An electrophile among the following is -

1. \(\mathrm{OH}^-\) 2. \(\mathrm{NC}^-\)
3. \(R_3C^-\) 4. Carbonyl group

Subtopic:  Nucleophile & Electrophile |
 71%
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Geometrical isomerism can be shown by:

1.
2.
3.
4.
Subtopic:  Stereo Isomers |
 88%
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Free radical formation will take place in :

1.
2.
3.
4.
Subtopic:  Reaction Intermediates ; Preparation & Properties |
 86%
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The effect that can explain the given order of acidity of the carboxylic acids is-

Cl3CCOOH > Cl2CHCOOH > ClCH2COOH

1. +I effect

2. -I effect

3. +E effect

4. -E effect

Subtopic:  Electron Displacement Effects |
 90%
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The purification method based on the difference in solubilities of the compound and the impurities in a solvent is -
1. Crystallisation
2. Distillation
3. Chromatography
4. Isolation

Subtopic:  Purification of Organic Compounds |
 68%
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 Functional isomer is not possible for -

1. Alcohols 2. Aldehydes
3. Alkyl halides 4. Cyanides
Subtopic:  Structural Isomers |
 78%
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The fragrance of flowers is due to the presence of some steam volatile organic compounds called essential oils. These are generally insoluble in water at room temperature but are miscible with water vapor in the vapor phase. A suitable method for the extraction of these oils from the flowers is

1.  Distillation

2.  Crystallisation

3.  Distillation under pressure

4.  Steam distillation

Subtopic:  Quantitative Analysis of Organic Compounds |
 65%
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During the hearing of a court case, the judge suspected that some changes in the documents had been carried out. He asked the forensic department to check the ink used at two different places. The technique that can give the best results is-

1. Column chromatography 2. Solvent extraction
3. Distillation 4. Thin layer chromatography
Subtopic:  Purification of Organic Compounds |
 66%
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The principle involved in paper chromatography is

1. Adsorption

2. Partition

3. Solubility 

4. Volatility

Subtopic:  Purification of Organic Compounds |
 58%
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The correct order of decreasing stability of the following carbocations is:

I \( \begin{aligned} &~~~~~~~~~~~~\oplus\\ & CH_3 - CH-CH_3 \end{aligned}\)
II \( \begin{aligned} &~~~~~~~~~~~~\oplus\\ & CH_3 - CH-OCH_3\end{aligned}\)
III \( \begin{aligned} & ~~~~~~~~~~~~\oplus\\ &CH_3 - CH-CH_2- OCH_3\end{aligned}\)
1. II>I>III 2. I>II>III
3. II<I<III 4. I<II<III
Subtopic:  Electron Displacement Effects |
 57%
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