- 1(current)
Q. No.The order of reactivity of alkyl halides (RCl, RBr, RI) with aliphatic amines is:
1. \(RCl > RI > RBr \)
2. \( RBr > RCl > RI \)
3. \(RI > RBr > RCl \)
4. \(RI > RCl > RBr \)
1. \(RCl > RI > RBr \)
2. \( RBr > RCl > RI \)
3. \(RI > RBr > RCl \)
4. \(RI > RCl > RBr \)
Subtopic: Â Mechanism |
 87%
Level 1: 80%+
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Hints
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The reagent required to convert acetamide into methyl amine is :
1. NaOH/ Br2
2. Sodalime
3. Hot conc. H2SO4
4. PCl5
Subtopic: Â Amines - Preparation & Properties |Â Mechanism |
 87%
Level 1: 80%+
AIPMT - 2010
Hints
Consider the given reaction and products:
The correct statement about the given chemical reaction is :
1. -NH2 group is ortho and para directive, so product (B) is not possible.
2. Reaction is possible and compound (B) will be the major product.
3. The reaction will form sulphonated product instead of nitration.
4. Reaction is possible and compound (A) will be major product.
Subtopic: Â Mechanism |
 84%
Level 1: 80%+
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Aniline + Benzoyl chloride \(\xrightarrow[]{Base}\) Product
The product produced in the reaction mentioned above is:
1. N-Phenylbenzamide
2. Chlorobenzene
3. N-Chlorobenzamide
4. None of the above
Subtopic: Â Mechanism |
 81%
Level 1: 80%+
Hints
Consider the following reaction:
A significant amount of meta-isomer forms because:
1. \(-NH_2 \) group is ortho- , para- , and meta-director.
2. Anilinium ions are formed during the reaction.
3. There is a less steric hindrance at meta-position.
4. Low temperature increases the amount of meta-isomer.
A significant amount of meta-isomer forms because:
1. \(-NH_2 \) group is ortho- , para- , and meta-director.
2. Anilinium ions are formed during the reaction.
3. There is a less steric hindrance at meta-position.
4. Low temperature increases the amount of meta-isomer.
Subtopic: Â Mechanism |
 80%
Level 1: 80%+
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Hints
Please attempt this question first.
- 1(current)
Q. No.
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