MEDIUM
Earn 100
What is the mechanism behind reduction of carboxylic acids to alcohol?
Important Questions on Aldehydes, Ketones and Carboxylic Acids
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chlorosodium acetate on boiling with aqueous sodium nitrite gives
HARD
In the reaction,
,
the product C is :
HARD
The major product of the following reaction is:
EASY
The correct structure of the product in the following reaction is
EASY
In the presence of a small amount of phosphorous, aliphatic carboxylic acid reacts with chlorine or bromine to yield a reaction in which, hydrogen is been replaced by halogen. This reaction is known as
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Propanoic acid undergoes reaction to give chloropropanoic acid. The product obtained is
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The major product of the following reaction is:
EASY
Why benzoic acid does not undergo Friedel-crafts reaction?
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How will you bring about the following conversion in not more than two steps?
Benzoic acid to m-Nitrobenzyl alcohol
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Which of the following derivatives of alcohols is unstable in an aqueous base?
EASY
Give the chemical equation for the reaction of with following:
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Which of the following acid will form an (a) Anhydride on heating and (b) Acid imide on strong heating with ammonia?
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The most suitable reagent for the given conversion is:
EASY
Which of the following acids, does NOT undergo Hell-Volhard-Zelinsky reaction?
EASY
Name the end product in the following series of reactions ections
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The major product of nitration of benzoic acid is
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The major product obtained in the reaction of aniline with acetic anhydride is
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An organic compound A upon reacting with gives B. On heating, B gives C. C in presence of KOH reacts with Br2 to give CH3CH2NH2. A is :
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With dehydrating agent present which dicarboxylic acid is least reactive towards forming an anhydride?
