Chemistry-
General
Easy
Question
The reactivity of acid derivatives in general follows the order :
The above order of reactivity can be explained in terms of the : (i) Basicity of leaving group (ii) Resonance effect (iii) Inductive effect Weaker is the basic character of leaving group, more is the reactivity of acid derivative. In general, all the acid derivatives show resonance as follows:
More is the stabilization, lesser is the reactivity and vice-versa.
Which of the most reactive acid derivative?
- RCOOR
The correct answer is:
Related Questions to study
chemistry-
The reactivity of acid derivatives in general follows the order :
The above order of reactivity can be explained in terms of the : (i) Basicity of leaving group (ii) Resonance effect (iii) Inductive effect Weaker is the basic character of leaving group, more is the reactivity of acid derivative. In general, all the acid derivatives show resonance as follows:
More is the stabilization, lesser is the reactivity and vice-versa.
Which among the following anions is the most basic ?
The reactivity of acid derivatives in general follows the order :
The above order of reactivity can be explained in terms of the : (i) Basicity of leaving group (ii) Resonance effect (iii) Inductive effect Weaker is the basic character of leaving group, more is the reactivity of acid derivative. In general, all the acid derivatives show resonance as follows:
More is the stabilization, lesser is the reactivity and vice-versa.
Which among the following anions is the most basic ?
chemistry-General
chemistry-
Observe the esterification mechanisms for primary and tertiary alcohols.
Type.1
Mechanism
Type. 2
Mechanism
Observe the esterification mechanisms for primary and tertiary alcohols.
Type.1
Mechanism
Type. 2
Mechanism
chemistry-General
chemistry-
Observe the esterification mechanisms for primary and tertiary alcohols.
Type.1
Mechanism
Type. 2
Mechanism
In the above reaction (P) and (Q) are respectively :
Observe the esterification mechanisms for primary and tertiary alcohols.
Type.1
Mechanism
Type. 2
Mechanism
In the above reaction (P) and (Q) are respectively :
chemistry-General
chemistry-
Observe the following sequence of reaction and answer the questions based on it
Which of the following compound give benzoic acid on KMnO4 oxidation
Observe the following sequence of reaction and answer the questions based on it
Which of the following compound give benzoic acid on KMnO4 oxidation
chemistry-General
chemistry-
Observe the following sequence of reaction and answer the questions based on it
Which of the following statement is not correct
Observe the following sequence of reaction and answer the questions based on it
Which of the following statement is not correct
chemistry-General
chemistry-
Observe the following sequence of reaction and answer the questions based on it
Compound z is :
Observe the following sequence of reaction and answer the questions based on it
Compound z is :
chemistry-General
chemistry-
In the Hofmann rearrangement an unsubstituted amide is treated with sodium hydroxide and bromine to give a primary amine that has one carbon lesser than starting amide.
General reaction :
Mechanism :
If the migrating group is chiral then its configuration is retained. Electron releasing effects in the migrating group increases reactivity of Hofmann rearrangement.
In the Hofmann rearrangement an unsubstituted amide is treated with sodium hydroxide and bromine to give a primary amine that has one carbon lesser than starting amide.
General reaction :
Mechanism :
If the migrating group is chiral then its configuration is retained. Electron releasing effects in the migrating group increases reactivity of Hofmann rearrangement.
chemistry-General
chemistry-
In the Hofmann rearrangement an unsubstituted amide is treated with sodium hydroxide and bromine to give a primary amine that has one carbon lesser than starting amide.
General reaction :
Mechanism :
If the migrating group is chiral then its configuration is retained. Electron releasing effects in the migrating group increases reactivity of Hofmann rearrangement.
Arrange the following amides according to their relative reactivity when reacted with Br2 in excess of strong base
I) 
II) 
III) 
IV) 
In the Hofmann rearrangement an unsubstituted amide is treated with sodium hydroxide and bromine to give a primary amine that has one carbon lesser than starting amide.
General reaction :
Mechanism :
If the migrating group is chiral then its configuration is retained. Electron releasing effects in the migrating group increases reactivity of Hofmann rearrangement.
Arrange the following amides according to their relative reactivity when reacted with Br2 in excess of strong base
I)
II)
III)
IV)
chemistry-General
physics-
The tube shown is of uniform cross–section. Liquid flows through it at a constant speed in the direction shown by the arrows. The liquid exerts on the tube
The tube shown is of uniform cross–section. Liquid flows through it at a constant speed in the direction shown by the arrows. The liquid exerts on the tube
physics-General
physics-
A bent arc shaped sealed glass tube filled with water is accelerated horizontally with acceleration a. A small air bubble inside it is found to be stuck at 1 cm from vertical axis. Neglect surface tension. What is the acceleration of the tube.
A bent arc shaped sealed glass tube filled with water is accelerated horizontally with acceleration a. A small air bubble inside it is found to be stuck at 1 cm from vertical axis. Neglect surface tension. What is the acceleration of the tube.
physics-General
physics-
