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Chapter 17: Q61P (page 848)

Show how 4-methyl-3-hexanol can be synthesised from 3-pentanone.

Short Answer

Expert verified

The answer is,

Reaction

Step by step solution

Chemical reaction

The reaction of 3-pentanone with a strong base like LDA (Lithium diisopropylamine) gives the enolate ion, which reacts with alkylation using alkyl chloride to give the product 4-methyl-3-hexanol.

Explanation

The reaction for the synthesis of 3-pentanone from 4-methyl-3-hexanol is as given below.

Reaction

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Most popular questions from this chapter

Indicate how the following compounds can be synthesized from cyclohexanone and any other necessary reagents:

Rank the compounds in each of the following groups from strongest acid to weakest acid

Design a synthesis for each of the following compounds using the given starting material:

Explain why the pK_aof a hydrogen bonded to the sp³carbon of propene is greater (pK_a= 42) than that of any of the carbon acids listed in Table 17.1, but is less than the pK_aof an alkane (pK_a> 60).

Show how the following compound can be prepared from starting materials that have no more than five carbons:

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Show how 4-methyl-3-hexanol can be synthesised from 3-pentanone.

Short Answer

Step by step solution

Chemical reaction

Explanation

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Most popular questions from this chapter

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