The reddish-brown precipitate formed in Fehling's test for aldehydes (RCHO) is due to the formation of the following compound :
1. \(\mathrm{Cu}\)
2. \(\mathrm{Cu}_2 \mathrm{O}\)
3. \(\mathrm{CuO}\)
4. \((\mathrm{RCOO})_2 \mathrm{Cu}\)

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 |
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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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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 |
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In the following reactions

      

1.  

2.  

3.  

4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
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The major product formed in the following reaction is:

 

1. 2.
3. 4.
Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
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The main product X formed in the following reaction is

        

1.        2.  

3.    4.  

Subtopic:  Name Reaction |
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Three isomeric compounds M, N and P (C5H10O) give the following tests

i.  M and P react with sodium bisulfite to form an adduct.

ii.  N consumes 1 mol of bromine and also gives turbidity with conc. HCl/anhydrous ZnCl2 after prolonged heating.

iii.  M reacts with an excess of iodine in an alkaline solution to give a yellow crystalline compound with a characteristic smell.

iv.  p-Rosaniline treated with sulfur dioxide develops pink color on shaking with P.

The structures of M, N, and P, respectively are

           M                N                P

1.  

2.  

3.  

4.  

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

1. 2.
3. 4.


 

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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The correct order of acidity of the following compounds is:

1. 1 > 2 > 3

2. 1 > 3 > 2

3. 3 > 1 > 2

4. 3 > 2 > 1

Subtopic:  Carboxylic Acids: Preparation & Properties |
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