Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion
Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion
3rd Edition
ISBN: 9781119340577
Author: Klein
Publisher: Wiley (WileyPLUS Products)
Question
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Chapter 13.8, Problem 13PTS

(a)

Interpretation Introduction

Interpretation: The reagents are to be identified for Synthesis of Racemic mixture of Epoxides.

Concept Introduction:

Epoxides are obtained by the conversion of Alkene using Peroxy acids and Halohydrins

Epoxides from Peroxy acids:

The commonly used Peroxy acids are meta-Chloroperoxybenzoic acid (MCPBA) and Peroxyacetic acid. This process is stereospecific.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  1

Specifically, the substituent are cis to each other in starting Alkene remains cis to each other in Epoxide, and the substituent’s are trans to each other in starting Alkene remains trans to each other in Epoxide.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  2

Epoxides from Halohydrins:

Epoxides can be obtained by the conversion of Alkene to Halohydrins. Halohydrins are formed when an Alkene is treated with halogen in presence of Water. Halohydrins formed are later treated with strong base to from Epoxides.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  3

(b)

Interpretation Introduction

Interpretation: The reagents are to be identified for Synthesis of Racemic mixture of Epoxides.

Concept Introduction:

Epoxides are obtained by the conversion of Alkene using Peroxy acids and Halohydrins

Epoxides from Peroxy acids:

The commonly used Peroxy acids are meta-Chloroperoxybenzoic acid (MCPBA) and Peroxyacetic acid. This process is stereospecific.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  4

Specifically, the substituent are cis to each other in starting Alkene remains cis to each other in Epoxide, and the substituent’s are trans to each other in starting Alkene remains trans to each other in Epoxide.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  5

Epoxides from Halohydrins:

Epoxides can be obtained by the conversion of Alkene to Halohydrins. Halohydrins are formed when an Alkene is treated with halogen in presence of Water. Halohydrins formed are later treated with strong base to from Epoxides.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  6

(c)

Interpretation Introduction

Interpretation: The reagents are to be identified for Synthesis of Racemic mixture of Epoxides.

Concept Introduction:

Epoxides are obtained by the conversion of Alkene using Peroxy acids and Halohydrins

Epoxides from Peroxy acids:

The commonly used Peroxy acids are meta-Chloroperoxybenzoic acid (MCPBA) and Peroxyacetic acid. This process is stereospecific.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  7

Specifically, the substituent are cis to each other in starting Alkene remains cis to each other in Epoxide, and the substituent’s are trans to each other in starting Alkene remains trans to each other in Epoxide.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  8

Epoxides from Halohydrins:

Epoxides can be obtained by the conversion of Alkene to Halohydrins. Halohydrins are formed when an Alkene is treated with halogen in presence of Water. Halohydrins formed are later treated with strong base to from Epoxides.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  9

(d)

Interpretation Introduction

Interpretation: The reagents are to be identified for Synthesis of Racemic mixture of Epoxides.

Concept Introduction:

Epoxides are obtained by the conversion of Alkene using Peroxy acids and Halohydrins

Epoxides from Peroxy acids:

The commonly used Peroxy acids are meta-Chloroperoxybenzoic acid (MCPBA) and Peroxyacetic acid. This process is stereospecific.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  10

Specifically, the substituent are cis to each other in starting Alkene remains cis to each other in Epoxide, and the substituent’s are trans to each other in starting Alkene remains trans to each other in Epoxide.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  11

Epoxides from Halohydrins:

Epoxides can be obtained by the conversion of Alkene to Halohydrins. Halohydrins are formed when an Alkene is treated with halogen in presence of Water. Halohydrins formed are later treated with strong base to from Epoxides.

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion, Chapter 13.8, Problem 13PTS , additional homework tip  12

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Chapter 13 Solutions

Organic Chemistry, 3e WileyPLUS Registration Card + Loose-leaf Print Companion

Ch. 13.5 - Prob. 9CCCh. 13.6 - Prob. 10CCCh. 13.7 - Prob. 11CCCh. 13.7 - Prob. 12CCCh. 13.8 - Prob. 3LTSCh. 13.8 - Prob. 13PTSCh. 13.8 - Prob. 14ATSCh. 13.9 - Prob. 15CCCh. 13.10 - Prob. 4LTSCh. 13.10 - Prob. 16PTSCh. 13.10 - Prob. 17ATSCh. 13.10 - Prob. 5LTSCh. 13.10 - Prob. 18PTSCh. 13.10 - The sequence below shows an enantioselective...Ch. 13.11 - Prob. 20CCCh. 13.11 - Prob. 21CCCh. 13.12 - Prob. 6LTSCh. 13.12 - Prob. 22PTSCh. 13.12 - Prob. 23ATSCh. 13.12 - Prob. 7LTSCh. 13.12 - Prob. 24PTSCh. 13.12 - Prob. 25ATSCh. 13 - Prob. 26PPCh. 13 - Prob. 27PPCh. 13 - Prob. 28PPCh. 13 - Prob. 29PPCh. 13 - Prob. 30PPCh. 13 - Prob. 31PPCh. 13 - Prob. 32PPCh. 13 - Methylmagnesium bromide reacts rapidly with...Ch. 13 - Prob. 34PPCh. 13 - Prob. 35PPCh. 13 - Prob. 36PPCh. 13 - Prob. 37PPCh. 13 - Prob. 38PPCh. 13 - Prob. 39PPCh. 13 - Prob. 40PPCh. 13 - Prob. 41PPCh. 13 - Prob. 42PPCh. 13 - Prob. 43PPCh. 13 - Prob. 44PPCh. 13 - Prob. 45PPCh. 13 - Prob. 46IPCh. 13 - Prob. 47IPCh. 13 - Prob. 48IPCh. 13 - Prob. 49IPCh. 13 - Prob. 50IPCh. 13 - Prob. 51IPCh. 13 - Prob. 52IPCh. 13 - Prob. 53IPCh. 13 - Prob. 54IPCh. 13 - Prob. 55IPCh. 13 - Prob. 56IPCh. 13 - Prob. 57IPCh. 13 - Prob. 58IPCh. 13 - Prob. 59IPCh. 13 - Prob. 60IPCh. 13 - Prob. 61IPCh. 13 - Prob. 62IPCh. 13 - Prob. 63IPCh. 13 - Prob. 64IPCh. 13 - Prob. 65IPCh. 13 - Prob. 66IPCh. 13 - Prob. 67IPCh. 13 - Prob. 68IPCh. 13 - Prob. 69IPCh. 13 - Prob. 70IPCh. 13 - The following procedure13 is part of a synthetic...Ch. 13 - Prob. 72CPCh. 13 - Prob. 73CPCh. 13 - Prob. 74CPCh. 13 - Prob. 75CP
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