The major product is
\(\xrightarrow{LiAlH_4}\)

1.  2.
3. 4.

Subtopic:  Isomers & Reaction Mechanism |
 58%

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Fehling solution gives red precipitated with

(a) Aromatic aldehyde

(b) Aliphatic aldehyde

(c) Ketone

(d) terminal α-Hydroxy ketone

1. b,d

2. a,b

3. a,d

4. b,c

 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 67%
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and can be distinguished by

1. I2+NaOH

2. NaSO3H

3. NaCN/HCl

4. 2,4-DNP

 

(1) a,b,d

(2) a,b

(3) a,c,d

(4) a,d

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Name Reaction |
 56%
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 Zn/H2OO3I mole PNaOH  Q; Q is

1.

2.

3.

4.

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
 57%

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I2+NaOH x + y(yellow ppt) yAg  z;z is

1. CHCH

2. CHI3

3. Ph-COONa

4. CH2=CH2

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 66%
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ii·i·K2Cr2O7X; X is

1. 

2.

3.

4.

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 62%

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Hex-3-ene2. Zn, H2O1. O3 A H+KMnO4 B Red PBr2 CKOH (aq)D

D is :-

1. CH3-CH|Br-COOH                           

2.  CH3-CH2-CHO

3. CH3-CH|Br-CHO                         

4.  CH3-CH|OH-COOH

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Carboxylic Acids: Preparation & Properties |
 78%

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The reaction

is fastest when X is-

1. Cl

2. NH2

3. OC2H5

4. OCOR

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 76%

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iiH+/H2OiNaOH/100°c

Major Product is:

1. 

2.

 

3.

4.

Subtopic:  Name Reaction |
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KMnO4Y

In the above reaction, X and Y are:

1. Identical

2. Homologes

3. Structural Isomers

4. Stereoisomers

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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