Chapter 19: Q86E (page 648)
The proton and carbon NMR spectra for each of three isomeric ketones with the formula C7H14Oare shown below. Assign a structure to each pair of spectra.
Short Answer
A)
B)
Assignment of the NMR spectrum
C)
Chapter 19: Q86E (page 648)
The proton and carbon NMR spectra for each of three isomeric ketones with the formula C7H14Oare shown below. Assign a structure to each pair of spectra.
A)
B)
Assignment of the NMR spectrum
C)
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Get started for freePropose structures for molecules that meet the following descriptions.
Assume that the kinds of carbons (1°, 2°, 3°, or 4°) have been assigned
by DEPT–NMR.
(a); IR: 1715; 13C NMR: 8.0 (1°), 18.5 (1°), 33.5(2°),
40.6 (3°), 214.0 (4°)
(b); IR: 1730; 13C NMR: 22.6 (1°), 23.6 (3°), 52.8 (2°),
202.4 (3°)
(c); IR: 1680; 13C NMR: 22.9(2°), 25.8 (2°), 38.2 (2°),
129.8 d(3°), 150.6 (3°), 198.7 (4°)
How would you use a Grignard reaction on an aldehyde or ketone to synthesize the following compounds?
The 1HNMR spectrum shown is that of a compound isomeric with the one in Problem 19-81. This isomer has an IR absorption at 1730 cm-1. Propose a structure.
[Note: Aldehyde protons (CHO) often show low coupling constants to adjacent hydrogens, so the splitting of aldehyde signals is not always apparent.]
One of the steps in metabolism of fats is the reaction of an unsaturated acyl coA with water to give a - hydroxyacyl CoA. Propose a mechanism.
How might conjugate addition reactions of lithium diorganocopper reagents be used to synthesize the following compounds?
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