An aldehyde which undergoes Cannizzaro's reaction and reduces Schiff's reagent but does not reduce Fehling's solution is:

(1) CH3CHO

(2) HCHO

(3) C6H5CHO

(4) salicylaldehyde

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Level 2: 60%+
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Which can be reduced to corresponding hydrocarbon by Zn/HCl ?

(a) Butan-2-one

(b) Acetic acid

(c) Acetamide

(d) Ethyl acetate

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 79%
Level 2: 60%+
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The IUPAC name of the CH3COCH(CH3)2 is:

(1) 4-methyl isopropyl ketone

(2) 3-methyl-2-butanone

(3) isopropylmethyl ketone

(4) 2-methyl-3-butanone

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Level 1: 80%+
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Major product maybe

1.     

 2.  

3.     

 4.  

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 64%
Level 2: 60%+
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Choose the correct statement(s) for the reaction

           

1.  (b) is more rapidly at the higher temperature

2.  (b) is more volatile than (a)

3.  (a) is more volatile than (b)

4.  (a) is formed higher yields at a lower temperature

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 64%
Level 2: 60%+
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1.       2.  

3.       4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 56%
Level 3: 35%-60%
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Major product 'A' ' is

1.       

2. 

3.         

4. 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
Level 3: 35%-60%
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The reagents that produce compound A mentioned below in a Diels-Aider reaction are

                         

1.       2.  

3.       4.  

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 53%
Level 3: 35%-60%
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The following reaction gives

1.       2.  

3.       4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
Level 3: 35%-60%
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The reaction 'A' is

1.       2.  

3.       4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 68%
Level 2: 60%+
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