TMS peak is this absorption in the 60-MHz spectrum? In the 500-MHz spectrum?

(a) Draw all five isomers of formula(including stereoisomers).

(b) For each structure, show how many types of would appear in the proton NMR spectrum.

(c) For each structure, show how many types ofwould appear in theNMR spectrum.

(d) If an unknown compound of formulashows three types of and three types of ,can you determine its structure from this information?

Predict the multiplicity (the number of peaks as a result of splitting) and the chemical shift for all the protons in the following compounds.

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