The stability of 2,3-dimethylbut-2-ene is more than 2-butene. This can be explained in terms of:
1. Resonance
2. Hyperconjugation
3. Electromeric effect
4. Inductive effect
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Among the following the most stable carbocation is:
1. | 2. | ||
3. | 4. |
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Silver sulphate solution is used to separate:
1. Nitrate and bromide
2. Nitrate and chlorate
3. Bromide and iodide
4. Nitrate and nitrite
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The IUPAC name of is:
1. 2,6-Dimethylhepta-2, 5-dienoic acid
2. 3,7-Dimethylhepta-2, 5-dienoic acid
3. 1-Hydroxy-2, 6-dimethylhepta-2, 5-dienone
4. None of the above
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The IUPAC name of the given compound is:
1. Ethyl 2-methylprop-2-enoate
2. Ethyl 2-methylprop-1-enoate
3. 1-Ethoxy 2-methylprop-2-enoate
4. 1-Ethoxy 2-methylprop-2-enal
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A compound that does not give a positive test in Lassaigne’s test for nitrogen is-
1. | Urea | 2. | Hydrazine |
3. | Azobenzene | 4. | Phenyl hydrazine |
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In Kjeldahl's method of estimation of nitrogen, K2SO4 acts as:
1. An oxidising agent
2. Catalytic agent
3. Hydrolysing agent
4. Boiling point elevator
Sodium nitroprusside when added to an alkaline solution of sulphide ions produces a colouration which is:
1. Red
2. Blue
3. Brown
4. Purple
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Most stable radical is
1. | 2. | ||
3. | 4. |
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Consider the acidity of the following carboxylic acids
(i) PhCOOH
(ii) o-NO2C6H4COOH
(iii) p-NO2C6H4COOH
(iv)m-NO2C6H4COOH
1. i>ii>iii>iv
2. ii>iv>iii>i
3. ii>iv>i>iii
4. ii>iii>iv>i
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