Select the correct option based on statements below:

Assertion (A):	The α -hydrogen atom in carbonyl compounds is less acidic.
Reason (R):	The anion formed after the loss of the α -hydrogen atom is resonance stabilized.

 

1.	Both (A) and (R) are True and (R) is the correct explanation of (A).
2.	Both (A) and (R) are True but (R) is not the correct explanation of (A).
3.	(A) is True but (R) is False.
4.	(A) is False but (R) is True.

What is the name of the below mentioned reaction?
\(\small{\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{OH}+\mathrm{CH}_3 \mathrm{COCl} \stackrel{\text { Pyridine }}{\longrightarrow} \mathrm{CH}_3 \mathrm{COOC}_2 \mathrm{H}_5+\mathrm{HCl}}\)

1. Acetylation

2. Cannizzaro reaction

3. Cross aldol condensation

4. Decarboxylation

The reaction that does not give benzoic acid as the major product is:

1.
2.
3.
4.

Select the correct option based on statements below:

Match the example in Column I with the name of the reaction in Column II.

Column l (Example)	Column ll (Reaction)
A.	1. Friedel-Crafts acylation
B.	2. HVZ reaction
C.	3. Aldol condensation
D.	4. Rosenmund Reaction

Match the reactions given in Column-I with the suitable reagents given in Column-II. 

Codes:

Match the acids given in Column I with their correct IUPAC names given in Column II and mark the appropriate option:

Codes:

Match the common names given in Column I with the IUPAC names given in Column II.

Codes:

What is the most suitable reagent for the below mentioned conversion?

\(\mathrm{CH_{3} — CH = CH — CH_{2} — \overset{\Large{O} \\~ ||}{C}—CH_{3} \rightarrow}\)
    
\(\mathrm{CH_{3} — CH = CH — CH_{2} — \overset{\Large{O} \\~ ||}{C}—OH}\)

1.  Tollens' reagent 

2.  Benzoyl peroxide

3.  \(\mathrm I_{2}\) and NaOH solution

4.  Sn and NaOH solution

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

1.
2.
3.
4.