Organic Chemistry, Books a la Carte Edition (9th Edition)
Organic Chemistry, Books a la Carte Edition (9th Edition)
9th Edition
ISBN: 9780134160382
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
Question
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Chapter 10, Problem 10.52SP

(a)

Interpretation Introduction

To determine: The synthesis of the given compound 1-methylcyclohexanol with methylenecyclohexane as a starting material.

Interpretation: The synthesis of the given compound 1-methylcyclohexanol with methylenecyclohexane as a starting material is to be devised.

Concept introduction: Methylenecyclohexane is a compound which has molecular formula C7H12. Its molar mass is 96.17g/mol. It is used in organic synthesis of many compounds. It is produced by different types of reactions such as Tebbe reaction from cyclohexanone or by the Wittig reaction.

(b)

Interpretation Introduction

To determine: The synthesis of the given compound with methylenecyclohexane as a starting material.

Interpretation: The synthesis of the given compound with methylenecyclohexane as a starting material is to be devised.

Concept introduction: Methylenecyclohexane is a compound which has molecular formula C7H12. It is used in organic synthesis of many compounds.

It is produced by different types of reactions such as Tebbe reaction from cyclohexanone or by the Wittig reaction. Its molar mass is 96.17g/mol.

(c)

Interpretation Introduction

To determine: The synthesis of the given compound 1-(hydroxymethyl)cyclohexanol with methylenecyclohexane as a starting material.

Interpretation: The synthesis of the given compound 1-(hydroxymethyl)cyclohexanol with methylenecyclohexane as a starting material is to be devised.

Concept introduction: Methylenecyclohexane is a compound which has molecular formula C7H12. It is used in organic synthesis of many compounds.

It is produced by different types of reactions such as Tebbe reaction from cyclohexanone or by the Wittig reaction. Its molar mass is 96.17g/mol.

(d)

Interpretation Introduction

To determine: The synthesis of the given compound trans-2-methylcyclohexanol with methylenecyclohexane as a starting material.

Interpretation: The synthesis of the given compound trans-2-methylcyclohexanol with methylenecyclohexane as a starting material is to be devised.

Concept introduction: Methylenecyclohexane is a compound which has molecular formula C7H12. It is used in organic synthesis of many compounds.

It is produced by different types of reactions such as Tebbe reaction from cyclohexanone or by the Wittig reaction. Its molar mass is 96.17g/mol.

(e)

Interpretation Introduction

To determine: The synthesis of the given compound 2-chloro-1-methylcyclohexanol with methylenecyclohexane as a starting material.

Interpretation: The synthesis of the given compound 2-chloro-1-methylcyclohexanol with methylenecyclohexane as a starting material is to be devised.

Concept introduction: Methylenecyclohexane is a compound which has molecular formula C7H12. It is used in organic synthesis of many compounds.

It is produced by different types of reactions such as by Tebbe reaction from cyclohexanone or by the Wittig reaction. Its molar mass is 96.17g/mol.

(f)

Interpretation Introduction

To determine: The synthesis of the given compound 1-(phenylmethyl)cyclohexanol with methylenecyclohexane as a starting material.

Interpretation: The synthesis of the given compound 1-(phenylmethyl)cyclohexanol with methylenecyclohexane as a starting material is to be devised.

Concept introduction: Methylenecyclohexane is a compound which has molecular formula C7H12. It is used in organic synthesis of many compounds.

It is produced by different types of reactions such as Tebbe reaction from cyclohexanone or by the Wittig reaction. Its molar mass is 96.17g/mol.

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Chapter 10 Solutions

Organic Chemistry, Books a la Carte Edition (9th Edition)

Ch. 10.8B - Prob. 10.11PCh. 10.8B - Prob. 10.12PCh. 10.9A - Prob. 10.13PCh. 10.9B - Prob. 10.14PCh. 10.9C - Show how you would synthesize each tertiary...Ch. 10.9D - Prob. 10.16PCh. 10.9D - Show how you would add Grignard reagents to acid...Ch. 10.9D - A formate ester, such as ethyl formate, reacts...Ch. 10.9E - Prob. 10.19PCh. 10.9E - In Section9-7B, we saw how acetylide ions add to...Ch. 10.9F - Prob. 10.21PCh. 10.10A - Prob. 10.22PCh. 10.10B - Prob. 10.23PCh. 10.11B - Predict the products you would expect from the...Ch. 10.11B - Prob. 10.25PCh. 10.11B - Prob. 10.26PCh. 10.12 - Prob. 10.27PCh. 10.12 - Prob. 10.28PCh. 10.12 - Authentic skunk spray has become valuable for use...Ch. 10 - Give a systematic (IUPAC) name for each alcohol....Ch. 10 - Give systematic (IUPAC) names for the following...Ch. 10 - Draw the structures of the following compounds...Ch. 10 - Predict which member of each pair has the higher...Ch. 10 - Predict which member of each pair is more acidic,...Ch. 10 - Predict which member of each group is most soluble...Ch. 10 - Draw the organic products you would expect to...Ch. 10 - Prob. 10.37SPCh. 10 - Show how you would synthesize the following...Ch. 10 - Show how you would use Grignard syntheses to...Ch. 10 - Show how you would accomplish the following...Ch. 10 - Show how you would synthesize the following: a....Ch. 10 - Complete the following acid-base reactions. In...Ch. 10 - Prob. 10.43SPCh. 10 - Prob. 10.44SPCh. 10 - Geminal diols, or 1,1-diols, are usually unstable,...Ch. 10 - Vinyl alcohols are generally unstable, quickly...Ch. 10 - Compound A (C7H11Br) is treated with magnesium in...Ch. 10 - Prob. 10.48SPCh. 10 - Prob. 10.49SPCh. 10 - Prob. 10.50SPCh. 10 - Prob. 10.51SPCh. 10 - Prob. 10.52SPCh. 10 - Prob. 10.53SPCh. 10 - Prob. 10.54SPCh. 10 - Prob. 10.55SPCh. 10 - Prob. 10.56SPCh. 10 - Show how this 1 alcohol can be made from the...Ch. 10 - Prob. 10.58SPCh. 10 - Prob. 10.59SPCh. 10 - Prob. 10.60SP
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