Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
Question
Book Icon
Chapter 11.2C, Problem 11.2P

(a)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(b)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(c)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(d)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(e)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(f)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(g)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

(h)

Interpretation Introduction

To determine: The products of the reactions with the given compound.

Interpretation: The products of the reactions with the given compounds are to be stated.

Concept introduction: The combination of chromic acid or excess sodium hypochlorite with acetic acid is used for the conversion of secondary alcohols into ketone and primary alcohols or aldehyde into carboxylic acid through oxidation reaction.

The combination of PCCorNaOCl(1equivalent) with TEMPO is used for the conversion of primary alcohols into aldehyde and secondary alcohol into ketone through selective oxidation reaction.

Blurred answer
Students have asked these similar questions
Why is diethyl ether used as a solvent for the reduction reaction of the keystone (3,3-dimethyl-2-butanone) utilizing the reducing agent sodium borohydride (NaBH4). what is the purpose of was repeated washes with water? What is the purpose of repeated washes with brine?
Describe how the product is purified. 4,4'-DIBROMOBIPHENYL [Biphenyl, 4,4'-dibromo-] Submitted by Robert E. Buckles and Norris G. Wheeler1. Checked by R. S. Schreiber, Wm. Bradley Reid, Jr., and Robert W. Jackson. 1. Procedure In a 15-cm. evaporating dish is placed 15.4 g. (0.10 mole) of finely powdered biphenyl (Note 1). The dish is set on a porcelain rack in a 30-cm. desiccator with a 10-cm. evaporating dish under the rack containing 39 g. (12 ml., 0.24 mole) of bromine. The desiccator is closed, but a very small opening is provided for the escape of hydrogen bromide (Note 2). The biphenyl is left in contact with the bromine vapor for 8 hours (or overnight). The orange solid is then removed from the desiccator and allowed to stand in the air under a hood for at least 4 hours (Note 3). At this point, the product weighs about 30 g. and has a melting point in the neighborhood of 152°. The crude 4,4'-dibromobiphenyl is dissolved in 75 ml. of benzene, filtered, and cooled to 15°. The…
A Grignard reaction of phenylmagnesium bromide with 3-pentanone gives 3-phenylpentan-3-ol as the major product. The crude product contains the 3-phenylpentan-3-ol product, unreacted 3-pentanone, and biphenyl (a side product). A developing solvent is found that separates the mixture into three spots on a silica gel TLC plate. Considering the functional groups present, predict which compounds would have the smallest and largest Rf values. Briefly justify your answer.

Chapter 11 Solutions

Organic Chemistry (9th Edition)

Ch. 11.6 - Predict the products of the following reactions....Ch. 11.7A - Propose a mechanism for the reaction of a....Ch. 11.7B - Prob. 11.13PCh. 11.7B - Show how you would use a simple chemical test to...Ch. 11.7C - Neopentyl alcohol, (CH3)3CCH2OH, reacts with...Ch. 11.7C - Prob. 11.16PCh. 11.7C - When cis-2-methylcyclohexanol reacts with the...Ch. 11.8 - Prob. 11.18PCh. 11.9 - Prob. 11.19PCh. 11.9 - Prob. 11.20PCh. 11.9 - Prob. 11.21PCh. 11.10A - Prob. 11.22PCh. 11.10A - Some alcohols undergo rearrangement or other...Ch. 11.10B - Prob. 11.24PCh. 11.10B - Explain why the acid-catalyzed condensation is a...Ch. 11.10B - Prob. 11.26PCh. 11.10B - When the following substituted cycloheptanol...Ch. 11.11A - Prob. 11.28PCh. 11.11A - Prob. 11.29PCh. 11.11B - Predict the products formed by periodic acid...Ch. 11.12 - Prob. 11.31PCh. 11.13A - Prob. 11.32PCh. 11.14 - Prob. 11.33PCh. 11.14 - a. Show how ethanol and cyclohexanol may be used...Ch. 11.14 - Prob. 11.35PCh. 11.14 - Phenols (pKa 10) are more acidic than other...Ch. 11.14 - To practice working through the early parts of a...Ch. 11.14 - Prob. 11.38PCh. 11 - Predict the major products of the following...Ch. 11 - Show how you would convert 2-methylcyclopentanol...Ch. 11 - In each case, show how you would synthesize the...Ch. 11 - Prob. 11.42SPCh. 11 - Prob. 11.43SPCh. 11 - Prob. 11.44SPCh. 11 - Both cis- and trans-2-methylcyclohexanol undergo...Ch. 11 - Prob. 11.46SPCh. 11 - Prob. 11.47SPCh. 11 - Show how you would make each compound, beginning...Ch. 11 - Predict the major products (including...Ch. 11 - Show how you would use simple chemical tests to...Ch. 11 - The compound shown below has three different types...Ch. 11 - Prob. 11.52SPCh. 11 - Prob. 11.53SPCh. 11 - Prob. 11.54SPCh. 11 - Prob. 11.55SPCh. 11 - Show how you would synthesize the following...Ch. 11 - Show how you would synthesize the following...Ch. 11 - The following pseudo-syntheses (guaranteed not to...Ch. 11 - Two unknowns, X and Y, both having the molecular...Ch. 11 - The Williamson ether synthesis involves the...Ch. 11 - Prob. 11.61SPCh. 11 - Prob. 11.62SPCh. 11 - Alcohols combine with ketones and aldehydes to...Ch. 11 - Prob. 11.64SPCh. 11 - Prob. 11.65SPCh. 11 - Prob. 11.66SP
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT