ORGANIC CHEM +SG +SAPLING >IP<
ORGANIC CHEM +SG +SAPLING >IP<
6th Edition
ISBN: 9781319171179
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 24, Problem 24.6P
Interpretation Introduction

(a)

Interpretation:

The reaction mechanism for the conversion of aldose into cyclic hemiacetals is to be stated.

Concept introduction:

Aldoses are the carbohydrates in which an aldehyde group is present. The aldehyde carbon is numbered one in Fischer projection. A carbohydrate consists of six carbon atoms chain and an aldehyde group is known as aldohexose. Carbohydrates in which the hydroxyl-aldehyde is present at the γ, or δ position, is usually exist as cyclic hemiacetals.

Interpretation Introduction

(b)

Interpretation:

The reaction mechanism for the conversion of aldose into cyclic hemiacetals is to be stated.

Concept introduction:

Aldoses are the carbohydrates in which an aldehyde group is present. The aldehyde carbon is numbered one in Fischer projection. A carbohydrate consists of six carbon atoms chain and an aldehyde group is known as aldohexose. Carbohydrates in which the hydroxyl-aldehyde is present at the γ, or δ position, is usually exist as cyclic hemiacetals.

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Part II. two unbranched ketone have molecular formulla (C8H100). El-ms showed that both of them have a molecular ion peak at m/2 =128. However ketone (A) has a fragment peak at m/2 = 99 and 72 while ketone (B) snowed a fragment peak at m/2 = 113 and 58. 9) Propose the most plausible structures for both ketones b) Explain how you arrived at your conclusion by drawing the Structures of the distinguishing fragments for each ketone, including their fragmentation mechanisms.
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