The compound on hydrolysis of 50% aqueous sodium hydroxide that produces the corresponding alcohol and acid is:

1. $C_6{H}_{5}C{H}_{2}CHO$

2. $C_6{H}_{5}CHO$

3. $C{H}_{3}C{H}_{2}C{H}_{2}CHO$

4. ${\mathrm{CH}}_3-\stackrel{\mathrm{O}}{\stackrel{\left|\right|}{\mathrm{C}}}-{\mathrm{CH}}_3$

Consider the following compounds:

(i)	C6H5COCl	(ii)
(iii)		(iv)

What is the correct decreasing order of their reactivity towards hydrolysis?

1. (ii) > (iv) > (iii) > (i)

2. (i) > (ii) > (iii) > (iv)

3. (iv) > (ii) > (i) > (iii)

4. (ii) > (iv) > (i) > (iii)

The nucleophilic addition reaction will be most favored among the given compounds is:

1. $C{H}_{3}C{H}_{2}C{H}_{2}COC{H}_3$

2. $(C{H}_3{)}_{2}C=O$

3. $C{H}_{3}C{H}_{2}CHO$

4. $C{H}_{3}CHO$

The correct statement among the following about HCOOH is:

1. It is a stronger acid than CH₃COOH

2. It reduces Tollen’s reagent

3. It gives CO and H₂O on heating with conc.H₂SO₄

4. All of the above

 is converted to  by

In a basic medium, acetophenone yields a stable compound A with C₂H₅ONa.

The structure of A is:

1.		2.
3.		4.

The Clemmensen reduction of a ketone is carried out in the presence of:

1. $\mathrm{Zn}$-$\mathrm{Hg}$ with $\mathrm{HCl}$

2. ${\mathrm{LiAlH}}_4$

3. ${\mathrm{H}}_2$ and $\mathrm{Pt}$ as a catalyst

4. Glycol with $\mathrm{KOH}$

CH₃CHO and C₆H₅CH₂CHO can be distinguished by:

1. Benedict test

2. Iodoform test

3. Tollen's reagent test

4. Fehling solution test

Predict the products in the given reaction, 

1.		2.
3.		4.

Benzaldehyde cannot be prepared by:

1.
2.
3.
4.