Ph-CH=CH-COOH 

The IUPAC name is:

1. 3-Phenyl prop-2-enoic acid

2. 3-Phenol prop-1-enoic acid

3. 3-Carboxy-prop-1-ene benzene

4. But-2-enoic acid

Subtopic:  Nomenclature |
 84%
Level 1: 80%+
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The IUPAC name iS'

1. Chloromethylbenzene 

2. Chlorophenylmethane

3. (1) and (2) both

4. None of the above

Subtopic:  Nomenclature |
 61%
Level 2: 60%+
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The IUPAC name of the following compound is:

(1) 4-Bromo-3-cyanophenol

(2) 2-Bromo-5-hydroxybenzonitrile

(3) 2-cyano-4-hydroxybromobenzene

(4) 6-Bromo-3-hydroxybenzonitrile

Subtopic:  Nomenclature |
 57%
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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The compound which forms one monochloro product when treated with chlorine is:

(1) n-pentane

(2) isopentane

(3) neo-pentane

(4) None of these

Subtopic:  Structural Isomers |
 74%
Level 2: 60%+
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Among the following anions (a) CH3, (b) NH2, (c) OH-, (d) F-, the order of basicity is:

1. a > b > c > d

2. b > a > c > d

3. c > b > a > d

4. c > a > b > d

Subtopic:  Nucleophile & Electrophile |
 56%
Level 3: 35%-60%
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The electromeric effect in organic compounds is a :

1. Temporary effect

2. Permanent effect

3. Electromeric effect is only observed in inorganic molecules

4. None of the above

Subtopic:  Electron Displacement Effects |
 80%
Level 1: 80%+
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The arrangement in decreasing order of stability of CH3C2H5,(CH3)2CH and (CH3)3 C free radicals is-

1. CH3C2H5 > (CH3)2CH > (CH3)3 C  

2. (CH3)3 C > (CH3)2CH > C2H5CH3

3. C2H5CH3 > (CH3)2CH > (CH3)3 C

4. (CH3)3 C > (CH3)2CH >  CH3  > C2H5 

Subtopic:  Reaction Intermediates ; Preparation & Properties |
 86%
Level 1: 80%+
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