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why is it necessary to control pH during the reaction of aldehydes and ketoes with ammonia?
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why is it necessary to control pH during the reaction of aldehydes and...
He addition of ammonia derivative (NH2−G) to aldehydes and ketones is done in weakly acidic medium (pH about 3.5). In case the medium is strongly acidic (pH close to 1), then the ammonia derivative will be also protonated and will not be able to act as a nucleophile.
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why is it necessary to control pH during the reaction of aldehydes and...
Introduction:
When aldehydes and ketones react with ammonia, various products can be formed depending on the reaction conditions. Controlling the pH of the reaction is necessary to ensure the desired product is obtained.

Importance of pH control:
1. Prevention of undesired side reactions: The control of pH is crucial to prevent unwanted side reactions that may occur at different pH levels. For example, at high pH, the formation of imines or enolates can take place rather than the intended reaction with ammonia. By maintaining the appropriate pH, the desired reaction can be favored.

2. Stability of reactants: Aldehydes and ketones can undergo various chemical transformations under different pH conditions. For instance, aldehydes can be oxidized to carboxylic acids in basic conditions, while ketones can undergo keto-enol tautomerism. By controlling the pH, the stability of the reactants can be maintained.

3. Optimal reaction rate: The reaction rate of aldehydes and ketones with ammonia can be influenced by pH. The optimal pH range favors the reaction kinetics, ensuring a reasonable rate of reaction without excessive side reactions or slow reaction rates.

Effect of pH on reaction outcome:
1. Acidic conditions: In acidic conditions, aldehydes and ketones are generally stable, and the reaction with ammonia is slow. However, under strongly acidic conditions, the formation of imine derivatives can occur.

2. Neutral conditions: At neutral pH, the reaction between aldehydes/ketones and ammonia predominantly leads to the formation of imine derivatives. These imines can further react with additional ammonia or undergo hydrolysis to form amines.

3. Basic conditions: In basic conditions, aldehydes are prone to oxidation, leading to the formation of carboxylic acids. Ketones can undergo keto-enol tautomerism. However, if the pH is carefully controlled, the reaction with ammonia can proceed to form imine derivatives.

Conclusion:
Controlling the pH during the reaction of aldehydes and ketones with ammonia is crucial to achieve the desired product and prevent unwanted side reactions. pH control ensures the stability of reactants, optimal reaction rates, and the formation of the intended imine derivatives. By maintaining the appropriate pH, the reaction conditions can be optimized for the desired outcome.
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Read the passage given below and answer the following questions:Reductive alkylation is the term applied to the process of introducing alkyl groups into ammonia or a primary or secondary amine by means of an aldehyde or ketone in the presence of a reducing agent. The present discussion is limited to those reductive alkylations in which the reducing agent is hydrogen and a catalyst or "nascent" hydrogen, usually from a metalacid combination; most of these reductive alkylations have been carried out with hydrogen and a catalyst. The principal variation excluded is that in which the reducing agent is formic acid or one of its derivatives; this modification is known as the Leuckart reaction. The process of reductive alkylation of ammonia consists in the addition of ammonia to a carbonyl compound and reduction of the addition compound or its dehydration product. The reaction usually is carried out in ethanol solution when the reduction is to be effected catalytically:Since the primary amine is formed in the presence of the aldehyde it may react in the same way as ammonia, yielding an additional compound, a Schiff's base (RCH= NCH2R) and finally, a secondary amine. Similarly, the primary amine may react with the imine, forming an addition product which also is reduced to a secondary amine Finally, the secondary amine may react with either the aldehyde or the imine to give products which are reduced to tertiary amines.Similar reactions may occur when the carbonyl compound employed is a ketone.Q. The reaction of ammonia and its derivatives with aldehydes is called

why is it necessary to control pH during the reaction of aldehydes and ketoes with ammonia?
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why is it necessary to control pH during the reaction of aldehydes and ketoes with ammonia? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared according to the Class 12 exam syllabus. Information about why is it necessary to control pH during the reaction of aldehydes and ketoes with ammonia? covers all topics & solutions for Class 12 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for why is it necessary to control pH during the reaction of aldehydes and ketoes with ammonia?.
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