Organic Chemistry
Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 10, Problem 10.57AP
Interpretation Introduction

Interpretation:

The compounds A,B,C and D formed in the reaction are to be stated.

Concept introduction:

The conversion of an alcohol to ketone and ketone to carboxylic is known as the oxidation reaction. The reaction in which either oxygen is being added or hydrogen is being removed is termed as the oxidation reaction. Enantiomers are the stereoisomers in which configuration of each carbon present in the molecule is reverse from that of the other pair.

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5. Compound A, C 10H 18O, undergoes reaction with dilute H 2SO 4 at 50 °C to yield a mixture of two alkenes, C 10H 16.  The major alkene B, gives only cyclopentanone after ozone treatment followed by reduction with zinc in acetic acid.  Which of the following reactions are correct.
A certain compound of molecular formula C19H38 was isolated from fish oil and from plankton. On hydrogenation it gave 2,6,10,14-tetramethylpentadecane. Ozonolysis gave (CH3)2C O and a 16-carbon aldehyde. What is the structure of the natural product? What is the structure of the aldehyde?
Compound A, C 10H 18O, undergoes reaction with dilute H 2SO 4 at 50 °C to yield a mixture of two alkenes, C 10H 16.  The major alkene B, gives only cyclopentanone after ozone treatment followed by reduction with zinc in acetic acid.  Which of the following reactions are correct. Can be more than one answer

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