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 In this reaction, the multiple carbon–carbon bond has been replaced by the boron group and at last to OH group on addition of hydrogen peroxide.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 In this reaction, the multiple carbon–carbon bond has been replaced by a carbonyl group while azo compounds form nitrosamines.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 In this reaction, the multiple carbon–carbon bond has been replaced by the OH group.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.

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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 In this reaction, the multiple carbon–carbon bond has been replaced by the boron group and at last to OH group on addition of hydrogen peroxide.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 In this reaction, the multiple carbon–carbon bond has been replaced by a carbonyl group while azo compounds form nitrosamines.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 In this reaction, the multiple carbon–carbon bond has been replaced by the OH group.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.

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