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

Subtopic:  Electron Displacement Effects |
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Among the following the most stable carbocation is:

1. 2.
3. 4.
Subtopic:  Electron Displacement Effects | Reaction Intermediates ; Preparation & Properties |
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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

Subtopic:  Qualitative Analysis of Organic Compounds |
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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

Subtopic:  Nomenclature |
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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

Subtopic:  Nomenclature |
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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
Subtopic:  Quantitative Analysis of Organic Compounds |
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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

Subtopic:  Qualitative Analysis of Organic Compounds |

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Sodium nitroprusside when added to an alkaline solution of sulphide ions produces a colouration which is:

1. Red

2. Blue

3. Brown

4. Purple

 

Subtopic:  Qualitative Analysis of Organic Compounds |
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Most stable radical is

1. 2.
3. 4.

Subtopic:  Electron Displacement Effects | Reaction Intermediates ; Preparation & Properties |
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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

Subtopic:  Acidic & Basic Character |
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