The major product in the following reaction is: 

1. 2.
3. 4.


 

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 53%
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Which of the following will not form a yellow precipitate on heating with an alkaline solution of iodine?

1. CH3CH(OH)CH3                                 

2. CH3CH2CH(OH)CH3

3. CH3OH                                               

4. CH3CH2OH

Subtopic:  Name Reaction |
 81%
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When propanoic acid is treated with aqueous sodium bicarbonate, CO2 is liberated. The ‘C’ of COcomes from:

1. Carboxylic acid group

2. Methylene group

3. Bicarbonate

4. Methyl group

Subtopic:  Isomers & Reaction Mechanism |
 56%
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A key step in the hydrolysis of acetamide in aqueous acid proceeds by nucleophilic addition of-

1. H3O+ to                          

2.  H2O to   

3. H3O+ to                          

4. HO- to 

Subtopic:  Isomers & Reaction Mechanism |
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The product of the below mentioned reaction is- 

1.  2.
3. 4.

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 67%
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The main product X formed in the following reaction is

        

1.        2.  

3.    4.  

Subtopic:  Name Reaction |
 66%
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In the following reactions

      

1.  

2.  

3.  

4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
 81%
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In the given below reaction

  

x, y, and z are: 

1.  x = Mg; dry ether; y = CH3Cl; z = H2O

2.  x = Mg; dry methanol; y = CO2; z = dil.HCl 

3.  x = Mg; dry ether; y = CO2; z = dil.HCl

4.  x = Mg; dry methanol; y = CH3Cl; z = H2O

Subtopic:  Carboxylic Acids: Preparation & Properties |
 75%
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4-Formylbenzoic acid on treatment with one equivalent of hydrazine followed by heating with alcoholic KOH gives, as major product:

1.  2. 
3. 4.

Subtopic:  Name Reaction |
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The major final product in the following reaction is

CH3CH2CN2H3O+1CH3MgBr

1.        2.  

3.       4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 67%
From NCERT
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