An alkene ‘A’ contains 3 C – Cσ bonds, 8 C – H σ bonds, and 1 C – C π bond,

 ‘A’ on ozonolysis gives two moles of an aldehyde of molar mass 44 u. The IUPAC name of ‘A’ is:

1. Prop-2-yne 2. But-2-ene
3. But-2-yne 4. Prop-2-ene

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 80%
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Propanal and pentane-3-one are the products of ozonolysis of an alkene. The structural formula of the alkene is  :

1. 2.  , 
3. 4.

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 83%
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Benzene is extraordinarily stable, though it contains three double bonds, because of :

1. Delocalized protons

2. Delocalized neutrons

3. Resonance

4. None of the above.

Subtopic:  Aromatic Hydrocarbons - Nomenclature, Isomerism & Huckel's Rule |
 92%
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Out of benzene, m-dinitrobenzene, and toluene, the one that will undergo nitration most easily is :

1. Benzene 2. m–Dinitrobenzene
3. Toluene 4. None of the above
Subtopic:  Aromatic Hydrocarbons - Reactions & Mechanism |
 71%
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Lewis acid(s) that can be used during the ethylation of benzene is/are:

1. FeCl3

2. SnCl4 

3. BF3

4. All of the above
Subtopic:  Aromatic Hydrocarbons - Reactions & Mechanism |
 64%
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The numbers of structural isomers of C4H8 (with one double bond) and C5H8 (with one triple bond) are:

1. C4H8 = 3 ; C5H8 = 3

2. C4H8 = 4 ; C5H8 = 4

3. C4H8 = 3 ; C5H8 = 4

4. C4H8 = 4 ; C5H8 = 3

Subtopic:  Aromatic Hydrocarbons - Nomenclature, Isomerism & Huckel's Rule |
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The balanced chemical equation for the combustion reaction of Butane is :

1. \(\mathrm{2 {C}_4 {H}_{10({g})}+13 {O}_{2({g})} \rightarrow 8 {CO}_{2({g})}+10 {H}_2 {O}}+\) Heat Butane
2. \(\mathrm{2 {C}_4 {H}_{10({g})}+13 {O}_{2({g})} \rightarrow 9 {CO}_{2({g})}+10 {H}_2 {O}+}\) Heat Butane
3. \(\mathrm{2 {C}_4 {H}_{10({g})}+14 {O}_{2({g})} \rightarrow 8 {CO}_{({g})}+10 {H}_2 {O}}+\) Heat Butane
4. \( \mathrm{{C}_4 {H}_{10({g})}+13 {O}_{2({g})} \rightarrow 8 {CO}_{({g})}+10 {H}_2 {O}}+\) Heat Butane
Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 83%
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 An alkene ‘A’ on ozonolysis gives a mixture of ethanal and pentan-3-one.
The IUPAC name of ‘A’ is :

1. 3-Ethylpent-2-ene

2. 3-Ethylpent-2- yne

3. 2-Ethylpent-3-ene

4. 3-Ethylpent-4-yne

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 81%
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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

Subtopic:  Aromatic Hydrocarbons - Reactions & Mechanism |
 71%
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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 

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 69%
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