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Chapter 6: Q53P (page 280)

Show how each of the following compounds can be synthesized from an alkene:

Short Answer

Expert verified

All the reactions are proceeded from alkene in the presence of some conditions.

In this markoniv and antimarkoniv addition takes place.

Markoniv addition= Positive ion will go to that double bonded carbon which has more no of hydrogens attached and negative ion will go towards that carbon which has less number of hydrogens attached.

Step by step solution

01

How the reaction proceed

All the reactions are proceeded from alkene in the presence of some conditions.

In this markoniv and antimarkoniv addition takes place.

Markoniv addition= Positive ion will go to that double bonded carbon which has more no of hydrogens attached and negative ion will go towards that carbon which has less number of hydrogens attached.

02

Final answer

a) Here markoniv addition takes place as OCH3-and H+ ions will form.

b) Here Br+ and Br- will form and attached with double bonded carbon atoms.

c) Antimarkoniv addition takes place.

d) Markoniv addition takes place.

e) Markoniv addition takes place.

f) Markoniv addition takes place.

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Most popular questions from this chapter

What reagents are needed to synthesize the following alcohols?

a. What is the major product obtained from the reaction of propene and Br2plus excess Cl-?

b. Indicate the relative amounts of the stereoisomers that are obtained.

What stereoisomers would you expect to obtain from each of the following reactions

What stereoisomers are obtained when (S)-3-methyl-1-pentene reacts with Cl2?

Which is more stable?
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