For the reaction:

Which reagent will be appropriate for the above conversion?

1. Zn-Hg/HCl

2. NH2-NH2/OH-

3. LiAlH4/H

4. HI/P

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 52%
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Identify (X) in the given sequential reaction.

1. CH3OH

2. Ethyl alcohol

3. Methyl cyanide

4. tert-Butyl alcohol

Subtopic:  Isomers & Reaction Mechanism |
 89%
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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 |
 59%
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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 |
 72%
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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 |
 53%
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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

Subtopic:  Carboxylic Acids: Preparation & Properties |
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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 |
 76%
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The reaction

is fastest when X is

1. Cl

2. NH2

3. OC2H5

4. OCOR

Subtopic:  Isomers & Reaction Mechanism |
 67%
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