The compound Y in the above sequence of reactions is:

 

1. 1-Phenylethene

2. 2-Phenyl-2-propanol

3. Acetophenone

4. Benzaldehyde

Subtopic:  Isomers & Reaction Mechanism |
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In the following reaction:

The structure of the major product 'X' is

(1)

(2)

(3)

(4)

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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The compound A can be exclusively oxidized into ​​​B by:
 

1. NaCN, followed by hydrolysis

2. NaOI, followed by H3O+

3. KMnO4(hot), followed by hydrolysis

4. K2Cr2O7, followed by H3O+

Subtopic:  Carboxylic Acids: Preparation & Properties |
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KMnO4Y

In the above reaction, X and Y are:

1. Identical

2. Homologous

3. Structural Isomers

4. Stereoisomers

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\(\xrightarrow[\left(ii\right) H^{+} / H_{2} O]{\left(i\right) NaOH / 100^{\circ}}\)

Major Product is:

1. 

2.

 

3.

4.

Subtopic:  Isomers & Reaction Mechanism |
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Which compound is most reactive towards nucleophilic addition?

1. CH3CHO

2. PhCOCH3

3. PhCOPh

4. CH3COCH3

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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The reaction

is fastest when X is

1. Cl

2. NH2

3. OC2H5

4. OCOR

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In a set of reaction propionic acid yielded a compound D.

CH3CH2COOHSOCl2 BNH3 CBr2KOH

The structure of D would be

1. CH3CH2NHCH3

2. CH3CH2NH2

3. CH3CH2CH2NH2

4. CH3CH2CONH2

Subtopic:  Carboxylic Acids: Preparation & Properties |
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Hex-3-ene2.Zn,H2O1.O3 A H+KMnO4 B RedPBr2 CKOH(aq)D

D is :-

1. CH3-CH|Br-COOH                           

2.  CH3-CH2-CHO

3. CH3-CH|Br-CHO                         

4.  CH3-CH|OH-COOH

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ii·i·K2Cr2O7X; X is

1. 

2.

3.

4.

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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