Incorrect statement regarding aromaticity among the following is:
1. | The compound should have a planar structure. |
2. | The π–electrons of the compound are completely delocalized in the ring. |
3. | The total number of π–electrons present in the ring should be equal to (4n + 2) π electrons, where n = 0, 1, 2 … etc. This is known as Huckel’s rule. |
4. | The compound should have a linear structure. |
Non aromatic molecule(s)among the following is/are :
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4. | All of the above |
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:
1. | It undergoes electrophilic substitution reactions very easily. |
2. | Nucleophiles are attracted by a benzene ring. |
3. | Benzene is a planar molecule. |
4. | It has 12 sigma bonds. |
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:
1. | a, b | 2. | b, c |
3. | a, c | 4. | a, b, c |
The correct order of decreasing reactivity of the following compounds:
Chlorobenzene, 2,4-Dinitrochlorobenzene, and p-Nitrochlorobenzene
with an electrophile (E+) is :
1. | Chlorobenzene > p–Nitrochlorobenzene > 2,4-Dinitrochlorobenzene |
2. | p – Nitro chlorobenzene > 2, 4-Dinitrochlorobenzene > Chlorobenzene |
3. | Chlorobenzene > 2, 4-Dinitrochlorobenzene > p-Nitrochlorobenzene |
4. | 2, 4-Dinitrochlorobenzene > Chlorobenzene > p-Nitrochlorobenzene |