Compound X in the above reaction is

(1)  
(2)
(3)
(4)

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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PhCOOH, PhMe can be separated by

(1) KMnO4

(2) aq. NaHCO3 + n–hexane

(3) H2O

(4) All of these

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Reactivity order towards a nucleophile is

(1) RCOCI > RCOOEt > (RCO)2O > RCONH2

(2) RCOCI > (RCO)2O > RCOOEt > RCONH2

(3) (RCO)2 > RCOCI > RCOOEt > RCONH2

(4) (RCO)2O > RCOOEt > RCOCI > RCONH2

Subtopic:  Isomers & Reaction Mechanism |
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When phenyl glyoxal is kept in a solution of aq. NaOH it is converted to

(1)  
(2)
(3)
(4)
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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In the given reaction, the number of isomeric products formed is–

(1) 1

(2) 2

(3) 3

(4) 4

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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The basicity order of I, II and III is

(1) III > I > II

(2) I > II > III

(3) III > II > I

(4) II > III > I

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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(1) CH3CH(OH)2, CH3CH(OH)COOH

(2) CH3CHO, CH3CH(OH)COOH

(3) CH3CH2COOH, CH3CH2OH

(4) CH3CH(OH)COOH, CH3CH2OH

Subtopic:  Isomers & Reaction Mechanism |
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What will be the kmost probable product when compound 'X' is treated with two equivalents of NaOH,

(1)  
(2)
(3)
(4)
Subtopic:  Carboxylic Acids: Preparation & Properties |
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Which pair of compounds on heating give isomeric products

(1)  
(2)
(3)
(4) All the above
Subtopic:  Carboxylic Acids: Preparation & Properties |
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The correct sequence of reagents for the following conversion is

(1)  
(2)
(3)
(4)
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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