The structures of the products formed when 1-methylcyclopentene reacts with the given reagents are to be written. Concept Introduction: Hydroboration-oxidation: An organic reaction in which the double bonds of alkenes or alkynes are broken by BH 3 . In this reaction, the multiple carbon–carbon bond has been replaced by the boron group and at last to OH group on addition of hydrogen peroxide. Reduction is a process in which hydrogen atoms are added to a compound. Usual reagents used in the reduction process are H 2 / Pt / pressure , or H 2 / Ni / pressure . Ozonolysis: An organic reaction in which the double bonds of alkenes, alkynes, or azo compounds are broken by ozone. In this reaction, the multiple carbon–carbon bond has been replaced by a carbonyl group while azo compounds form nitrosamines. Oxymercuration-demercuration: An organic reaction in which the double bonds of alkenes or alkynes are broken by HgOAc . In this reaction, the multiple carbon–carbon bond has been replaced by the OH group. Alkenes or alkynes undergo halogenation reaction in the presence of halides like Br 2 and form substituted products.

Question

Want to see the full answer?

Answer 1

Question

Chapter 8, Problem 27P

Interpretation Introduction

Interpretation:

The structures of the products formed when 1-methylcyclopentene reacts with the given reagents are to be written.

Concept Introduction:

Hydroboration-oxidation: An organic reaction in which the double bonds of alkenes or alkynes are broken by BH3. In this reaction, the multiple carbon–carbon bond has been replaced by the boron group and at last to OH group on addition of hydrogen peroxide.

Reduction is a process in which hydrogen atoms are added to a compound.

Usual reagents used in the reduction process are H2/Pt/pressure, or H2/Ni/pressure.

Ozonolysis: An organic reaction in which the double bonds of alkenes, alkynes, or azo compounds are broken by ozone. In this reaction, the multiple carbon–carbon bond has been replaced by a carbonyl group while azo compounds form nitrosamines.

Oxymercuration-demercuration: An organic reaction in which the double bonds of alkenes or alkynes are broken by HgOAc. In this reaction, the multiple carbon–carbon bond has been replaced by the OH group.

Alkenes or alkynes undergo halogenation reaction in the presence of halides like Br2 and form substituted products.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

5) Compound A reacted with Mg in ether to give B. Compound B is with Ethyl bromide to give Ethyl cyclohexane. What are the structures of A and B?

Explain the role strain plays on stability and reactivity of a cyclic alkane such as cyclopropane.

The heat of combustion of decahydronaphthalene(C10H18) is -6286 kJ/mol. The heat of combustion ofnaphthalene (C10H8) is -5157 kJ/mol. (In both casesCO2(g) and H2O(l) are the products.) Calculate the heat of hydrogenationand the resonance energy of naphthalene.