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Chapter 8: Q15P (page 418)

Sketch the expected proton NMR spectra of 3,3- dimethylbutanal.

Short Answer

Expert verified

The compound 3,3-dimethylbutanal has a functional group aldehyde.

The structure of 3,3-dimethylbutanal is as shown below:

Step by step solution

01

The structure of 3,3-dimethylbutanal

The compound 3,3-dimethylbutanal has a functional group aldehyde.

The structure of 3,3-dimethylbutanal is as shown below:

02

The proton NMR spectrum of 3,3-dimethylbutanal

The given compound 3,3-dimethylbutanal has the following chemical shift values for chemically different protons.

It has three sets of chemically different protons.

The graph of NMR spectrum is shown below:

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Most popular questions from this chapter

Predict the carbenoid addition products of the following reactions.

(a) trans-hex-3-ene+ CH2I2, Zn(Cu)

(b) ciz-hept-2-ene+ CH2I2, Zn(Cu)

Predictthe major products of the following reactions.

a. E- 3-methyloct-3-ene+ ozone, then Me3S

b. Z- 3-methyloct-3-ene+ ozone, then Me3S

e. 1-ethylcycloheptene + ozone, then Me2S

f. 1-ethylcycloheptene + warm, then KMnO4

g. 1-ethylcycloheptene + cold,, dil.KMnO4

Question: Show how you would accomplish the following synthetic conversions.

  1. 3-methylpent-2-ene to 2-chloro-3-methylpentan-3-ol
  2. Chlorocyclohexane to trans-2-chlorocyclohexaol
  3. 1-methylcyclopentanol to 2-chloro-1-methylcyclopentanol

Show how you would accomplish each of the following synthetic conversions.

Propose a mechanism to show how 3,3-dimethylbut-1-ene reacts with dilute aqueous H2SO4to give 2,3-dimethylbutan-2-ol and a small amount of 2,3-dimethylbut-2-ene.
See all solutions

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