Which of the following statements is not correct for a nucleophile?
1. Nucleophile is a Lewis acid.
2. Ammonia is a nucleophile.
3. Nucleophiles attack low electron density sites.
4. Nucleophiles are not electron-seeking.
Two possible stereo-structures of CH3CHOH.COOH, that are optically active, called:
1. | Diastereomers | 2. | Atropisomers |
3. | Enantiomers | 4. | Mesomers |
In which of the following compounds, the C—Cl bond ionization shall give the most stable carbonium ion?
1. | 2. | ||
3. | 4. |
1. | 4 | 2. | 8 |
3. | 12 | 4. | 16 |
Which structure corresponds to the IUPAC name 3-Ethyl-2-hydroxy-4-methylhex-3-en-5-ynoic acid?
1. | 2. | ||
3. | 4. |
The correct order of increasing bond length of C-H, C-O, C-C and C=C is:
1.
2.
3.
4.
The most reactive compound towards electrophilic reagent among the following is:
1. | 2. | ||
3. | 4. |
The most stable conformation of n-butane among the following is:
1. | 2. | ||
3. | 4. |
Which of the following compounds will exhibit cis-trans (geometrical) isomerism?
1. 2-butene
2. Butanol
3. 2-butyne
4. 2-butenol
The following compounds are given for reference
(1) CH3-CH2–
(2) H2C=CH–
(3) HC≡C–
The increasing order of basic strength is:
1. (2)>(1)>(3)
2. (3) >(2) >(1)
3. (1) >(3) >(2)
4. (1) >(2)>(3)