ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
9th Edition
ISBN: 9781337034623
Author: McMurry
Publisher: CENGAGE C
Question
Book Icon
Chapter 17.SE, Problem 63AP
Interpretation Introduction

a)

ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<, Chapter 17.SE, Problem 63AP , additional homework tip  1

Interpretation:

Starting from testosterone how to prepare the compound shown is to be shown.

Concept introduction:

Pyridiniumchlorochromate in dichloromethane oxidizes 10 alcohols to aldehydes and 20 alcohols to ketones.

To show:

Starting from testosterone how to prepare the compound shown is to be stated.

Interpretation Introduction

b)

ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<, Chapter 17.SE, Problem 63AP , additional homework tip  2

Interpretation:

Starting from testosterone how to prepare the compound shown is to be stated.

Concept introduction:

LiAlH4 in ether reduces unsaturated aldehydes, acids and esters to 10 alcohols. It reduces ketones to 20 alcohols. The double bond remains unaffected during the reduction.

To state:

Starting from testosterone how to prepare the compound shown.

Interpretation Introduction

c)

ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<, Chapter 17.SE, Problem 63AP , additional homework tip  3

Interpretation:

Starting from testosterone how to prepare the compound shown is to be stated.

Concept introduction:

Pyridiniumchlorochromate in dichloromethane oxidizes 10 alcohols to aldehydes and 20 alcohols to ketones. H2, Pd/C can reduce the double bond in a compound without affecting aldehydic or keto group present in the compound.

To state:

Starting from testosterone how to prepare the compound shown.

Interpretation Introduction

d)

ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<, Chapter 17.SE, Problem 63AP , additional homework tip  4

Interpretation:

Starting from testosterone how to prepare the compound shown is to be stated.

Concept introduction:

LiAlH4 in ether reduces unsaturated aldehydes, acids and esters to 10 alcohols. It reduces ketones to 20 alcohols. The double bond remains unaffected during the reduction. The double bond can be reduced using H2, Pd/C.

To state:

Starting from testosterone how to prepare the compound shown.

Blurred answer
Students have asked these similar questions
How would you prepare the following substances from 1-butanol? Butylamine N,N-dimethylbutylamine Propene
Starting with 3-nitroaniline, show how to prepare the following compounds. Q.) 1,3-Dihydroxybenzene (resorcinol)
Starting with methyl propanoate, how could you prepare 4-methyl-3-heptanone?

Chapter 17 Solutions

ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<

Ch. 17.5 - Use the reaction of a Grignard reagent with a...Ch. 17.6 - How would you carry out the following...Ch. 17.6 - What products(s) would you expect from dehydration...Ch. 17.7 - What alcohols would give the following products on...Ch. 17.7 - What products would you expect from oxidation of...Ch. 17.8 - TMS ethers can be removed by treatment with...Ch. 17.9 - Show the mechanism for the reaction of...Ch. 17.11 - Prob. 18PCh. 17.11 - When the 1HNMR spectrum of an alcohol is run in...Ch. 17.SE - Give IUPAC names for the following compounds:Ch. 17.SE - Draw the structure of the carbonyl compound(s)...Ch. 17.SE - Prob. 22VCCh. 17.SE - Prob. 23VCCh. 17.SE - Name and assign R or S stereochemistry to the...Ch. 17.SE - Evidence for the intermediate carbocations in the...Ch. 17.SE - Acid-catalyzed dehydration of 2,...Ch. 17.SE - Prob. 27MPCh. 17.SE - Treatment of the following epoxide with aqueous...Ch. 17.SE - Prob. 29MPCh. 17.SE - Prob. 30MPCh. 17.SE - Identify the type of substitution mechanism (SN1,...Ch. 17.SE - The conversion of 3 alcohols into alkenes under...Ch. 17.SE - Prob. 33MPCh. 17.SE - The trimethylsilyl (TMS) protecting group is one...Ch. 17.SE - When the alcohol below is treated with POCI3 and...Ch. 17.SE - Phenols generally have lower pKa’s than...Ch. 17.SE - Give IUPAC names for the following compounds:Ch. 17.SE - Draw and name the eight isomeric alcohols with...Ch. 17.SE - Prob. 39APCh. 17.SE - Named bombykol, the sex pheromone secreted by the...Ch. 17.SE - Carvacrol is a naturally occurring substance...Ch. 17.SE - What Grignard reagent and what carbonyl compound...Ch. 17.SE - What carbonyl compounds would you reduce to...Ch. 17.SE - What carbonyl compounds might you start with to...Ch. 17.SE - Prob. 45APCh. 17.SE - What products would you obtain from reaction of...Ch. 17.SE - Prob. 47APCh. 17.SE - How would you prepare the following compounds from...Ch. 17.SE - Prob. 49APCh. 17.SE - What products would you expect to obtain from...Ch. 17.SE - Prob. 51APCh. 17.SE - Propose structures for alcohols that have the...Ch. 17.SE - Propose a structure consistent with the following...Ch. 17.SE - The 1HNMR spectrum shown is that of...Ch. 17.SE - A compound of unknown structure gave the following...Ch. 17.SE - Propose a structure for a compound C15H24O that...Ch. 17.SE - Prob. 57APCh. 17.SE - Prob. 58APCh. 17.SE - Rank the following substituted phenols in order of...Ch. 17.SE - Benzvl chloride can be converted into benzaldehvde...Ch. 17.SE - Prob. 61APCh. 17.SE - Prob. 62APCh. 17.SE - Prob. 63APCh. 17.SE - Prob. 64APCh. 17.SE - Prob. 65APCh. 17.SE - Prob. 66APCh. 17.SE - Dehydration of trans-2-methylcyclopentanol with...Ch. 17.SE - 2, 3-Dimethyl-2, 3-butanediol has the common name...Ch. 17.SE - As a rule, axial alcohols oxidize somewhat faster...Ch. 17.SE - Prob. 70APCh. 17.SE - A problem often encountered in the oxidation of...Ch. 17.SE - Identify the reagents a-f in the Following scheme:Ch. 17.SE - Prob. 73APCh. 17.SE - Prob. 74APCh. 17.SE - Compound A, C8H10O, has the IR and 1H NMR spectra...Ch. 17.SE - Prob. 76APCh. 17.SE - Prob. 77AP
Knowledge Booster
Background pattern image
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning