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Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079

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Chapter
Section
BuyFindarrow_forward

Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079
Textbook Problem

Draw the structure of the alcohol produced when each of the following compounds is reduced using molecular H2 and a Ni catalyst.

Chapter 4, Problem 4.83EP, Draw the structure of the alcohol produced when each of the following compounds is reduced using , example  1

Chapter 4, Problem 4.83EP, Draw the structure of the alcohol produced when each of the following compounds is reduced using , example  2

Chapter 4, Problem 4.83EP, Draw the structure of the alcohol produced when each of the following compounds is reduced using , example  3

Chapter 4, Problem 4.83EP, Draw the structure of the alcohol produced when each of the following compounds is reduced using , example  4

(a)

Interpretation Introduction

Interpretation:

Structure of alcohol that is formed when the given compound undergoes reduction with molecular hydrogen and nickel catalyst have to be drawn.

Concept Introduction:

In organic chemistry, oxidation reaction is referred to the number CO bonds increase and/or number of CH bonds decrease.

In organic chemistry, reduction reaction is referred to the number CO bonds decrease and/or number of CH bonds increase.

Alcohols undergo oxidation reaction and reduction reaction.  This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom.  Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction.  Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product.  Secondary alcohol undergoes oxidation to give ketone as the product.

Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.

The reverse of oxidation reaction is reduction reaction.  Reduction of aldehyde gives primary alcohol as the product and reduction of ketone gives secondary alcohol as the product.  Reduction can be accomplished using hydrogen gas and a metal catalyst namely nickel.

Explanation

Given compound is,

The given compound is an aldehyde.  Reduction of aldehyde gives primary alcohol as the product.  The general scheme of reduction of aldehyde can be given as shown below,

(b)

Interpretation Introduction

Interpretation:

Structure of alcohol that is formed when the given compound undergoes reduction with molecular hydrogen and nickel catalyst have to be drawn.

Concept Introduction:

In organic chemistry, oxidation reaction is referred to the number CO bonds increase and/or number of CH bonds decrease.

In organic chemistry, reduction reaction is referred to the number CO bonds decrease and/or number of CH bonds increase.

Alcohols undergo oxidation reaction and reduction reaction.  This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom.  Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction.  Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product.  Secondary alcohol undergoes oxidation to give ketone as the product.

Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.

The reverse of oxidation reaction is reduction reaction.  Reduction of aldehyde gives primary alcohol as the product and reduction of ketone gives secondary alcohol as the product.  Reduction can be accomplished using hydrogen gas and a metal catalyst namely nickel.

(c)

Interpretation Introduction

Interpretation:

Structure of alcohol that is formed when the given compound undergoes reduction with molecular hydrogen and nickel catalyst have to be drawn.

Concept Introduction:

In organic chemistry, oxidation reaction is referred to the number CO bonds increase and/or number of CH bonds decrease.

In organic chemistry, reduction reaction is referred to the number CO bonds decrease and/or number of CH bonds increase.

Alcohols undergo oxidation reaction and reduction reaction.  This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom.  Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction.  Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product.  Secondary alcohol undergoes oxidation to give ketone as the product.

Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.

The reverse of oxidation reaction is reduction reaction.  Reduction of aldehyde gives primary alcohol as the product and reduction of ketone gives secondary alcohol as the product.  Reduction can be accomplished using hydrogen gas and a metal catalyst namely nickel.

(d)

Interpretation Introduction

Interpretation:

Structure of alcohol that is formed when the given compound undergoes reduction with molecular hydrogen and nickel catalyst have to be drawn.

Concept Introduction:

In organic chemistry, oxidation reaction is referred to the number CO bonds increase and/or number of CH bonds decrease.

In organic chemistry, reduction reaction is referred to the number CO bonds decrease and/or number of CH bonds increase.

Alcohols undergo oxidation reaction and reduction reaction.  This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom.  Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction.  Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product.  Secondary alcohol undergoes oxidation to give ketone as the product.

Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.

The reverse of oxidation reaction is reduction reaction.  Reduction of aldehyde gives primary alcohol as the product and reduction of ketone gives secondary alcohol as the product.  Reduction can be accomplished using hydrogen gas and a metal catalyst namely nickel.

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Sect-4.4 P-3QQSect-4.4 P-4QQSect-4.4 P-5QQSect-4.5 P-1QQSect-4.5 P-2QQSect-4.5 P-3QQSect-4.5 P-4QQSect-4.5 P-5QQSect-4.6 P-1QQSect-4.6 P-2QQSect-4.6 P-3QQSect-4.7 P-1QQSect-4.7 P-2QQSect-4.8 P-1QQSect-4.8 P-2QQSect-4.9 P-1QQSect-4.9 P-2QQSect-4.10 P-1QQSect-4.10 P-2QQSect-4.10 P-3QQSect-4.10 P-4QQSect-4.11 P-1QQSect-4.11 P-2QQSect-4.11 P-3QQSect-4.11 P-4QQSect-4.11 P-5QQSect-4.12 P-1QQSect-4.12 P-2QQCh-4 P-4.1EPCh-4 P-4.2EPCh-4 P-4.3EPCh-4 P-4.4EPCh-4 P-4.5EPCh-4 P-4.6EPCh-4 P-4.7EPCh-4 P-4.8EPCh-4 P-4.9EPCh-4 P-4.10EPCh-4 P-4.11EPCh-4 P-4.12EPCh-4 P-4.13EPCh-4 P-4.14EPCh-4 P-4.15EPCh-4 P-4.16EPCh-4 P-4.17EPCh-4 P-4.18EPCh-4 P-4.19EPCh-4 P-4.20EPCh-4 P-4.21EPCh-4 P-4.22EPCh-4 P-4.23EPCh-4 P-4.24EPCh-4 P-4.25EPCh-4 P-4.26EPCh-4 P-4.27EPCh-4 P-4.28EPCh-4 P-4.29EPCh-4 P-4.30EPCh-4 P-4.31EPCh-4 P-4.32EPCh-4 P-4.33EPCh-4 P-4.34EPCh-4 P-4.35EPCh-4 P-4.36EPCh-4 P-4.37EPCh-4 P-4.38EPCh-4 P-4.39EPCh-4 P-4.40EPCh-4 P-4.41EPCh-4 P-4.42EPCh-4 P-4.43EPCh-4 P-4.44EPCh-4 P-4.45EPCh-4 P-4.46EPCh-4 P-4.47EPCh-4 P-4.48EPCh-4 P-4.49EPCh-4 P-4.50EPCh-4 P-4.51EPCh-4 P-4.52EPCh-4 P-4.53EPCh-4 P-4.54EPCh-4 P-4.55EPCh-4 P-4.56EPCh-4 P-4.57EPCh-4 P-4.58EPCh-4 P-4.59EPCh-4 P-4.60EPCh-4 P-4.61EPCh-4 P-4.62EPCh-4 P-4.63EPCh-4 P-4.64EPCh-4 P-4.65EPCh-4 P-4.66EPCh-4 P-4.67EPCh-4 P-4.68EPCh-4 P-4.69EPCh-4 P-4.70EPCh-4 P-4.71EPCh-4 P-4.72EPCh-4 P-4.73EPCh-4 P-4.74EPCh-4 P-4.75EPCh-4 P-4.76EPCh-4 P-4.77EPCh-4 P-4.78EPCh-4 P-4.79EPCh-4 P-4.80EPCh-4 P-4.81EPCh-4 P-4.82EPCh-4 P-4.83EPCh-4 P-4.84EPCh-4 P-4.85EPCh-4 P-4.86EPCh-4 P-4.87EPCh-4 P-4.88EPCh-4 P-4.89EPCh-4 P-4.90EPCh-4 P-4.91EPCh-4 P-4.92EPCh-4 P-4.93EPCh-4 P-4.94EPCh-4 P-4.95EPCh-4 P-4.96EPCh-4 P-4.97EPCh-4 P-4.98EPCh-4 P-4.99EPCh-4 P-4.100EPCh-4 P-4.101EPCh-4 P-4.102EPCh-4 P-4.103EPCh-4 P-4.104EPCh-4 P-4.105EPCh-4 P-4.106EPCh-4 P-4.107EPCh-4 P-4.108EPCh-4 P-4.109EPCh-4 P-4.110EPCh-4 P-4.111EPCh-4 P-4.112EPCh-4 P-4.113EPCh-4 P-4.114EPCh-4 P-4.115EPCh-4 P-4.116EPCh-4 P-4.117EPCh-4 P-4.118EP

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