An acid that forms an anhydride (X) on heating and an acid imide (Y) on strong heating with ammonia is:

1.		2.
3.		4.

 A yellow precipitate with iodine and alkali is given by:

(i).  Methyl acetate

(ii).  Acetamide

(iii).  2-Hydroxypropane

(iv).  Acetophenone

1. (i), and (ii)
2. (ii), and (iii)
3. (iii), and (iv)
4. (iv), and (i)

Consider the following reaction:

The product 'A' is:

1. $C_6{H}_{5}OH$

2. $C_6{H}_{5}COC{H}_3$

3. $C_6{H}_{5}Cl$

4. $C_6{H}_{5}CHO$

Match the compounds given in List-I with List-II and select the suitable option from the code given below:

Codes:

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

1.	\(\xrightarrow{K_2Cr_2O_7}\)	2.	\(\xrightarrow[(ii)H_3O^+]{(i)NaOCl}\)
3.	\(\xrightarrow{PCC}\)	4.	\(\xrightarrow{KMnO_4/H^+}\)

The compound that does not give an iodoform test is:

1. 3-Pentanone

2.  2-Pentanone

3.  Ethanol

4.  Ethanal

Ethylbenzene is obtained from phenyl methyl ketone by using:

1. Zn–Hg+HCl

2. LiAlH₄

3. KMnO₄

4. None of the above

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

An organic compound with the molecular formula C₉H₁₀O forms a 2,4-DNP derivative, reduces Tollens’ reagent, and undergoes the Cannizzaro reaction. On vigorous oxidation, it gives 1,2-benzenedicarboxylic acid. This organic compound will be:

1. 2-Methyl benzaldehyde

2. 2-Hydroxy benzaldehyde

3. 2-Ethyl benzaldehyde

4. 4-Ethyl benzaldehyde

The below structure is an example of :