In the reaction

CH3-CH=CH-CHOagentoxidizing 
CH3-CH=CH-COOH

the oxidizing agent can be

1. Alkaline KMnO4

2. Acidified K2Cr2O7

3. Benedict’s solution

4. All of the above

Subtopic:  Carboxylic Acids: Preparation & Properties |

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The appropriate reagent for the transformation is

1. Zn (Hg)/HCl

2. NH2–NH2/OH

3. Both 1. and 2.

4. None of the above

Subtopic:  Name Reaction |
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In a Cannizzaro’s reaction, the intermediate that will
be the best hydride donor is

Subtopic:  Name Reaction |
 54%

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What is the product (Y) formed in the following sequence of reactions?

oxidationvigorousXheatingDry


 

1. 
2. 
3. 
4. 


Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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An organic compound (A) (MF C4H10O) upon dehydrogenation gives a compound (B) which forms phenyl hydrazone with phenylhydrazine and both the compounds (A) and (B) respond to iodoform test. Hence, the compound (A) is

Subtopic:  Isomers & Reaction Mechanism | Name Reaction |
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The major product of the following reaction is:

strong heating

1.  

 

2.  

 

3.  

 

4.  

Subtopic:  Carboxylic Acids: Preparation & Properties |
 88%
From NCERT
NEET - 2019
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Self condensation of two moles of ethyl acetate in presence of sodium ethoxide yields :

1. Ethyl butyrate

2. Acetoacetic ester

3. Methyl acetoacetate

4. Ethyl propionate

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Name Reaction |
 55%
AIPMT - 2006
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Nucleophilic addition reaction will be most favoured in-

1. CH3CH2CH2COCH3

2. (CH3)2C=O

3. CH3CH2CHO

4. CH3CHO

Subtopic:  Isomers & Reaction Mechanism |
 72%
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AIPMT - 2006
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A carbonyl compound reacts with hydrogen cyanide to form cyanohydrins which on hydrolysis forms a racemic mixture of α-hydroxy acid. The carbonyl compound is :

1. Acetaldehyde

2. Acetone

3. Diethyl ketone

4. Formaldehyde

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
 66%
From NCERT
AIPMT - 2006
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In a set of reactions propanoic acid yielded a compound D

CH3CH2COOHSOCl2BNH3CBr2KOHD 
The structure of D would be :

1. CH3CH2CH2NH2

2. CH3CH2CONH2

3. CH3CH2NHCH3

4. CH3CH2NH2

Subtopic:  Amines - Preparation & Properties |
 74%
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AIPMT - 2006
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