The correct order of –I effect is:
| 1. | -NR3+ > -OR > -F |
| 2. | -F > -NR3+ > -OR |
| 3. | -NR3+ > -F > -OR |
| 4. | -OR > -NR3+ > -F |
The correct order of stability is:
| 1. | 1–butene > Trans–2–butene > Cis–2–butene |
| 2. | Trans–2–butene > 1–butene > Cis–2–butene |
| 3. | Trans–2–butene > Cis–2-butene > 1–butene |
| 4. | Cis-2–butene > Trans–2–butene > 1–butene |
IUPAC name of is:
1. 2-Chloro-3-iodo-2-pentene
2. 2-Chloro-3-iodo-3-pentene
3. 2-Iodo-3-chloro-pentene
4. None of the above
2-Butene shows geometrical isomerism due to:
1. Restricted rotation about double bond
2. Free rotation about double bond
3. Free rotation about single bond
4. Chiral carbon
Find the dihedral angle in the staggered form of ethane.
1.
2.
3.
4.
Which of the following is most reactive towards electrophilic substitution reaction?
| 1. | 2. | ||
| 3. | 4. |
The best method for the separation of naphthalene and benzoic acid from their mixture is:
1. Sublimation
2. Chromatography
3. Crystallisation
4. Distillation
Which amongst the following is the most stable carbocation:
| 1. | 2. | ||
| 3. | 4. |
The chiral centre is absent in:
1. DCH2-CH2-CH2-Cl
2. CH3-CHD-CH2-Cl
3. CH3-CHCl-CH2D
4. CH3-CHOH-CH2-CH3
Which one of the following compounds is most acidic:
| 1. | 2. | ||
| 3. | 4. | \(\mathrm{Cl}-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{OH} \) |