Which of the following will give yellow precipitate with I2/NaOH?

1. CH3-CO-O-CO-CH3 2.
3. 4. Both (2) and (3)
Subtopic:  Aldehydes & Ketones |
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Identify (X) in the sequence :

C3H8O(X)H2SO4K2Cr2O7C3H6OWarmI2+NaOHCHI3

1. CH3-CH2-CH2OH

2. CH3-CH-CH3
|
OH

3. CH3-O-CH2-CH3

4. CH3-CH2-CHO

Subtopic:  Aldehydes & Ketones |
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An organic compound X on treatment with acidified K2Cr2O7, gives compound Y which reacts with I2, and NaOH to form CHI3. The compound X can be-

1. CH3OH

2. CH3CHO 

3. CH3COCH3

4. CH3CH(OH)CH3

Subtopic:  Aldehydes & Ketones |
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Which compound would give 5-keto-2-methyl hexanal upon ozonolysis?

1. 2.
3. 4.

Subtopic:  Aldehydes & Ketones |
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CH3CH=CHCHO is oxidized to CH3CH=CHCOOH using:

1. Alkaline permanganate

2. Ammoniacal silver nitrate

3. Selenium dioxide

4. Osmium tetroxide

Subtopic:  Aldehydes & Ketones |
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Ozonolysis of propyne gives:

1. CH3CHO               

2. CH3COCHO

3. HCHO                   

4. CHOCHO

Subtopic:  Aldehydes & Ketones |
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Propyne on oxidation with SeO2 gives:

1. CHOCHO                   

2. CH3CH2CHO

3. CH3COCHO               

4. CHOCH2CHO

Subtopic:  Aldehydes & Ketones |
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Acetylene and HCHO react in the presence of copper acetylide catalyst to form:

(1) 2-Butyne-1,4-diol

(2) 1-Butyne-1,4-diol

(3) 2-Butyne-1,2-diol

(4) None of these

Subtopic:  Aldehydes & Ketones |
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Level 3: 35%-60%
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An organic compound X having molecular formula C5H10O yields phenyl hydrazone and

gives negative response to the iodoform test and Tollen's test. It produces n-pentane on

reduction. X could be:

1. Pentenal

2. 2-Pentanone

3. 3-Pentanone

4. n-Amyl alcohol

Subtopic:  Aldehydes & Ketones |
 69%
Level 2: 60%+
NEET - 2015
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CH3CHO and C6H5CH2CHO can be distinguished chemically by:

1. Benedict test

2. Iodoform test

3. Tollen's reagent test

4. Fehling solution test

Subtopic:  Aldehydes & Ketones |
 69%
Level 2: 60%+
NEET - 2012
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