ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
2nd Edition
ISBN: 9780393664034
Author: KARTY
Publisher: NORTON
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Chapter 20, Problem 20.48P
Interpretation Introduction

(a)

Interpretation:

How the given transformation can be carried out is to be explained.

Concept introduction:

The diisobutylaluminum hydride (DIBAH, or DIBAL-H) is the reducing agent that can stop the reduction of ester or carboxylic acid to aldehyde. A conjugated ester can be reduced to an aldehyde without reducing it further to alcohol using a specific reagent such as DIBAH, then H3O+. The single hydride ion from DIBAH, then H3O+ adds to the carbonyl of a carboxylic acid, reducing it to an aldehyde in acidic condition. It does not reduce the C=C bond in the compound.

Interpretation Introduction

(b)

Interpretation:

How the given transformation can be carried out is to be explained.

Concept introduction:

The Lithiumaluminum hydride (LiAlH4) is the reducing agent that can reduce carbonyls to corresponding alcohol. The conjugated ester can be reduced to an aldehyde, which is further reduced to an alcohol using a specific reagent as (LiAlH4). It does not reduce the C=C bond in the compound.

Interpretation Introduction

(c)

Interpretation:

How the given transformation can be carried out is to be explained.

Concept introduction:

An acid chloride can be converted to an aldehyde by reacting it with LiAlH(O-t-Bu)3. The LiAlH(O-t-Bu)3 is a source of hydride ion, which acts as a nucleophile and reduces the acid derivative to an aldehyde by elimination of chloride ion. It does not reduce the C=C bond in the compound.

Interpretation Introduction

(d)

Interpretation:

How the given transformation can be carried out is to be explained.

Concept introduction:

The Lithiumaluminum hydride (LiAlH4) is the reducing agent that can reduce carbonyls to corresponding alcohols. The acid chloride can be reduced to an aldehyde, which is further reduced to alcohol using a specific reagent as (LiAlH4). It does not reduce the C=C bond in the compound.

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Chapter 20 Solutions

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5

Ch. 20 - Prob. 20.11PCh. 20 - Prob. 20.12PCh. 20 - Prob. 20.13PCh. 20 - Prob. 20.14PCh. 20 - Prob. 20.15PCh. 20 - Prob. 20.16PCh. 20 - Prob. 20.17PCh. 20 - Prob. 20.18PCh. 20 - Prob. 20.19PCh. 20 - Prob. 20.20PCh. 20 - Prob. 20.21PCh. 20 - Prob. 20.22PCh. 20 - Prob. 20.23PCh. 20 - Prob. 20.24PCh. 20 - Prob. 20.25PCh. 20 - Prob. 20.26PCh. 20 - Prob. 20.27PCh. 20 - Prob. 20.28PCh. 20 - Prob. 20.29PCh. 20 - Prob. 20.30PCh. 20 - Prob. 20.31PCh. 20 - Prob. 20.32PCh. 20 - Prob. 20.33PCh. 20 - Prob. 20.34PCh. 20 - Prob. 20.35PCh. 20 - Prob. 20.36PCh. 20 - Prob. 20.37PCh. 20 - Prob. 20.38PCh. 20 - Prob. 20.39PCh. 20 - Prob. 20.40PCh. 20 - Prob. 20.41PCh. 20 - Prob. 20.42PCh. 20 - Prob. 20.43PCh. 20 - Prob. 20.44PCh. 20 - Prob. 20.45PCh. 20 - Prob. 20.46PCh. 20 - Prob. 20.47PCh. 20 - Prob. 20.48PCh. 20 - Prob. 20.49PCh. 20 - Prob. 20.50PCh. 20 - Prob. 20.51PCh. 20 - Prob. 20.52PCh. 20 - Prob. 20.53PCh. 20 - Prob. 20.54PCh. 20 - Prob. 20.55PCh. 20 - Prob. 20.56PCh. 20 - Prob. 20.57PCh. 20 - Prob. 20.58PCh. 20 - Prob. 20.59PCh. 20 - Prob. 20.60PCh. 20 - Prob. 20.61PCh. 20 - Prob. 20.62PCh. 20 - Prob. 20.63PCh. 20 - Prob. 20.64PCh. 20 - Prob. 20.65PCh. 20 - Prob. 20.66PCh. 20 - Prob. 20.67PCh. 20 - Prob. 20.68PCh. 20 - Prob. 20.69PCh. 20 - Prob. 20.70PCh. 20 - Prob. 20.71PCh. 20 - Prob. 20.1YTCh. 20 - Prob. 20.2YTCh. 20 - Prob. 20.3YTCh. 20 - Prob. 20.4YTCh. 20 - Prob. 20.5YTCh. 20 - Prob. 20.6YTCh. 20 - Prob. 20.7YTCh. 20 - Prob. 20.8YTCh. 20 - Prob. 20.9YTCh. 20 - Prob. 20.10YTCh. 20 - Prob. 20.11YTCh. 20 - Prob. 20.12YTCh. 20 - Prob. 20.13YT
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How to Design a Total Synthesis; Author: Chemistry Unleashed;https://www.youtube.com/watch?v=9jRfAJJO7mM;License: Standard YouTube License, CC-BY