When hydrolyzed with aqueous KOH, compounds that undergoes racemization are:

(i)		(ii)	CH3CH2CH2Cl
(iii)		(iv)

1.	(i) and (ii)	2.	(ii) and (iv)
3.	(iv) only	4.	(i) and (iv)

The end product (C) in the below-mentioned reaction is:
\(H_3C-Br\xrightarrow{\bf KCN }A\xrightarrow{ \bf H_3O^+~~}B\xrightarrow[\bf\text{Ether}]{~~LiAlH_4~~}C\)

The correct order of increasing C-X bond reactivity toward nucleophiles among the following is:

I		II
III	\(\left(\mathrm{CH}_3\right)_3 \mathrm{C}-\mathrm{X}\)	IV	\(\left(\mathrm{CH}_3\right)_2 \mathrm{CH}-\mathrm{X}\)

Which of the following reactions cannot form new carbon-carbon bonds?

1. Reimer-Tiemann reaction

2. Cannizaro reaction

3. Wurtz reaction

4. Friedel-Crafts acylation

Which of the options is correct about product (A)?

1. Product is aromatic  

2. Product has a high dipole moment

3. Product has less resonance energy          

4. Both A and B

A few reactions are given below:

i.	\(\small{\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{Br}+\mathrm{KOH} \rightarrow \mathrm{CH}_3 \mathrm{CH}=\mathrm{CH}_2+\mathrm{KBr}+\mathrm{H}_2 \mathrm{O}}\)
ii.
iii.

Consider the reaction,

This reaction will be the fastest in:

1. Ethanol

2. Methanol

3. N, N'-dimethylformamide (DMF)

4. Water

Compound among the following that can be used as
the halide component in the Friedel-Crafts reaction :

1. Chlorobenzene

2. Bromobenzene

3. Chloroethene

4. Isopropyl chloride

Products (A) and (B) in the given below reactions, respectively, are:
 

	(A)	(B)
1.
2.
3.
4.	None of the above

How is m-Bromotoluene prepared?