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Product (x) will be:
(a) 
(b) 
(c) 
(d) 

Product (P) is:

1.		2.
3.		4.

Identify the major product,

1.     
2.   
3.    
4. 

The structure of A in the below mentioned reaction is:
 

1.		2.
3.		4.

$\underset{100°\mathrm{C}}{\overset{{\mathrm{AC}}_2\mathrm{O}}{\to }}$(A); Product (A) of reaction is:
(a) 
(b) 
(c) 
(d) 

$\underset{\mathrm{dimethoxy} \mathrm{ethane}}{\overset{\mathrm{LiH}}{\to }}$L$\stackrel{{\mathrm{CH}}_3\mathrm{Li}}{\to }$M$\stackrel{{\mathrm{H}}_3{\mathrm{O}}^{+}}{\to }$ N + CH₃OH
Product (N) is:
1. 
2. 
3.       
4. 

$\underset{\mathrm{Pyridine}}{\overset{\mathrm{TsCl}}{\to }}$(A)$\stackrel{{\mathrm{LiAlH}}_4}{\to }$(B)    
Product (B) of the above reaction is:

Product Z of above reaction is :

Which of the following compounds give positive Tollen's Test?
       
1. 
2. 
3. 
4.                       

In the reaction  + CH₃OH $\stackrel{{\mathrm{CH}}_3\mathrm{ONa}}{\to }$Product.
The product is:
(1) 
(2) 
(3) 
(4) 

An ester cannot be prepared by -
1. RCOOH + R'OH + OH^-
2. RCOCl+R'OH +Pyridine
3. RCOOH+ R’OH +H⁺
4. (RCO)₂O + R'OH + Pyridine

The product of the reaction is:-
(1)
(2)
(3)
(4)

Diethyl ether may be regarded as anhydride of:-
1. C₂H₅COOH
2. C₂H₅OH
3. C₂H₅CHO
4. C₂H₅COOC₂H₅

Which one of the following will most readily be dehydrated in acidic conditions?
1. 
2. 
3. 
4. 

1-propanol and 2-propanol can be best distinguished by:-
(1) oxidation with alkaline KMnO₄ followed by reaction with Fehling's solution
(2) oxidation with acidic dichromate followed by reaction with Fehling’s solution
(3) oxidation by heating with copper followed by reaction with Fehling’s solution
(4) oxidation with conc. H₂SO₄ followed by reaction with Fehling’s solution

Phenyl magnesium bromide reacts with methanol to give a mixture of:-
1. Anisole and Mg(OH)Br
2. Benzene and Mg(OMe)Br
3. Toluene and Mg(OH)Br
4. Phenol and Mg(Me)Br

The main product of the following reaction is:
C₆H₅CH₂CH(OH)CH(CH₃)₂$\stackrel{\mathrm{Conc}. {\mathrm{H}}_2{\mathrm{SO}}_4}{\to }$?
(1) 
(2) 
(3) 
(4)

When phenol is treated with excess bromine water, it gives:
(1) m-bromophenol
(2) o- and p-bromophenol
(3) 2,4-dibromophenol
(4) 2,4,6-tribromophenol

Resorcinol and conc. H₂SO₄ in presence of phthalic anhydride produce a compound which is:
1. a dye                             
2. an antiseptic
3. an indicator                   
4. a detergent

In the given transformation, which of the following is the most appropriate reagent ?

(1) Zn-Hg/HCl
(2) Na, Liq. NH₃
(3) NaBH₄
(4) NH₂NH₂,OH
 

Sodium phenoxide when heated with CO₂ under pressure at 125°C yields a product which on acetylation produces C.

The major product C would be :
(1) 
(2) 
(3) 
(4) 

A compound with molecular formula C₄H₁₀O₃ is converted by the action of acetyl chloride to a compound with molar mass 190. The original compound has: 
(1) one OH group
(2) two OH groups
(3) three OH groups
(4) no OH group

Acetophenone when reacted with a base, C₂H₅ONa, yields a stable compound which has the structure


 

Phenyl ethyl ether with concentrated hydrobromic acid on boiling yields:-
1. Phenol and ethyl bromide
2. Bromobenzene and ethanol
3. Phenol and ethane
4. Bromobenzene and ethane

Which of the following is not the product of dehydration of

1. 
2. 
3. 
4. 
 

The reaction:
${\mathrm{CH}}_3-\stackrel{{\mathrm{CH}}_3}{\stackrel{|}{\mathrm{CH}}}-{\mathrm{CH}}_2-\mathrm{O}-{\mathrm{CH}}_2-{\mathrm{CH}}_3 + \mathrm{HI} \stackrel{\mathrm{heated}}{\to }?$
Which of the following compounds will be formed?
(1) ${\mathrm{CH}}_3-\stackrel{\stackrel{{\mathrm{CH}}_3}{|}}{\mathrm{C}}\mathrm{H}-{\mathrm{CH}}_2-\mathrm{I}+{\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{OH}$
(2) ${\mathrm{CH}}_3-\underset{\underset{{\mathrm{CH}}_3}{|}}{\mathrm{C}}\mathrm{H}-{\mathrm{CH}}_3+{\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{OH}$
(3) ${\mathrm{CH}}_3-\underset{\underset{{\mathrm{CH}}_3}{|}}{\mathrm{C}}\mathrm{H}-{\mathrm{CH}}_2\mathrm{OH}+{\mathrm{CH}}_3{\mathrm{CH}}_3$
(4) ${\mathrm{CH}}_3-\stackrel{\stackrel{{\mathrm{CH}}_3}{|}}{\mathrm{C}}\mathrm{H}-{\mathrm{CH}}_2\mathrm{OH}+{\mathrm{CH}}_3-{\mathrm{CH}}_2-\mathrm{I}$