The dihedral angle of the least stable conformer of ethane is:

1. 60° 2.
3. 120° 4. 180°

Subtopic:  Aliphatic Hydrocarbon -Nomenclature, Isomerism & Mechanism |
 67%
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The major product of the following chemical reaction is:

1.
2.
3.
4.
Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 69%
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Reactant A in the following reaction is-

A  + NaOH \(\xrightarrow[\Delta ]{CaO}\) CH3CH2CH3 + Na2CO3

1. Sodium ethanoate

2. Sodium propanoate

3. Sodium butanoate

4. Sodium methanoate

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 74%
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The balanced chemical equation for the combustion reaction of Butane is :

1. \(2 \mathrm{C}_4 \mathrm{H}_{10(\mathrm{~g})}+13 \mathrm{O}_{2(\mathrm{~g})} \rightarrow 8 \mathrm{CO}_{2(\mathrm{~g})}+10 \mathrm{H}_2 \mathrm{O}+\text { Heat }\)
Butane
2. \(2 \mathrm{C}_4 \mathrm{H}_{10(\mathrm{~g})}+13 \mathrm{O}_{2(\mathrm{~g})} \rightarrow 9 \mathrm{CO}_{2(\mathrm{~g})}+10 \mathrm{H}_2 \mathrm{O}+\text { Heat }\)
Butane
3. \(2 \mathrm{C}_4 \mathrm{H}_{10(\mathrm{g})}+14 \mathrm{O}_{2(\mathrm{g})} \rightarrow 8 \mathrm{CO}_{(\mathrm{g})}+10 \mathrm{H}_2 \mathrm{O}+\text { Heat }\)
Butane
4. \( \mathrm{C}_4 \mathrm{H}_{10(\mathrm{~g})}+13 \mathrm{O}_{2(\mathrm{g})} \rightarrow 8 \mathrm{CO}_{(\mathrm{g})}+10 \mathrm{H}_2 \mathrm{O}+\text { Heat }\)
Butane

 

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 83%
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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 IUPAC names of the following compounds are?

(a) CH3CH=C(CH3)2

(b) CH2=CH-CC-CH3

 

(c)

(d)

(e)

 

(g) CH3 – CH = CH – CH2 – CH = CH – CH – CH2 – CH = CH2

                                                                  |

                                                             C2H5

 

1.  2-Methylbut-2-ene, Pen-1-ene-3-yne, 1, 3-Butadiene, 4-Phenyl but-1-ene , 2-Methyl phenol, 5-(2-Methylpropyl)-decane and 4-Ethyldeca-1, 5, 8-triene

2. 4-Phenyl but-1-ene, Pen-1-ene-3-yne, 1, 3-Butadiene, 2-Methylbut-2-ene, Pen-1-ene-3-yne, 2-Methyl phenol, 5-(2-Methylpropyl)-decane and 4-Ethyldeca-1, 5, 8-triene

3. 2-Methylbut-2-ene, 4-Phenyl but-1-ene, 1, 3-Butadiene, Pen-1-ene-3-yne, 2-Methyl phenol, 5-(2-Methylpropyl)-decane and 4-Ethyldeca-1, 5, 8-triene

4. 4-Ethyldeca-1, 5, 8-triene, Pen-1-ene-3-yne, 1, 3-Butadiene, 4-Phenyl but-1-ene, 2-Methyl phenol, 5-(2-Methylpropyl)-decane and 2-Methylbut-2-ene

Subtopic:  Aromatic Hydrocarbons - Nomenclature, Isomerism & Huckel's Rule |
 80%
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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 |
 65%
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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 these

Subtopic:  Aromatic Hydrocarbons - Reactions & Mechanism |
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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 these

Subtopic:  Aromatic Hydrocarbons - Nomenclature, Isomerism & Huckel's Rule |
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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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