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Chapter 21: Q80E (page 726)

Draw the structure of the compound that produced the spectra below.

The infrared spectrum has strong bands at1720 and 1738 cm-1

Short Answer

Expert verified

The Structure should be

Step by step solution

01

Step 1: Apply the given Formula

The Given Formula Molecular formula is C7H12O3.

Therefore, The Compound is acid and alcohol.

02

Draw the Structure of the reaction

The IR values correspond to these functional group.

The Structure should be

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Most popular questions from this chapter

How would you convert N-ethylbenzamide to each of the following products?

(a) Benzoic acid (b) Benzyl alcohol (c)C6H5CH2NHCH2CH3

21-50 Answer Problem 21-48 for the reaction of the listed reagents withpropanamide

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The hydrolysis of a biological thioester to the corresponding carboxylate is often more complex than the overall result might suggest. The conversion of succinyl CoA to succinate in the citric acid cycle, for instance, occurs by initial formation of an acyl phosphate, followed by reaction with guanosine diphosphate (GDP, a relative of adenosine diphosphate [ADP]) to give succinate and guanosine triphosphate (GTP, a relative of ATP). Suggest mechanisms for both steps.

21-75 One frequently used method for preparing methyl esters is by reactionof carboxylic acids with diazomethane, CH2N2

The reaction occurs in two steps: (1) protonation of diazomethane bythe carboxylic acid to yield methyldiazonium ion,, CH3N2+plus a carboxylate ion; and (2) reaction of the carboxylate ion with CH3N2+.
(a) Draw two resonance structures of diazomethane, and account forstep 1.
(b) What kind of reaction occurs in step 2?
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