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Column I | Column II | |
(a) CH2Cl2 | (i) | neo-Pentyl chloride |
(b) (CH3)3CCH2Cl | (ii) | Ethylidene chloride |
(c) CH3CHCl2 | (iii) | Ethylene dichloride |
(d) |
(iv) | Methylene chloride |
1. | (IV) > (III) > (II) > (I) |
2. | (I) > (II) > (III) > (IV) |
3. | (I) > (III) > (II) > (IV) |
4. | (IV) > (II) > (III) > (I) |
List I Reaction |
List II Type of reaction |
A. |
I. Nucleophilic substitution |
B. |
II. Saytzeff elimination |
C. |
III. Electrophilic addition |
D. |
IV. Electrophilic substitution |
(A) | (B) | (C) | (D) | |
!. | (II) | (IV) | (III) | (I) |
2. | (IV) | (II) | (III) | (I) |
3. | (IV) | (II) | (I) | (III) |
4. | (II) | (IV) | (I) | (III) |
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The product formed in the following reaction sequence is:
1. | |
2. | \(CH_3-CH=CH-CH_3 \) |
3. | \(CH_3 -CH_2 -CH = CH_2 \) |
4. | \(CH_3 -CH_2 -CH_2 -CH_2 -OH \) |
The correct reaction among the following is:
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1. | A racemic mixture shows zero optical rotation |
2. | SN1 reaction yields a 1:1 mixture of both enantiomers |
3. | The product obtained by SN2 reaction of haloalkane having chirality at the reactive site shows the inversion of configuration |
4. | Enantiomers are superimposable mirror images on each other |