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 :

1. Increases its boiling point

2. Decreases its boiling point

3. Doesn’t change its boiling point

4. None of the above

The product obtained on the addition of HBr to propene in the absence and presence of benzoyl peroxide are 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

Non aromatic molecule(s)among the following is/are :

1.		2.
3.		4.	All of the above