The slowest step of Cannizarro's reaction is

1. Attack of nucleophilic

2. Hydride shift

3. Formation of anion

4. Transfer of proton

Subtopic:  Name Reaction |
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+Br2 CCl4?

1.

2.

3.

4.

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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  H3O+CH3MgBrexcessProduct,

Product is:-

1.

2.

3.

4.

 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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The structure of the product is:

1. 2.
3. 4.
Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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HCNA (excess)KCNB;B is

1.

2.

3.

4.

 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 73%
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Which shows decarboxylation by heating

1.

2.

3.

4.

 

Subtopic:  Carboxylic Acids: Preparation & Properties |
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The major product is
\(\xrightarrow{LiAlH_4}\)

1.  2.
3. 4.
Subtopic:  Isomers & Reaction Mechanism |
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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 |
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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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