The dihedral angle of the least stable conformer of ethane is:
1. | 60° | 2. | 0° |
3. | 120° | 4. | 180° |
The major product of the following chemical reaction is:
1. | |
2. | |
3. | |
4. |
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
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 |
The numbers of structural isomers of (with one double bond) and (with one triple bond) are:
1.
2.
3.
4.
The IUPAC names of the following compounds are?
(a) CH3CH=C(CH3)2
(b) CH2=CH-C≡C-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
Lewis acid(s) that can be used during the ethylation of benzene is/are:
1.
2.
3.
4. All of the above
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
Benzene is extraordinarily stable, though it contains three double bonds, because of -
1. Delocalized protons
2. Delocalized neutrons
3. Resonance
4. None of these
Propanal and pentane-3-one are the products of ozonolysis of an alkene. The structural formula of the alkene is :
1. | 2. | , | |
3. | 4. |