ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
3rd Edition
ISBN: 9781119497479
Author: Klein
Publisher: WILEY
Question
Book Icon
Chapter 12, Problem 60IP

(a)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

(b)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

(c)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

(d)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

(e)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

(f)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

(g)

Interpretation Introduction

Interpretation:

The synthesis of the given product transformation should be identified.

Concept introduction:

Bromination:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using Br2 which provides corresponding brominated products.

Oxidation: Alcohols undergoing oxidation by using oxidizing agent like Na2Cr2O7 which provides ketone or carboxylic acid.

9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols

Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.

Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol

Hydrogenation: Molecular hydrogen ( H2 ) and element, usually in the presence of a catalyst such as nickel, palladium or platinum are used for hydrogenation process.

Blurred answer
Students have asked these similar questions
Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 IZ IN Molecule 4 Molecule 5 ZI none of the above ☐ Molecule 3 Х IN www Molecule 6 NH G
Highlight each chiral center in the following molecule. If there are none, then check the box under the drawing area. There are no chiral centers. Cl Cl Highlight
A student proposes the following two-step synthesis of an ether from an alcohol A: 1. strong base A 2. R Is the student's proposed synthesis likely to work? If you said the proposed synthesis would work, enter the chemical formula or common abbreviation for an appropriate strong base to use in Step 1: If you said the synthesis would work, draw the structure of an alcohol A, and the structure of the additional reagent R needed in Step 2, in the drawing area below. If there's more than one reasonable choice for a good reaction yield, you can draw any of them. ☐ Click and drag to start drawing a structure. Yes No ロ→ロ 0|0 G Х D : ☐ ப

Chapter 12 Solutions

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)

Ch. 12.4 - Prob. 3LTSCh. 12.4 - Prob. 9PTSCh. 12.4 - Prob. 10ATSCh. 12.4 - Prob. 4LTSCh. 12.4 - Prob. 11PTSCh. 12.4 - Prob. 12ATSCh. 12.6 - Prob. 5LTSCh. 12.6 - Prob. 13PTSCh. 12.6 - Prob. 14PTSCh. 12.7 - Prob. 16CCCh. 12.9 - Prob. 6LTSCh. 12.9 - Prob. 17PTSCh. 12.9 - Prob. 18ATSCh. 12.9 - Prob. 19CCCh. 12.10 - Prob. 7LTSCh. 12.10 - PRACTICE the skill Predict the major organic...Ch. 12.10 - Prob. 21ATSCh. 12.13 - Prob. 8LTSCh. 12.13 - Prob. 22PTSCh. 12.13 - Prob. 23ATSCh. 12.13 - Prob. 24CCCh. 12.13 - Prob. 9LTSCh. 12.13 - Prob. 25PTSCh. 12.13 - Prob. 26ATSCh. 12 - Prob. 27PPCh. 12 - Prob. 28PPCh. 12 - Prob. 29PPCh. 12 - Prob. 30PPCh. 12 - Prob. 31PPCh. 12 - Predict the major product of the reaction between...Ch. 12 - Prob. 33PPCh. 12 - Prob. 34PPCh. 12 - Using a Grignard reaction, show how you could...Ch. 12 - Each of the following alcohols can be prepared via...Ch. 12 - Prob. 37PPCh. 12 - Prob. 38PPCh. 12 - Prob. 39PPCh. 12 - Prob. 40PPCh. 12 - Prob. 41PPCh. 12 - Prob. 42PPCh. 12 - Prob. 43PPCh. 12 - Prob. 44PPCh. 12 - Prob. 45PPCh. 12 - Prob. 46PPCh. 12 - Prob. 47PPCh. 12 - Prob. 48PPCh. 12 - Prob. 49PPCh. 12 - Prob. 50PPCh. 12 - Prob. 51IPCh. 12 - Prob. 52IPCh. 12 - Prob. 53IPCh. 12 - Prob. 54IPCh. 12 - Prob. 55IPCh. 12 - Prob. 56IPCh. 12 - Prob. 57IPCh. 12 - Prob. 58IPCh. 12 - Prob. 59IPCh. 12 - Prob. 60IPCh. 12 - Prob. 61IPCh. 12 - Prob. 62IPCh. 12 - Prob. 63IPCh. 12 - Prob. 64IPCh. 12 - Prob. 65IPCh. 12 - The compound duryne was one of several...Ch. 12 - Estragole is an insect repellant that has been...Ch. 12 - Prob. 68IPCh. 12 - Prob. 70IPCh. 12 - Prob. 71IPCh. 12 - Prob. 72IPCh. 12 - Prob. 73IPCh. 12 - Prob. 74IPCh. 12 - Prob. 75CPCh. 12 - Prob. 76CPCh. 12 - Prob. 77CP
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY