Compounds A and C in the following reaction are:
\(\mathrm{\small{{CH}_3 {CHO} \xrightarrow[{(ii) ~H_{2}O}]{(i) ~CH_{3}MgBr}({A}) \stackrel{{H}_2 {SO}_4}{\longrightarrow}({B}) \xrightarrow[]{Hydroboration \ oxidation}(C)}}\)

1. Identical                               

2. Positional isomers

3. Functional isomers       

4. Optical isomers

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

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

1.  Tollens' reagent 

2.  Benzoyl peroxide

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

4.  Sn and NaOH solution

Which of the following compounds will give butanone on oxidation with alkaline ${\mathrm{KMnO}}_4$ solution?

1. Butan-1-o1                 
2. Butan-2-ol
3. Both (a) and (b)             
4. None of the above

Carbonyl compound is treated with--- in Clemmensen reduction .

1.  Zinc amalgam + HCl

2.  Sodium amalgam + HCl

3. Zinc amalgam + nitric acid

4.  Sodium amalgam + ${\mathrm{HNO}}_3$

Which of the following compounds do not undergo aldol condensation?

(a)		(b)
(c)		(d)

Options are as follows:

1. a, b

2. b, d

3. b, c

4. c, d

The product (P) and (Q) of the given reaction are:
 

1. (a, b)
2. (b, c)
3. (c, d)
4. (a, d)

Identify the conversions that are possible with Clemmensen reduction:

a. Benzaldehyde to benzyl alcohol.

b. Cyclohexanone to cyclohexane.

c. Benzoyl chloride to benzaldehyde.

d. Benzophenone to diphenylmethane.

Which of the following reactions increase the number of carbon atoms in the carbon chain?
a. Grignard reaction
b. Cannizzaro’s reaction
c. Aldol condensation
d. HVZ reaction

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

Benzophenone can be obtained by:
a.  Benzoyl chloride + Benzene 
b.  Benzoyl chloride + Diphenyl cadmium
c.  Benzoyl chloride + Phenyl magnesium chloride
d.  Benzene + Carbon monoxide 

Choose the correct option

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

Codes: