ii·i·K2Cr2O7X; X is

1. 

2.

3.

4.

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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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 |
 55%

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The compound  can be exclusively oxidized into by

1. NaCN followed by hydrolysis

2. NaOI followed by H3O+

3. Hot KMnO4 followed by hydrolysis

4. K2Cr2O7 followed by H3O+

Subtopic:  Name Reaction |
 56%
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Phenolphthalein is produced on heating phthalic anhydride and conc. sulphuric acid with

1. Salicylic acid

2. Phenol

3. Phenacetin

4. Phenanthrene

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 66%

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A mixture of benzaldehyde and formaldehyde on heating with aqueous (conc.)NaOH solution gives

1. Benzyl alcohol and sodium formate

2. Sodium benzoate and methyl alcohol

3. Sodium benzoate and sodium formate

4. None of the above

Subtopic:  Name Reaction |
 67%
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Ethyl acetate on reaction with excess of methyl magnesium chloride and dil. H2SO4 gives-

1. Dimethyl ketone

2. Iso-propyl alcohol

3. Ethyl aceto acetate

4. t-Butyl alcohol

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 51%

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Cyanohydrin of 'X' gives lactic acid on hydrolysis. The compound 'X' will be:

1. Acetone                                 

2. Acetaldehyde

3. Propanal                                 

4. HCHO

Subtopic:  Isomers & Reaction Mechanism |
 65%
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