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Chapter 9: Q. 9-9-3 P-a (page 265)

What products would you expect from the following reactions?

a. CH3CH2CH2C鈮�CH+Cl2

Short Answer

Expert verified

a.

Step by step solution

01

Markovnikov reactions

In this the alkyne is converted to alkene by the halogenation that the three out of one triple bond is break foe the addition of halogen but the halogen are added always in trans geometry.

02

Reaction of alkyne with halide CH3CH2CH2C≡CH+Cl2

When alkyne reacts with halide they undergo an additional reaction to form a halogen-substituted alkene. Alkyne follows Markovnikov regiochemistry in which two added halogen atoms are always in a trans relationship with each other as shown:

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Most popular questions from this chapter

What alkynes would you start with to prepare the following ketones?

Terminal alkynes react with and water to yield bromo ketones. For example:

Propose a mechanism for the reaction. To what reaction of alkenes is

the process analogous?

Using any alkyne needed, how would you prepare the following alkenes?

(b) cis-3-Heptene

Show the terminal alkyne and alkyl halide from which the following products can be obtained. If two routes look feasible, list both.

b.(CH3)2CHC鈮�CCH2CH3

There are seven isomeric alkynes with the formulaC6H10 . Draw and name them.
See all solutions

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