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Chapter 12: Q.63. (page 492)

Question:Devise a synthesis of each compound from acetylene and any other required reagents.

Short Answer

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Answer

Step by step solution

01

Retrosynthetic analysis

Retrosynthesis is the stepwise breakdown of the product to determine the starting materials used in the reaction. It also gives an idea about the pathway of the reaction and the reagents used.

02

Determination of synthetic pathway and reagents

The retrosynthetic analysis of the given compound is given below:

Retrosynthesis of compound b

The synthetic pathway is:

Synthesis of compound b

c.

The retrosynthetic analysis of the given compound is given below:

Retrosynthesis of compound c.

The synthetic pathway is:

Synthesis of compound c.

d.

The retrosynthetic analysis of the given compound is given below:

Retrosynthesis of compound d.

The synthetic pathway is:

Synthesis of compound d

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Most popular questions from this chapter

Question: Identify compounds A, B, and C.

a. Compound A has molecular formula C8H12 and reacts with two equivalents of H2. A gives HCOCH2CH2CHOas the only product of oxidative cleavage with O3followed byCH3SCH3.

b. Compound B has molecular formula C6H10and gives (CH3)2CHCH2CH2CH3 when treated with excess H2 in the presence of Pd. B reacts with NaNH2and CH3Ito form compound C (molecular formula C7H12).

Question:Devise a synthesis of (E)-hex-2-ene from pent-1-ene and any needed organic compounds or inorganic reagents.

Question: Draw the product of each asymmetric epoxidation reaction.

Question: Draw the structure of two different epoxides that would yield 2-methylpentan-2-ol [ (CH3)2CH(OH)CH2CH2CH3] when reduced with LiAlH4 .

Question: Draw all alkenes that react with one equivalent of H2 in the presence of a palladium catalyst to form each alkane. Consider constitutional isomers only

a.

b.

c.
See all solutions

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