The IUPAC name of the given structure is: 
  

1. (N-Bromo)-2-keto-3-methylbutanamide

2. (Bromo) -2-keto-4-methylbutanamide

3. (N-Bromo)-1, 2-diketo-3-methylbutanamine carboxamide

4. (N-Bromo)-1-keto-2-methylpropane

Subtopic:  Nomenclature |
 55%
Level 3: 35%-60%
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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 |
 82%
Level 1: 80%+
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The reagent that is used to remove SO42- and Clis -

1. NaOH             

2. Pb(NO3)2

3. BaSO4             

4. KOH

Subtopic:  Properties of Glass, Pb & Sn compounds |
 58%
Level 3: 35%-60%
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The 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 |
Level 3: 35%-60%
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Find the method used for the preparation of soda extract.

1. Fusing sodium carbonate with the organic compound mixture, followed by extraction with water

2. Dissolving NaHCO₃ and the organic compound mixture in dilute HCl

3. Boiling Na₂CO₃ and the organic compound mixture with dilute HCl

4. Boiling Na2COand a mixture of hydrocarbons in distilled water

Subtopic:  Qualitative Analysis of Organic Compounds |
Level 3: 35%-60%
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The most stable carbocation among the following is:

1. 2.
3. 4.
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 78%
Level 2: 60%+
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Find the correct statement regarding the electromeric effect in organic compounds.

1. It is a temporary effect.
2. It is a permanent effect.
3. It is both temporary and permanent.
4. None of the above.

Subtopic:  Electron Displacement Effects |
 80%
Level 1: 80%+
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H2C = O behaves as:

1. Nucleophile

2. Electrophile

3. Both (1) and (2)

4. None of the above 

Subtopic:  Nucleophile & Electrophile |
Level 3: 35%-60%
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Which of the following is strongest nucleophile?

1. Br-

2. O..H

3. C..N

4. C2H5O..

Subtopic:  Nucleophile & Electrophile |
Level 3: 35%-60%
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The stability of 2,3-dimethyl but-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 |
 80%
Level 1: 80%+
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