Which of the following is the correct representation for intermediate of nucleophilic addition reaction to the given carbonyl compound (A) :

a. 

b. 

c. 

d. 

Choose the correct option
1. (a, b)
2. (b, c)
3. (c, d)
4. (a, d)

Addition of water to alkynes occurs in acidic medium and in the presence of ${\mathrm{Hg}}^{2+}$ ions as a catalyst. Which of the following products will be formed on addition of water to but-1-yne under these conditions?

1.
2.
3.
4.

Which of the following compounds is most reactive towards nucleophilic addition reaction?

1.		2.
3.		4.

The correct order of increasing acidic strength is:

Compound$$ can  be prepared by the reaction of-
1. Phenol and benzoic acid in the presence of NaOH
2. Phenol and benzoyl chloride in the presence of pyridine
3. Phenol and benzoyl chloride in the presence of ${\mathrm{ZnCl}}_2$
4. Phenol and benzaldehyde in the presence of palladium

The reagent which does not react with both, acetone and benzaldehyde?

1. Sodium hydrogen sulphite   

2. Phenyl hydrazine

3. Fehling's solution                 

4. Grignard reagent

Cannizzaro’s reaction is not given by:
 

1.		2.
3.	HCHO	4.	CH3CHO

The compound below is treated with a concentrated aqueous KOH solution. The products obtained are:

1.
2.
3.
4.

The structure of ‘A’ and type of isomerism in the above reaction are respectively: 

Compounds A and C in the following reaction are:

\(\small{\mathrm{CH}_3 \mathrm{CHO} \xrightarrow[{(ii) H_{2}O}]{(i)CH_{3}MgBr}(\mathrm{A}) \stackrel{\mathrm{H}_2 \mathrm{SO}_4}{\longrightarrow}(\mathrm{B}) \xrightarrow[]{Hydroboration \ oxidation}(C)}\)

1.  Identical                               

2.  Positional isomers

3.  Functional isomers       

4.  Optical isomers