The correct order of basicities of the following compounds is:

(1)

(2) CH3-CH2-NH2

(3) (CH3)2NH

(4) CH3-C||O-NH2

1. 2>1>3>4         

2. 1>3>2>4

3. 3>1>2>4         

4. 1>2>3>4

Subtopic:  Acidic & Basic Character |
 57%
Level 3: 35%-60%
Hints

The most reactive of these compounds towards sulphonation is

1. Toluene                2. Chlorobenzene

3. Nitrobenzene        4. m-Xylene

Subtopic:  Nucleophile & Electrophile |
Level 3: 35%-60%
Hints

How many geometrical isomers are possible of the following?

 CH3-CH=CH-CH=CH-CH3

1. 2             2. 3

3. 4             4. 6

Subtopic:  Stereo Isomers |
Level 3: 35%-60%
Hints

advertisementadvertisement

The configuration of given tartaric acid is

 

1. 2R, 3R         2. 2R, 3S

3. 2S, 3S         4. 2S, 3R

Subtopic:  Stereo Isomers |
 64%
Level 2: 60%+
Hints

Correct IUPAC name of the compound 

1. 4-(Ethyl methanolyonxy)phenylpropanoate

2. Ethyl 4-propanoyloxybenzenecarboxylate

3. 4-(1-Oxo-2-oxabutyl)phenylpropanoate

4. 1-(1-Oxo-2-oxbutyl)-4-(1-oxopropoxy)benzene

Subtopic:  Nomenclature |
Level 3: 35%-60%
Hints

The IUPAC name of the following compound is

1. 2-(Ethoxycarbonyl)benzoylchloride

2. Ethyl 2-(chlorocarbonyl)benzoate

3. Ethyl 2-(chloromethanoyl)benzoate

4. Methyl 2-(Chlorocarbonyl)benzene carboxylate.

Subtopic:  Nomenclature |
Level 3: 35%-60%
Hints

advertisementadvertisement

 and are

1. Position isomers

2. Chain isomers

3. Functional isomers

4. Metamers

Subtopic:  Structural Isomers |
 65%
Level 2: 60%+
Hints

Which of the following statements about the inductive effect is correct?

1.  The inductive effect transfers electrons from one carbon atom to another.
2.   The inductive effect operates in both \(\sigma\)- and \(\pi\)-bonds.
3.     The inductive effect does not create any charge in the molecule.
4.      The inductive effect creates partial charges and is distance-dependent.

Subtopic:  Electron Displacement Effects |
 86%
Level 1: 80%+
Hints

The IUPAC name of the following compounds is:
 

1. 1-Bromocyclohexane carboxylic acid

2. 3-Bromocyclohexanoic acid

3. 3-Bromoheptanoic acid

4. 3-Bromocyclohexanecarboxylic acid

Subtopic:  Nomenclature |
 52%
Level 3: 35%-60%
Hints

advertisementadvertisement

The correct increasing order of carbon-carbon bond length in the given compounds is: 

1. III<II<I<IV

2. IV<I<II<III

3. I<II<III<IV

4. I<IV<III<II

Subtopic:  Hybridisation & Structure of Carbon Compounds |
 83%
Level 1: 80%+
Hints