The catalyst used in the conversion of benzene into acetophenone is:

1. Anhydrous AlCl₃

2. HNO₃

3. HCl

4. Heating

The effect of branching on an alkane is:
1. It increases its boiling point
2. It decreases its boiling point
3. It doesn’t change its boiling point
4. None of the above

What are the products obtained when \(\text{HBr}\) is added to propene in the absence and presence of benzoyl peroxide, respectively?

1. 1-Bromopropane, 2-Bromopropane

2. 2-Bromopropane, 1-Bromopropane

3. 1-Bromopropanol, 2-Bromopropanone

4. 2-Bromopropanone, 1-Bromopropanol

Decreasing order of acidic behavior of benzene, n-hexane, and ethyne is:

1. Hexane > Ethyne > Benzene

2. Benzene > Hexane > Ethyne

3. Ethyne > Benzene > Hexane

4. Benzene > Ethyne > Hexene

Incorrect statement towards reactivity of benzene is:

$\mathrm{Ethyne} \stackrel{?}{\to }$ $\mathrm{Benzene}$ 

The reagent used in the above conversion is:

1. Cr₂O₃

2. Alc. KOH

3. Red hot Fe

4. NaNH₂/liq.NH₃

Out of the above alkenes, the ones that can give 2-methyl butane on hydrogenation are:

The correct order of decreasing reactivity of the following compounds:

Chlorobenzene, 2,4-Dinitrochlorobenzene, and p-Nitrochlorobenzene

with an electrophile (E⁺)  is :

The products of ozonolysis of 1,2-dimethyl benzene (o-xylene) are:

1. Methylglyoxal, 1, 2-dimethylglyoxal, and glyoxal

2. Methylglyoxal, 1, 3-dimethylglyoxal, and glyoxal

3. Methylglyoxal, 1, 4-dimethylglyoxal, and glyoxal

4. Methylglyoxal, 1, 5-dimethylglyoxal, and glyoxal

Match the hydrocarbons in Column I with the boiling points given in Column II.

Codes